Skip to main content
BMC Endocrine Disorders logoLink to BMC Endocrine Disorders
. 2026 Feb 25;26:94. doi: 10.1186/s12902-026-02207-z

The effect of dietary approaches to stop hypertension (DASH) diet on cardiometabolic and atherogenic indices in subjects with metabolic syndrome: a randomized clinical trial

Xun Wei 1, Alireza Takzare 2, Rafat Rezapour-Nasrabad 3, Abbas Ali Sangouni 4,5, Mahdieh Hosseinzadeh 5, Karim Parastouei 4,✉
PMCID: PMC13041230  PMID: 41742133

Abstract

Background

Dietary approaches to stop hypertension (DASH) diet as a balanced dietary pattern is designed to help manage hypertension. The scientific evidence hypothesized that following the DASH diet may lead to reductions in cardiometabolic risk. We aimed to design a clinical trial to assess the impact of the DASH diet on cardiometabolic and atherogenic indices in individuals with metabolic syndrome (MetS).

Methods

Sixty participants diagnosed with MetS were randomly divided into two groups: the intervention group (adhering to DASH diet) or the control group (following a common healthy diet). Key outcomes of the present study including cardiometabolic index (CMI) as our primary outcome, and atherogenic index of plasma (AIP), atherogenic coefficient (AC) and castelli risk index II (CRI-II) as secondary outcomes were evaluated at the baseline and at the end of the study.

Results

While one participant excluded from the trial, 59 subjects completed the study. Baseline values of CMI (p = 0.33), AIP (p = 0.27), AC (p = 0.44) and CRI-II (p = 0.17) showed no significant difference between the intervention group and the control group. After adjusting for confounding factors, the intervention group demonstrated a significant decrease compared to the control group in CMI (−0.38±0.29 vs. −0.02±0.47; p = 0.001), AIP (−0.04±0.04 vs. 0.01 ± 0.07; p = 0.001), AC (−0.31±0.54 vs. 0.01 ± 0.72; p = 0.04) and CRI-II (−0.30±0.37 vs. −0.03±0.39; p = 0.009).

Conclusions

Adherence to the DASH diet appears to be effective in reducing CMI and some atherogenic indices. Further well-designed clinical trials with longer intervention durations are needed.

Trial registration

The trial was registered on 21 October 2022 at Iranian Registry of Clinical Trials (IRCT20180201038585N12, https://irct.behdasht.gov.ir/trial/66161).

Keywords: Metabolic syndrome, DASH diet, Cardiometabolic risk

Introduction

The worldwide prevalence of metabolic syndrome (MetS) is more than 20% [1]. Due to its widespread prevalence and its association with the occurrence of various non-communicable diseases, MetS imposes a significant economic burden on the healthcare system [1, 2]. The number of prevalent cases of cardiovascular diseases (CVDs) has more than doubled from 1990 to 2023, rising from 311 million to 626 million globally [3]. It has been indicated that the probability of cardiovascular risk is higher among individuals suffering from MetS than individuals without MetS [4]. The cardiometabolic index (CMI), derived from anthropometric measurements and lipid profile, serves as a reliable scoring system for assessing cardiovascular risk [5]. In addition, atherogenic index of plasma (AIP), atherogenic coefficient (AC) and castelli risk index (CRI) have been established to predict cardiometabolic risk [6, 7]. Following healthy dietary patterns can be a useful strategy to manage cardiovascular risk and MetS [8, 9].

The dietary approaches to stop hypertension (DASH) diet as a plant-based diet relies on low consumption of fat, red meat, sugar-sweetened beverages, and sodium [10]. Instead, the DASH diet emphasizes consuming healthy food groups such as vegetables, whole grains, fruits, low-fat dairy products and legumes [11]. It has been shown that adherence to healthy diets such as DASH diet could prevent excessive use of antihypertensive drugs, reduce the dose or number of drugs employed, and improve the efficacy of the pharmacological treatment [12]. The study of Siervo et al. [13] suggested that DASH diet may have greater beneficial effects in subjects with an increased cardiometabolic risk. Some clinical trials have evaluated the effect of DASH diet among individuals suffering from non-communicable diseases [14–17]. A few numbers of studies have explored the effect of DASH diet on individuals with MetS, yielding inconsistent findings [18, 19]. The DASH diet is hypothesized to play a significant role in managing CMI and atherogenic indices. We aimed to examine the effect of DASH diet on CMI and atherogenic indices in subjects with MetS.

Methods

Participants

We conducted a randomized controlled trial (RCT) for 12 weeks. Recruitment of subjects was performed from October 2022 to November 2022 in Yazd, Iran. Individuals aged between 30 and 60 years, with MetS according to the International Diabetes Federation (IDF) criteria [20], and who signed a written informed consent were included in the study. According to the IDF criteria, MetS is defined by the presence of central obesity (waist circumference (WC) in male ≥ 94 cm and female ≥ 80 cm) plus any two of the following four factors: 1) raised triglycerides (TG) (≥150 mg/dL) or specific treatment for this lipid abnormality; 2) reduced high-density lipoprotein cholesterol (HDL-c) (<40 mg/dL in males, <50 mg/dL in females) or specific treatment for this lipid abnormality; 3) raised blood pressure (systolic/diastolic blood pressure ≥ 130/85 mmHg) or treatment of previously identified hypertension; and 4) raised fasting plasma glucose (≥100 mg/dL) or previously diagnosed type 2 diabetes mellitus (T2DM). Individuals who met the following criteria were excluded from the study: hypothyroidism, Cushing’s syndrome, Wilson disease, kidney diseases, history of hepatitis, hemochromatosis, bypass surgery, pregnancy and lactation, and consuming calcium channel blockers, synthetic estrogens, vitamin D, vitamin E, and omega-3.

Trial design

The present study aimed to assess the impact of adhering DASH diet for 12 weeks on CMI (as primary outcome) and atherogenic indices including AIP, AC and CRI-II (as secondary outcomes) among individuals with MetS. Previously, our research team reported the effect of DASH diet on fatty liver, insulin resistance, lipid accumulation product and cardiovascular risk factors [21, 22]. The research protocol was approved by the ethical committee of Baqiyatallah University of Medical Sciences Tehran, Iran. We registered the study protocol at Iranian Registry of Clinical Trials (IRCT20180201038585N12, URL: https://irct.behdasht.gov.ir/trial/66161).

This study was done in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. A stratified randomization method based on sex (male/female) and age (30–45 and 45–60 years) was used and the subjects were divided into the groups by a computer-generated random numbers table. Opaque sealed envelopes were used to perform allocation concealment. Using a 95% confidence interval with α = 0.05 and β = 0.2 and based on the WC values reported by Razavi Zade et al. [17] a sample size of 60 was determined to be sufficient. A retrospective power analysis was performed for outcomes of the present article, and we observed sufficient power.

Both the intervention group (following DASH diet) and control group (following a common healthy diet) received energy-restricted diet with similar macronutrients distribution (50–55% carbohydrate, 15–20% protein, and 30% total fat). The DASH diet compared to the healthy diet has higher amounts of food groups such as vegetables, fruits, low-fat dairy products, nuts, seeds and legumes. Thus, the participants in the intervention group (DASH diet) receive higher amounts of fibers and micronutrients especially potassium, magnesium, vitamin C, vitamin A and folate. In addition, the DASH diet has lower amounts of meats, fats and oils. In general, we aimed to control the effects of energy restriction and macronutrient distribution to clarify the effects of DASH diet compared to a common healthy diet. The dietary intakes of participants were checked every 4 weeks via phone interviews and the participants were trained to follow the intervention. The participants received text messages twice a week to maintain an appropriate level of adherence to the intervention.

Assessments

Dietary intakes of participants were assessed at baseline and post-intervention utilizing a food record [23]. The collected data were analyzed via Nutritionist IV (N-Squared Computing, Salem, OR, USA) customized for Iranian foods. Physical activity was assessed using metabolic equivalent of task (MET) questionnaire [24, 25].

Participants’ weight was recorded at the baseline and after intervention using a digital Seca scale (Seca, Germany), while height and waist circumference were determined by a stadiometer (Seca, Hamburg, Germany) and a tape measure, respectively. We computed body mass index (BMI) using its equation: weight (kg)/height squared (m2).

Laboratory analysis

After an overnight fasting, 10 cc of blood was drawn from each participant at baseline and post-intervention for laboratory analyses. We evaluated total cholesterol (TC), TG, low-density lipoprotein cholesterol (LDL-c) and HDL-c using Pars Azmoon kits (manufactured in Iran) and an autoanalyzer (Siemens, United Kingdom).

We computed the CMI [5], AIP [26], AC [7] and CRI-II [27] using following equations:

  • CMI = (TG/HDL-c) × waist-to-height ratio (WHtR)

  • AIP = log (TG/HDL-c)

  • AC = (TC – HDL-c)/HDL-c

  • CRI-II = LDL-c/HDL-c

Statistical analysis

Statistical analysis was conducted utilizing the statistical package for social science (SPSS) software version 24 and an intention-to-treat (ITT) approach was used for analyses. The normality of indices was assessed with the Kolmogorov-Smirnov test. An independent t-test (for continuous variables) was used to compare the differences between groups, while categorical variables were analyzed using chi-square test. Within-group changes from baseline to post-intervention were analyzed utilizing paired t-tests. Analysis of Covariance (ANCOVA) was employed to control confounding factors such as physical activity and energy intake. A p-value equal to or less than 0.05 was deemed statistically significant.

Results

Characteristics and dietary intakes

After excluding one subject (non-referral) from the control group, 59 participants completed the study (Fig. 1). Characteristics of groups were represented at Table 1.

Fig. 1.

Fig. 1

Eligibility, screening, and follow-up

Table 1.

Characteristics of subjects with MetS

Variables Intervention group
(n = 30)
Control group
(n = 30)
P
Age, y 44.43 ± 6.06 45.60 ± 7.07 0.49
Height, cm 165.33 ± 9.12 163.70 ± 10.57 0.52
Sex Male, n (%) 15 (50.0) 15 (50.0) 0.99
Female, n (%) 15 (50.0) 15 (50.0)
Smoking No, n (%) 21 (70.0) 22 (73.3) 0.77
Yes, n (%) 9 (30.0) 8 (26.7)
Education Under diploma, n (%) 5 (16.7) 7 (23.4) 0.87
Diploma, n (%) 9 (30.0) 10 (33.3)
Bachelor’s degree, n (%) 11 (36.6) 9 (30.0)
Master’s degree, n (%) 5 (16.7) 4 (13.3)
Physical activity Low, n (%) 21 (70.0) 22 (73.3) 0.95
Moderate, n (%) 8 (26.7) 7 (23.4)
High, n (%) 1 (3.3) 1 (3.3)
Frequency of MetS components WC, n 30 30
DBP/SBP, n 19 23
TG, n 18 27
HDL-c, n 21 16
FPG, n 25 26
DBP Baseline 86.26 ± 6.53 86.43 ± 10.02 0.93
After intervention 81.10 ± 7.22 84.93 ± 7.83 0.06
Mean change of DBP −5.16 ± 3.92 −1.50 ± 7.04 0.01
SBP Baseline 125.13 ± 10.42 130.56 ± 10.96 0.06
After intervention 118.16 ± 11.30 129.20 ± 13.74 0.001
Mean change of SBP −6.97 ± 8.21 −1.36 ± 6.83 0.006
TG Baseline 180.03 ± 65.42 207.16 ± 81.23 0.16
After intervention 161.53 ± 64.78 207.76 ± 89.06 0.02
Mean change of TG −18.50 ± 14.32 0.60 ± 23.81 <0.001
HDL-c Baseline 43.23 ± 7.51 45.06 ± 9.93 0.42
After intervention 42.33 ± 6.88 43.66 ± 7.93 0.48
Mean change of HDL-c −0.90 ± 3.40 −1.40 ± 5.46 0.67
FPG Baseline 114.26 ± 18.90 129.13 ± 31.58 0.03
After intervention 106.40 ± 17.85 130.10 ± 24.73 <0.001
Mean change of FPG −7.86 ± 10.08 0.97 ± 15.51 0.01
WC Baseline 105.53 ± 7.94 105.0 ± 9.80 0.81
After intervention 99.51 ± 7.85 102.76 ± 8.62 0.13
Mean change of WC −6.02 ± 4.24 −2.24 ± 4.28 0.001
Weight Baseline 83.37 ± 11.22 80.46 ± 11.90 0.33
After intervention 79.98 ± 11.19 78.95 ± 11.87 0.72
Mean change of weight −3.39 ± 2.53 −1.51 ± 2.72 0.008
BMI Baseline 30.49 ± 3.12 29.98 ± 3.11 0.52
After intervention 29.24 ± 3.11 29.42 ± 3.15 0.82
Mean change of BMI −1.25 ± 0.93 −0.56 ± 1.01 0.008

P values of age, height, DBP, SBP, TG, HDL-c, FPG, WC, weight and BMI are computed by independent t-test and data are expressed as mean ± standard deviation (SD), while p values of sex, smoking, education and physical activity are computed by chi-square and data are expressed as numbers (percentage)

MetS: metabolic syndrome; PA: physical activity; DBP: diastolic blood pressure; SBP: systolic blood pressure; TG: triglyceride; HDL-c: high-density lipoprotein cholesterol; FPG: fasting plasma glucose; WC: waist circumference; BMI: body mass index

We demonstrated the intake of energy, macronutrients, food groups and micronutrients of two groups at the baseline and after intervention in Table 2. The intervention group received higher amounts of vegetables, fruits, nuts, seeds and legumes, dairy products, fibers, potassium, magnesium, vitamin C, vitamin A and folate, and also lower amounts of meats as well as fats and oils (p ≤ 0.05 for all). There was no side effect related to the intervention.

Table 2.

Dietary intakes in subjects with MetS

Variables Intervention group (n = 30) Control group (n = 30) P
Energy intake, kcal/d
 Baseline 2117.50 ± 130.54 2093.16 ± 118.67 0.45
 After intervention 1540.16 ± 283.92 1481.16 ± 284.84 0.42
Carbohydrate, g/d
 Baseline 293.96 ± 24.36 289.26 ± 25.26 0.46
 After intervention 199.31 ± 36.48 193.07 ± 37.13 0.51
Protein, g/d
 Baseline 65.74 ± 10.78 66.92 ± 9.91 0.66
 After intervention 69.37 ± 12.79 64.60 ± 12.42 0.14
Fat, g/d
 Baseline 75.40 ± 17.48 74.25 ± 15.18 0.78
 After intervention 51.77 ± 9.54 50.04 ± 9.62 0.48
Potassium, g/d
 Baseline 1845.55 ± 357.04 1982.91 ± 360.65 0.14
 After intervention 3376.62 ± 562.29 2634.73 ± 748.65 <0.001
Sodium, g/d
 Baseline 2279.67 ± 426.55 2147.75 ± 279.76 0.16
 After intervention 1622.37 ± 550.83 1752.78 ± 623.25 0.39
Magnesium, g/d
 Baseline 317.60 ± 71.53 311.33 ± 54.09 0.70
 After intervention 407.73 ± 79.56 344.82 ± 92.38 0.006
Vitamin C, g/d
 Baseline 44.90 ± 5.62 46.33 ± 4.19 0.26
 After intervention 65.32 ± 5.06 53.78 ± 7.17 <0.001
Vitamin A, g/d
 Baseline 331.09 ± 69.35 348.87 ± 70.74 0.33
 After intervention 525.62 ± 44.23 460.14 ± 69.24 <0.001
Folate, g/d
 Baseline 202.78 ± 40.76 207.36 ± 31.30 0.62
 After intervention 347.07 ± 61.43 277.97 ± 74.71 <0.001
Fiber, g/d
 Baseline 16.54 ± 5.91 16.90 ± 4.34 0.78
 After intervention 31.85 ± 8.45 21.67 ± 10.06 <0.001
Vegetables, serving/d
 Baseline 1.26 ± 0.64 1.23 ± 0.67 0.69
 After intervention 3.73 ± 0.44 2.73 ± 0.73 <0.001
Fruits, serving/d
 Baseline 2.06 ± 0.76 1.93 ± 0.69 0.33
 After intervention 4.06 ± 0.63 2.73 ± 0.74 <0.001
Grains, serving/d
 Baseline 13.03 ± 0.55 12.30 ± 0.74 <0.001
 After intervention 6.36 ± 1.40 6.96 ± 1.47 0.11
Nuts, seeds and legumes, serving/d
 Baseline 0.23 ± 0.50 0.26 ± 0.52 0.80
 After intervention 1.46 ± 0.51 0.53 ± 0.50 <0.001
Dairy products, serving/d
 Baseline 1.33 ± 0.60 1.66 ± 0.47 0.02
 After intervention 2.10 ± 0.30 1.70 ± 0.46 <0.001
Meats, serving/d
 Baseline 4.96 ± 0.85 4.93 ± 0.82 0.87
 After intervention 2.73 ± 0.44 4.10 ± 0.30 <0.001
Fats and oils, serving/d
 Baseline 5.96 ± 0.66 6.03 ± 0.61 0.68
 After intervention 2.63 ± 1.03 4.26 ± 0.44 <0.001
Simple sugars, serving/d
 Baseline 4.90 ± 0.71 4.63 ± 1.06 0.25
 After intervention 1.10 ± 0.30 1.16 ± 0.37 0.45

Values are presented as mean ± standard deviation (SD)

presulted from comparisons between two groups by independent t-test

MetS: metabolic syndrome

Outcomes

At the baseline, we found no significant difference between groups in CMI (2.74 ± 1.17 vs. 3.06 ± 1.33; p = 0.33), AIP (0.23 ± 0.17 vs. 0.28 ± 0.17; p = 0.27), AC (3.97 ± 0.96 vs. 3.74 ± 1.37; p = 0.44) and CRI-II (3.31 ± 0.74 vs. 3.0 ± 0.98; p = 0.17). At the end of the trial, the values of CMI (2.36 ± 1.08 vs. 3.04 ± 1.27; p = 0.03) and AIP (0.19 ± 0.18 vs. 0.29 ± 0.16; p = 0.02) were significantly lower in the group receiving DASH diet than the control group; however, the values of AC (3.66 ± 0.99 vs. 3.75 ± 1.52; p = 0.79) and CRI-II (3.01 ± 0.61 vs. 2.97 ± 1.05; p = 0.84) were statistically similar (Table 3).

Table 3.

Effect of DASH diet on cardiometabolic and atherogenic indices in subjects with MetS

Variables Intervention group
(n = 30)
Control group
(n = 30)
P † P ††
CMI
 Baseline 2.74 ± 1.17 3.06 ± 1.33 0.33 0.001
 After intervention 2.36 ± 1.08 3.04 ± 1.27 0.03
 P <0.001 0.82
 Mean change of CMI −0.38 ± 0.29 −0.02 ± 0.47 0.001
 Mean change of EMM (95%CI) −0.38 (−0.52, −0.23) −0.02 (−0.16, 0.12)
AIP
 Baseline 0.23 ± 0.17 0.28 ± 0.17 0.27 0.001
 After intervention 0.19 ± 0.18 0.29 ± 0.16 0.02
 P <0.001 0.46
 Mean change of AIP −0.04 ± 0.04 0.01 ± 0.07 0.001
 Mean change of EMM (95%CI) −0.04 (−0.06, −0.02) 0.01 (−0.01, 0.03)
AC
 Baseline 3.97 ± 0.96 3.74 ± 1.37 0.44 0.04
 After intervention 3.66 ± 0.99 3.75 ± 1.52 0.79
 P 0.004 0.94
 Mean change of AC −0.31 ± 0.54 0.01 ± 0.72 0.06
 Mean change of EMM (95%CI) −0.31 (−0.54, −0.08) 0.01 (−0.21, 0.24)
CRI-II
 Baseline 3.31 ± 0.74 3.0 ± 0.98 0.17 0.009
 After intervention 3.01 ± 0.61 2.97 ± 1.05 0.84
 P <0.001 0.66
 Mean change of CRI-II −0.30 ± 0.37 −0.03 ± 0.39 0.01
 Mean change of EMM (95%CI) −0.30 (−0.43, −0.15) 0.03 (−0.17, −0.11)

Values are presented as mean ± standard deviation (SD)

P: resulted from comparisons within groups by paired t-test. P†: resulted from comparisons between two groups by independent t-test. P††: resulted from comparisons between two groups by Univariate analysis of covariance after adjusting for physical activity and energy intake. We reported the results as estimated marginal means with 95% confidence intervals, lower bound and upper bound

DASH: dietary approaches to stop hypertension; MetS: metabolic syndrome; EMM: estimated marginal means; CMI: cardiometabolic index; AIP: atherogenic index of plasma; AC: Atherogenic coefficient; CRI: castelli risk index

After adjusting for confounding factors, the group receiving DASH diet showed a significant reduction in CMI (−0.38 ± 0.29 vs. −0.02 ± 0.47; p = 0.001), AIP (−0.04 ± 0.04 vs. 0.01 ± 0.07; p = 0.001), AC (−0.31 ± 0.54 vs. 0.01 ± 0.72; p = 0.04) and CRI-II (−0.30 ± 0.37 vs. −0.03 ± 0.39; p = 0.009) (Table 3).

Discussion

This study has shown that adhering to the DASH diet for 12 weeks can be effective in reducing CMI and some atherogenic indices.

CMI and atherogenic indices, established as valid scoring systems for assessing cardiometabolic risk, are derived from on anthropometric variables and lipid profile [5–7]. To date, no research has specifically examined the effect of DASH diet on these indices. However, some studies have explored the effect of DASH diet on either anthropometric variable or lipid profile. For instance, A study found that adherence to DASH diet for 12 weeks reduced body weight and body fat mass among obese people [28]. Similarly, it has been shown that adhering to the DASH diet for 12 weeks effectively decreased BMI [29]. Contrary to these findings, it has been reported that a 6-week adherence to DASH diet showed no significant effect on anthropometric measurements in individuals suffering from MetS [19]. In line with the results of the present study, the meta-analysis of Lari et al. [15] highlighted the positive impact of DASH diet on several anthropometric parameters such as weight, BMI, and waist circumference (WC).

A clinical trial reported that 6-month adherence to DASH diet is an effective approach for managing lipid profile parameters such as TC, TG and LDL-c, though it showed no effect on HDL-c [16]. A study revealed the beneficial effect of DASH diet on TG [14]. In addition, another meta-analysis reported reductions in TC and LDL-c, though no impact was observed on HDL-c [15]. It’s worth mentioning that the DASH diet is characterized as a low-fat dietary pattern, and some evidence suggest that dietary patterns with low-fat content are ineffective in raising HDL-c levels [30–32].

The health benefits of DASH diet are primarily linked to the its nutrient-rich food groups. Antioxidant compounds like polyphenols, abundantly present in vegetables and fruits, attenuate lipid production and β-oxidation in the liver [33, 34]. Additionally, polyphenols enhance hepatic clearance of lipids while decreasing fat accumulation in the liver [35, 36]. Whole grains can diminish intrahepatic fat production [37, 38]. Fibers content found in whole grains and vegetables play an important role in decreasing both hepatic lipid production and lipid peroxidation [39]. Soluble dietary fiber is effective in absorbing dietary cholesterol, reducing absorption of cholesterol and increasing lipid excretion [39, 40]. Moreover, fibers influences macronutrient absorption, gastric emptying time, satiety and appetite regulation, all of which improve obesity [39]. Furthermore, replacing low-energy food groups like fruits and vegetables with meats and processed foods allows for a reduction in energy intake without altering the overall food volume consumed [40]. In general, DASH diet may be effective in reducing cardiovascular risk factors.

As an important strength, our study investigated the impact of DASH diet on novel cardiometabolic and atherogenic indices. This study had some limitations. An important limitation was the relatively short duration of the intervention. In addition, the effect of the DASH diet was not assessed at the middle of intervention period (week 6). Given the nature of the intervention (diet), there were two other important limitations. 1) There was no possibility of blinding the participants. 2) It was difficult to accurately assess the level of compliance of the participants.

Conclusions

The present study suggests that following DASH diet for 12 weeks may decrease CMI and some atherogenic indices. Further studies with longer intervention durations must be conducted in this area.

Acknowledgements

We acknowledge the contribution of the participants and co-researchers.

Author contributions

K.P and A.S: conducted the study; M.H: provided material and technical support; X.W, A.T and R.R: carried out the statistical analysis, and interpreted the finding; X.W: drafted the manuscript; K.P: critically revised the manuscript and supervised the study. All authors reviewed the final manuscript.

Funding

There is no financial funding for this study.

Data availability

The data and materials of the current study is available from the corresponding author upon reasonable request.

Declarations

Ethics approval and consent to participate

The ethical committee of Baqiyatallah University of Medical Sciences in Tehran confirmed the study protocol and written informed consent. All participants provided their informed consent prior to the start of the trial.

Consent for publication

Not applicable.

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.

References

  • 1.Saklayen MG. The global epidemic of the metabolic syndrome. Curr Hypertens Rep. 2018;20(2):12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.McCracken E, Monaghan M, Sreenivasan S. Pathophysiology of the metabolic syndrome. Clin Dermatol. 2018;36(1):14–20. [DOI] [PubMed] [Google Scholar]
  • 3.Collaborators GBDCD. Global, regional, and national burden of cardiovascular diseases and risk factors in 204 countries and territories, 1990-2023. J Am Coll Cardiol. 2025;S0735–1097(25)07428–5. [DOI] [PubMed]
  • 4.Silveira Rossi JL, Barbalho SM, de Araujo R R, Bechara MD, Sloan KP, Sloan LA. Metabolic syndrome and cardiovascular diseases: going beyond traditional risk factors. Diabetes Metab Res Rev. 2022;38(3):e3502. [DOI] [PubMed]
  • 5.Wakabayashi I, Daimon T. The “cardiometabolic index” as a new marker determined by adiposity and blood lipids for discrimination of diabetes mellitus. Clin Chim Acta. 2015;438:274–78. [DOI] [PubMed] [Google Scholar]
  • 6.Sangouni AA, Sasanfar B, Ghadiri-Anari A, Hosseinzadeh M. Effect of l-carnitine supplementation on liver fat content and cardiometabolic indices in overweight/obese women with polycystic ovary syndrome: a randomized controlled trial. Clin Nutr ESPEN. 2021;46:54–59. [DOI] [PubMed] [Google Scholar]
  • 7.Sujatha R, Kavitha S. Atherogenic indices in stroke patients: a retrospective study. Iran J Neurol. 2017;16(2):78–82. [PMC free article] [PubMed] [Google Scholar]
  • 8.Fahed G, Aoun L, Bou Zerdan M, Allam S, Bou Zerdan M, Bouferraa Y, et al. Metabolic syndrome: updates on Pathophysiology and management in 2021. Int J Mol Sci. 2022;23(2):786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Sangouni AA, Nadjarzadeh A, Rohani FS, Sharuni F, Zare Z, Rahimpour S, et al. Dietary approaches to stop hypertension (DASH) diet improves hepatic fibrosis, steatosis and liver enzymes in patients with non-alcoholic fatty liver disease: a randomized controlled trial. Eur J Nutr. 2024;63(1):95–105. [DOI] [PubMed] [Google Scholar]
  • 10.Wickman BE, Enkhmaa B, Ridberg R, Romero E, Cadeiras M, Meyers F, et al. Dietary management of heart failure: DASH diet and precision Nutrition perspectives. Nutrients. 2021;13(12):4424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Panbehkar-Jouybari M, Mollahosseini M, Salehi-Abargouei A, Fallahzadeh H, Mirzaei M, Hosseinzadeh M. The Mediterranean diet and dietary approach to stop hypertension (DASH)-style diet are differently associated with lipid profile in a large sample of Iranian adults: a cross-sectional study of shahedieh cohort. BMC Endocr Disord. 2021;21(1):192. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Cicero AFG, Veronesi M, Fogacci F. Dietary intervention to improve blood pressure control: beyond salt restriction. High Blood Press Cardiovasc Prev. 2021;28(6):547–53. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Siervo M, Lara J, Chowdhury S, Ashor A, Oggioni C, Mathers JC. Effects of the dietary approach to stop hypertension (DASH) diet on cardiovascular risk factors: a systematic review and meta-analysis. Br J Nutr. 2015;113(1):1–15. [DOI] [PubMed] [Google Scholar]
  • 14.Guo R, Li N, Yang R, Liao XY, Zhang Y, Zhu BF, et al. Effects of the modified DASH diet on adults with elevated blood pressure or hypertension: a systematic review and meta-analysis. Front Nutr. 2021;8:725020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lari A, Sohouli MH, Fatahi S, Cerqueira HS, Santos HO, Pourrajab B, et al. The effects of the dietary approaches to stop hypertension (DASH) diet on metabolic risk factors in patients with chronic disease: a systematic review and meta-analysis of randomized controlled trials. Nutr Metab Cardiovasc Dis. 2021;31(10):2766–78. [DOI] [PubMed] [Google Scholar]
  • 16.Lima ST, Souza BS, Franca AK, Salgado JV, Salgado-Filho N, Sichieri R. Reductions in glycemic and lipid profiles in hypertensive patients undergoing the Brazilian dietary approach to break hypertension: a randomized clinical trial. Nutr Res. 2014;34(8):682–87. [DOI] [PubMed] [Google Scholar]
  • 17.Razavi Zade M, Telkabadi MH, Bahmani F, Salehi B, Farshbaf S, Asemi Z. The effects of DASH diet on weight loss and metabolic status in adults with non-alcoholic fatty liver disease: a randomized clinical trial. Liver Int. 2016;36(4):563–71. [DOI] [PubMed] [Google Scholar]
  • 18.Azadbakht L, Mirmiran P, Esmaillzadeh A, Azizi T, Azizi F. Beneficial effects of a dietary approaches to stop hypertension eating plan on features of the metabolic syndrome. Diabetes Care. 2005;28(12):2823–31. [DOI] [PubMed] [Google Scholar]
  • 19.Saneei P, Hashemipour M, Kelishadi R, Rajaei S, Esmaillzadeh A. Effects of recommendations to follow the dietary approaches to stop hypertension (DASH) diet v. usual dietary advice on childhood metabolic syndrome: a randomised cross-over clinical trial. Br J Nutr. 2013;110(12):2250–59. [DOI] [PubMed] [Google Scholar]
  • 20.Alberti KG, Zimmet P, Shaw J, Idfetfc G. The metabolic syndrome-a new worldwide definition. Lancet. 2005;366(9491):1059–62. [DOI] [PubMed] [Google Scholar]
  • 21.Sangouni AA, Hosseinzadeh M, Parastouei K. The effect of dietary approaches to stop hypertension (DASH) diet on fatty liver and cardiovascular risk factors in subjects with metabolic syndrome: a randomized controlled trial. BMC Endocr Disord. 2024;24(1):126. 10.1186/s12902-024-01661-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Sangouni AA, Hosseinzadeh M, Parastouei K. Effect of dietary approaches to stop hypertension diet on insulin resistance and lipid accumulation product in subjects with metabolic syndrome. Sci Rep. 2025;15(1):17025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Sangouni AA, Sangsefidi ZS, Yarhosseini F, Hosseinzadeh M, Akhondi-Meybodi M, Ranjbar A, et al. Effect of cornus mas L. fruit extract on lipid accumulation product and cardiovascular indices in patients with non-alcoholic fatty liver disease: a double-blind randomized controlled trial. Clin Nutr ESPEN. 2022;47:51–57. [DOI] [PubMed] [Google Scholar]
  • 24.Aadahl M, Jorgensen T. Validation of a new self-report instrument for measuring physical activity. Med Sci Sports Exercise. 2003;35(7):1196–202. [DOI] [PubMed] [Google Scholar]
  • 25.Ainsworth BE, Haskell WL, Whitt MC, Irwin ML, Swartz AM, Strath SJ, et al. Compendium of physical activities: an update of activity codes and MET intensities. Med Sci Sports Exercise. 2000;32(9 Suppl):S498–504. [DOI] [PubMed]
  • 26.Fernandez-Macias JC, Ochoa-Martinez AC, Varela-Silva JA, Perez-Maldonado IN. Atherogenic index of plasma: novel predictive biomarker for cardiovascular illnesses. Arch Med Res. 2019;50(5):285–94. [DOI] [PubMed] [Google Scholar]
  • 27.Koca TT, Tugan CB, Seyithanoglu M, Kocyigit BF. The clinical importance of the plasma atherogenic index, other lipid indexes, and urinary Sodium and potassium excretion in patients with stroke. Eurasian J Med. 2019;51(2):172–76. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Perry CA, Van Guilder GP, Kauffman A, Hossain M. A Calorie-restricted DASH diet reduces body fat and maintains muscle strength in obese older adults. Nutrients. 2019;12(1):102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Said MS, El Sayed IT, Ibrahim EE, Khafagy GM. Effect of DASH diet versus healthy dietary advice on the estimated atherosclerotic cardiovascular disease risk. J Prim Care Community Health. 2021;12:2150132720980952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Hashemi R, Mehdizadeh Khalifani A, Rahimlou M, Manafi M. Comparison of the effect of dietary approaches to stop hypertension diet and American Diabetes Association nutrition guidelines on lipid profiles in patients with type 2 Diabetes: a comparative clinical trial. Nutr Diet. 2020;77(2):204–11. [DOI] [PubMed] [Google Scholar]
  • 31.Mooradian AD, Haas MJ, Wong NC. The effect of select nutrients on serum high-density lipoprotein cholesterol and apolipoprotein A-I levels. Endocr Rev. 2006;27(1):2–16. [DOI] [PubMed] [Google Scholar]
  • 32.Qian F, Korat AA, Malik V, Hu FB. Metabolic effects of monounsaturated fatty Acid-Enriched Diets compared with Carbohydrate or polyunsaturated fatty Acid-Enriched Diets in patients with type 2 Diabetes: a systematic review and meta-analysis of randomized controlled trials. Diabetes Care. 2016;39(8):1448–57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Dzah CS, Asante-Donyinah D, Letsyo E, Dzikunoo J, Adams ZS. Dietary polyphenols and obesity: a review of polyphenol effects on lipid and glucose metabolism, mitochondrial homeostasis, and starch digestibility and absorption. Plant Foods Hum Nutr. 2023;78(1):1–12. [DOI] [PubMed] [Google Scholar]
  • 34.Momtazi-Borojeni AA, Katsiki N, Pirro M, Banach M, Rasadi KA, Sahebkar A. Dietary natural products as emerging lipoprotein(a)-lowering agents. J Cell Physiol. 2019;234(8):12581–94. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Aghemo A, Alekseeva OP, Angelico F, Bakulin IG, Bakulina NV, Bordin D, et al. Role of silymarin as antioxidant in clinical management of chronic liver diseases: a narrative review. Ann Med. 2022;54(1):1548–60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Yang K, Chen J, Zhang T, Yuan X, Ge A, Wang S, et al. Efficacy and safety of dietary polyphenol supplementation in the treatment of non-alcoholic fatty liver disease: a systematic review and meta-analysis. Front Immunol. 2022;13:949746. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Zhou AL, Hergert N, Rompato G, Lefevre M. Whole grain oats improve insulin sensitivity and plasma cholesterol profile and modify gut microbiota composition in C57BL/6J mice. J Nutr. 2015;145(2):222–30. [DOI] [PubMed] [Google Scholar]
  • 38.Zhou H, Liu K, Liu W, Wu M, Wang Y, Lv Y, et al. Diets Enriched in sugar, refined, or whole grain differentially influence plasma cholesterol concentrations and cholesterol Metabolism pathways with concurrent changes in bile acid profile and gut microbiota composition in ApoE(-/-) mice. J Agric Food Chem. 2023;71(25):9738–52. [DOI] [PubMed] [Google Scholar]
  • 39.Waddell IS, Orfila C. Dietary fiber in the prevention of obesity and obesity-related chronic diseases: from epidemiological evidence to potential molecular mechanisms. Crit Rev Food Sci Nutr. 2023;63(27):8752–67. [DOI] [PubMed] [Google Scholar]
  • 40.Del Rio-Celestino M, Font R. The Health benefits of fruits and vegetables. Foods. 2020;9(3). [DOI] [PMC free article] [PubMed]

Associated Data

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

Data Availability Statement

The data and materials of the current study is available from the corresponding author upon reasonable request.


Articles from BMC Endocrine Disorders are provided here courtesy of BMC

RESOURCES