Abstract
Objective
The recommendation of free sugar reduction in dental practice is mostly given with regard to caries prevention but has also further health impacts. This umbrella review aimed to comprehensively display the shared health consequences of sugar consumption in both oral and general health.
Materials and methods
Within an umbrella review, two independent reviewers identified and analysed systematic reviews examining free sugar consumption alone or as a part of dietary patterns and its association to described diseases in three databases (Epistemonikos, Pubmed, Cochrane Library). Electronic databases were searched up to March 2026, findings were synthesised narratively. Risk of bias was assessed using AMSTAR-2.
Results
The literature search identified 10,593 articles, of which 633 were further assessed for eligibility. Finally, 228 articles were included after full-text analysis. Results showed that sugar intake was consistently associated with increased risks of 18 generalised negative health outcomes. Strongest evidence was found for type 2 diabetes, obesity, cardiovascular and all-cause mortality, oral diseases, irritable bowel syndrome, and cognitive disorders. Furthermore, a positive association was found between excessive sugar consumption and cancer, non-alcoholic fatty liver disease, kidney disease, gout, asthma, poor sleep, reduced bone density, mood disorders, telomere shortening, and fertility impairments. AMSTAR-2 showed that most reviews had low or critically low methodological quality, while about one third demonstrated moderate to high confidence. Most studies (68%) investigated sugar in form of sugar-sweetened beverages.
Conclusions
Within the limitations of this umbrella review, available evidence indicates that avoiding free sugar intake contributes to both reduced chronic disease burden and improved oral health. Against this background, avoiding free sugar, as recommended by dentists, is a key shared health factor that should be emphasized in the context of caries, periodontal disease, and in terms of general primary prevention.
Clinical relevance
Dental advised and assisted sugar reduction is an important preventive measure not only for oral health but also for several general health outcomes. After synthesizing and evaluating the available systematic reviews, this study highlights the crucial need to reduce sugar consumption as an important factor in improving both systemic and oral health.
Systematic review registration
The systematic review was registered in the international register for systematic reviews Prospero. Systematic review registration CRD42023380458.
Supplementary Information
The online version contains supplementary material available at https://doi.org/10.1007/s00784-026-07191-1.
Keywords: Sugar, Sugar-sweetened beverages, Artificially sweetened beverages, Oral health, Obesity, Cardiometabolic risk factors
Introduction
Excessive sugar consumption has become a significant public health issue since the start of industrial sugar production. A growing body of evidence links high sugar intake (particularly sugar-sweetened beverages (SSB)) to obesity, type 2 diabetes mellitus (T2DM), cardiovascular diseases, non-alcoholic fatty liver disease (NAFLD), and several oral health conditions, such as dental caries [1–7] and periodontitis [8–10]. These associations are explained by multifactorial mechanisms which include chronic inflammation, oxidative stress, total calories overload, insulin resistance, disproportionate satiety, changes in oral and gut microbiota and bacterial metabolism/metabolites [11, 12]. The World Health Organization (WHO) estimates that dental caries affects approximately 60–90% of school-aged children and most adults worldwide [4]. Meanwhile, periodontal diseases, with a global prevalence of around 50%, are a leading cause of tooth loss and reduced quality of life and are increasingly associated with multiple systemic conditions [8]. Periodontal disease affects approximately 3.9 billion people worldwide and ranks as the 11th most prevalent disease [10].
Dental caries is defined as the destruction of tooth enamel caused by acids produced by cariogenic bacteria during the fermentation of sugars and starches [13]. Caries develops through the interaction of bacteria, fermentable carbohydrates, and susceptible tooth surfaces and progresses when demineralization exceeds the protective effects of saliva and remineralization. High and frequent consumption of free sugars promotes acid production by oral bacteria, leading to enamel demineralisation and an increased risk of dental caries. According to the World Health Organization, free sugars comprise monosaccharides and disaccharides added to foods and beverages by manufacturers, cooks or consumers, together with sugars naturally present in honey, syrups, fruit juices and fruit juice concentrates [14]. In contrast, sugars naturally present in whole foods are typically less harmful to oral health, as they are consumed with fibres and nutrients that reduce their cariogenic potential [15]. In addition, Western diets rich in saturated fats and processed carbohydrates are associated with chronic inflammation and, consequently, an increased incidence of periodontal diseases [10]. Based on moderate-quality evidence, a strong recommendation supports limiting free sugar intake to less than 10% of total energy intake, while especially the focus on oral health underpins a conditional recommendation to further reduce intake to below 5% of energy intake [14]. Accordingly, lowering free sugar intake to these values can be recommended to improve health outcomes [5]. High intake of non-milk extrinsic sugars increases the risk of dental caries and is also linked to obesity and diabetes, which is why their reduction is recommended for both oral and general health [16]. Consistently, dental caries experience is lower in children and adults when free sugar intake is below the WHO recommendation, although the cariogenicity of other fermentable carbohydrates remains debated. Starches, particularly wheat-based grains, constitute a major component of Western diets and account for approximately 40–75% of total energy intake [7]. Despite the WHO recommendation, sugar consumption in industrialised regions like the European Union remains far above the recommended thresholds with approximately 60–120 g of total sugar intake [17].
There is evidence that the recommendation to avoid sugar has changed in dentistry in terms of its severity and strength, particularly due to the widespread introduction of fluoride in caries prevention. While the standard recommendation of dentists before World War II was a low-carbohydrate diet and vitamin D check, in the following decades, the central recommendation of fluoridated oral hygiene became increasingly dominant [18]. This shift in the prioritization of preventive approaches is particularly relevant in light of the common risk factor approach [16]. The concept of the common risk factor approach proposes that several chronic diseases share a limited number of modifiable behavioural risk factors. Excessive free sugar intake represents one of the most important examples of such shared risk factors because it contributes to both oral diseases and multiple non-communicable diseases. Consequently, dietary counselling delivered in dental practice may provide benefits extending far beyond oral health.
Umbrella reviews, which systematically evaluate and synthesize evidence from existing systematic reviews, provide an opportunity to concentrate an evidence-based summary of the overall strength, consistency, and quality of associations between sugar intake and health outcomes. To the best of the authors’ knowledge, there is currently only one existing umbrella review by Huang et al. that has summarised and analysed the negative health effects of regular sugar consumption [19]. The authors were able to include 73 studies, showing significant associations of sugar consumption with T2DM, body weight, obesity, metabolic syndrome, coronary heart disease (CHD), LDL-cholesterol, hypertension, and pancreatic cancer. However, their review mainly focused on metabolic outcomes and only included systematic reviews eligible for secondary quantitative analyses. Consequently, oral diseases, oral microbiome alterations and several additional systemic outcomes were only incompletely represented.
Therefore, the aims of this umbrella review were [1] to systematically summarise evidence from systematic reviews investigating sugar consumption and health [2], to compare evidence across oral and systemic health domains [3], to discuss the implications for preventive dentistry within the framework of the common risk factor approach supporting sugar reduction as a relevant public health and preventive strategy [9].
We hypothesised that higher dietary sugar intake, particularly free sugars and sugar-sweetened beverages, is consistently associated with adverse oral and systemic health outcomes across the available systematic review evidence.
Materials and methods
Study design
The umbrella review systematically searched relevant scientific databases for eligible studies, including Epistemonikos, PubMed, and the Cochrane Library, in accordance with Cochrane methodological criteria. There were no restrictions on study design, and included articles that investigated the intake of different types of sugars and reported on human health outcomes. Duplicates were removed both manually and using Covidence (Veritas Health Innovation Ltd, Australia). The systematic review was registered in the international register for systematic reviews Prospero (CRD42023380458).
For the literature analysis, a search strategy was developed to achieve the broadest possible inclusion of studies addressing the effects of sugar consumption. The search term “sugar” was applied across the MeSH term (keyword search), text word, and title/abstract fields. Combined using the Boolean operator “OR”, the resulting search string was:
((sugar[Text Word]) OR (sugar[Title/Abstract])) OR (sugar[MeSH Terms]). No filters or limits were applied.
Eligibility criteria
To be included in the umbrella-review, studies were supposed to meet the following inclusion criteria:
systematic review, with or without meta-analysis.
focus on human populations.
examination of any health outcome related to sugar intake.
Sugar could be investigated in various chemical forms, including monosaccharides, disaccharides, oligosaccharides, and polysaccharides; from different sources, including free and added sugars; and as part of dietary patterns involving sugar-sweetened beverages (SSB), soft drinks, sweets, chocolate, fruits, vegetables, or milk. Studies asserting the effects of honey and orange juice were included as well.
Exclusion criteria were:
Primary studies (including randomized controlled trials, quasi-experimental studies, cohort studies, case–control studies, and cross-sectional studies).
Studies lacking a clearly defined systematic methodology (reproducible literature search, predefined eligibility criteria and a structured evidence synthesis).
Studies based on animal or in vitro models.
Studies with insufficiently defined populations, interventions/exposures, comparators, outcomes, or study designs.
Studies not reporting outcomes related to the effects of sugar consumption on human health.
Studies where the full text was not accessible.
Publications not available in English or German.
Studies related to the pain relief in neonates (were excluded during outcomes assessment).
Screening process, data extraction and evidence synthesis
The systematic literature search was conducted independently by two reviewers (ADZ, NW). During the first screening phase, studies were independently assessed based on their titles and abstracts and categorized as “include,” “exclude,” or “maybe.“. Regular meetings involving the entire study group (ADZ, NW, CT, and JPW) were held to discuss the review process and to resolve disagreements regarding study selection and methodological assessment. The screening process was supported by Covidence (Veritas Health Innovation Ltd., Australia), which was used to automatically remove duplicate records and to document the study selection process. In the second screening phase, full-text articles were assessed independently by both reviewers, and a final decision regarding study inclusion or exclusion was made. Within this process, grey literature and reference lists of the included reviews were also screened. After full texts were uploaded and assessed for eligibility, data extraction was performed. During data extraction, two reviewers (ADZ, NW) independently analysed primarily found studies. Disagreements were solved within the whole study group (ADZ, NW, CT, JPW).
Due to the broad scope of this umbrella review, no additional quantitative evidence synthesis was performed. Findings were synthesised narratively and all included studies were classified into predefined subtopics (based on [19]) according to health outcomes and reported effects, and these categories were expanded as necessary. Studies addressing more than one health outcomes were assigned to multiple sections. The various types of sugar listed in the inclusion criteria were noted in the results table and interpreted separately whenever possible. The study followed the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) 2020 protocol.
Risk of bias analysis
The risk of bias analysis was conducted independently by two reviewers (ADZ and NW) using the AMSTAR-2 [20] (A Measurement Tool to Assess Systematic Reviews). Any discrepancies between reviewers were discussed and resolved by consensus. Afterwards, all the studies were categorized into four levels of confidence in quality according to AMSTAR-2 [20] classification.
Results
Data search conducted between July 2025 up to March 2026 revealed a total of 10,593 original articles, of which 9,387 were excluded during the title and abstract screening phase. Of the 633 studies assessed for full-text eligibility, 378 were excluded based on the predefined criteria, including insufficient study setting, outcomes, interventions or study design, use of animal models, lack of access to the full text, absence of English or German language versions, or insufficient reporting on the effects of sugar consumption on human health (see Fig. 1).
Fig. 1.

PRISMA flow diagram of the study selection process, including identification, screening, eligibility assessment, and final inclusion of systematic reviews
Inter-rater reliability between the two primary reviewers (ADZ and NW) showed a Cohen’s kappa (κ) of 0.492, indicating moderate agreement in screening decisions. In cases of uncertainty regarding study inclusion or exclusion, discrepancies were discussed among the reviewers, and consensus was reached through consultation with two other reviewers (CT and JPW).
Finally, a total of 228 included studies which met predefined eligibility criteria were included (Supplementary Table 1). The outcomes were categorized into 18 subtopics (metabolic disorders n = 95, reproduction n = 6, oral health n = 21, cancer n = 14, cardiometabolic risk factors n = 47, all-cause-mortality n = 15, kidney diseases n = 3, blood values n = 13, bone health n = 3, cognition and psyche n = 19, inflammation n = 3, asthma n = 2 and sleep n = 1) to provide the most comprehensive overview to the topic. The Fig. 2 illustrates the distribution of included studies across 18 subtopics, summarizing the types of effects of sugar intake reported in these studies. To the extent that detailed data were available, 132 (68%) studies examined sugar in the form of SSBs, 17 examined sugar in solid form, 12 examined sugar in form of juice, 13 examined fructose, and 20 examined FODMAPs.
Fig. 2.

The total number of studies per health outcome and indicates how many reported significant positive, significant negative, non-significant, or mixed associations with sugar intake. Studies without quantitative analyses are also indicated. A few beneficial health outcomes were associated with fruit juice intake
Metabolic disorders and weight management
Most of the studies (n = 95) focused on the association between sugar intake and metabolic or functional gastrointestinal disorders (type 2 diabetes mellitus (T2DM), gout, irritable bowel syndrome, non-alcoholic fatty liver (NAFLD) and weight management.
Type 2 diabetes mellitus
The research yielded 19 studies [21–39] which focused on the relationship between SSB intake and the risk of and T2DM. Ten studies demonstrated statistically significant positive association between high sugar-sweetened beverage (SSB) intake and T2DM, while two studies confirmed that excessive sugar consumption was associated with elevated blood glucose, insulin resistance, and higher incidence of diabetes [36, 37]. The incidence of T2DM per serving (250–355 ml) of SSB was associated with a 18% increase in normal weighted participants and by 13% in obese ones [31]. The dose-response analyses showed a 25% to 26% increased T2DM risk per serving (approx. 350 ml) per day [22, 29]. Several authors also concluded that metabolic syndrome and obesity were mediators between SSB intake and T2DM [22, 29, 33, 34]. Two articles identified a 21% increased risk of acquired insulin resistance per serving of SSB (250 ml), but no linear dose-response relationship was found [21, 33]. In summary, the included studies demonstrated a risk increase range of 13–31% per serving of SSB per day. Although no significant association was found for fruit juices. The available evidence was based on four studies [33–35, 38] with low and one study [36] with moderate AMSTAR-2 rating, 14 studies showed critically low quality (Supplementary Table 2). Table 1 shows the risk ratio of T2DM caused by SSB intake.
Table 1.
Summary of systematic reviews reporting the association between sugar-sweetened beverage intake and the risk of type 2 diabetes mellitus (T2DM)
Gout and hyperuricemia
A total of eight systematic reviews were found regarding the association between sugar consumption and gout or hyperuricemia [40–47]. All studies found that SSB and fructose consumption were linked to uric acid production. The highest fructose intake (> 11.8% to > 11.9% total energy) was associated with a 65% increased risk of gout development compared with the lowest intake (< 6.9% to < 7.5% total energy) [40]. The risk of gout increased by 28% [45] −77% [41] due to fruit juice intake and from 35% [46] to 108% [43] due to SSB intake, while there was no significant association between whole fruit intake and gout [43]. Evidence regarding uric acid levels was mixed, with some studies suggesting a possible increase, but no consistent harmful effect was demonstrated [47]. The highest SSB intake significantly increased the level of uric acid [41, 42, 45]. There was an overall significant positive association between SSB intake and increased risk of both hyperuricemia and gout. The available evidence was based on three studies [41, 46, 47] with low, one study [45] with moderate, and four studies [40, 42–44] with high AMSTAR-2 quality rating, no study showed critically low quality (Supplementary Table 2).
Irritable bowel syndrome
20 studies were found investigating sugar intake and irritable bowel syndrome (IBS) [48–67]. Eight studies confirmed that low-FODMAP (Fermentable Oligo-, Di-, Monosaccharides and Polyols) diets significantly reduced global IBS symptoms [48–50, 60, 61] and improved abdominal pain (OR = 1.81; [53, 58], bloating, and stool consistency [59]. Three reviews did not find any positive effect of low-FODMAP diets compared to habitual (including regular rye bread and no dietary education) diets [49, 51, 66]. Several reviews reported reduced levels of Bifidobacterium associated with a high-FODMAP diet, with no significant effects on gut microbial diversity or fecal short-chain fatty acids [55, 57]. High sugar intake was significantly associated with increased risk of ulcerative colitis (UC) by 59% [52, 65] and Crohn’s disease by 66% [65]. SSB intake was associated with Crohn’s disease by 58% and UC by 72% [65]. The available evidence was based on five studies [51–53, 58, 63] with low, two studies [50, 65] with moderate, and seven studies [48, 49, 56, 57, 59–61] with high AMSTAR-2 quality rating, five studies [54, 62, 64, 66, 67] showed critically low quality (Supplementary Table 2).
Non-alcoholic fatty liver disease
Six studies investigating the effects of sugar consumption on non-alcoholic fatty liver disease (NAFLD) were included [68–73]. A statistically significant positive association was found in all studies except one [69]. Three studies investigated the association between SSB intake and NAFLD and reported that SSB consumption increased the risk of NAFLD by 39% [68] and 40% [73] compared to non-SSB-consumers. Two meta-analyses found that intrahepatocellular lipids (IHCL) levels increased up to 54% on a hypercaloric high-fructose diet compared to a weight-maintaining diet [70, 71]. No change in liver values was recorded in isocaloric trials [69]. The available evidence was based on one study [71] with low AMSTAR-2 quality rating and five studies [68–70, 72, 73] showing critically low quality (Supplementary Table 2).
Weight management and metabolic syndrome
A total of 43 systematic reviews were found regarding the relationship between sugar consumption and different aspects of weight gain and weight management [34, 74–115]. Of these, 35 reviews analysed the association between SSB intake and obesity/overweight/body weight change across age groups and consistently confirmed a significant positive association. At least one additional serving (250 ml) of SSB per day significantly increased obesity risk up to 18% [75] and waist circumference (WC) by/up to 20% [75]. However, consuming two or more soft drinks per day was associated with an increased risk of obesity up to 50% [84]. The risk of increased body mass index (BMI) caused by SSB intake varied between 31% and 38% [76, 83]. Experimental studies found a weight gain of 1.6 kg over 10 weeks with daily sucrose consumption [81]. A significant positive association was found between SSB intake and higher body fat, whereas 100% fruit juice generally did not show this effect [89, 114]. Each SSB serving was associated to a 5% increase of obesity risk and a 12% risk of abdominal obesity [96]. When SSB intake continued for more than two weeks, it was linked to 0.04 kg/m2 BMI increase in 13-year-old children which contributed to increased body fat in early adulthood [94, 97]. Hypercaloric fructose intake was significantly associated with increased ectopic fat, particularly in the liver and muscles [100] and triglycerides [107]. Breastfeeding was concluded as a factor which was associated with a decreased obesity risk in adulthood [94], whereas early SSB exposure was linked to obesity in adult age [113]. High sugar snack foods were associated with overweight when combined with low vegetable intake [109]. In contrary, one study found that ready-to-eat cereals with added sugar were associated with lower BMI in some groups [112]. Six systematic reviews investigated the link between sugar consumption and metabolic syndrome. Metabolic syndrome (MetS) is defined as a cluster of major health risk factors such as cardiovascular disease and type 2 diabetes [34, 105]. The findings demonstrated that all SSB, total sweetened beverage (TSB), and ASB intake increased the risk of MetS by 56%, 51% and 44%, respectively [104]. Each additional 250 ml of SSB per day increased the risk of MetS by 19%−46% [104, 105]. Additional 335 ml of SSB per day increased the risk of MetS by 14%, whereas 100% fruit juice demonstrated a low risk of metabolic syndrome outcomes [108]. Table 2 shows the summary of systematic reviews reporting the association between SSBs, TSB intake and the risk of weight or metabolic related outcomes.
Table 2.
Summary of systematic reviews reporting the association between sugar-sweetened beverages (SSBs), total sweetened beverages (TSBs) intake and the risk of weight or metabolic related outcomes
| Study | Exposition | Type of outcome | Risk ratio |
|---|---|---|---|
| Qin et al. [74] | SSB | obesity | 12% |
| Ruanpeng et al. [75] | SSB | obesity | 18% |
| Ruanpeng et al. [75] | SSB | increased WC | 20% |
| Malik et al. [81] | SSB | obesity | 60% |
| Neelakantan et al. [83] | SSB | higher BMI | 38% |
| Santos et al. [84] | SSB | obesity | 17%−50% |
| Abbasalizad Farhangi et al. [85] | SSB | obesity | 14% |
| Eugenia Pérez-Morales [90] | SSB | obesity in early childhood | 4% |
| Schlesinger et al. [96] | SSB | overweight/obesity | 20% |
| Schlesinger et al. [96] | SSB | abdominal obesity | 12% |
| Schlesinger et al. [96] | SSB | gaining weight | 23% |
| Te Morenga et al. [98] | SSB | overweight/obesity | 55% |
| Yang et al. [99] | SSB | overweight/obesity | 60% |
| Poorolajal et al. [101] | SSB | obesity | 24% |
| Zhang et al. [104] | SSB | MetS | 56% |
| Zhang et al. [104] | TSB | MetS | 51% |
| Narain et al. [105] | SSB | MetS | 46% |
| Semnani-Azad et al. [108] | SSB | MetS | 14% |
In conclusion, sugar intake, particularly from sugar-sweetened beverages, was consistently associated with weight gain, obesity, and an increased risk of metabolic syndrome. The available evidence was based on 14 studies [34, 74, 77, 82, 84, 85, 94, 95, 103, 104, 109, 111, 112, 114] with low, seven studies [80, 83, 91, 98, 101, 106, 110] with moderate, and four studies [93, 96, 107, 109] with high AMSTAR-2 quality rating, 18 studies [75–79, 81, 87–90, 92, 97, 99, 100, 105, 108, 113, 115] showed critically low quality (Supplementary Table 2).
Reproduction and sugar intake
The umbrella review yielded six articles regarding the general topic reproduction and sugar intake. All articles can be organised in three subtopics: male fertility [116, 117], pregnancy and birth outcomes [118–121].
Male fertility
The umbrella review yielded two systematic reviews which investigated the association between sugar intake and fertility in men [116, 117]. Both highlighted the negative impact of excessive sugar consumption, particularly from sweets and SSBs in form of adversely affected sperm parameters and overall reproductive health [116]. Poor sperm quality (volume, vitality, motility, morphology, and concentration), hormonal levels, the number of spermatozoa and concentration were positively associated with a diet that included processed meat, soy foods, potatoes, full-fat dairy, total dairy products, cheese, coffee, alcohol, SSBs, and sweets. Higher SSB intake was associated with lower sperm motility, though it was unrelated to other semen quality parameters or reproductive hormone levels [117]. Regarding sugar, the study outcomes were limited because the study did not analyse the sugar effects separately. The available evidence was two studies [116, 117] with high AMSTAR-2 quality rating, no studies showed critically low quality (Supplementary Table 2).
Pregnancy and birth outcomes
The literature analysis identified four systematic reviews which investigated the effects of sugar consumption during pregnancy on birth weight and allergies [121]. Three of them included studies yielded inconsistent results. One study found higher birth weight [120], one found lower birth weight [119], and one found no correlation [118]. There was no significant association between high-sugary food or drink intake during pregnancy and obesity risk in offspring up to 18 years of age [120]. One study focused on prenatal sugar intake and childhood allergies and reported a weak, borderline 7% increase in asthma risk associated with maternal sugar intake during pregnancy [121]. Moreover, a potential risk of allergic rhinitis, eczema, wheezing and food intolerances was found [121]. One study investigated dietary patterns during pregnancy and potential birth outcomes, such as preterm birth, small-for-gestational-age, and birth weight [119]. Unhealthy dietary patterns, which included higher sugar consumption, were significantly associated with lower birth weight (mean difference: −40 g) and a 17% higher risk of preterm birth [119]. The available evidence was based on three studies [118, 120, 121] with moderate and one study [119] with high AMSTAR-2 quality rating, no studies showed low nor critically low quality (Supplementary Table 2).
Cancer
The literature analysis revealed a total of 14 studies on the effects of sugar consumption on various cancers, as well as a study on the effects of high-sugar foods on cancer therapy [122–135].
Overall SSB intake was statistically significantly associated with increased general cancer risk by 12%, moreover each SSB serving per day increased the risk by 4% [129]. Fruit juice was linked to an increased overall risk of cancer by 14% [109]. Women who consumed no sugar-sweetened beverages compared with those who consumed more than 250 g SSB per day had a 27% lower risk of breast cancer [128]. The risk of prostate cancer increased by 14–18% with SSB intake [129, 130]. Due to insufficient data, none of the studies was able to demonstrate a significant association between endometrial/ovarian cancers and sugar consumption. Table 3 shows the association between sugar intake particularly with SSB and the risk of development of certain cancer types.
Table 3.
Summary of systematic reviews reporting the association between sugar intake and the risk of different types of cancer
| Study | Exposition | Type of cancer | Risk ratio |
|---|---|---|---|
| Li et al. [129] | SSB | total cancer risk | 12% |
| Makarem et al. [128] | 50-g increase in total sugar intake | total cancer risk | 36% |
| Li et al. (2022) | SSB | colorectal carcinomas | 14% |
| Makarem et al. [128] | total sugar intake | hepatocellular carcinomas | 88% |
| Li et al. [129] | SSB | hepatocellular carcinomas | 100% |
| Llaha et al. [130] | SSB | hepatocellular carcinomas | 89% |
| Li et al. [129] | SSB | breast carcinomas | 21% |
| Llaha et al. [130] | SSB | breast carcinomas | 14% |
| Li et al. [133] | SSB | breast carcinomas | 4% |
| Li et al. [129] | SSB | prostate carcinomas | 14% |
| Llaha et al. [130] | SSB | prostate carcinomas | 18% |
| Llaha et al. [130] | fruit juice | prostate carcinomas | 3% |
| Carroll et al. [125] | fructose | colorectal carcinomas | 30% |
In summary, statistically significant positive associations between sugar consumption and an increased risk of certain cancers including pancreatic, colorectal, liver, breast and prostate cancer were observed. In particular, the consumption of SSBs and fruit juices appeared to increase the risk of cancer. However, the significance for individual cancer type was limited due to insufficient evidence. The available evidence was based on three studies [128, 130, 131] with moderate AMSTAR-2 quality rating, ten studies [122–127, 129, 130, 133] showed critically low quality. No studies were available in moderate or high quality (Supplementary Table 2).
Cardiometabolic risk factors
The literature review identified a total of 47 studies on cardiometabolic and cardiovascular risk factors [32, 74, 83, 84, 136–178]. The risk ratio for cardiometabolic and cardiovascular outcomes associated with SSB consumption are shown in Table 4. Of these, 13 studies investigated the effects of sugar consumption on blood pressure. Eleven studies found a positive association between added sugar and hypertension [141, 146, 153, 157–162, 173, 178], and two did not [155, 170]. Consumption of SSB was associated with increased risk of hypertension by 6–21% [141, 146, 157–160, 175, 176]. Five studies found a statistically significant association between SSB intake and stroke risk, with an increase between 6% and 13% per serving [84, 154, 159, 166, 171]. Eleven studies associated SSB consumption with cardiovascular disease, of which ten studies found a statistically significant positive association [32, 74, 83, 145, 147, 149, 165, 167, 172, 179]. Cardiovascular mortality was found associated to increase between 8 and 24% due to high consumption of SSB [142]. Another study found a 17% higher risk of coronary heart disease, 7% for stroke, and 8% for heart failure per 250 ml SSB per day [172]. Findings regarding fruit juice consumption showed neutral, beneficial effects or no statistically significant associations [143, 148, 164, 169]. Overall, a statistically significant associations between fruit juice consumption and cardiovascular disease were observed. However, higher orange juice intake (> 500 ml/day) was associated to lower cholesterol levels and inflammation markers, whereas a statistically significant reduction in fasting blood glucose was found with cherry juice [143]. No effect was found for other factors such as LDL or HDL. Eight studies addressed the relationship between added/free sugars and the risk of cardiometabolic disease [136, 137, 139, 140, 144, 152, 163, 168], two of which found a positive association [137, 152]. In summary, 25 included studies show a statistically significant positive association between SSBs and the risk of hypertension, stroke, coronary heart syndrome, heart failure and cardiovascular mortality. The available evidence was based on 15 studies [74, 84, 141, 143, 150, 152, 155–157, 160, 162, 165, 169, 174, 175] with low, four studies [83, 136, 137, 168] with moderate, and three studies [138, 176, 178] with high AMSTAR-2 quality rating, 23 studies [32, 139, 142–149, 151, 153, 154, 158, 159, 161, 163, 164, 166, 167, 170, 171, 177] showed critically low quality (Supplementary Table 2).
Table 4.
Summary of systematic reviews reporting the association between sugar intake and the risk of cardiometabolic outcomes
| Study | Exposition | Cardiometabolic and cardiovascular outcome | Risk ratio |
|---|---|---|---|
| Cheungpasitporn et al. [161] | SSB | hypertension | 12% |
| Kim and Je [157] | SSB | hypertension | 8%−12% |
| Schwingshackl et al. [141] | SSB | hypertension | 7% |
| Xi et al. [159] | SSB | hypertension | 8% |
| Jayalath et al. [158] | SSB | hypertension | 12% |
| Kim et al. [175] | SSB | hypertension | 21% |
| Jamali et al. [176] | SSB | hypertension | 13% |
| Malik et al. [160] | SSB | hypertension | 6% |
| Santos et al. [84] | SSB | stroke | 10% |
| Narain et al. [171] | SSB | stroke | 13% |
| Wang et al. [166] | SSB | stroke | 9%−12% |
| Xi et al. [159] | SSB | stroke | 6% |
| Qin et al. [74] | SSB | hypertension | 10% |
| Meng et al. [32] | SSB | cardiovascular disease | 9% |
| Bechthold et al. [172] | SSB | coronary heart syndrome | 17% |
| Kazemi et al. [165] | SSB | cardiovascular mortality | 10%−16% |
| Sun et al. [179] | SSB | cardiovascular risk | 8%−13% |
| Bhagavathula et al. [142] | SSB | cardiovascular mortality | 6%−24% |
| Huang et al. [145] | SSB | coronary heart disease | 17% |
| Khan et al. [144] | total sugars | cardiovascular mortality | 9% |
| Khan et al. [144] | fructose | cardiovascular mortality | 8% |
Cognition and psyche
A total of 19 systematic reviews were included evaluating the effect of sugar consumption and different cognitive performances or disorders, e.g. attention deficit hyperactivity disorder (ADHD), depression, anxiety Parkinson’s disease (PD), mood, and hippocampal function [166, 173, 180–196]. SSB consumption was significantly associated with a higher risk (17%) of cognitive disorders [189]. Two studies investigated the effects of sugar consumption on ADHD [181, 191]. Sugar and SSB consumption was significantly associated with an increased risk of ADHD symptoms by 22% [191]. Unhealthy dietary patterns or Western diets including refined cereals, high-fat dairy, desserts, sugar, sweets, and soft drinks were associated with a 41% increased risk of ADHD [181]. Sugar consumption was associated with an immediate improvement in mood, while its long-term effects were significantly detrimental to overall cognitive health [192]. The risk of all-cause dementia in middle-aged and older people increased 2.8-fold when consuming two and more servings of SSB per day [187]. Three studies provided dose-response meta-analyses which demonstrated similar results with an increased risk of depression by 5%−25% caused by SSB intake [173, 190, 195]. Two studies which investigated the association between SSB intake and anxiety did not find any statistically significant results [194, 196] and one confirmed higher SSB intake increased the risk of anxiety by 34% [193].
Summarized, higher sugar intake, especially from SSB, was associated with decreased cognitive performance, including executive function, attention, memory, and decision-making, and was associated with an increased risk of depression, attention deficit hyperactivity disorder and Parkinson’s disease. The available evidence was based on five studies [182, 189, 191, 192, 196] with low, two studies [183, 193] with moderate, and six studies [173, 181, 187, 188, 190, 197] with high AMSTAR-2 quality rating, six studies [166, 180, 184, 186, 194, 195] showed critically low quality (Supplementary Table 2).
Other diseases and health outcomes
All-cause mortality and telomere length
Of the 15 included studies, eight systematic reviews examined the effects of consuming sugar-sweetened beverages (SSBs) or fruit juices [74, 165, 176, 198–202] and four examined the consumption of highly processed foods, sweets and added sugars in relation to all-cause mortality [163, 203–205]. All studies showed an increased risk in mortality associated with increased consumption of sugar. High consumption of SSB increased the all-cause mortality risk by 4–12% [74, 165, 176, 198, 199] and cardiovascular risk by 8–20% [199, 200, 204]. A daily sugar reduction of 5–40% or 100% substitution with sweeteners was associated with a 0.2–4% reduction in the prevalence of obesity and a 3.7–5.5% reduction in all-cause mortality from chronic diseases [206]. However, unlike SSB, no significant association was found for an equivalent amount of fruit juice consumption [201]. Two systematic reviews highlighted key dietary influences on telomere length in children and adolescents [207, 208]. There was a positive association between longer telomeres and the Mediterranean diet, higher intake of whole grains, coffee, and tea, along with a reduced intake of red meat. In contrast, the consumption of dairy products, sugars, SSBs, and refined cereals – particularly white bread – was associated with a 37% increased risk of telomeres shortening. Additionally, a diet with a high glycaemic load was negatively associated with telomere length. With regard to the current research question on the influence of sugar on general health, the included systematic reviews had limited informative value due cofounding nutritional factors. The available evidence was based on six studies [199–203, 205] with low and three studies [176, 207, 208] with high AMSTAR-2 quality rating, five studies [74, 163, 165, 198, 204] showed critically low quality (Supplementary Table 2).
Blood values
The current review yielded 13 studies that investigated blood value changes associated with sugar intake [103, 164, 178, 209–218]. The studies demonstrated that consumption of SSB and sweets were associated with increased levels of uric acid, whereas 100% fruit juice was associated with decreased uric acid levels [209]. There was a significant rise in postprandial triglycerides in hypercaloric trials linked to high fructose consumption [210, 217]. One study focusing on intermediate disease markers found that SSBs were associated with worsening lipid markers and increased risk coronary heart disease [211]. Furthermore, high SSB consumption was significantly associated with an increase in low-density lipoprotein cholesterol, decrease in high-density lipoprotein cholesterol and decrease in total cholesterol [213, 215].
The included studies showed that high sugar intake, particularly in the form of fructose and SSBs, were significantly associated with negative effects on lipid profiles, including increased LDL-C, decreased HDL-C, and increased triglycerides. The available evidence was based on three studies [103, 209, 219] with low and nine studies 1 [178, 211, 212, 214–219] with high AMSTAR-2 quality rating, one study [164] showed critically low quality (Supplementary Table 2).
Bone health
A total of three studies were found regarding sugar intake and bone health [220, 221]. The studies demonstrated that high sugar consumption, particularly SSB, was significantly associated with reduced bone health. A carbonated beverage or cola intake was linked to increase the fracture risk by 39% [220]. Increased consumption of SSB was associated with a significantly higher risk of hip fractures in men, while a modified Mediterranean Diet, which is low in sugar, demonstrated a decreased risk of hip fractures [222]. Higher SSB intake was associated with an 5–20% reduction in bone mineral density in adults [221]. In summary, SSB consumption was associated with an increased fracture risk in children and adults, lower bone mineral density, and lack of essential elements caused by milk replacement through SSB. The available evidence was based on one study [221] with low and two studies [203, 220] with moderate AMSTAR-2 quality rating, no studies showed critically low or high quality (Supplementary Table 2).
Inflammation
A total of three studies regarding sugar consumption and inflammation were found [223–225]. Fructose-containing sugars foods (SSB; sweetened dairy; sweetened dairy alternative [soy], 100% fruit juice, fruit, dried fruit, mixed fruit forms, sweetened cereal grains and bars, sweets and desserts, added nutritive sweetener, mixed sources with SSBs, and mixed sources without SSBs) did not demonstrate any significant influence on the level of C-reactive protein (CRP). However, some sources of fructose, such as sweetened soy beverages and 100% fruit juice, showed anti-inflammatory effects, while other sources, e.g. SSBs were associated with increased CRP levels [224]. Orange juice intake was associated with a significant decrease in the inflammatory cytokine IL-6 levels. However, markers such as C-reactive protein and malondialdehyde (MDA) and general oxidative stress did not show any significant decline [223].
In summary, the included studies showed a positive association between sugar consumption and increased levels of pro-inflammatory markers such as interleukin-6 (IL-6), and CRP. The available evidence was based on three studies [223–225] with high AMSTAR-2 quality rating, no studies showed critically low, low, nor moderate quality (Supplementary Table 2).
Kidney disease
The literature analysis revealed three studies on the effects of sugar consumption on kidney disease and urine production [226–228]. A constant or reduced urine volume was observed when 1 L of orange juice (10.5 g sugar/100 ml), cola (10.6 g sugar/100 ml) or sucrose (5–20 g sugar/100 ml) were consumed. The intake of 100–1000 mg honey per kilogram body weight caused an increase in urine volume [226]. The risk of chronic kidney disease was associated with an increase by 30%−58% linked to high SSB intake [227, 228]. In summary, the two included studies on chronic kidney disease showed a positive association with sugar consumption. However, the significance is limited due to the limited data available. The available evidence was based on one study [228] with moderate AMSTAR-2 quality rating, two studies [226, 227] showed critically low quality. No studies were available with high AMSTAR quality (Supplementary Table 2).
Sleep duration
One study investigated the relationship between sugar consumption and sleep [229]. Short sleep duration was defined as less than 7–8 h per night in adults and less than 9–10 h per night in children. An inverse relationship was found between sleep duration and consumption of SSB. Children with insufficient sleep duration consumed on average 16% more sugar, 18% more SSB, and 92% more energy drinks. In adults, a 58% increase in sugar consumption (including sugary energy drinks) was found to be significantly associated with shorter sleep duration. Since only cross-sectional studies were included in this study, a significant association was observed, but no conclusion on the causality of sugar consumption and sleep. The available evidence was based on one study [229] with moderate AMSTAR-2 quality rating, no studies showed critically low, low, nor high quality (Supplementary Table 2).
Asthma
The umbrella review yielded two systematic reviews regarding the relationship between SSB consumption and asthma [230, 231]. In adults, a meta-analysis of five studies found a significant associated increase in the prevalence of asthma by 37% with higher SSB intake. For children, ten studies indicated a 14% higher risk of asthma with high SSB consumption. SSB consumption was also significantly associated with a 9% increased risk of wheezing in children [230]. SSB intake was associated with an increased risk of asthma by 28%, while 100% fruit juice intake did not show any statistically significant association [231]. Overall, the included studies found that SSB consumption was significantly associated with an increased risk of asthma and respiratory issues in both children and adults. The available evidence was based on one study [231] with moderate, and one study [230] with high AMSTAR-2 quality rating, no studies showed critically low quality (Supplementary Table 2).
Oral health
Caries and erosion
The literature review revealed 15 studies investigating the effects of sugar consumption on the dental hard tissues, such as caries or erosion [1–7, 164, 173, 232–237]. Apart from one study, all reviews found a significant positive association between sugar intake and caries. A significant positive association with higher caries risk was found for both sugary drinks and foods [1–5, 173, 232]. One study found a positive association between the consumption of processed sugary and starchy foods and caries incidence [7]. A 18% [236] − 57% increased risk of caries and 43% increased risk of erosion were found, when comparing moderate to low sugar consumption [4]. Moderate sugar consumers (1–2 SSB servings per day) showed a 22% higher DMFT value compared to low sugar consumers (0–1 SSB serving per day). In the same study, a further risk increase of 53% for caries and 209% for erosions was observed when comparing high with moderate sugar consumers. A strong increase in the risk of caries was found up to a daily intake of 150 ml of SSBs comparing to no intake [4]. One study reported that RCTs showed reduced enamel hardness and increased erosion with 100% fruit juice consumption, whereas prospective cohort studies found no associations with erosive or carious lesions [6]. Two studies focused on sugar intake and early childhood caries (ECC) and confirmed a strong statistically significant association [235, 237]. Sugar intake increases the risk of ECC by 224% [237].
In summary, a significant positive association was found between sugar consumption and caries and/or erosions. The available evidence was based on six studies [4, 5, 232, 235, 237, 238] with low, one study [3] with moderate, and three studies [6, 7, 173] with high AMSTAR-2 quality rating, five studies [1, 164, 233, 234, 236] showed critically low quality (Supplementary Table 2).
Periodontal diseases
Four studies on sugar consumption and periodontal disease were included [8–10, 15]. Three of these found a significant positive association, one did not find a significant association [10], however, the consumption of SSBs was associated to increase gingival bleeding and thus an increase in the risk of periodontitis. Therefore, the authors described added sugars from SSB as a risk factor in the development of periodontitis [8]. The findings from one study demonstrated a significant association between high-frequency intake of sugary drinks or foods and an increased incidence of periodontitis. A meta-analysis of the two included studies indicated an increased risk of periodontal disease [9]. Sugar reduction was associated with a significant reduction in gingival inflammation [15]. One study did not find any significant association between sugar consumption and periodontal diseases [10]. The available evidence was based on two studies [10, 15] with low and one study [8] with moderate AMSTAR-2 quality rating, one study [9] showed critically low quality (Supplementary Table 2).
Oral microbiome
Two reviews on the effects of sugar consumption on the oral microbiome were included, which found a significant positive association [11, 12]. Both reviews found a significantly associated reduced diversity of the oral microbiome under high sugar consumption and a predominance of certain species such as Streptococci, Scardovia, Veillonella, Rothia, Actinomyces and Lactobacilli. The available evidence was based on one study [11] with moderate AMSTAR-2 quality rating, one study [12] showed critically low quality (Supplementary Table 2).
Overall, the evidence consistently indicated that higher sugar consumption was associated with an increased risk of oral diseases, including caries, dental erosion, periodontal disease, and unfavourable changes in the oral microbiome, whereas sugar reduction appeared to have protective effects on oral health.
Risk of bias analysis
All included articles were evaluated using AMSTAR-2 [20]. The methodological quality assessment classified the included reviews into four categories: regarding methodological quality, 98 reviews were rated as critically low, 64 as low, 22 as moderate, and 44 as high according to AMSTAR-2 [20] which are represented in the Fig. 3. Overall, 71% of the reviews were classified as having low or critically low confidence in the results, indicating methodological weaknesses, whereas only 29% reached a moderate or high level of confidence.
Fig. 3.

Risk of bias of the included studies assessed using AMSTAR-2
Discussion
This umbrella review aimed to summarise the evidence from systematic reviews and meta-analyses regarding the effects of sugar consumption on oral and general health. The results revealed a consistent association between sugar consumption, particularly from SSBs, and a wide range of negative health outcomes, such as type 2 diabetes mellitus (T2DM), gout, non-alcoholic fatty liver disease (NAFLD), obesity, metabolic syndrome, dental caries, periodontal diseases, and increased all-cause mortality. Figure 4 summarizes these negative outcomes visually. The most consistent evidence with best AMSTAR-2 quality across the included reviews was found for cardiometabolic outcomes, particularly obesity-related measures and type 2 diabetes mellitus, which were repeatedly confirmed by several independent meta-analyses [19, 82, 150, 160]. Additionally, the associations with cardiovascular diseases, certain types of cancer and declined bone health, cognitive and mental health disorders were observed. However, the AMSTAR-2 quality rating revealed a need for further high-quality systematic reviews for outcomes regarding cancer, bone health, kidney diseases, sleep, non-alcoholic fatty liver disease, fertility, and the oral microbiome (Supplementary Table 2).
Fig. 4.

Illustration of the multisystem oral and general health outcomes associated with high sugar consumption found in this umbrella review
The findings of this umbrella review are consistent with the WHO [14] recommendations and the conclusions of Huang et al. [19], which indicate that high dietary sugar consumption is generally more harmful than beneficial for health and reduced intake is recommended to mitigate adverse outcomes. Reducing sugar consumption and limiting SSB intake further underline the need for both behavioural prevention (e.g. in kindergartens, schools, hospitals, nursing homes, dental practices, medical settings, workplaces) and structural prevention measures, such as sugar taxes and other policy regulations.
The included reviews repeatedly reported associations between sugar consumption and metabolic disorders as well as weight gain. High consumption of SSB was associated a significant increase in T2DM risk (13–31% per serving/day) and insulin resistance. Obesity or metabolic syndrome were described as mediators between the consumption of SSBs and T2DM [29, 34, 81, 205]. High blood glucose levels lead to increased levels of inflammation markers, such as C-reactive protein, which is also linked to the risk of diabetes [25]. Similarly, the positive association between SSB intake and NAFLD risk (~ 39–40%) can be explained by the fact that excessive fructose intake promotes hepatic triglyceride accumulation, leading to oxidative stress in hepatocytes and subsequent inflammatory responses in the liver [69]. Under conditions of excess energy intake, fructose-containing sugar-sweetened beverages may further promote de novo lipogenesis and intrahepatocellular fat accumulation [70, 71]. The primary mechanism by which increased sugar consumption promotes weight gain seems to be excessive calorie intake. Liquid sugars such as SSB may increase the risk of weight gain compared to solid foods because of reduced satiety of liquid sugary foods and intensified total energy intake [81]. The AMSTAR-2 rating showed several moderate to high quality studies in the field of metabolic disorders. However, especially in the field of T2DM and NAFLD additional high-quality studies would further strengthen the evidence base.
Metabolic syndrome is characterized by central obesity, hypertension, hyperglycaemia, elevated triglycerides, and low levels of HDL cholesterol [105]. Excess calorie intake, high fructose, ASB, or SSB consumption can lead to increased triglyceride synthesis, reduced insulin sensitivity, and hyperglycaemia. High fructose intake is associated with increased systolic and diastolic blood pressure and weight gain, particularly visceral obesity. All these factors are associated with unhealthy dietary patterns and lifestyles. Diet, especially high intake of fructose, seems to play a key role [104–106, 108].
The authors of several systematic reviews described different pathomechanisms of inflammation as a response to sugar consumption. Sugar, particularly fructose, lead to metabolic processes that initiate increased production of uric acid in the liver and free fatty acids, which can activate immunological responses as well as oxidative stress [223–225]. The increased level of uric acid activates reactive oxygen species, which, can cause damage to cellular structures. Regular sugar intake is associated with chronic inflammatory conditions such as type 2 diabetes, IBS and cardiovascular disease. Moreover, sugar intake is associated with gut microbiome disbalance, specifically, decreased microbiotic diversity and associated with an increased amount of harmful bacteria, which initiate the production of lipopolysaccharides, increased intestinal permeability, immune system activation, another trigger of high cytokine production [67].
High sugar intake seems to negatively affect sperm quality through increased blood sugar and insulin production. In long-term, this may lead to insulin resistance and affect the hypothalamic-pituitary-gonadal (HPG) axis, which regulates male reproductive function and leads to imbalance in the testosterone-estrogen ratio in the body. Furthermore, increased sugar consumption was found to be associated with higher production of reactive oxygen species, which may lead to DNA damage in sperm and to lower sperm production [116, 117]. Beyond this, high sugar intake may accelerate biological ageing by increasing oxidative stress and chronic inflammation, which are associated with accelerated telomere shortening and reduced cellular longevity [207, 208].
The significant association of sugar consumption to cancer forms such as pancreatic [128, 130, 198], colorectal [128, 198], liver [130, 198], breast [130, 198], and prostate cancers [130, 198] was a major finding of the umbrella review. The range of the increase in risk was strongly depending on the type of cancer and the sugar source (total cancer risk varied between 12 and 36%). A link between colorectal cancer and sugar or sugar-sweetened beverage consumption may be mediated by increased insulin production and the associated accumulation of visceral adipose tissue leading to obesity. Insulin is a growth factor for colon cells and increases the risk of colorectal cancer. Patients with gastric cancer showed increased IGF-1 levels compared to healthy patients [135]. However, there seem to be still a need of high-quality systematic reviews in this field to strengthen the evidence base.
Higher sugar intake, especially from SSB, was associated with poorer cognitive performance, increased risk of ADHD, depression, and neurodegenerative diseases. The included studies suggested that SSB and sugar consumption were associated with anxiety, depression, stress, and negative emotions. Moreover, there was a bidirectional relationship between depression and obesity and between depression and type 2 diabetes [173]. The possible pathomechanism of anxiety/depression and soft drink consumption can be explained by endothelial dysfunction or a higher level of inflammation. Furthermore, glucose boosts the production and release of acetylcholine in the hippocampus which may also lead to gamma-aminobutyric acid release. High sugar consumption seemed to provoke gastrointestinal discomfort or reactive hypoglycemia and activated neurotransmitter functions and seems to be linked to a lack of essential nutrients such as iron and zinc. All these factors are known to worsen ADHD symptoms [181, 191].
SSB consumption was associated with lower bone mineral density and increased fracture risk because of increased urinary calcium loss and bone mineralization disorders. The phosphoric acid in SSB can also impair calcium absorption, raising the risk of fractures and osteoporosis. Additionally, higher levels of C-reactive protein may lead to increased bone resorption and chronic inflammation [220–222]. With regard to the high prevalence of both osteoporosis and high sugar consumption, more high-quality systematic reviews are needed. SSB intake may also significantly increase the risk of asthma. Regarding the underlying mechanisms, sugar has been shown to trigger inflammatory reactions which are associated with C-reactive protein and additives such as sodium benzoate and sulfites, which could also play a part in asthma development.
Based on the presented associations between sugar intake and multiple chronic diseases, it is not surprising that sugar consumption was also linked to increased all-cause mortality (increased risk ~ 4–12%), particularly through its contribution to cardiovascular risk. High sugar intake negatively affected lipid profiles, increasing LDL, decreasing HDL, and raising triglycerides [103, 213]. High consumption of SSBs and ASBs may contribute to increased mortality risk, through cardiovascular mechanisms. This highlights the potential importance of limiting sweetened beverage intake as part of strategies to reduce long-term health risks [198]. Because of their high caloric content, moderate-to-high glycemic index, and low satiety effect, increased intake of sugar-sweetened beverages is associated with weight gain, insulin resistance, inflammation, and atherogenic dyslipidemia [200]. Additionally, both sugar- and artificially sweetened beverages may contribute to metabolic disturbances through appetite dysregulation, altered gut microbiota, potentially leading to excess energy intake and increased cardiometabolic and mortality risk (~ 8–24% increased risk) [74].
Finally, the results of this umbrella review demonstrated a consistent association between higher intake of free sugar and adverse oral health outcomes, including dental caries (~ 18–43% increased risk), ECC, dental erosion, and periodontal diseases. The risk increased proportionally with sugar consumption levels. The frequent intake of sugar, especially more than 5% of the daily energy intake, was associated with a higher risk of caries and dental erosion [5–7, 232]. Dental caries arises when oral bacteria metabolise sugars into acids that lower biofilm pH below the critical threshold for enamel demineralisation. Sugar-sweetened beverages further increase caries risk by combining high sugar content with intrinsic acidity, leading to sustained tooth surface loss [4]. Early childhood caries (ECC) is common worldwide in preschool children and can negatively affect health, nutrition, and quality of life [237]. Sugar intake can promote gingivitis by increasing plaque accumulation and by bacterial sugar metabolism into pro-inflammatory acids that irritate the gingiva. In addition, systemic effects of free sugars, such as hyperglycaemia and impaired immune responses, may further increase gingival inflammation [15]. Periodontal diseases were also linked to sugar intake, possibly due to its effect on chronic gingival inflammation, impaired bone metabolism, which together increase susceptibility to alveolar bone loss and microbiome changes [10]. Due to the production of adhesins and polysaccharides, the bacteria easily attach to the tooth surface, making them one of the triggers of dental caries. The authors described Streptococci as one of the dominant genera in the oral microbiome [11, 12]. While the evidence base and the quality of studies on dental caries with 15 included studies can be considered robust, more high-quality systematic reviews on periodontal diseases and the oral microbiome are needed, as only four and two studies could be included, respectively.
Implications for oral and general health, and dental professionals
Oral diseases seem to represent the earliest and most consistently documented health consequences of excessive sugar consumption. In contrast to many presented chronic non-communicable diseases, which often develop over decades, adverse effects on oral tissues—including dental caries, alterations of the oral microbiome and periodontal inflammation—may occur within relatively short periods of sustained high sugar intake. Consequently, oral diseases may serve as early clinical indicators of an unhealthy dietary pattern. While the association between free sugar intake and dental caries has long been established, the present umbrella review demonstrates that the potential oral consequences of excessive sugar consumption extend beyond caries alone. The available evidence further indicates that dietary sugar may contribute to gingival and periodontal inflammation, although the certainty of evidence is lower than for dental caries. Experimental and clinical studies suggest that excessive free sugar intake may promote a pro-inflammatory environment through systemic metabolic effects, altered immune responses and microbiome-mediated mechanisms. However, the methodological quality of the currently available systematic reviews remains heterogeneous, and further high-quality prospective studies are required to clarify these associations.
From a clinical perspective, these findings reinforce the central role of dental professionals in dietary counselling. Because dental practitioners routinely examine patients throughout life and frequently identify early manifestations of sugar-related diseases, they are uniquely positioned to promote dietary modification before systemic complications become clinically apparent. Integrating dietary counselling into routine dental care therefore represents an important opportunity to simultaneously improve oral health and contribute to the prevention of chronic non-communicable diseases within the framework of the common risk factor approach (Fig. 5).
Fig. 5.

Shared health effects of a sugar reduction promoted by the dental professional based on the findings of the umbrella review
Strengths and Limitations
Most included studies confirmed the adverse health effects of sugar consumption in its multiple forms. Most of the investigations were related to SSB consumption. However, during data extraction, particularly in relation to sugar-specific exposures, it became apparent that several studies (excluding those investigating neonatal analgesia) examined sugar intake only as a part of dietary patterns. In consequence, the reported negative outcomes are likely related not only to sugar, but to a cluster of lifestyle factors, including consumption of SSB and ASB, excessive caloric-, processed foods- and saturated fats, lower level of physical activity, and increased screen time. These factors may represent a generalized lifestyle pattern, often related to the populations with lower health awareness. Additionally, under real-life conditions, accurately quantifying individual sugar intake remains methodologically challenging.
It should be noted that two reviews [69, 71] reported conflicts of interest with beverage/food manufacturers (e.g. Coca-Cola, Dr. Pepper Snapple Group, Unilever), the Canadian Sugar Institute or the International Life Sciences Institute (ILSI). Some studies were funded by The Peanut Institute, Barilla, Unilever, Unico, Primo, Loblaw Companies, Quaker (PepsiCo), Pristine Gourmet, Bunge Limited, Kellogg Canada, WhiteWave Foods [209], Unilever, a commercial food and beverage manufacturer [61]. Liska et al. [6] stated cooperation with juice product associations but found a positive association of fruit juice consumption with erosion in their review. Seven studies regarding cardiometabolic risk factors reported conflicts of interest with the sugar industry or associations such as the World Sugar Research Organization [139, 140, 144, 146, 155, 158, 165, 170]. It is striking that, except for the review by Gibson et al., all studies involved the same authors with a conflict of interest. Of these seven studies with conflict of interest, four found no positive associations, while Jayalath et al., Kazemi et al. and Liu et al. found positive associations of sugar-sweetened beverages with cardiovascular disease.
Several methodological limitations should be considered. First, several included systematic reviews were rated as low or critically low according to AMSTAR-2. Second, overlap of primary studies between reviews was not formally quantified and may therefore have increased the apparent amount of evidence. Third, exposure definitions and heterogeneity varied considerably across reviews, including free sugars, added sugars, sugar-sweetened beverages, total sugars and dietary patterns. Fourth, as this umbrella review aimed to summarise and compare findings from published systematic reviews rather than to re-evaluate the certainty of evidence for individual associations, no additional GRADE assessment was conducted. Instead, the methodological quality of the included systematic reviews was assessed using the AMSTAR-2 tool. For further meta-analysis we refer to Huang et al. [19]. Finally, because most underlying evidence originated from observational studies, causal conclusions cannot be drawn. The search results were limited to English and German publications.
Conclusions
High sugar intake, particularly from sugar-sweetened beverages, was consistently associated with an increased risk of oral diseases such as dental caries, gingivitis and periodontitis, as well as systemic conditions including obesity, type 2 diabetes mellitus, cardiovascular diseases, non-alcoholic fatty liver disease, and metabolic syndrome. These findings indicate the clinical relevance of sugar reduction for maintaining oral health, underlining the specific preventive role of dentistry through early identification, patient education, and support for reducing free sugar intake. Consequently, limiting sugar consumption constitutes a key strategy not only for improving oral health but also for contributing to comprehensive public health prevention efforts. Dental professionals help prevent disease by supporting patients in reducing sugar intake, which is important for both oral and general health.
Supplementary Information
Below is the link to the electronic supplementary material.
Acknowledgements
The authors like to thank Ines Badertscher and Bernadette Ravyler for their support with figure 1, and Aaron Frische for his support with Figure 2.
Authors’ contributions
JPW: Conceptualization, literature search, data extraction, data analysis, drafting of the manuscript; NW: Literature search, data extraction, drafting of the manuscript; AD-Z: Literature search, data extraction, drafting of the manuscript; CT: Conceptualization, data extraction, data analysis, interpretation, drafting of the manuscript, organization.
Funding
The study was based on institutional funding.
Data availability
The results of the literature search and risk of bias assessment are available in the supplementary material.
Declarations
Competing interests
The authors declare no competing interests.
Footnotes
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
J. P. Woelber, N. Wirth, A. Dallmer-Zerbe and C. Tennert share first/last authorship
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Supplementary Materials
Data Availability Statement
The results of the literature search and risk of bias assessment are available in the supplementary material.
