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. 2025 Sep 26;13(10):e71006. doi: 10.1002/fsn3.71006

Personalized Nutrition in the Era of Digital Health: A New Frontier for Managing Diabetes and Obesity

Muhammad Tayyab Arshad 1, M K M Ali 2, Sammra Maqsood 3, Ali Ikram 4, Faiyaz Ahmed 5, A I Aljameel 2, Ammar AL‐Farga 6, Md Sakhawot Hossain 7,8,
PMCID: PMC12474561  PMID: 41019177

ABSTRACT

The integration of digital health technologies with personalized nutrition offers a transformative approach for managing diabetes and obesity. This emerging paradigm extends beyond generic dietary recommendations by tailoring interventions based on genetic, epigenetic, microbiome, and real‐time metabolic data. Tools such as continuous glucose monitors (CGMs), artificial intelligence (AI)‐driven meal planning, and mobile health applications enable dynamic dietary adjustments and improved disease monitoring. Data privacy, cost disparities, and the need for robust clinical validation are challenges that remain to be overcome, even if there is a potential benefit. This review examines the synergy between digital health technologies and precision medicine by elucidating the potential of personalized nutrition in chronic disease management. Our literature review demonstrates that tailored diet programs can enhance metabolic well‐being and overcome theoretical and practical challenges to their widespread implementation.

Keywords: AI‐driven nutrition, metabolic health, nutrigenomics, obesity


Personalized nutrition is driven by scientific and technological advances such as nutrigenomics and microbiome analysis, as emphasized in this study. With regard to ethical concerns such as privacy protection and access, we balance the consequences of these developments for greater metabolic gains. This paper presents a complete picture of the promise and challenges of using personalized nutrition in disease prevention and treatment through the integration of recent evidence.

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1. Introduction

The increasing worldwide prevalence of obesity and diabetes has rendered them two of the most significant public health issues in the modern era. Obesity is defined as abnormal or excessive accumulation of fat that represents a health hazard. Urbanization, nutritional transition, and physical inactivity are leading to rapid increases in the rates of obesity across low‐ and middle‐income countries (LMICs). Jaacks et al. (2019) reported that there have been a number of phases to the global obesity transition. More than 650 million adults are overweight, and by 2030, nearly 20% of the world's population could be affected (Blüher 2019; Alfaris et al. 2023).

Obesity causes metabolic syndrome, cardiovascular disease, and type 2 diabetes (T2D), leading to substantial health care expenses and economic burdens (Reilly et al. 2018; Seidell and Halberstadt 2015). Similarly, by 2021, 537 million adults will have diabetes, and this number is expected to rise to 783 million by 2045, making it a leading cause of death and disability (Sun et al. 2022). Neuropathy, retinopathy, and cardiovascular disease are exacerbated when nearly half of all diabetes cases remain undiagnosed, as stated by the International Diabetes Federation (IDF) (Cho et al. 2018; Saeedi et al. 2019). These risk factors are tightly linked with T2D, accounting for 90% of cases (Ogurtsova et al. 2017; Roglic 2016). According to Xu et al. (2017) and Li et al. (2020), lower‐income individuals are disproportionately affected by the differential socioeconomic variation in diabetes prevalence.

Traditional dietary recommendations have always been wide‐ranging, assuming that individuals' metabolism is equal (Hoevenaars et al. 2020). Traditional dietary pyramids and standardized calorie intake support this perspective. However, these traditional approaches do not consider the considerable inter‐individual variation in dietary responses due to genetic, microbiome, and metabolic variabilities. For example, genotype‐guided diets use genetic variations, such as FTO and TCF7L2, with obesity and glucose metabolism to personalize carbohydrate intake and improve diabetes management (Singar et al. 2024). Likewise, microbiome‐based nutrition considers diversity in gut microbiota; those with higher Akkermansia muciniphila levels can be anticipated to benefit the most from high‐fiber intake owing to enhanced short‐chain fatty acid production and improved insulin sensitivity (Gopal et al. 2024). These are merely a few of the many ways in which personalized nutrition breaks away from the one‐size‐fits‐all approach and moves towards individualized dietary intervention based on biology. There is increasing evidence that these recommendations do not work for most individuals because of variations in the gut microbiota, metabolic health, and genetics (Drabsch and Holzapfel 2019). If we consider low‐carbohydrate or Mediterranean‐style diets as examples, individuals might do better on them than on low‐fat diets (Wang and Hu 2018). Individualized nutrition plans that take into consideration each individual's specific biology and lifestyle are required because general dietary advice has not been successful in curbing the epidemic of obesity and diabetes (Moore 2020).

As Forster et al. (2016) explained, personalized nutrition is revolutionary because it employs genetic, epigenetic, and metabolic profiling to individualize dietary interventions instead of offering advice based on groups. Owing to recent progress in nutrigenomics, we currently know which genes are involved in how food acts on an individual to raise or lower the risk of developing diabetes and obesity (Mathers 2019). Conversely, wearable devices, artificial intelligence (AI)‐based meal planning apps, and continuous glucose monitors (CGMs) provide users with instant feedback, allowing them to adjust their nutrition plans in real time (Michel and Burbidge 2019; Celis‐Morales et al. 2017). Specifically, in diabetes prevention programs, digital health interventions such as gamification, nudges, and remote monitoring have been shown to enhance behavioral adherence (Partridge and Redfern 2018). Data privacy, accessibility, and clinical validation continue to be substantial hurdles toward broad implementation (Abrahams et al. 2019; O'connor et al. 2016). Notwithstanding such impediments, digital health intertwined with precision nutrition can revolutionize healthcare by addressing chronic diseases. It does this by introducing solutions that are more sustainable, effective, and customized than any of its predecessors (Johnson et al. 2021; Goetz and Schork 2018). The current investigation discovers a blend of digital health and personalized nutrition for diabetes and obesity care. It looks back at the current investigation, technological innovations, and potential future directions of this rapidly evolving topic.

1.1. Aim of the Review

With a focus on how practical it is for diabetes and obesity management, the investigation aims to explore the cumulative role of personalized nutrition in the information age. A break from traditional dietary advice and personalized nutrition offers personalized therapies by integrating genetic, epigenetic, and real‐time metabolic information. We believe that AI‐based meal planning, CGMs, and behavioral nudges have the potential to close the gaps in accessibility and clinical validation and simultaneously improve accuracy and compliance at the same time. Personalized nutrition is driven by scientific and technological advances such as nutrigenomics and microbiome analysis, as emphasized in this study. With regard to ethical concerns such as privacy protection and access, we balance the consequences of these developments for greater metabolic gains. This paper presents a complete picture of the promise and challenges of using personalized nutrition in disease prevention and treatment through the integration of recent evidence.

2. What Is Personalized Nutrition?

Based on the genetic makeup, gut microbiota, and live metabolic reactions of a person, customized nutrition calls for a transition from one‐size‐fits‐all dietary recommendations to personalized practices (Bashiardes et al. 2018; Drabsch and Holzapfel 2019). As persons are diverse in terms of gene expression (e.g., FTO, TCF7L2), gut microbiota (e.g., A. muciniphila ), and glucose tolerance, personalized nutrition differs from usual “one‐size‐fits‐all” practice (Zeevi et al. 2015; Kolodziejczyk et al. 2019). For example, nutrigenomic analysis can tell one who would familiarize themselves with losing weight and controlling diabetes on low‐glycemic or high‐protein diets (de Toro‐Martín et al. 2017; Ferguson et al. 2016).

Metabolic well‐being can be improved with personalized prebiotic and probiotic therapy using microbiome profiling (Guizar‐Heredia et al. 2023). Novel digital health technologies, such as wearable sensors, AI apps, and CGMs, improve personalized nutrition by offering instantaneous feedback on the effect of food choices (Sempionatto et al. 2021; Shamanna et al. 2024). According to Ben‐Yacov and Rein (2022), the first tools enable people with obesity or diabetes to tailor their macronutrient content, meal timing, and food portions according to their own physiological response. Although concerns regarding data privacy, affordability, and clinical proof persist, additional indications and regulatory frameworks are essential to guarantee fair usage (Kohlmeier et al. 2016; Verma et al. 2018). Personalized nutrition can potentially revolutionize the prevention and management of chronic diseases, particularly with the emergence of precision medicine (Figure 1) (Moore 2020). Figure 1 shows the components of personalized nutrition.

FIGURE 1.

FIGURE 1

Components of personalized nutrition.

2.1. Personalized Nutrition Based on Genetics

Personalized nutrition is a revolution that displaces blanket dietary advice with individualized meal plans based on metabolic, microbial, and genetic information (Bashiardes et al. 2018). Genetic variation has a significant influence on nutritional metabolism and affects the risk of obesity and diabetes (Drabsch and Holzapfel 2019). For example, de Toro‐Martín et al. (2017) established that SNPs in FTO and TCF7L2 are correlated with an increased risk of obesity and impaired glucose metabolism. As nutrigenomics science authorizes, carbohydrate sensitivity has a genetic origin, and low‐glycemic foodstuffs are better for some than for others (Zeisel 2020).

Personalized gene‐driven meals are superior to generic approaches for weight loss and glucose control (Matusheski et al. 2021). One study found that people who carried a mutation within PPARG gained additional benefit from consuming a Mediterranean diet that confined advanced amounts of monounsaturated fat (Ferguson et al. 2016). Correspondingly, to avoid metabolic disorders, patients with APOA2 polymorphisms must decrease saturated fat consumption (Lagoumintzis and Patrinos 2023). Depending on these results, personalized nutrition therapy for obesity and diabetes management can be achieved via nutrigenetic testing (Goni et al. 2016). The translation of genetic information into effective dietary plans continues to be plagued by several issues (Verma et al. 2018). Data protection and the risk of genetic determinism are two ethical issues that must be considered (Kohlmeier et al. 2016). Individualized nutrition plans can be augmented by merging genomic information with digital health technology despite these challenges (Moore 2020).

2.2. The Role of the Gut Microbiome in Personalized Nutrition

Nutrient uptake, inflammation, and metabolic health are considerably exaggerated by the gut flora (Kolodziejczyk et al. 2019). Certain bacterial species, as per a study by Guizar‐Heredia et al. (2023), comprising A. muciniphila , have been associated with improved insulin sensitivity, indicating that microbial diversity plays a role in obesity and diabetes pathogenesis. Leshem et al. (2020) established that augmented obesity and glucose intolerance are linked to dysbiosis, which is a disturbance in gut microorganisms. To facilitate microbial balance, personalized nutrition applies microbiome profiling to recommend prebiotic‐ and probiotic‐rich foods (Yeşilyurt et al. 2022). Individuals who are predisposed to diabetes can benefit from a high‐fiber diet because it enhances the production of short‐chain fatty acids (SCFAs) by the body (Christensen et al. 2018).

Zeevi et al. (2015) reported that nutritional advice based on microbiota enhanced postprandial glucose responses better than low‐carbohydrate recommendations. This evidence is reinforced by trials such as the PREDICT trials. New technologies, including microbiome analysis driven by AI, enable instantaneous dietary modification (Romero‐Tapiador et al. 2023). The high cost of microbiome testing prevents it from being widely adopted, and more research is required to ascertain its long‐term effectiveness (Torres and Tovar 2021). Palmnäs et al. (2020) stated that metabolic diseases can be treated with a microbiome‐targeted diet in the future, as metabolomics and metagenomics are still evolving.

2.3. Metabolic Response Monitoring and Digital Tools

Through real‐time metabolic feedback, wearable sensors and CGMs enable dynamic dietary modifications (Sempionatto et al. 2021). CGMs enable diabetics to optimize the timing and macronutrient composition of meals by showing the impact of different foods on blood glucose (Ben‐Yacov and Rein 2022). Individualized CGM‐based meals are more effective in reducing HbA1c levels than are standard treatments (Table 1) (Schembre et al. 2020). Table 1 shows the key components and tools for personalized nutrition: insights from current research.

TABLE 1.

Key components and tools of personalized nutrition: insights from current research.

Aspect Description Tools used Key insight References
Genetics Use of DNA variations to guide diet Genotyping tests Tailored nutrition plans based on genetic predisposition Bashiardes et al. (2018)
Microbiome Role of gut flora in dietary responses Microbiome sequencing Microbial diversity impacts nutrient absorption Kolodziejczyk et al. (2019)
Metabolic response Individual postprandial glucose variability Continuous glucose monitors (CGMs) Predicting glycemic response to foods Zeevi et al. (2015)
Personalized apps Mobile applications for tracking diet and metabolism Mobile apps User feedback loops for diet adjustments Mortazavi and Gutierrez‐Osuna (2023)
Wearables Real‐time health monitoring devices Wearables (e.g., Fitbit) Integrating physical activity with dietary intake Sempionatto et al. (2021)
Precision nutrition Customized diets based on metabolism Biomarker analysis tools Metabolic heterogeneity addressed through diets Zeisel (2020)
Diet–microbiota interactions Effects of diet on gut microbiota Stool sample analysis Personalized prebiotic and probiotic use Torres and Tovar (2021)
Nutrigenomics Gene–diet interactions Genomic databases Prevention strategies for chronic diseases Ferguson et al. (2016)
Metabotyping Phenotypic grouping for nutrition strategies Blood biomarker profiling Targeted dietary interventions Palmnäs et al. (2020)
Postprandial responses Glycemic and lipid response to foods CGMs Individualized meal planning Guizar‐Heredia et al. (2023)
Nutritional AI AI‐driven dietary recommendations AI‐powered mobile apps Predictive analytics for diet success Romero‐Tapiador et al. (2023)
Digital biomarkers Predictive models for meal timing Wearable sensors Enhancing diet timing precision van den Brink et al. (2022)
Epigenetics Nutritional effects on gene expression DNA methylation analysis tools Diet‐driven epigenetic modifications Goni et al. (2016)
Consumer genomics Rise of direct‐to‐consumer genetic testing At‐home test kits Democratization of personalized nutrition Moore (2020)
Behavioral monitoring Tracking user habits for dietary adaptation Mobile/wearable integration Behavior‐informed diet adjustment Zahedani et al. (2023)
Digital twins Predictive glycemic modeling for individuals Digital twin platforms Improved diabetes remission via nutrition Shamanna et al. (2024)
Wearable validation Accuracy of nutrition‐tracking wearables Controlled trials Validating intake measurement devices Dimitratos et al. (2020)
Gut microbiome enterotypes Categorizing users by gut types for diets Metagenomic analysis Precision probiotics for obesity management Christensen et al. (2018)
Future of personalized nutrition Integrating IoT and AI for diet plans Smart devices and cloud analytics Tailored dietary solutions via smart systems Priyadharshini et al. (2025)
Challenges in implementation Ethical, scientific, and technical challenges Multimodal data collection platforms Balancing innovation with validation Verma et al. (2018)

To develop individualized meal plans, AI platforms and mobile applications integrate information on glucose, microbiota, and genetics (Mortazavi and Gutierrez‐Osuna 2023).

Zahedani et al. (2023) referred to ZOE's personalized nutrition program as an example that employs CGM data and microbiota analysis to predict glycemic responses. Biosensors and smartwatches track calorie intake, sleep, and exercise, which enhance compliance (Dimitratos et al. 2020). Digital technologies hold promise, but there are barriers to their use and availability (Liao and Schembre 2018). Additionally, the triglyceride–glucose (TyG) index and its derivatives (e.g., TyG–WHtR) have emerged as independent predictors of all‐cause and cardiovascular mortality in hypertensive patients, suggesting their application in digital risk assessment models (Li et al. 2025). Such markers, along with CGM and AI systems, can be used to advance personalized risk stratification for metabolic disease care.

Through the simulation of metabolic reactions, emerging technologies such as digital twins can further enhance individualized nutrition in the future (Shamanna et al. 2024). A new game‐changing model for managing diabetes and obesity is personalized nutrition, which is powered by genetics, microbiome science, and digital health. This paradigm moves attention away from generic diets and toward targeted, individualized interventions based on the biology of each individual. To achieve full potential, problems concerning price, data privacy, and clinical evidence must be addressed.

3. Genetic and Epigenetic Influences on Nutrition

Obesity and diabetes can be more easily understood by reviewing the intricate dynamics of diet, epigenetics, and inheritance. Boland et al. (2019) and Mansour et al. (2024) reported that genetic variations, such as single nucleotide polymorphisms (SNPs), can affect metabolism, appetite regulation, and fat accumulation by altering the way individuals react to different nutrients. For instance, many indications are associated with the risk of obesity with gene polymorphisms, such as FTO and MC4R, predominantly when coupled with high‐calorie diets (Heianza and Qi 2017; Gkouskou et al. 2024). Diet can affect genetic risk, as shown by nutrigenomics (the study of nutrient impact on gene expression), which demonstrates that personalized nutrition can decrease the severity of disease (Marcum 2020).

Furthermore, recent advancements in genomics and bioinformatics have made it possible to discover how diverse nutrients affect gene expression. This has opened the door for precision nutrition methods that aim to minimize the load of metabolic diseases (Vincenti et al. 2024; Ndimele et al. 2017). With respect to modulation of the impact of early‐life and lifetime dietary acquaintance, epigenetic modifications—heritable alterations in gene expression that are not DNA sequence changes—are as essential as genetic susceptibility (Burgio et al. 2015). Dietary circumstances can influence non‐coding RNAs, DNA methylation, and histone modifications, thus influencing metabolic well‐being from generation to generation (Franzago et al. 2019; Mishra et al. 2022). If the mother does not eat enough while pregnant, she might have genes that are “hardwired” to create children who become diabetic, obese, and predisposed to other metabolic disorders (Miraghajani et al. 2017). Folate and polyphenols are two recently discovered nutrients that can reverse pathogenic epigenetic markers and have potential therapeutic applications (Elsayed and Saleh 2024; Zeinalian et al. 2022). Understanding the dual actions of genetic susceptibility and nutritional epigenetics is crucial for appropriate intervention in the multifactorial etiology of diabetes and obesity.

3.1. Nutrigenomics and Obesity/Diabetes Risk

Increasing evidence suggests that diet and genetic predispositions contribute significantly to the development of metabolic syndrome and T2D. Nutrigenomics, according to Boland et al. (2019), is all about how various individuals' genes influence their bodies' responses to nutrition and how this impacts their metabolic health. Others are more prone to developing diabetes or obesity even when eating the same diet, and scientists have begun to grasp this by examining gene expression differences due to specific dietary factors. An example is the link between high‐fat diets and specific genetic variations, such as those in the FTO and TCF7L2 genes, which make a person more likely to develop diabetes (Marcum 2020). Increasing evidence is revealing that environmental and genetic interactions result in obesity and diabetes, not vice versa (Burgio et al. 2015).

Genetically influenced nutritional impacts controlled by gene mutations and SNPs have been the focus of increasing research owing to advances in nutrigenomic technologies. The way in which nutrients are digested and utilized by the organism is influenced by genetic differences; these differences influence the emergence and progression of metabolic disorders, specifically (Zeinalian et al. 2022).

Recent studies have demonstrated that epigenetic alterations, including modifications of DNA methylation and histone changes, control the long‐term influence of early food exposure on the risk of disease. An example is the association between metabolic dysregulation and epigenetic programming in children, which can arise when mothers fail to eat nutritious food throughout pregnancy (Franzago et al. 2019). This aids in designating the vulnerable time of pregnancy, where nutrition–gene interactions determine the trajectory of future health. In particular, there are food remedies with the motivation of plummeting the risk of illness via epigenetic indicators. Studies have shown that certain nutrients, such as folate, choline, and polyphenols, can moderate the patterns of DNA methylation complexes in the development of obesity and diabetes (Mishra et al. 2022). These explanations support the argument that personalized dietary advice can benefit from the amalgamation of epigenetic data. Currently, genetic, epigenetic, and microbiome data are obtained using high‐throughput technologies such as genome‐wide association studies (GWAS), DNA methylation profiling, and 16S rRNA gene sequencing (Demirkan et al. 2024). These platforms enable the detection of polymorphisms (e.g., FTO and TCF7L2), methylation signatures, and gut microbial profiles associated with metabolic dysfunction. Personalized nutrition sites integrate omics information with evidence‐based approaches that translate biological profiles into dietary recommendations (Ramos‐Lopez et al. 2022). For example, nutrigenetic tests translate SNPs to personalized macronutrient recommendations, whereas microbiome‐assisted applications screen taxa such as A. muciniphila and Faecalibacterium prausnitzii to forecast glycemic effects (Singar et al. 2024). The major biomarkers of diabetes and obesity are fasting glucose, HbA1c, the triglyceride–glucose (TyG) index, HOMA‐IR, pro‐inflammatory cytokines (e.g., IL‐6 and TNF‐α), and microbiota‐derived SCFAs (Anachad et al. 2023). In addition to genetic and epigenetic elements, bile acids (BAs) are being increasingly identified as regulators of obesity. Mendelian randomization analyses suggest a potential inverse causal association of glycolithocholate (GLCA) trunk fat percentage, indicating a role for BA metabolism in obesity control (Huang et al. 2024). These observations broaden our understanding of metabolic targets for precision nutrition interventions.

More strongly, diet has been associated with a greater risk of T2D, leading to large cohort studies. The prospective dietary lifestyle to nullify genetic predispositions was emphasized in an exploration by Jia et al. (2021), where high fruit consumption abridged the genetic risk for T2D. A new area of study referred to as “precision nutrition” is using genetic data to tailor treatments that can avert or postpone metabolic disease. According to Gkouskou et al. (2024), this strategy goes beyond simple food recommendations by providing individualized programs that render individual genetic profiles to each person. With the global rise in noncommunicable diseases, such innovation is more crucial than ever.

The translation of nutrigenomic results into clinical application remains plagued by challenges, even with encouraging progress. There must be heterogeneity in cohort studies and methodological standardization to address study design heterogeneity, demographic heterogeneity, and uneven replication of findings (Mondal and Panda 2021). Issues regarding genetic privacy must be resolved as precision nutrition has become increasingly prevalent in medicine. Nonetheless, a revolutionary advancement in the management of diabetes and obesity is the acknowledgment of nutrigenomic effects. Mansour et al. (2024) advise that scientists continue to refine gene‐diet models and that nutritional interventions aimed at specific diseases should be tested and confirmed through extensive clinical trials. Tailor‐made intervention strategies may be elevated to the next level by integrating omics information with machine learning (ML) and wearable electronics (Ndimele et al. 2017).

3.2. Gene–Diet Interactions

Individuals have various vulnerabilities to illness and varying reactions to diet therapies, which are largely a result of gene–diet interactions. Heianza and Qi (2017) state that these interactions are conditions in which an individual's genetics determine how dietary components influence health outcomes. For example, individuals carrying certain FTO variants are likely to become obese if they consume high amounts of calories, but the risk can be minimized if they maintain healthy eating behaviors (Zhuang et al. 2021).

Research on metabolic issues has indicated that genetics can elevate or reduce the influence of food constituents on disease risk. Of particular note regarding diabetes therapy, Westerman et al. (2021) employed the UK Biobank data to illustrate how certain dietary–gene pairings influence hemoglobin A1c. These results reinforce the potential for dramatic improvement in disease outcomes with customized diet plans based on genetic information. Furthermore, food influences on obesity and the growth of diabetes are regulated by differences in genes regulating inflammatory processes, glucose metabolism, and lipid metabolism (Crovesy and Rosado 2019). The risk of diabetes is controlled by triglyceride levels, which are regulated by polymorphisms in the APOA5 gene and ingestion of dietary fats (Ortega et al. 2017). To predict the risk of obesity with better precision, investigators have progressively turned to ML methods to examine intricate gene–diet interactions (Lee et al. 2022). Using these approaches, investigators can obtain vast amounts of genetic and nutritional data so that they are capable of detecting slight interface effects that have not been observed with more conventional approaches. Investigations suggest that exposure to the environment and genetics could affect interactions between diet and gene populations. Sekar et al. (2023) reported that research into interactions between genes and food in Southeast Asian populations has identified population‐specific genetic variations that affect the risk of diabetes compared to Western populations. These results highlight the importance of learning about numerous ethnic populations in an effort to develop personalized nutritional recommendations that are applicable globally (Table 2). Table 2 shows the genetic and epigenetic influences on nutrition: nutrigenomics and gene–diet interactions in obesity and diabetes risk.

TABLE 2.

Genetic and epigenetic influences on nutrition: nutrigenomics and gene–diet interactions in obesity and diabetes risk.

Topic Key findings Nutritional implications Future directions References
Nutrigenomics and obesity Genetic variants impact obesity risk via nutrient metabolism pathways Personalized diets can reduce obesity risk Integrating genetic testing into routine care Boland et al. (2019)
Nutrigenomics in athletes Genetics may dictate optimal macronutrient ratios for performance Tailored diets enhance athletic outcomes Further exploration of sports‐specific nutrigenomics Vincenti et al. (2024)
Genetics of obesity Epigenetic changes can predispose individuals to obesity Early nutritional interventions can reverse epigenetic marks Preventive nutrition strategies Burgio et al. (2015)
Gestational diabetes & epigenetics Maternal diet influences fetal epigenome and diabetes risk Nutritional counseling in pregnancy is vital Long‐term monitoring of offspring Franzago et al. (2019)
Mineral deficiencies & nutrigenomics Electrolyte imbalances interact with genetic predispositions Correction of deficiencies may lower metabolic risks Mineral‐genetics studies Mondal and Panda (2021)
Personalized nutrition in diabetes Genetic profiles can guide dietary management Precision diets can improve glycemic control Wider application of nutrigenomics Zeinalian et al. (2022)
Nutrigenetics in healthcare Personalized nutrition can transform healthcare systems Disease prevention through diet Policy implementation Marcum (2020)
Microbiota and obesity genetics Gut microbiota interplay with gene–nutrient interactions Microbiota modulation for obesity treatment Probiotic‐genetic interventions Mansour et al. (2024)
Nutritional genomics review Different genes respond uniquely to the same nutrient Need for genotype‐specific recommendations Expansion of databases Elsayed and Saleh (2024)
Gene‐nutrition‐health interface Nutrigenomics links diet, gene expression, and disease Holistic nutritional approaches Interdisciplinary research Mishra et al. (2022)
Prenatal nutrition exposure Intrauterine diet programs future obesity risk Targeting maternal nutrition Preventive public health policies Miraghajani et al. (2017)
OMICS platforms in metabolism Integrated OMICS improve precision nutrition Data‐driven dietary interventions Technological integration in clinics Ndimele et al. (2017)
Childhood obesity & precision nutrition Early‐life genetics influence obesity risk Personalized interventions in childhood Lifelong nutritional monitoring Wu et al. (2020)
Obesity genomics and cardiometabolic risk Metabolomic profiles reveal obesity–genetics connections Metabolite‐targeted diets Biomarker discovery Regan and Shah (2020)
Genetics, nutrition, and disease prevention Genetic understanding can predict disease risk Preventive nutrition strategies Genomic literacy in nutritionists Agrawal et al. (2024)
Nutrigenomics prospects Nutrigenomics can redefine nutritional sciences Emerging field with vast applications Global nutrigenomic initiatives Bahinipati et al. (2021)
Nutrigenomics in public health Mass customization of diets based on genetics is possible Public health nutrition programs Feasibility studies Reddy et al. (2018)
Personalized obesity prevention Genomic insights enable obesity prevention Early risk identification Genome‐guided dietary planning Gkouskou et al. (2024)
Gene‐diet interaction in obesity Specific gene variants interact with diets to affect obesity Tailored interventions based on risk alleles Longitudinal studies needed Heianza and Qi (2017)
Diet quality and genetic predisposition Poor diet amplifies genetic risk for diabetes High‐quality diets mitigate genetic risks Gene–environment modification studies Zhuang et al. (2021)

Diet patterns, rather than individual nutrients, are the targets of genetic risk research. Adherence to a healthy dietary pattern lowers the risk of obesity regardless of genetic predisposition, as demonstrated by Nettleton et al. (2015). This supports the contention that promoting healthy eating habits overall remains important, even when personalization is taken into account. In addition, the effectiveness of public health nutrition interventions can be influenced by gene–environment interactions. Recent experimental research has shown that microcystin‐LR (MC‐LR), a cyanotoxin, accelerates liver lipid metabolic disorders in obese mice through the PI3K/AKT/mTOR/SREBP1 pathway (Chu et al. 2022). The findings emphasize the interaction of environmental dietary toxins and metabolic gene regulation as central problems in personalized nutrition design.

For instance, universal dietary interventions that seek to reduce sugar intake may not be as effective for individuals who are genetically inclined to eat more sugar (Haslam et al. 2018). Therefore, to enhance the effectiveness of interventions, public health recommendations can be individualized based on genetic risk profiles. Encouraging results have been found, but a large challenge is the inconsistency across studies investigating gene–diet interactions. To approve deductions and create stable gene‐diet connections with applicability to real life, Dietrich et al. (2019) underscored the consequences of large‐scale, high‐quality studies. Personalized nutrition is achievable because of the enhanced understanding of gene‐diet connections, as well as the creation of new opportunities for diabetes and obesity treatment. Based on the latest examination (Vincenti et al. 2024; Elsayed and Saleh 2024), the successful determination and control of metabolic disease will most positively comprise the blending of genomic information with the continuous assessment of nutrition utilizing digital health technologies.

4. Real‐Time Data and Glucose Monitoring

Diabetes and obesity control have been greatly improved by the real‐time data collected through CGM. Glucose is measured minute by minute using CGMs, and people can see the impact of food, exercise, and medications in real time (Alfadhli et al. 2016; Hegedus et al. 2021). Patients can improve, take care of their diabetes themselves, and stick to their new way of life after being provided with constant feedback about their separate glycemic patterns. Patients with insulin‐treated diabetes had better quality glucose levels and more severe acute metabolic problems when they used real‐time CGMs, as described by Karter et al. (2021). In addition, CGM technology has been critical to obesity examination in revealing the connection between glucose variability and health risks linked to weight (Brummer et al. 2024). The course of T2D development from obesity can be slowed by incorporating CGMs into the standard medical practice. This makes early intrusion possible, which consequently allows for diet alteration and behavioral modification. The educational function of the CGM is also extremely important. Examinations have shown that access to real‐time glucose data can help people make healthier lifestyle and food choices. It is also used as an instrument to directly alter behavior directly (Ehrhardt and Al Zaghal 2019; Engler et al. 2022).

For instance, Alfian et al. (2018) highlighted how intelligent healthcare systems increase diabetes patients' self‐observational competences and condition monitoring by processing in‐the‐moment information from wearables. Additionally, studies have shown that CGM‐based treatments are helpful for patients who are not on insulin. This means that obese people can be helped by initial exposure to real‐time glucose response to avoid metabolic drop (Moon et al. 2023). In general, connecting real behavior with metabolic reactions and real‐time glucose monitoring is a paradigm shift in precision medicine.

4.1. Role of CGMs

By permitting them to track real‐time blood glucose changes, CGMs have been developed for diabetes management (Karter et al. 2021). They concentrate on the trends of hyperglycemia or hypoglycemia, while glucose is continuously measured day and night using this technology. By presenting the immediate effect of changes in food, exercise, stress, and medicine, this real‐time response has an important advantage over conventional fingerstick testing in diabetic patients (Engler et al. 2022).

Expanding the scope of glucose‐responsive innovation, a novel therapeutic gel has shown promise in healing diabetic subcutaneous abscesses through the synergistic action of photodynamic therapy, oxygen release, and pain killing induced by elevated glucose levels (Huang, An, et al. 2025; Huang, Huhulea, et al. 2025). These intelligent materials illustrate how metabolic signals can directly guide personalized care as an add‐on to digital feedback.

Consequently, CGMs are not only devices for more than analysis but can also be used as behavioral interferences to encourage people to uphold a better lifestyle. CGMs have been used extensively in obesity studies. The correlation between deranged glucose dynamics and weight management was explained by Hegedus et al. (2021), who found that even among obese non‐diabetic persons, real‐time glucose monitoring can detect personalized glycemic patterns. Obesity predisposes individuals to the development of T2D, and subtle disturbances in glucose control are often present before clinical diagnosis; therefore, these results are predominantly significant. Preventive treatment can be allowed through the use of CGMs by noticing the dysregulation of metabolism early on, prior to instigating irreparable harm. Furthermore, CGMs are used as educational tools, allowing patients to comprehend the impact of specific meals on their blood glucose levels (Alfadhli et al. 2016). For instance, CGM‐supported education allows individuals with gestational diabetes to augment their control of glucose and, perhaps, decrease the risk of adverse pregnancy outcomes. In addition, by illustrating the physiological impact of food selection graphically, CGMs may promote swift behavior changes in individuals with T2D and prediabetes (Ehrhardt and Al Zaghal 2020).

Both the precision and user experience of CGMs have been significantly enhanced by technological innovations. One of the devices that minimizes the user burden is a factory‐calibrated CGM (Tripyla et al. 2020). Teenagers, adults, and non‐insulin users have found such novelty acceptable to studies (Moon et al. 2023; Liao and Schembre 2018). As they become more reachable, CGMs will be in a better position to influence public health interventions for opposing growing rates of obesity and diabetes. One crucial integral of diabetes treatment is behavior modification, and CGMs deliver a novel process to encourage behavioral change through feedback‐based data (Ehrhardt and Al Zaghal 2019). Continuously guided mats assist individuals in developing habits and adhering to good lifestyle decisions over time, as long as they have real‐life significance for their exercise and food choices. Better than broad dietary advice would be to present to a patient how a meal that is high in carbohydrates causes a rapid rise in blood sugar. Greater compensation has been observed when CGMs are part of lifestyle interference programs. A pilot study by Taylor et al. (2019) proved that CGMs enhanced glycemic control in patients with T2D more than lifestyle counseling. Participants could personalize their responses based on real‐time information, resulting in a more adaptive and individualized approach to diabetes management. Not only will CGMs be useful for modifying behavior, they will also reduce the likelihood of long‐term diabetic complications by reducing glucose variability as a risk factor for cardiovascular complications (Jamiołkowska et al. 2016). These patients can minimize the risk of developing diabetic cardiovascular complications by minimizing their blood glucose excursions and, in return, decreasing their risk for oxidative stress and endothelial dysfunction. Other applications of CGMs beyond glucose control have been explored. New avenues for the examination of eating behavior in obesity studies have become available since Brummer et al. (2024) highlighted the potential for CGMs to automatically register eating episodes. Key information that is often lost using conventional food diaries, this device is able to offer quantitative and qualitative information regarding eating patterns, meal frequency, and glucose responses. Finally, CGMs can become an ordinary instrument in diabetes treatment and preventive health care, given that their costs continue to decline as insurance coverage increases. There is hope that CGMs have the potential to reduce the social burden of obesity and T2D by monitoring those at risk and enabling them to make early, individualized interventions (Porter et al. 2022).

4.2. AI‐Driven Meal Planning and Feedback Loops

New innovative meal planning software has been introduced by AI, which provides personalized dietary recommendations based on health information, lifestyle behavior, and metabolic requirements. A significant component of AI‐based meal planning for obesity and diabetes is the generation of personalized nutritional therapy that assists in blood glucose level regulation and the maintenance of weight management (Mehrotra and Mehrotra 2024). For example, a new research study by Xiong et al. (2024) developed a personalized light‐based prediction model for the prediction of postprandial glycemic response (PPGR) of type 1 diabetes patients with significantly better predictive performance (R = 0.63) than traditional carbohydrate‐counting models (R = 0.14) and traditional insulin infusion techniques (R = 0.43) (Xiong et al. 2024).

In another study, Bhadouria and Ahirwar (2024) employed a Random Forest classifier in the Nutrition Diet Expert System (NDES) to offer personalized dietary recommendations to diabetic patients with 96.48% accuracy, 0.98 precision, 0.96 recall, and an F1‐score of 0.97, indicating the potential of AI to improve glycemic control and patient outcomes (Bhadouria and Ahirwar 2024).

Unlike the general nature of the traditional diet plans, AI models can analyze real‐time CGM data and modify recommendations to maximize glycemic control (Joachim et al. 2022). The ability of AI to scan enormous amounts of individual health information, including real‐time glucose readings, activity levels, and sleep patterns, to provide personalized nutritional advice is a significant advantage of AI for meal planning. Considering the advantages of AI‐based nutrition apps for diet and health improvement, Prasad et al. (2025) highlighted the manner in which such apps enable individuals with diabetes to manage their blood sugar levels better and more effectively by adapting recommendations according to user‐specific glycemic responses. Several clinical and real‐world studies have demonstrated the efficacy of digital nutritional interventions in improving metabolic outcomes. For instance, CGM‐based dietary feedback has been shown to significantly lower HbA1c levels in T2D patients compared to standard self‐monitoring (Shamanna et al. 2024; De Luca et al. 2023). Similarly, mobile health apps combined with remote counseling have led to notable reductions in body weight and improvements in insulin sensitivity (Kitazawa et al. 2024), supporting their integration into broader dietary risk mitigation strategies.

Obese individuals, whose metabolic responses to food vary widely, stand to gain significantly from such tailoring (Nehete 2023). In addition, feedback loops brought about by AI systems allow for ongoing learning and real‐time eating plan refinement (Nehete 2023) for consumers. One of the novel mobile app prototypes, HealthyBaby by Al‐Massoudi et al. (2022), uses a logistic regression classifier and deep learning regression combined to provide personalized pregnancy diet recommendations with improved performance over conventional static methods. The integrated model accounted for user‐specific dietary restrictions and nutritional needs, indicating the growing applications of AI in managing maternal nutrition (Al‐Massoudi et al. 2022).

Glucose excursions can be evaluated, and real‐time feedback and meal adjustment recommendations can be provided by the system following every meal. Owing to this continuous feedback loop, individuals are likely to eat healthily and are able to make adjustments prior to any opposing metabolic consequences. Once AI enables patients to accomplish their own diabetes management, active self‐management is the outcome of passive compliance (Huang, An, et al. 2025; Huang, Huhulea, et al. 2025). Scientists have also established that AI‐based predictive models can prevent obese people from developing diabetes. According to Huang, An, et al. (2025) and Huang, Huhulea, et al. (2025), AI may use biomarker data in real time to forecast the risk of obesity‐related situations such as diabetes and propose diet modifications to delay them. AI‐supported dietary interventions in the early stages can delay or prevent the development of obesity in T2D by improving metabolic flexibility and maintaining glucose homeostasis (Nehete 2023).

Further, AI‐powered platforms have engaged in behavior modification techniques, such as gamification, nudges, and motivational feedback, to sustain individuals on the diet track. Such plans promote a user interface with diabetes self‐management applications, which result in lasting lifestyle changes (Priesterroth et al. 2019). People with diabetes and obesity can benefit significantly from intelligence's capability to keep them on their toes about their long‐term work towards altering their behavior (Hemanth et al. 2025). AI‐powered meal plans can be as intricate as desired, more than just calorie and macronutrient distribution. Diet plans that exploit hormonal equilibrium, fullness, and glycemic burden are recommended by AI systems (Hemanth et al. 2025), which are critical parameters in diabetes and obesity management. AI can plan diets that provide blood sugar and enhance metabolic health by considering the complex interactions between nutrients and metabolic pathways.

Polyphenols from Myrica rubra pomace have also exhibited hypoglycemic and gut microbiota‐modulating effects in T2D mouse models by modulating the PI3K and AMPK signaling pathways and enhancing GLUT‐4 and IRS‐1 expression (Chang et al. 2025). Such bioactive compounds can be utilized as key components in algorithm‐based meal planning in precision nutrition systems.

With the advent of mobile apps, wearable devices, and CGM integration, AI‐based diet management is becoming more common. In their impression of AI's role in diabetes management, Sarma and Devi (2025) emphasized how technology is streamlining patient‐doctor communication, leading the way for remote monitoring and real‐time decision support. To inspire quicker and healthier eating habits, they allow users to receive meal suggestions based on their current glucose patterns. People may more readily heed dietary advice without feeling deprived as a result of AI's adjustability, respecting cultural, territorial, and personal eating habits. For improving insulin sensitivity and lowering the threat of obesity, chrononutrition (diet in accordance with natural circadian cycles) plays an important part, and AI's potential was examined by Bajaj and Lata (2024) in this application. Both the quantity and timing of individuals' consumption can be further optimized in such a manner so as to stimulate the best overall metabolic health (Table 3). Table 3 shows the role of CGM‐ and AI‐driven nutrition in diabetes and obesity management.

TABLE 3.

The role of continuous glucose monitoring (CGM) and AI‐driven nutrition in diabetes and obesity management.

Technology Application Key findings Population studied References
CGM Educational tool for gestational diabetes Improved glycemic control and patient understanding of food impacts Pregnant women with GDM Alfadhli et al. (2016)
CGM Obesity research and dietary behavior tracking Identified postprandial glucose variability linked to obesity Adults with obesity Hegedus et al. (2021)
CGM + AI Real‐time eating event detection Automated meal logging reduced user burden and improved accuracy General population Brummer et al. (2024)
AI/ML algorithms Obesity and heart disease risk prediction Enhanced real‐time risk stratification using glucose patterns High‐risk cardiometabolic patients Devarapu et al. (2019)
Bluetooth‐enabled CGM Personalized diabetes monitoring system Reduced hypoglycemia episodes through real‐time alerts T2D patients Alfian et al. (2018)
CGM Behavioral intervention for T2D Increased physical activity and dietary adherence Adults with T2D Engler et al. (2022)
Digital tracker + CGM Glucose regulation improvement Significant HbA1c reduction in healthy and T2D users Healthy adults & T2D patients Zahedani et al. (2023)
CGM Prediabetes behavior modification Enhanced patient engagement in lifestyle changes Prediabetic adults Ehrhardt and Al Zaghal (2019)
CGM Glycemic control in insulin‐treated diabetes Reduced severe hypoglycemia events T1D and insulin‐dependent T2D Karter et al. (2021)
CGM Pilot self‐care support for T2D Improved meal timing and portion control T2D patients Porter et al. (2022)
AI‐driven meal planning Nudge‐based diabetes self‐management Increased adherence to Mediterranean diet T2D patients Joachim et al. (2022)
AI nutrition assistant Personalized diet recommendations Optimized macronutrient distribution based on glucose trends T2D and obese patients Nehete (2023)
AI + CGM integration Dynamic meal planning Reduced postprandial glucose spikes by 27% T2D patients Mehrotra and Mehrotra (2024)
AI analytics Obesity risk prediction Early identification of metabolic deterioration patterns High‐BMI adults Huang, An, et al. (2025) and Huang, Huhulea, et al. (2025)
Gamification + CGM Diabetes self‐management apps Improved long‐term engagement through reward systems T1D and T2D patients Priesterroth et al. (2019)
Social incentive apps Lifestyle modification in diabetes 15% greater weight loss vs. control group Uncontrolled T2D Patel et al. (2021)
AI‐powered WHO guidelines Interactive nutrition education Improved dietary knowledge retention General and diabetic populations Ojo et al. (2025)
Machine learning Precision meal plans for PCOS Balanced insulin and androgen levels through customized diets PCOS patients Hemanth et al. (2025)
AI‐driven chrononutrition Circadian‐based meal timing Reduced nocturnal glucose variability Shift workers with T2D Bajaj and Lata (2024)
CGM + wearable sensors Metabolite tracking for wellness Real‐time micronutrient adjustment based on glucose‐metabolite correlations Health‐conscious users Banka et al. (2025)

Although AI meal planning promises much, there are challenges ahead, including concerns regarding data privacy and algorithm transparency. Mackenzie et al. (2024) emphasized the need to address any biases in AI models and to ensure ethical use. Despite some challenges, the assistance of AI in enhancing nutrition approaches for diabetes and obesity control is substantial, pointing towards a good future for precision health interference. Finally, diabetes and obesity care have experienced a paradigm shift with the advent of AI‐driven feedback loops and meal planning. They allow people to play an active and educated role in their own healthcare process via hyper‐personalized real‐time nutritional guidance, enhancing glycemic control and weight loss (Kassem et al. 2025).

4.3. Comparison of Digital Tools for Dietary Monitoring and Exposure Management

The recent past has witnessed a speeding up in the adoption of digital technologies within diet assessment and health surveillance, particularly in managing the consumption of harmful food substances and improving metabolic outcomes. Digital health technologies, such as CGMs, mobile applications, wearable physical activity monitors, and AI systems, offer promising tools for personalized nutrition counseling and enabling behavior‐change interventions (Table 4) (Edelman et al. 2018; Pang et al. 2018; Dhar et al. 2023; Fanelli et al. 2023; Vegesna 2024). These online tools have the potential to reduce the intake of detrimental dietary components such as heavy metals by encouraging healthy food choices, tracking packaged food intake, and offering personal alerts or education. Table 4 summarizes the major tools, their purposes, target populations, primary features, and current limitations.

TABLE 4.

Comparison of digital tools for dietary monitoring and exposure management.

Technology/tool Function Target users Key features Limitations References
CGMs Tracks glucose response to diet T1DM, T2DM Real‐time alerts, dietary trend detection Not specific to heavy metals; may cause skin irritation or discomfort Edelman et al. (2018)
Mobile health apps Logs food intake and risks General public, obesity, T2DM Barcode scanning, alerts on additives/metals Limited database coverage; user adherence often declines over time Pang et al. (2018)
Wearable trackers Monitors physical activity & calorie intake Obesity, fitness‐focused individuals Real‐time health data, sync with diet apps Doesn't measure contaminants; overestimation or underestimation of energy expenditure Dhar et al. (2023)
AI‐based nutrition apps Generates personalized diet plans Obesity, metabolic syndrome AI‐driven recommendations, food risk evaluation Varying accuracy; recommendations may not be culturally or regionally tailored Vegesna (2024)
Telenutrition platforms Offers remote dietary counseling At‐risk, chronically ill populations Expert guidance, behavior modification Requires digital access and literacy; limited in physical assessment capabilities Fanelli et al. (2023)

5. Behavioral Change Through Technology

To decrease the severity of diabetes and obesity, digital adherence policies, gamification, and nudges can be employed to stimulate healthy lifestyles. Including game‐like elements such as rewards, challenges, and social competition in gamification policies has been found to meaningfully improve engagement and support good behavior. Gamification‐based DM applications employ behavior‐change techniques to empower patients to adhere to treatment (Priesterroth et al. 2019). Correspondingly, for people with uncontrolled diabetes, a randomized clinical trial combining gamification with social incentives showed that such people accomplished significant lifestyle alterations. Nudges, or small design vicissitudes that quietly encourage healthier choices, have also been shown to be essential in this field. Nudges, comprising social comparisons and goal reminders, can influence health behaviors without constraining separate choices (Kwan et al. 2020). This makes them an operative tool for the management and prevention of diabetes.

Digital channels modified by incorporating AI and ML boost behavioral change policies significantly. Banka et al. (2025) recognized the significance of AI‐driven customization in the distribution of tailored, responsive diet and physical activity treatments, as their investigation established that interventions improved compliance and health outcomes. Experts have recognized that gamification, if added to incentives or simulations, significantly improves the chance that people will exercise and adhere to medication according to instructions (Agrawal et al. 2024; Agarwal et al. 2021). Current digital health technologies often lack an in‐depth behavioral theory, as stated by Klonoff (2019), although such a theory is significant for sustaining change over the long term. To exploit the efficiency of digital interventions in diabetes and obesity deterrence programs, they should ideally be informed by behavioral science, clinically established (Gomis‐Pastor et al. 2024), and centered on user preferences (Berger and Jung 2024).

5.1. Gamification, Nudges, and Adherence

Over the past few years, gamification has emerged as an effective tool for engaging individuals with diabetes and obesity to change their behavior. As Priesterroth et al. (2019) report, patients will be more inclined to participate and adhere to treatment programs if self‐management apps feature game elements, such as points, levels, and rewards. Users of the diabetes app indicated greater levels of app use, self‐efficacy, and glycemic control following gamified therapy participation. By incorporating interactive and personalized elements, Orte et al. (2023) developed a gamified mobile health framework to promote healthy eating behaviors. Diabetes control has also been gained from the inclusion of nudges, which are small design cues that nudge individuals towards improved choices without encroaching upon their autonomy (Orte et al. 2023).

Personalized reminders, social comparisons, and default options significantly boosted health behavior among people managing diabetes, as established by Kwan et al.'s (2020) wide‐ranging review of nudge strategies. Digital health interventions that include behavioral nudges, as noted by Shah and Adusumalli (2020), can significantly increase the adoption and continuous use of health interventions, which are crucial for the prevention of diabetes and obesity. The impact of gamification interventions aimed at specific behaviors has been established through large‐scale clinical studies. Overweight and obese adults in the United States experienced a significant increase in their physical activity levels after they were randomly assigned to participate in STEP UP, as conducted by Patel et al. (2019). Similarly, the MOVE‐MORE program showed the potential for a mix of digital and environmental interventions by prompting office workers to take walking breaks through web‐based gamification and physical nudges (Mamede et al. 2021).

A new realization is that customized gamification is the most effective. As Banka et al. (2025) point out, one of the ways to enhance accuracy in wellness methods is through the application of AI and ML to customize gamification according to each individual's habits, preferences, and health goals. Individuals with diabetes and obesity are more likely to adhere to the lifestyle modifications required, such as consuming healthier foods and exercising more, if they have a plan specifically tailored to their requirements. However, it is also important to add behavioral theory to digital platforms to achieve effective behavioral changes. Most digital health interventions fail, as Klonoff (2019) opines, because they fail to integrate the three pillars of behavior change: goal setting, self‐monitoring, and reinforcement. Adding these theories to gamified platforms increases participation and encourages users to keep up their behavior in the long term, which is fundamental in preventing chronic diseases. Further gains were found when gamification was combined with financial incentives. Agarwal et al. (2021) found that gamified exercise programs with financial incentives support a significantly greater level of adherence. This indicates that gamified experiences can add to intrinsic motivation, particularly in populations that are at risk for obesity and diabetes, when paired with properly designed extrinsic motivators.

There has been limited research on implementing gamified behavior simulations in class. Grimani et al. (2024) illustrated that applying game simulation to medication adherence and non‐adherence improved understanding, and consequently, real‐world medication adherence rates. These findings illustrate the gamification potential of diabetes education interventions to improve self‐care and adherence through simulations. When creating gamified interventions, it is important to consider patient preferences. A “one‐size‐fits‐all” strategy could be counterproductive, as Berger and Jung (2024) discovered that individuals have varying preferences for gaming mechanics within diet and health apps. User segmentation can be better understood so that digital interventions are more inclusive and effective. Even though gamification and nudges hold much promise, there remain challenges to overcome. Digital fatigue, disparity in access to technology, and varying levels of health literacy are variables that may influence the impact of these resources (Fleming et al. 2020). Electronic health products require stringent clinical testing and rigorous evaluation of these attributes prior to population‐level gamified behavior‐change interventions to address obesity and diabetes (Gomis‐Pastor et al. 2024).

5.2. Use in Diabetes Prevention Programs (e.g., NDPP)

Interventions such as the National Diabetes Prevention Program (NDPP) have begun to incorporate behavior‐change technologies into their integrated efforts towards diabetes prevention. The NDPP is an intervention endorsed by the CDC. Its emphasis lies on behavioral changes, including enhanced physical activity and diet, in a bid to prevent or delay T2D. Gamification strategies have been incorporated into NDPP programs to enhance participation and engagement (Patel et al. 2021).

Social rewards, leaderboards, and points are a few of the strategies employed to maintain individuals' interest in creating positive behavioral changes throughout the program's year‐long operation. A key step in developing an NDPP is the application of nudges. Behavioral nudges, such as reminders of daily activity or coaching sessions, increase program adherence and reduce dropout (Kwan et al. 2020). Today, digital replicas of the NDPP employ app‐based nudge strategies to engage participants, keep them motivated, and track their progress toward their health objectives through numerous touchpoints. Gamification significantly enhances the effectiveness of diabetes prevention programs, says clinical research. Based on a study by Patel et al. (2021), gamified behavior‐based lifestyle change programs resulted in greater weight loss and improved glycemic control than more traditional, non‐digitally interactive interventions.

These findings facilitate the inclusion of gamified strategies within broader public health initiatives, such as the NDPP. AI and ML have revolutionized the provision of personalized therapies as part of diabetes prevention programs. According to Banka et al. (2025), making nutrition counseling and exercise recommendations more personalized with the help of AI algorithm‐generated personalized feedback would render the NDPP more effective and useful for diverse populations. These developments ensure that individuals receive interventions that match their preferences and lifestyles.

These interventions are even stronger when grounded in behavioral economics. By illustrating how clinician choices can be informed by behavioral economics modules within electronic health records, Belli et al. (2020) illustrated how such integration can foster the best preventive care for older adults at risk of diabetes while minimizing overtreatment. One method to enhance risk assessment and intervention tailoring is to apply the same principles to NDPP digital platforms.

However, extensive validation must be performed to ensure that digital treatments are credible in preventative programs. Mathews et al. (2019) emphasized the importance of clinical validation pathways to ensure the security, efficacy, and satisfaction of digital health solution users. Without rigorous validation, computational tools are at risk of being ineffective or even detrimental to the battle against disease. New trials are proving promising, including FOOTSTEPS (Suzuki et al. 2024), a trial that utilizes behavioral economic feedback processes to motivate exercise in individuals at risk for cardiovascular disease and diabetes, two populations with many commonalities. NDPP and similar programs could greatly benefit from what can be learned from such trials. Further support for introducing technology‐enhanced NDPP models was provided through scoping reviews by Kearns et al. (2025), which clearly show the substantial effectiveness of digital technologies that assist in the transfer of mental health and obesity knowledge when integrated with clinical practice. In view of this, mounting consensus now exists that digital health technologies, in the right circumstances, can add to more traditional methods of averting diabetes. Finally, as noted by Gomis‐Pastor et al. (2024), technology‐driven customized coaching, increased integration of gamification with wearable technology, and real‐time analysis of health data are all possible directions for technology to prevent diabetes. Collectively, these elements can create an adaptive prevention environment that enables users to control their metabolic well‐being before disease onset.

6. Limitations and Ethical Issues

Although digital health technologies are increasingly being used for diabetes and obesity management, they also present several limitations and ethical issues. The most significant aspect of such issues is data privacy. There is a valid reason to worry about data breaches, unauthorized access, and the secondary use of data without patient consent because of the massive amounts of sensitive health data accumulated by digital tools (Grande et al. 2020). The challenge of ensuring equal protection for everyone is compounded by the lack of equal rules in different regions, fueling these issues. Unfortunately, users must trust that their information is being handled properly. However, if there are any violations or abuses, this trust could be greatly undermined, which would deter individuals from engaging in digital health programs. The high cost of most digital health solutions is also a significant drawback that prevents many from accessing them. Digital treatments can be helpful in treating obesity, but their benefits usually accrue to individuals with a higher socioeconomic status who can afford them, as stated by Hinchliffe et al. (2022). Rather than curtailing health disparities, disadvantaged communities might experience them in enhanced ways because of the exorbitant price of devices such as CGMs, wearable trackers, and subscriptions to apps. For digital health benefits to be universal, we need to eliminate economic barriers. Infrastructure and technical knowledge issues are also included in the accessibility. Kearns et al. (2025) stated that numerous individuals, especially rural dwellers and elderly individuals, struggle to utilize complex health apps properly. User‐unfriendly interfaces, poor Internet connectivity, and insufficient knowledge of mobile technologies also restrict the impact of digital interventions. If these practical factors are not considered, digital health innovations risk failing to reach those who would benefit the most from them. To make digital health available to everyone, developers and legislators must prioritize inclusive design and support services.

Digital health technologies continue to require clinical validation, which is often overlooked even though it is extremely important. Even with the growing digital tool market, various products have not been adequately tested scientifically, raising questions regarding their effectiveness and credibility (Mathews et al. 2019). To ensure the effectiveness of the technologies and to establish the credibility desirable for physician and patient uptake, clinical validation is critical (Gomis‐Pastor et al. 2024). Without confirmation by extensive trials, such technologies risk ending up being called gimmicks instead of effective medical treatments. Another major drawback is that digital health technologies have no established assessment framework. It is difficult to associate, advise on, and control digital tools optimally because of the lopsided health technology assessment, according to a systematic review by von Huben et al. (2022). It is necessary to systematically evaluate safety, effectiveness, and worth, chiefly in the case of treatments that cure chronic conditions such as diabetes and obesity, and this becomes an added concern because there is no clear and evident criterion used for their evaluations. Stringent evaluation standards demand collective efforts from healthcare regulators, practitioners, and technology companies. Commercialization and commodification of health data have ethical consequences. The desire to sell patient data commercially for profit increases as wearable technology becomes more deeply embedded in clinical care (Figure 2) (Ginsburg et al. 2024). Patient choice and well‐versed consent have become less of an issue with the commercialization of intimate health information. To maintain ethical restraints in place as the industry develops, explicit data regulations and patient‐centered governance structures are essential. Finally, it is important to consider the broader context of how the integration of healthcare technology affects society. Notwithstanding the radical potential of digital health technologies, as Solomon and Rudin (2020) put it, their unconsidered adoption risks exacerbating the current inequities. If digital health innovation is going to bring authentic transformation in healthcare, as Bhavnani et al. (2017) state, then it must not let go of the values of presence, equity, and patient‐centeredness. The value of digital health may go unrewarded to many unless active measures are taken to address social and ethical concerns. Figure 2 shows the limitations and ethical issues of personalized nutrition implementation.

FIGURE 2.

FIGURE 2

Limitations and ethical issues of personalized nutrition implementation.

6.1. Ethical and Equity Considerations in Personalized Nutrition

The intersection of personalized diet with digital health infrastructure catalyzes landmark ethical and equity issues that must be addressed methodically to facilitate real‐world momentum. A key ethical issue is the ownership of data, informed consent, and transparency of algorithms. Given that users enter personal biometric, genomic, and behavioral data through apps and wearable sensors, open governance structures must be in place to prevent misuse and unlawful commodification (Maeckelberghe et al. 2023). Equity concerns are pressing. The application of digital technologies such as CGMs, AI‐driven meal planning apps, and microbiome testing largely preserves more prosperous, urban‐dwelling populations, further widening the digital divide and potentially perpetuating existing health inequities (Paccoud et al. 2024). Marginalized populations, including rural dwellers, elderly citizens, and less digitally informed people, face systemic barriers such as inferior connectivity, ambiguous interfaces, and extortionate pricing plans (Sin et al. 2021). In the interest of justice, subsidized pricing, universal design, and culturally appropriate nutritional guidance are needed. Finally, algorithmic bias trained on small demographic datasets can perpetuate prejudicial diet suggestions. Hence, policymakers and developers must create ethically focused AI frameworks, promote participatory design, and integrate regulatory processes to ensure that personalized nutrition is inclusive and equitable in implementation.

6.2. Reimbursement and Regulation Environment

The successful use of digital health tools in personalized nutrition is contingent on clear‐cut regulatory policies and long‐term reimbursement models. However, there are a broad range of differences between geographic markets in evaluating and funding these technologies. The United States Food and Drug Administration (FDA) has provided regulations for software as a medical device (SaMD) that include certain nutrition‐specific digital solutions. However, reimbursement remains patchy, and the majority of nutrition apps and AI platforms are not reimbursable under standard insurance until recommended by healthcare professionals in specific codes (Watson et al. 2023). In contrast, the European Union has adopted the Medical Device Regulation (MDR) model, which deems the majority of AI‐based nutritional aids as Class IIa or greater, necessitating more robust clinical trials. Some EU countries, such as Germany, have also created digital health application (DiGA) pathways where registered apps can become eligible for reimbursement through statutory health insurance if they demonstrate positive health outcomes (Bond et al. 2023).

Regulatory pathways for digital nutrition tools in LMICs are immature. Constraints in infrastructure, a lack of digital health legislation, and unclear approval processes deter innovation adoption. Out‐of‐pocket spending is also dominant in the health financing system, making the reimbursement of digital nutrition interventions non‐existent (Abeltino et al. 2025). To guarantee both scalability and equity, global stakeholders must ensure harmonized standards for the authorization of digital nutrition tools, develop performance‐based reimbursement models, and integrate these tools into primary care systems. Clear regulation and evidence‐based pricing policies will be essential to ensure innovation and access in the new digital world of nutrition.

7. Conclusions and Future Perspectives

The use of digital health technology to deliver personalized diets is transforming diabetes and obesity management. Personalized diet interventions involving genetic data, real‐time blood glucose, and AI‐powered feedback can recover metabolic consequences more than unguided recommendations. The use of behavioral interventions as part of an application can make a personalized diet a long‐term strategy for chronic disease management. Data protection, expense, and the need for extensive clinical validation are barriers that need to be addressed. To have a maximum public health impact, it is essential to provide equal access and incorporate these strategies into mainstream medicine. There is increasing evidence that individualized diets can transform strategies for the prevention and treatment of metabolic diseases.

For hyper‐personalized eating advice, the science of personalized nutrition will have to move ahead with multi‐omics integration (genomics, metabolomics, and microbiome) and digital health tools. Augmenting predictive models using AI and ML will enable real‐time adjustment of person‐specific metabolic reactions. Even if regulatory steps are needed to reduce price and availability disparities, wearable technology and mobile health platforms will make it more democratized. Longitudinal research and randomized large‐scale trials are required to validate its efficacy and cost‐effectiveness. Researchers, clinicians, and policymakers must cooperate to standardize procedures and ascertain ethical use. The use of personalized nutrition in public health initiatives could entirely transform the treatment and prevention of metabolic diseases, such as diabetes and obesity.

Author Contributions

Muhammad Tayyab Arshad: writing – original draft (equal). M. K. M. Ali: conceptualization (equal), data curation (equal). Sammra Maqsood: writing – review and editing (equal). Ali Ikram: supervision (equal). Faiyaz Ahmed: methodology (equal). A. I. Aljameel: data curation (equal), visualization (equal). Ammar AL‐Farga: data curation (equal), resources (equal). Md. Sakhawot Hossain: validation (equal).

Disclosure

The authors have nothing to report.

Ethics Statement

This study did not involve humans or animals.

Consent

This study did not involve humans.

Conflicts of Interest

The authors declare no conflicts of interest.

Acknowledgments

This work was supported and funded by the Deanship of Scientific Research at Imam Mohammad Ibn Saud Islamic University (IMSIU) (grant number IMSIU‐DDRSP2502).

Arshad, M. T. , Ali M. K. M., Maqsood S., et al. 2025. “Personalized Nutrition in the Era of Digital Health: A New Frontier for Managing Diabetes and Obesity.” Food Science & Nutrition 13, no. 10: e71006. 10.1002/fsn3.71006.

Funding: This work was supported by the Deanship of Scientific Research at Imam Mohammad Ibn Saud Islamic University (IMSIU) (grant number IMSIU‐DDRSP2502).

Contributor Information

Ali Ikram, Email: ali.ikram@uifst.uol.edu.pk.

Md. Sakhawot Hossain, Email: sakhawot.jnft@gmail.com.

Data Availability Statement

The data supporting the findings of this study is available from the corresponding author upon reasonable request.

References

  1. Abeltino, A. , Riente A., Bianchetti G., et al. 2025. “Digital Applications for Diet Monitoring, Planning, and Precision Nutrition for Citizens and Professionals: A State of the Art.” Nutrition Reviews 83, no. 2: e574–e601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Abrahams, M. , Frewer L. J., Bryant E., and Stewart‐Knox B.. 2019. “Personalised Nutrition Technologies and Innovations: A Cross‐National Survey of Registered Dietitians.” Public Health Genomics 22, no. 3–4: 119–131. [DOI] [PubMed] [Google Scholar]
  3. Agarwal, A. K. , Waddell K. J., Small D. S., et al. 2021. “Effect of Gamification With and Without Financial Incentives to Increase Physical Activity Among Veterans Classified as Having Obesity or Overweight: A Randomized Clinical Trial.” JAMA Network Open 4, no. 7: e2116256. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Agrawal, P. , Kaur J., Singh J., et al. 2024. “Genetics, Nutrition, and Health: A New Frontier in Disease Prevention.” Journal of the American Nutrition Association 43, no. 4: 326–338. [DOI] [PubMed] [Google Scholar]
  5. Alfadhli, E. , Osman E., and Basri T.. 2016. “Use of a Real Time Continuous Glucose Monitoring System as an Educational Tool for Patients With Gestational Diabetes.” Diabetology & Metabolic Syndrome 8: 1–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Alfaris, N. , Alqahtani A. M., Alamuddin N., and Rigas G.. 2023. “Global Impact of Obesity.” Gastroenterology Clinics 52, no. 2: 277–293. [DOI] [PubMed] [Google Scholar]
  7. Alfian, G. , Syafrudin M., Ijaz M. F., Syaekhoni M. A., Fitriyani N. L., and Rhee J.. 2018. “A Personalized Healthcare Monitoring System for Diabetic Patients by Utilizing BLE‐Based Sensors and Real‐Time Data Processing.” Sensors 18, no. 7: 2183. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Al‐Massoudi, Y. M. A. , Mariya Shah U. E., Anjum S. S., and Cherukuru P.. 2022. “HealthyBaby: Prototype of an AI‐Based Nutrition Recommendation Mobile Application for Pregnant Women.” In Congress on Smart Computing Technologies, 129–143. Springer Nature Singapore. [Google Scholar]
  9. Anachad, O. , Taha W., Bennis F., and Chegdani F.. 2023. “The Implication of Short‐Chain Fatty Acids in Obesity and Diabetes.” Microbiology Insights 16. 10.1177/11786361231162720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Bahinipati, J. , Sarangi R., Mishra S., and Mahapatra S.. 2021. “Nutrigenetics and Nutrigenomics: A Brief Review With Future Prospects.” Biomedicine 41, no. 4: 714–719. [Google Scholar]
  11. Bajaj, P. , and Lata K.. 2024. “Artificial Intelligence and Chrononutrition: A Review Study on Role of AI in Revolutionizing Dietary Recommendations.” In 2024 11th International Conference on Computing for Sustainable Global Development (INDIACom), 548–552. IEEE. [Google Scholar]
  12. Banka, R. , Das P., Das S., and Ghosh J.. 2025. “Tailored Nutrition and Diet Plan Using AI and Machine Learning for Precision Wellness.” In Harnessing AI and Machine Learning for Precision Wellness, edited by Banka R., Das P., Das S., and Ghosh J., 185–214. IGI Global Scientific Publishing. [Google Scholar]
  13. Bashiardes, S. , Godneva A., Elinav E., and Segal E.. 2018. “Towards Utilization of the Human Genome and Microbiome for Personalized Nutrition.” Current Opinion in Biotechnology 51: 57–63. [DOI] [PubMed] [Google Scholar]
  14. Belli, H. M. , Chokshi S. K., Hegde R., et al. 2020. “Implementation of a Behavioral Economics Electronic Health Record (BE‐EHR) Module to Reduce Overtreatment of Diabetes in Older Adults.” Journal of General Internal Medicine 35: 3254–3261. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ben‐Yacov, O. , and Rein M.. 2022. “Precision Nutrition for Type 2 Diabetes.” In Precision Medicine in Diabetes: A Multidisciplinary Approach to an Emerging Paradigm, 233–249. Springer International Publishing. [Google Scholar]
  16. Berger, M. , and Jung C.. 2024. “Gamification Preferences in Nutrition Apps: Toward Healthier Diets and Food Choices.” Digital Health 10. 10.1177/20552076241260482. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Bhadouria, A. S. , and Ahirwar A.. 2024. Predictive Model Approach for Enhancing Diet Management for Diabetes Patients Through Artificial Intelligence. Advances in Medical Technologies and Clinical Practice Book Series, 335–366. IGI Global Scientific Publishing. [Google Scholar]
  18. Bhavnani, S. P. , Parakh K., Atreja A., et al. 2017. “2017 Roadmap for Innovation—ACC Health Policy Statement on Healthcare Transformation in the Era of Digital Health, Big Data, and Precision Health: A Report of the American College of Cardiology Task Force on Health Policy Statements and Systems of Care.” Journal of the American College of Cardiology 70, no. 21: 2696–2718. [DOI] [PubMed] [Google Scholar]
  19. Blüher, M. 2019. “Obesity: Global Epidemiology and Pathogenesis.” Nature Reviews Endocrinology 15, no. 5: 288–298. [DOI] [PubMed] [Google Scholar]
  20. Boland, M. , Alam F., and Bronlund J.. 2019. “Modern Technologies for Personalized Nutrition.” In Trends in Personalized Nutrition, 195–222. Elsevier. [Google Scholar]
  21. Bond, A. , Mccay K., and Lal S.. 2023. “Artificial Intelligence & Clinical Nutrition: What the Future Might Have in Store.” Clinical Nutrition ESPEN 57: 542–549. [DOI] [PubMed] [Google Scholar]
  22. Brummer, J. , Glasbrenner C., Hechenbichler Figueroa S., Koehler K., and Höchsmann C.. 2024. “Continuous Glucose Monitoring for Automatic Real‐Time Assessment of Eating Events and Nutrition: A Scoping Review.” Frontiers in Nutrition 10: 1308348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Burgio, E. , Lopomo A., and Migliore L.. 2015. “Obesity and Diabetes: From Genetics to Epigenetics.” Molecular Biology Reports 42: 799–818. [DOI] [PubMed] [Google Scholar]
  24. Celis‐Morales, C. , Livingstone K. M., Marsaux C. F., et al. 2017. “Effect of Personalized Nutrition on Health‐Related Behaviour Change: Evidence From the Food4Me European Randomized Controlled Trial.” International Journal of Epidemiology 46, no. 2: 578–588. [DOI] [PubMed] [Google Scholar]
  25. Chang, G. , Tian S., Luo X., et al. 2025. “Hypoglycemic Effects and Mechanisms of Polyphenols From Myrica rubra Pomace in Type 2 Diabetes (Db/Db) Mice.” Molecular Nutrition & Food Research 69, no. 10: e202400523. [DOI] [PubMed] [Google Scholar]
  26. Cho, N. H. , Shaw J. E., Karuranga S., et al. 2018. “IDF Diabetes Atlas: Global Estimates of Diabetes Prevalence for 2017 and Projections for 2045.” Diabetes Research and Clinical Practice 138: 271–281. [DOI] [PubMed] [Google Scholar]
  27. Christensen, L. , Roager H. M., Astrup A., and Hjorth M. F.. 2018. “Microbial Enterotypes in Personalized Nutrition and Obesity Management.” American Journal of Clinical Nutrition 108, no. 4: 645–651. [DOI] [PubMed] [Google Scholar]
  28. Chu, H. , Du C., Yang Y., et al. 2022. “MC‐LR Aggravates Liver Lipid Metabolism Disorders in Obese Mice Fed a High‐Fat Diet via PI3K/AKT/mTOR/SREBP1 Signaling Pathway.” Toxins 14, no. 12: 833. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Crovesy, L. , and Rosado E. L.. 2019. “Interaction Between Genes Involved in Energy Intake Regulation and Diet in Obesity.” Nutrition 67: 110547. [DOI] [PubMed] [Google Scholar]
  30. De Luca, V. , Bozzetto L., Giglio C., et al. 2023. “Clinical Outcomes of a Digitally Supported Approach for Self‐Management of Type 2 Diabetes Mellitus.” Frontiers in Public Health 11: 1219661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. de Toro‐Martín, J. , Arsenault B. J., Després J. P., and Vohl M. C.. 2017. “Precision Nutrition: A Review of Personalized Nutritional Approaches for the Prevention and Management of Metabolic Syndrome.” Nutrients 9, no. 8: 913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Demirkan, A. , van Dongen J., Finnicum C. T., et al. 2024. “Linking the Gut Microbiome to Host DNA Methylation by a Discovery and Replication Epigenome‐Wide Association Study.” BMC Genomics 25, no. 1: 1224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Devarapu, K. , Rahman K., Kamisetty A., and Narsina D.. 2019. “MLOps‐Driven Solutions for Real‐Time Monitoring of Obesity and Its Impact on Heart Disease Risk: Enhancing Predictive Accuracy in Healthcare.” International Journal of Reciprocal Symmetry and Theoretical Physics 6: 43–55. [Google Scholar]
  34. Dhar, R. , Kumar A., and Karmakar S.. 2023. “Smart Wearable Devices for Real‐Time Health Monitoring.” Asian Journal of Medical Sciences 14, no. 12: 1–3. [Google Scholar]
  35. Dietrich, S. , Jacobs S., Zheng J. S., Meidtner K., Schwingshackl L., and Schulze M. B.. 2019. “Gene‐Lifestyle Interaction on Risk of Type 2 Diabetes: A Systematic Review.” Obesity Reviews 20, no. 11: 1557–1571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Dimitratos, S. M. , German J. B., and Schaefer S. E.. 2020. “Wearable Technology to Quantify the Nutritional Intake of Adults: Validation Study.” JMIR mHealth and uHealth 8, no. 7: e16405. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Drabsch, T. , and Holzapfel C.. 2019. “A Scientific Perspective of Personalised Gene‐Based Dietary Recommendations for Weight Management.” Nutrients 11, no. 3: 617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Edelman, S. V. , Argento N. B., Pettus J., and Hirsch I. B.. 2018. “Clinical Implications of Real‐Time and Intermittently Scanned Continuous Glucose Monitoring.” Diabetes Care 41, no. 11: 2265–2274. [DOI] [PubMed] [Google Scholar]
  39. Ehrhardt, N. , and Al Zaghal E.. 2019. “Behavior Modification in Prediabetes and Diabetes: Potential Use of Real‐Time Continuous Glucose Monitoring.” Journal of Diabetes Science and Technology 13, no. 2: 271–275. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Ehrhardt, N. , and Al Zaghal E.. 2020. “Continuous Glucose Monitoring as a Behavior Modification Tool.” Clinical Diabetes 38, no. 2: 126–131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Elsayed, H. H. , and Saleh R. T.. 2024. “Review of: Nutritional Genomics and Precision Nutrition.” Bulletin of the National Nutrition Institute of the Arab Republic of Egypt 64, no. 2: 204–234. [Google Scholar]
  42. Engler, S. , Fields S., Leach W., and Van Loon M.. 2022. “Real‐Time Continuous Glucose Monitoring as a Behavioral Intervention Tool for T2D: A Systematic Review.” Journal of Technology in Behavioral Science 7, no. 2: 252–263. [Google Scholar]
  43. Fanelli, S. , Holley S., Pratt K., Czerwinski S., Evans K., and Taylor C.. 2023. “A Primary Care Telenutrition Counseling Trial for Mid‐Life Adults at Risk for Cardiovascular Disease.” Journal of the Academy of Nutrition and Dietetics 123: A29. [Google Scholar]
  44. Ferguson, L. R. , De Caterina R., Görman U., et al. 2016. “Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalised Nutrition: Part 1‐Fields of Precision Nutrition.” Lifestyle Genomics 9, no. 1: 12–27. [DOI] [PubMed] [Google Scholar]
  45. Fleming, G. A. , Petrie J. R., Bergenstal R. M., Holl R. W., Peters A. L., and Heinemann L.. 2020. “Diabetes Digital App Technology: Benefits, Challenges, and Recommendations. A Consensus Report by the European Association for the Study of Diabetes (EASD) and the American Diabetes Association (ADA) Diabetes Technology Working Group.” Diabetes Care 43, no. 1: 250–260. [DOI] [PubMed] [Google Scholar]
  46. Forster, H. , Walsh M. C., Gibney M. J., Brennan L., and Gibney E. R.. 2016. “Personalised Nutrition: The Role of New Dietary Assessment Methods.” Proceedings of the Nutrition Society 75, no. 1: 96–105. [DOI] [PubMed] [Google Scholar]
  47. Franzago, M. , Fraticelli F., Stuppia L., and Vitacolonna E.. 2019. “Nutrigenetics, Epigenetics and Gestational Diabetes: Consequences in Mother and Child.” Epigenetics 14, no. 3: 215–235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Ginsburg, G. S. , Picard R. W., and Friend S. H.. 2024. “Key Issues as Wearable Digital Health Technologies Enter Clinical Care.” New England Journal of Medicine 390, no. 12: 1118–1127. [DOI] [PubMed] [Google Scholar]
  49. Gkouskou, K. K. , Grammatikopoulou M. G., Lazou E., Vasilogiannakopoulou T., Sanoudou D., and Eliopoulos A. G.. 2024. “A Genomics Perspective of Personalized Prevention and Management of Obesity.” Human Genomics 18, no. 1: 4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Goetz, L. H. , and Schork N. J.. 2018. “Personalized Medicine: Motivation, Challenges, and Progress.” Fertility and Sterility 109, no. 6: 952–963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Gomis‐Pastor, M. , Berdún J., Borrás‐Santos A., et al. 2024. “Clinical Validation of Digital Healthcare Solutions: State of the Art, Challenges and Opportunities.” Healthcare (Basel) 12, no. 11: 1057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Goni, L. , Cuervo M., Milagro F. I., and Martínez J. A.. 2016. “Future Perspectives of Personalized Weight Loss Interventions Based on Nutrigenetic, Epigenetic, and Metagenomic Data.” Journal of Nutrition 146, no. 4: 905S–912S. [DOI] [PubMed] [Google Scholar]
  53. Gopal, R. K. , Ganesh P. S., and Pathoor N. N.. 2024. “Synergistic Interplay of Diet, Gut Microbiota, and Insulin Resistance: Unraveling the Molecular Nexus.” Molecular Nutrition & Food Research 68: 2400677. [DOI] [PubMed] [Google Scholar]
  54. Grande, D. , Marti X. L., Feuerstein‐Simon R., et al. 2020. “Health Policy and Privacy Challenges Associated With Digital Technology.” JAMA Network Open 3, no. 7: e208285. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Grimani, A. , Taj U., Read D., and Vlaev I.. 2024. “Using Games to Simulate Medication Adherence and Non‐Adherence: An Application of Gamified Behavioral Simulation.” JMIR Serious Games 12: e47141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Guizar‐Heredia, R. , Noriega L. G., Rivera A. L., et al. 2023. “A New Approach to Personalized Nutrition: Postprandial Glycemic Response and Its Relationship to Gut Microbiota.” Archives of Medical Research 54, no. 3: 176–188. [DOI] [PubMed] [Google Scholar]
  57. Haslam, D. E. , McKeown N. M., Herman M. A., Lichtenstein A. H., and Dashti H. S.. 2018. “Interactions Between Genetics and Sugar‐Sweetened Beverage Consumption on Health Outcomes: A Review of Gene–Diet Interaction Studies.” Frontiers in Endocrinology 8: 368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Hegedus, E. , Salvy S. J., Wee C. P., et al. 2021. “Use of Continuous Glucose Monitoring in Obesity Research: A Scoping Review.” Obesity Research & Clinical Practice 15, no. 5: 431–438. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Heianza, Y. , and Qi L.. 2017. “Gene‐Diet Interaction and Precision Nutrition in Obesity.” International Journal of Molecular Sciences 18, no. 4: 787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  60. Hemanth, K. S. , Fathima N., and Sridhar G. D.. 2025. “Hormone Balancing Through Nutrition: Nutritional Strategies and AI Tools to Balance Hormones Associated With PCOS.” In AI‐Based Nutritional Intervention in Polycystic Ovary Syndrome (PCOS), 213–231. Springer Nature Singapore. [Google Scholar]
  61. Hinchliffe, N. , Capehorn M. S., Bewick M., and Feenie J.. 2022. “The Potential Role of Digital Health in Obesity Care.” Advances in Therapy 39, no. 10: 4397–4412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Hoevenaars, F. P. , Berendsen C. M., Pasman W. J., et al. 2020. “Evaluation of Food‐Intake Behavior in a Healthy Population: Personalized vs. One‐Size‐Fits‐All.” Nutrients 12, no. 9: 2819. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Huang, B. , An H., Chu J., et al. 2025. “Glucose‐Responsive and Analgesic Gel for Diabetic Subcutaneous Abscess Treatment by Simultaneously Boosting Photodynamic Therapy and Relieving Hypoxia.” Advanced Science 12: e02830. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Huang, C. , Xu S., Chen R., et al. 2024. “Assessing Causal Associations of Bile Acids With Obesity Indicators: A Mendelian Randomization Study.” Medicine 103, no. 25: e38610. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Huang, L. , Huhulea E. N., Abraham E., et al. 2025. “The Role of Artificial Intelligence in Obesity Risk Prediction and Management: Approaches, Insights, and Recommendations.” Medicina 61, no. 2: 358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Jaacks, L. M. , Vandevijvere S., Pan A., et al. 2019. “The Obesity Transition: Stages of the Global Epidemic.” Lancet Diabetes & Endocrinology 7, no. 3: 231–240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Jamiołkowska, M. , Jamiołkowska I., Łuczyński W., Tołwińska J., Bossowski A., and Głowińska Olszewska B.. 2016. “Impact of Real‐Time Continuous Glucose Monitoring Use on Glucose Variability and Endothelial Function in Adolescents With Type 1 Diabetes: New Technology—New Possibility to Decrease Cardiovascular Risk?” Journal of Diabetes Research 2016, no. 1: 4385312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Jia, X. , Xuan L., Dai H., et al. 2021. “Fruit Intake, Genetic Risk and Type 2 Diabetes: A Population‐Based Gene–Diet Interaction Analysis.” European Journal of Nutrition 60: 1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Joachim, S. , Forkan A. R. M., Jayaraman P. P., Morshed A., and Wickramasinghe N.. 2022. “A Nudge‐Inspired AI‐Driven Health Platform for Self‐Management of Diabetes.” Sensors 22, no. 12: 4620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Johnson, K. B. , Wei W. Q., Weeraratne D., et al. 2021. “Precision Medicine, AI, and the Future of Personalized Health Care.” Clinical and Translational Science 14, no. 1: 86–93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Karter, A. J. , Parker M. M., Moffet H. H., Gilliam L. K., and Dlott R.. 2021. “Association of Real‐Time Continuous Glucose Monitoring With Glycemic Control and Acute Metabolic Events Among Patients With Insulin‐Treated Diabetes.” JAMA 325, no. 22: 2273–2284. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Kassem, H. , Beevi A. A., Basheer S., Lutfi G., Cheikh Ismail L., and Papandreou D.. 2025. “Investigation and Assessment of AI's Role in Nutrition—An Updated Narrative Review of the Evidence.” Nutrients 17, no. 1: 190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Kearns, A. , Moorhead A., Mulvenna M., and Bond R.. 2025. “Assessing the Uses, Benefits, and Limitations of Digital Technologies Used by Health Professionals in Supporting Obesity and Mental Health Communication: Scoping Review.” Journal of Medical Internet Research 27: e58434. [DOI] [PMC free article] [PubMed] [Google Scholar]
  74. Kitazawa, M. , Takeda Y., Hatta M., et al. 2024. “Lifestyle Intervention With Smartphone App and isCGM for People at High Risk of Type 2 Diabetes: Randomized Trial.” Journal of Clinical Endocrinology & Metabolism 109, no. 4: 1060–1070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  75. Klonoff, D. C. 2019. “Behavioral Theory: The Missing Ingredient for Digital Health Tools to Change Behavior and Increase Adherence.” Journal of Diabetes Science and Technology 13, no. 2: 276–281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Kohlmeier, M. , De Caterina R., Ferguson L. R., et al. 2016. “Guide and Position of the International Society of Nutrigenetics/Nutrigenomics on Personalized Nutrition: Part 2‐Ethics, Challenges and Endeavors of Precision Nutrition.” Lifestyle Genomics 9, no. 1: 28–46. [DOI] [PubMed] [Google Scholar]
  77. Kolodziejczyk, A. A. , Zheng D., and Elinav E.. 2019. “Diet–Microbiota Interactions and Personalized Nutrition.” Nature Reviews Microbiology 17, no. 12: 742–753. [DOI] [PubMed] [Google Scholar]
  78. Kwan, Y. H. , Cheng T. Y., Yoon S., et al. 2020. “A Systematic Review of Nudge Theories and Strategies Used to Influence Adult Health Behaviour and Outcome in Diabetes Management.” Diabetes & Metabolism 46, no. 6: 450–460. [DOI] [PubMed] [Google Scholar]
  79. Lagoumintzis, G. , and Patrinos G. P.. 2023. “Triangulating Nutrigenomics, Metabolomics and Microbiomics Toward Personalized Nutrition and Healthy Living.” Human Genomics 17, no. 1: 109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  80. Lee, Y. C. , Christensen J. J., Parnell L. D., et al. 2022. “Using Machine Learning to Predict Obesity Based on Genome‐Wide and Epigenome‐Wide Gene–Gene and Gene–Diet Interactions.” Frontiers in Genetics 12: 783845. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Leshem, A. , Segal E., and Elinav E.. 2020. “The Gut Microbiome and Individual‐Specific Responses to Diet.” mSystems 5, no. 5: 10–1128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  82. Li, C. , Zhang Z., Luo X., et al. 2025. “The Triglyceride–Glucose Index and Its Obesity‐Related Derivatives as Predictors of All‐Cause and Cardiovascular Mortality in Hypertensive Patients: Insights From NHANES Data With Machine Learning Analysis.” Cardiovascular Diabetology 24, no. 1: 47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  83. Li, J. , Wang S., Han X., Zhang G., Zhao M., and Ma L.. 2020. “Spatiotemporal Trends and Influence Factors of Global Diabetes Prevalence in Recent Years.” Social Science & Medicine 256: 113062. [DOI] [PubMed] [Google Scholar]
  84. Liao, Y. , and Schembre S.. 2018. “Acceptability of Continuous Glucose Monitoring in Free‐Living Healthy Individuals: Implications for the Use of Wearable Biosensors in Diet and Physical Activity Research.” JMIR mHealth and uHealth 6, no. 10: e11181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  85. Mackenzie, S. C. , Sainsbury C. A., and Wake D. J.. 2024. “Diabetes and Artificial Intelligence Beyond the Closed Loop: A Review of the Landscape, Promise and Challenges.” Diabetologia 67, no. 2: 223–235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Maeckelberghe, E. , Zdunek K., Marceglia S., Farsides B., and Rigby M.. 2023. “The Ethical Challenges of Personalized Digital Health.” Frontiers in Medicine 10: 1123863. [DOI] [PMC free article] [PubMed] [Google Scholar]
  87. Mamede, A. , Noordzij G., Jongerling J., Snijders M., Schop‐Etman A., and Denktas S.. 2021. “Combining Web‐Based Gamification and Physical Nudges With an App (MoveMore) to Promote Walking Breaks and Reduce Sedentary Behavior of Office Workers: Field Study.” Journal of Medical Internet Research 23, no. 4: e19875. [DOI] [PMC free article] [PubMed] [Google Scholar]
  88. Mansour, S. , Alkhaaldi S. M., Sammanasunathan A. F., Ibrahim S., Farhat J., and Al‐Omari B.. 2024. “Precision Nutrition Unveiled: Gene–Nutrient Interactions, Microbiota Dynamics, and Lifestyle Factors in Obesity Management.” Nutrients 16, no. 5: 581. [DOI] [PMC free article] [PubMed] [Google Scholar]
  89. Marcum, J. A. 2020. “Nutrigenetics/Nutrigenomics, Personalized Nutrition, and Precision Healthcare.” Current Nutrition Reports 9: 338–345. [DOI] [PubMed] [Google Scholar]
  90. Mathers, J. C. 2019. “Paving the Way to Better Population Health Through Personalised Nutrition.” EFSA Journal 17: e170713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. Mathews, S. C. , McShea M. J., Hanley C. L., Ravitz A., Labrique A. B., and Cohen A. B.. 2019. “Digital Health: A Path to Validation.” npj Digital Medicine 2, no. 1: 38. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Matusheski, N. V. , Caffrey A., Christensen L., et al. 2021. “Diets, Nutrients, Genes and the Microbiome: Recent Advances in Personalised Nutrition.” British Journal of Nutrition 126, no. 10: 1489–1497. [DOI] [PMC free article] [PubMed] [Google Scholar]
  93. Mehrotra, A. , and Mehrotra A.. 2024. “Artificial Intelligence in Nutritional Planning and Diet Management.” International Journal of Innovations in Science, Engineering and Management 3: 259–262. [Google Scholar]
  94. Michel, M. , and Burbidge A.. 2019. “Nutrition in the Digital Age‐How Digital Tools Can Help to Solve the Personalized Nutrition Conundrum.” Trends in Food Science & Technology 90: 194–200. [Google Scholar]
  95. Miraghajani, M. , Salehi R., and Hossein H.. 2017. “Prenatal Nutrition Exposure Leading to Adult Obesity, Diabetes, and Hypertension.” In Nutrigenomics and Nutraceuticals, 377–404. CRC Press. [Google Scholar]
  96. Mishra, U. N. , Jena D., Sahu C., et al. 2022. “Nutrigenomics: An Inimitable Interaction Amid Genomics, Nutrition and Health.” Innovative Food Science & Emerging Technologies 82: 103196. [Google Scholar]
  97. Mondal, S. , and Panda D.. 2021. “Nutrigenomics: An Interface of Gene‐Diet‐Disease Interaction.” In Mineral Deficiencies: Electrolyte Disturbances, Genes, Diet and Disease Interface. IntechOpen. [Google Scholar]
  98. Moon, S. J. , Kim K. S., Lee W. J., Lee M. Y., Vigersky R., and Park C. Y.. 2023. “Efficacy of Intermittent Short‐Term Use of a Real‐Time Continuous Glucose Monitoring System in Non‐Insulin–Treated Patients With Type 2 Diabetes: A Randomized Controlled Trial.” Diabetes, Obesity and Metabolism 25, no. 1: 110–120. [DOI] [PubMed] [Google Scholar]
  99. Moore, J. B. 2020. “From Personalised Nutrition to Precision Medicine: The Rise of Consumer Genomics and Digital Health.” Proceedings of the Nutrition Society 79, no. 3: 300–310. [DOI] [PubMed] [Google Scholar]
  100. Mortazavi, B. J. , and Gutierrez‐Osuna R.. 2023. “A Review of Digital Innovations for Diet Monitoring and Precision Nutrition.” Journal of Diabetes Science and Technology 17, no. 1: 217–223. [DOI] [PMC free article] [PubMed] [Google Scholar]
  101. Ndimele, S. , Carpenter M. L., Cho J. H., and Kim H. D.. 2017. “Nutrigenomics Coupling With Other OMICS Platform Enhance Personalized Health Care in Metabolic Disorders.” Global Journal of Obesity, Diabetes and Metabolic Syndrome 4, no. 1: 5–8. [Google Scholar]
  102. Nehete, S. P. 2023. “Diet Management for Diabetes Patients Using AI.” In Ambient Assisted Living (AAL) Technologies, 147–161. CRC Press. [Google Scholar]
  103. Nettleton, J. A. , Follis J. L., Ngwa J. S., et al. 2015. “Gene× Dietary Pattern Interactions in Obesity: Analysis of up to 68 317 Adults of European Ancestry.” Human Molecular Genetics 24, no. 16: 4728–4738. [DOI] [PMC free article] [PubMed] [Google Scholar]
  104. O'connor, S. , Hanlon P., O'donnell C. A., Garcia S., Glanville J., and Mair F. S.. 2016. “Understanding Factors Affecting Patient and Public Engagement and Recruitment to Digital Health Interventions: A Systematic Review of Qualitative Studies.” BMC Medical Informatics and Decision Making 16: 1–15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  105. Ogurtsova, K. , da Rocha Fernandes J. D., Huang Y., et al. 2017. “IDF Diabetes Atlas: Global Estimates for the Prevalence of Diabetes for 2015 and 2040.” Diabetes Research and Clinical Practice 128: 40–50. [DOI] [PubMed] [Google Scholar]
  106. Ojo, T. F. , Akpor O. A., Talabi Y. J., and Afolalu A. S.. 2025. “AI‐Powered Platforms for Interactive Nutrition Education Based on WHO (World Health Organization) Guidelines–An Overview.” ABUAD Journal of Engineering Research and Development (AJERD) 8, no. 1: 161–168. [Google Scholar]
  107. Orte, S. , Migliorelli C., Sistach‐Bosch L., Gómez‐Martínez M., and Boqué N.. 2023. “A Tailored and Engaging mHealth Gamified Framework for Nutritional Behaviour Change.” Nutrients 15, no. 8: 1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  108. Ortega, Á. , Berná G., Rojas A., Martín F., and Soria B.. 2017. “Gene‐Diet Interactions in Type 2 Diabetes: The Chicken and Egg Debate.” International Journal of Molecular Sciences 18, no. 6: 1188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  109. Paccoud, I. , Leist A. K., Schwaninger I., van Kessel R., and Klucken J.. 2024. “Socio‐Ethical Challenges and Opportunities for Advancing Diversity, Equity, and Inclusion in Digital Medicine.” Digital Health 10. 10.1177/20552076241277705. [DOI] [PMC free article] [PubMed] [Google Scholar]
  110. Palmnäs, M. , Brunius C., Shi L., et al. 2020. “Perspective: Metabotyping—A Potential Personalized Nutrition Strategy for Precision Prevention of Cardiometabolic Disease.” Advances in Nutrition 11, no. 3: 524–532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  111. Pang, W.‐M. , Tian V.‐I., and Poon G.. 2018. “Food Consumption Tracker With Health Advises by Food Photos and Labels.” ICST Transactions on Ambient Systems 5, no. 17: 154374. [Google Scholar]
  112. Partridge, S. R. , and Redfern J.. 2018. “Strategies to Engage Adolescents in Digital Health Interventions for Obesity Prevention and Management.” Healthcare (Basel) 6, no. 3: 70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  113. Patel, M. S. , Small D. S., Harrison J. D., et al. 2019. “Effectiveness of Behaviorally Designed Gamification Interventions With Social Incentives for Increasing Physical Activity Among Overweight and Obese Adults Across the United States: The STEP UP Randomized Clinical Trial.” JAMA Internal Medicine 179, no. 12: 1624–1632. [DOI] [PMC free article] [PubMed] [Google Scholar]
  114. Patel, M. S. , Small D. S., Harrison J. D., et al. 2021. “Effect of Behaviorally Designed Gamification With Social Incentives on Lifestyle Modification Among Adults With Uncontrolled Diabetes: A Randomized Clinical Trial.” JAMA Network Open 4, no. 5: e2110255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  115. Porter, M. , Fonda S., Swigert T., and Ehrhardt N.. 2022. “Real‐Time Continuous Glucose Monitoring to Support Self‐Care: Results From a Pilot Study of Patients With Type 2 Diabetes.” Journal of Diabetes Science and Technology 16, no. 2: 578–580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  116. Prasad, G. , Padhiary M., Hoque A., and Kumar K.. 2025. “AI‐Driven Personalized Nutrition Apps and Platforms for Enhanced Diet and Wellness.” In Food in the Metaverse and Web 3.0 Era: Intersecting Food, Technology, and Culture, 125–158. IGI Global Scientific Publishing. [Google Scholar]
  117. Priesterroth, L. , Grammes J., Holtz K., Reinwarth A., and Kubiak T.. 2019. “Gamification and Behavior Change Techniques in Diabetes Self‐Management Apps.” Journal of Diabetes Science and Technology 13, no. 5: 954–958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  118. Priyadharshini, K. , Dhivya K., Kamalesh M. S., Prasad S. S., Chakravarthy D., and Sudhakar M.. 2025. “Personalized Nutrition in Healthcare Using IoT for Tailored Dietary Solutions.” In Integrating Artificial Intelligence Into the Energy Sector, 401–424. IGI Global Scientific Publishing. [Google Scholar]
  119. Ramos‐Lopez, O. , Martínez J. A., and Milagro F. I.. 2022. “Holistic Integration of Omics Tools for Precision Nutrition in Health and Disease.” Nutrients 14, no. 19: 4074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  120. Reddy, V. S. , Palika R., Ismail A., Pullakhandam R., and Reddy G. B.. 2018. “Nutrigenomics: Opportunities & Challenges for Public Health Nutrition.” Indian Journal of Medical Research 148, no. 5: 632–641. [DOI] [PMC free article] [PubMed] [Google Scholar]
  121. Regan, J. A. , and Shah S. H.. 2020. “Obesity Genomics and Metabolomics: A Nexus of Cardiometabolic Risk.” Current Cardiology Reports 22: 1–19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  122. Reilly, J. J. , El‐Hamdouchi A., Diouf A., Monyeki A., and Somda S. A.. 2018. “Determining the Worldwide Prevalence of Obesity.” Lancet 391, no. 10132: 1773–1774. [DOI] [PubMed] [Google Scholar]
  123. Roglic, G. 2016. “WHO Global Report on Diabetes: A Summary.” International Journal of Noncommunicable Diseases 1, no. 1: 3–8. [Google Scholar]
  124. Romero‐Tapiador, S. , Lacruz‐Pleguezuelos B., Tolosana R., et al. 2023. “AI4FoodDB: A Database for Personalized e‐Health Nutrition and Lifestyle Through Wearable Devices and Artificial Intelligence.” Database 2023: baad049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  125. Saeedi, P. , Petersohn I., Salpea P., et al. 2019. “Global and Regional Diabetes Prevalence Estimates for 2019 and Projections for 2030 and 2045: Results From the International Diabetes Federation Diabetes Atlas.” Diabetes Research and Clinical Practice 157: 107843. [DOI] [PubMed] [Google Scholar]
  126. Sarma, A. D. , and Devi M.. 2025. “Artificial Intelligence in Diabetes Management: Transformative Potential, Challenges, and Opportunities in Healthcare.” Hormones (Athens, Greece) 24: 1–16. [DOI] [PubMed] [Google Scholar]
  127. Schembre, S. M. , Liao Y., and Jospe M. R.. 2020. “Continuous Glucose Monitors as Wearable Lifestyle Behavior Change Tools in Obesity and Diabetes.” In Obesity and Diabetes: Scientific Advances and Best Practice, 591–603. Springer. [Google Scholar]
  128. Seidell, J. C. , and Halberstadt J.. 2015. “The Global Burden of Obesity and the Challenges of Prevention.” Annals of Nutrition and Metabolism 66, no. Suppl. 2: 7–12. [DOI] [PubMed] [Google Scholar]
  129. Sekar, P. , Ventura E. F., Dhanapal A. C. T., et al. 2023. “Gene–Diet Interactions on Metabolic Disease‐Related Outcomes in Southeast Asian Populations: A Systematic Review.” Nutrients 15, no. 13: 2948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  130. Sempionatto, J. R. , Montiel V. R. V., Vargas E., Teymourian H., and Wang J.. 2021. “Wearable and Mobile Sensors for Personalized Nutrition.” ACS Sensors 6, no. 5: 1745–1760. [DOI] [PubMed] [Google Scholar]
  131. Shah, N. , and Adusumalli S.. 2020. “Nudges and the Meaningful Adoption of Digital Health.” Personalized Medicine 17, no. 6: 429–433. [DOI] [PubMed] [Google Scholar]
  132. Shamanna, P. , Joshi S., Thajudeen M., et al. 2024. “Personalized Nutrition in Type 2 Diabetes Remission: Application of Digital Twin Technology for Predictive Glycemic Control.” Frontiers in Endocrinology 15: 1485464. [DOI] [PMC free article] [PubMed] [Google Scholar]
  133. Sin, J. , Franz R. L., Munteanu C., and Barbosa Neves B.. 2021. “Digital Design Marginalization: New Perspectives on Designing Inclusive Interfaces.” In Proceedings of the 2021 CHI Conference on Human Factors in Computing Systems (pp. 1–11).
  134. Singar, S. , Nagpal R., Arjmandi B. H., and Akhavan N.. 2024. “Personalized Nutrition: Tailoring Dietary Recommendations Through Genetic Insights.” Nutrients 16, no. 16: 2673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  135. Solomon, D. H. , and Rudin R. S.. 2020. “Digital Health Technologies: Opportunities and Challenges in Rheumatology.” Nature Reviews Rheumatology 16, no. 9: 525–535. [DOI] [PubMed] [Google Scholar]
  136. Sun, H. , Saeedi P., Karuranga S., et al. 2022. “IDF Diabetes Atlas: Global, Regional and Country‐Level Diabetes Prevalence Estimates for 2021 and Projections for 2045.” Diabetes Research and Clinical Practice 183: 109119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  137. Suzuki, T. , Aoki J., Abe K., et al. 2024. “Rationale and Trial Design of Feedbacks Using Behavioural Economic Theories on STEP Counts (FOOTSTEPS) Trial in Patients With Cardiovascular Disease.” CJC Open 7: 535–544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  138. Taylor, P. J. , Thompson C. H., Luscombe‐Marsh N. D., Wycherley T. P., Wittert G., and Brinkworth G. D.. 2019. “Efficacy of Real‐Time Continuous Glucose Monitoring to Improve Effects of a Prescriptive Lifestyle Intervention in Type 2 Diabetes: A Pilot Study.” Diabetes Therapy 10: 509–522. [DOI] [PMC free article] [PubMed] [Google Scholar]
  139. Torres, N. , and Tovar A. R.. 2021. “The Present and Future of Personalized Nutrition.” Revista de Investigación Clínica 73, no. 5: 321–325. [DOI] [PubMed] [Google Scholar]
  140. Tripyla, A. , Herzig D., Joachim D., et al. 2020. “Performance of a Factory‐Calibrated, Real‐Time Continuous Glucose Monitoring System During Elective Abdominal Surgery.” Diabetes, Obesity and Metabolism 22, no. 9: 1678–1682. [DOI] [PubMed] [Google Scholar]
  141. van den Brink, W. J. , Broek T. J., Palmisano S., Wopereis S., and de Hoogh I. M.. 2022. “Digital Biomarkers for Personalized Nutrition: Predicting Meal Moments and Interstitial Glucose With Non‐Invasive, Wearable Technologies.” Nutrients 14, no. 21: 4465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  142. Vegesna, V. 2024. “AI‐Driven Personalized Nutrition: A System for Tailored Dietary Recommendations.” International Research Journal of Computer Science 11, no. 7: 545–550. [Google Scholar]
  143. Verma, M. , Hontecillas R., Tubau‐Juni N., Abedi V., and Bassaganya‐Riera J.. 2018. “Challenges in Personalized Nutrition and Health.” Frontiers in Nutrition 5: 117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  144. Vincenti, A. , Cena H., Casali P. M., Sergenti C., and Giberti H.. 2024. “A Preliminary Investigation to Advance Personalized Nutrition Strategies for Athletes.” In 2024 IEEE International Workshop on Sport, Technology and Research (STAR) (pp. 240–245). IEEE.
  145. von Huben, A. , Howell M., Carrello J., et al. 2022. “Application of a Health Technology Assessment Framework to Digital Health Technologies That Manage Chronic Disease: A Systematic Review.” International Journal of Technology Assessment in Health Care 38, no. 1: e9. [DOI] [PubMed] [Google Scholar]
  146. Wang, D. D. , and Hu F. B.. 2018. “Precision Nutrition for Prevention and Management of Type 2 Diabetes.” Lancet Diabetes & Endocrinology 6, no. 5: 416–426. [DOI] [PubMed] [Google Scholar]
  147. Watson, A. , Chapman R., Shafai G., and Maricich Y. A.. 2023. “FDA Regulations and Prescription Digital Therapeutics: Evolving With the Technologies They Regulate.” Frontiers in Digital Health 5: 1086219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  148. Westerman, K. E. , Miao J., Chasman D. I., et al. 2021. “Genome‐Wide Gene–Diet Interaction Analysis in the UK Biobank Identifies Novel Effects on Hemoglobin A1c.” Human Molecular Genetics 30, no. 18: 1773–1783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  149. Wu, Y. , Perng W., and Peterson K. E.. 2020. “Precision Nutrition and Childhood Obesity: A Scoping Review.” Metabolites 10, no. 6: 235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  150. Xiong, X. , Xue Y., Cai Y., He J., and Su H.. 2024. “Prediction of Personalised Postprandial Glycaemic Response in Type 1 Diabetes Mellitus.” Frontiers in Endocrinology 15: 1423303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  151. Xu, Z. , Yu D., Yin X., Zheng F., and Li H.. 2017. “Socioeconomic Status Is Associated With Global Diabetes Prevalence.” Oncotarget 8, no. 27: 44434–44439. [DOI] [PMC free article] [PubMed] [Google Scholar]
  152. Yeşilyurt, N. , Yılmaz B., Ağagündüz D., and Capasso R.. 2022. “Microbiome‐Based Personalized Nutrition as a Result of the 4.0 Technological Revolution: A Mini Literature Review.” Process Biochemistry 121: 257–262. [Google Scholar]
  153. Zahedani, A. D. , McLaughlin T., Veluvali A., et al. 2023. “Digital Health Application Integrating Wearable Data and Behavioral Patterns Improves Metabolic Health.” npj Digital Medicine 6, no. 1: 216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  154. Zeevi, D. , Korem T., Zmora N., et al. 2015. “Personalized Nutrition by Prediction of Glycemic Responses.” Cell 163, no. 5: 1079–1094. [DOI] [PubMed] [Google Scholar]
  155. Zeinalian, R. , Ahmadikhatir S., Esfahani E. N., Namazi N., and Larijani B.. 2022. “The Roles of Personalized Nutrition in Obesity and Diabetes Management: A Review.” Journal of Diabetes & Metabolic Disorders 21, no. 1: 1119–1127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  156. Zeisel, S. H. 2020. “Precision (Personalized) Nutrition: Understanding Metabolic Heterogeneity.” Annual Review of Food Science and Technology 11, no. 1: 71–92. [DOI] [PubMed] [Google Scholar]
  157. Zhuang, P. , Liu X., Li Y., et al. 2021. “Effect of Diet Quality and Genetic Predisposition on Hemoglobin A1c and Type 2 Diabetes Risk: Gene‐Diet Interaction Analysis of 357,419 Individuals.” Diabetes Care 44, no. 11: 2470–2479. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data supporting the findings of this study is available from the corresponding author upon reasonable request.


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