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Systematic Review

Impact of the Level of Adherence to the DASH Diet on Blood Pressure: A Systematic Review and Meta-Analysis

by
Xenophon Theodoridis
1,2,
Areti Triantafyllou
2,
Lydia Chrysoula
1,
Fotios Mermigkas
1,
Violeta Chroni
1,
Konstantina Dipla
3,
Eugenia Gkaliagkousi
2 and
Michail Chourdakis
1,*
1
Laboratory of Hygiene, Social and Preventive Medicine and Medical Statistics, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece
2
3rd Clinic of Internal Medicine, Papageorgiou Hospital, School of Medicine, Faculty of Health Sciences, Aristotle University of Thessaloniki, 56403 Thessaloniki, Greece
3
Exercise Physiology & Biochemistry Laboratory, Department of Sport Sciences at Serres, Aristotle University of Thessaloniki, 62110 Thessaloniki, Greece
*
Author to whom correspondence should be addressed.
Metabolites 2023, 13(8), 924; https://doi.org/10.3390/metabo13080924
Submission received: 19 June 2023 / Revised: 17 July 2023 / Accepted: 20 July 2023 / Published: 7 August 2023
(This article belongs to the Special Issue Advances in Dietary Nutrition Intervention on Metabolic Diseases)

Abstract

:
Introduction: the objective of our study was to systematically review the current literature and perform a meta-analysis to evaluate the effect of the level of adherence to the DASH diet on blood pressure. Methods: The identification of relevant studies, data extraction and critical appraisal of the included studies were performed independently by two reviewers. A random-effects model was employed to synthesize the available evidence using the standardized mean difference (SMD) as the appropriate effect size. Results: A total of 37 and 29 articles were included in the qualitative and quantitative analysis, respectively. The pooled effect for systolic blood pressure was SMD = −0.18 (95%CI: −0.32 to −0.04; I2 = 94%; PI: −0.93 to 0.57) and for diastolic blood pressure it was SMD = −0.13 (95%CI: −0.19 to −0.06; I2 = 94%; PI: −0.42 to 0.17). Conclusions: Our findings showed that greater adherence to the DASH diet has a beneficial effect on blood pressure compared to the lowest adherence. Increased compliance with DASH diet recommendations might also have a positive effect on cardiometabolic factors and overall health status. Future studies should aim to standardize the tools of adherence to the DASH diet and utilize rigorous study designs to establish a clearer understanding of the potential benefits of the level of adherence to the DASH diet in blood pressure management.

1. Introduction

Hypertension, defined as the consistently high pressure of blood flow within vessels, is the leading cause of cardiovascular events and all-cause mortality worldwide. Hypertension bears a correlation with the incidence of cardiovascular and renal detriment [1]. As of 2010, nearly one third of adults worldwide had hypertension. The increasing prevalence of hypertension is mainly attributed to the growing number of elderly people, the preference for unhealthy food options (diets rich in sodium and poor in potassium), smoking and the absence of exercise [2].
According to the current literature, the cornerstone of hypertension treatment includes anti-hypertensive drugs [3], as well as lifestyle alterations that consist of salt moderation, the restriction of alcohol and cigarettes, body weight diminution, exercise and dietary approaches [4]. Specifically, the Dietary Approaches to Stop Hypertension (DASH) diet, which comprises fruits, vegetables, fiber and low-fat dairy products in abundance, has been recommended as an efficient diet for regulating normal blood pressure measurements [5,6]. On the other hand, adherence to the DASH diet can be defined as the extent to which an individual may follow nutritional recommendations according to the DASH dietary pattern [7]. Accordingly, the DASH Score is calculated using information obtained from validated food frequency questionnaires in which low and high scores indicate poor and good adherence, respectively.
Several studies have demonstrated that the DASH diet holds a pivotal role in decreasing blood pressure, taking into consideration that people must be able and inclined to ensue this dietary pattern [5,8]. Therefore, proper adherence to the DASH diet is important in the prevention and treatment of elevated blood pressure measurements. Recently, a considerable number of observational studies have been conducted, regarding the effect of the DASH diet on cardiovascular events, including blood pressure measurements [9]. Nevertheless, the results of the available studies are contradictory.
Thus, the aim of our study was to systematically review the current literature and perform a meta-analysis to evaluate the effect of the level of adherence to the DASH diet on blood pressure values.

2. Methods

2.1. Protocol

This systematic review and meta-analysis follow the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA, 2020) [10] and Meta-Analysis of Observational Studies in Epidemiology Guidelines (MOOSE) (Supplementary Tables S1 and S2) [11]. The study protocol was registered in PROSPERO with ID CRD42022368688.

2.2. Search Strategy

The electronic databases PubMed, Scopus and Web of Science Core Collection were searched for the identification of eligible studies from inception to November 2022. We also searched the gray literature and the references of the included studies. Only studies published in the English language without a restriction on publication date were included. Keywords related to DASH diet and hypertension, such as “DASH diet”, “hypertension”, “blood pressure” and “diet” were used for PubMed and were modified accordingly for the remaining databases. The full search string can be found in Supplementary Table S3.

2.3. Eligibility Criteria

Observational and interventional studies, investigating the association between the level of adherence (high versus low) to the DASH diet and changes in blood pressure measurements in the adult population were included in our review. Studies that did not report any data for raw blood pressure measurements in adults were excluded. We also excluded studies involving the pregnant or pediatric population.

2.4. Outcomes

The primary outcome of our review was the difference in systolic and diastolic blood pressure measurements according to the adherence level to the DASH diet.

2.5. Data Extraction

Data from the included studies were extracted independently by two researchers (LC and VC) using an identical standardized data extraction form. Information regarding the study design, first author’s name, publication year, country, sample size, participant’s characteristics (age, sex, BMI, physical activity, smoking), comorbidities, use of anti-hypertensive medication, blood pressure measurements (systolic and diastolic) and the level of adherence to the DASH diet as reported by an assessment tool were abstracted for each study. With regard to the statistical data, we extracted the mean difference and standard deviations, as well as baseline and post-treatment values. In case of any missing data, authors were contacted for additional clarifications regarding data collection and accuracy. Any conflicts were resolved by consensus.

2.6. Quality Appraisal

The quality appraisal regarding the methodological validity of all included studies was evaluated by two independent researchers using the checklists developed by the Joanna Briggs Institute (JBI). Checklists were employed according to the study design of each included record (cohort, case–control and cross-sectional studies). The quality assessment was completed by answering the 11 questions of the JBI tool related to the study design, methodological validity and reliability. The risk of bias (RoB 2.0) tool and the Critical Appraisal Skills Programme (CASP) for the randomized controlled trial checklist were used to evaluate the quality of interventional studies. Any disagreement was resolved by a third reviewer.

2.7. Statistical Analysis

A meta-analysis was conducted for our outcome of interest. Blood pressure measurements were considered as a continuous variable. We used the mean, standard deviation and number of participants in each arm. When the included studies reported standard errors or 95% confidence intervals (95% CI) we transformed them to standard deviation following the guidelines by Cochrane. Furthermore, median values were transformed to mean values according to Wan and colleagues’ [12] approach. A random effects model was employed due to the expected heterogeneity between the included studies. Standardized mean differences (SMDs) and 95% confidence intervals (Cis) were used to present our findings. Heterogeneity was measured using tau-square (τ2) and the I2 index and estimated using the restricted maximum likelihood method. Funnel plots and Egger’s test were used for the evaluation of publication bias. We also performed subgroup and sensitivity analyses to explain heterogeneity and assess the robustness of our findings, respectively. All of the analyses were performed in the statistical software R Studio (version 2022.12.0 + 353) using the meta package.

2.8. Quality of the Evidence

The quality of our findings was assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE), as recommended by the Cochrane handbook [13]. Domains such as the risk of bias, publication bias, heterogeneity, imprecision of the results and indirectness of the evidence were taken into consideration for the total evaluation.

3. Results

3.1. Study Selection

Through the electronic database search, a total of 4319 records were identified, and after the removal of duplicates, 628 articles were reviewed for eligibility. Of those, 527 were excluded based on the title and abstract, 21 were removed due to a lack of access to the full-text articles and a total of 80 records remained for full-text assessment. In the qualitative synthesis, we included 37 papers, and of which, 3 were randomized trials, 20 were cohort studies, 1 was a case–control study and 14 were cross-sectional studies, while only 29 studies were included in the quantitative analysis (Figure 1).

3.2. Study and Patient Characteristics

The socio-demographic characteristics of the included studies are summarized in Table 1 [14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50]. Fourteen studies were conducted in the U.S. [14,20,21,27,29,30,36,38,39,41,43,48,49,50], two studies were conducted in the U.K. [33,42], Spain [26,45] and Italy [15,16], one study was conducted in Greece [18], Brazil [22], Ireland [28], Korea [34], the Netherlands [41], Sweden [46] and Turkey [37], six were conducted in Iran [25,31,32,35,44,47], three were conducted in China [19,23,24] and one study was conducted in four different countries [17]. The number of participants identified in the low- and high-adherence groups in each study ranged from 25 to 19,503 individuals. Adherence to the DASH diet was assessed using the tool constructed by Fung et al. (2008) [51] in 28 studies [15,16,17,18,19,20,23,24,26,27,28,29,30,31,32,33,35,36,38,40,41,42,43,45,46,47,49,50] and the tool developed by Mellen at al. (2008) [52] in three studies [14,39,48], while one study [25] implemented the tool by Valipour et al. (2017) [53], one study [34] implemented the tool by Lee et al. (2017) [54], one study [21] implemented the tool by Folsom et al. (2007) [55], one study [44] utilized principal component analysis (PCA) by Fransen et al., (2014) [56] and two studies [22,37] developed their DASH Score based on the guidelines produced by the National Institutes of Health and the National Heart Lung and Blood Institute (2018) [57]. Moreover, 18 studies [14,17,20,26,29,30,31,32,33,36,38,41,43,44,46,48,49,50] reported an intake of anti-hypertensive medication treatment by the participants including angiotensin-converting-enzyme inhibitors (ACEIs), angiotensin receptor blockers (ARBs) or any other anti-hypertensive agents.
Regarding patient characteristics, all details can be found in Table 2. In only one study [15] were participants disease-free, while in the remaining 35 studies [14,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,46,47,48,49,50], participants were diagnosed with depression, insomnia and cardiometabolic diseases including diabetes, obesity, hypertension, dyslipidemia, metabolic syndrome (MetS), chronic kidney disease (CKD), hyperuricemia, atrial fibrillation or diabetic nephropathy or had undergone surgery for leg amputation; for two [30,45] studies, relevant details were not provided. The mean BMI of all individuals ranged from 23.1 to 32.8 kg/m2, the mean SBP ranged from 102.5 to 154.1 mmHg and the DBP ranged from 45.8 to 88.8 mmHg.

3.3. SBP and DBP Levels

The forest plots for SBP and DBP are presented in Figure 2 and Figure 3, respectively. The pooled effect for SBP favored the high adherence to the DASH diet compared to low adherence (SMD = −0.18; 95%CI −0.32 to −0.04; I2 = 94%; PI: −0.93 to 0.57). Regarding DBP, a significant difference was also observed favoring high adherence to the DASH diet (SMD = −0.13; 95%CI: −0.19 to −0.06; I2 = 94%; PI: −0.42 to 0.17).

3.4. Subgroup Analysis

There was a difference between the two groups regarding both SBP and DBP levels according to the use of drug prescription for hypertension. More specifically, high adherence to the DASH diet was associated with SBP values compared to low adherence for the participants that did not receive any anti-hypertensive medication (SMD = −0.14; 95%CI −0.22 to −0.06, I2 = 91%) (Supplementary Figure S1). Furthermore, a similar association was also observed for DBP values (SMD = −0.23; 95%CI −0.34 to −0.13, I2 = 84%) (Supplementary Figure S2).
Furthermore, a subgroup analysis according to the study design of the included studies was conducted. There was no difference between the high and low adherence to the DASH diet on SBP when cohort or cross-sectional studies were pooled together. On the other hand, there was a significant difference favoring high adherence to the DASH diet based on the randomized controlled trial (Supplementary Figure S3). As far as DBP is concerned, a difference was observed when cohort or cross-sectional studies were synthesized. In contrast, a difference was absent in the randomized controlled trial (Supplementary Figure S4).
Lastly, we performed a subgroup analysis for subsets of studies such as different continents for the SBP and DBP outcomes. There was no difference in SBP between high and low adherence to the DASH diet when studies performed in North America, Europe and South America were synthesized. A significant difference was observed in one study, which was a multicenter one, and in the studies from Asia (Supplementary Figure S5). Regarding DBP, a difference between the two groups was present in the studies that were conducted in North and South America, as well as in the multicenter one (Supplementary Figure S6).

3.5. Sensitivity Analysis

To explore high heterogeneity, we conducted a leave-one-out analysis for both of our outcomes. The findings of this sensitivity analysis showed that regarding SBP there was no significant change in heterogeneity values when omitting one study each time (Supplementary Figure S7). The same findings apply to the DBP outcome (Supplementary Figure S8).

3.6. Risk of Bias Assessment

As depicted in Supplementary Tables S4–S6, almost all cohort and cross-sectional studies successfully performed the recruitment process of participants, identified the potential confounding factors, and used valid methods for measuring the exposures and outcomes. However, information on the sufficient follow-up time, the potential reasons regarding incomplete follow-up, and information on the implementation of strategies for addressing this matter were either missing or were not described clearly. With reference to the interventional studies (Supplementary Table S7), the overall quality was rated as having “some concerns”, according to the RoB 2.0 tool.

3.7. Publication Bias

According to the funnel plots, there were no signs of publication bias in our review (Supplementary Figures S9–S10). Moreover, Egger’s test for the SBP was p = 0.355 and for DBP it was p = 0.232, indicating the absence of publication bias.

3.8. Certainty of Findings

Based on the GRADE approach, the certainty of our evidence was judged as being very low for both of our outcomes of interest.

4. Discussion

The present systematic review and meta-analysis aimed to evaluate the impact of the level of adherence to the DASH diet on blood pressure based on synthesizing the available data from observational and interventional studies. Our findings demonstrate a difference in the reported values of SBP and DBP between participants in the highest and lowest adherence group.
The results of our review support the notion that higher adherence to the DASH diet may have a favorable effect on SBP. However, they should be interpreted with caution due to the high heterogeneity among the included studies. This beneficial effect of the DASH diet could be attributed to its dietary characteristics and the combination of various foods including the high consumption of fruits, vegetables, whole grains, and nuts and the limited salt intake, which have been associated with numerous studies with a reduction in blood pressure [58].
With regard to SBP, high adherence to the DASH diet had a beneficial effect compared to low adherence. It should be stated that few of the included studies presented a mean SBP > 140 mmHg, while in parallel, the majority of them presented a mean DBP < 130 mmHg. This finding is essential, as it supports the protective role of high adherence to the DASH diet in SBP even in subjects with normal SBP.
Regarding DBP, the level of adherence to the DASH diet led to a difference between the highest and lowest adherence group. It should be noted that none of the included studies presented a mean DBP > 90 mmHg, while in parallel, the majority of them presented a mean DBP < 80 mmHg. This finding is of great importance, as it supports that high adherence to the DASH diet could reduce DBP values even in subjects with normal DBP.
In line with our results, published systematic reviews and meta-analyses investigating the effectiveness of the DASH diet provided as an intervention, compared to the usual diet group, showed that the DASH diet is effective in reducing both systolic and diastolic blood pressure [58,59,60]. Furthermore, the DASH diet is also effective in lessening other cardiovascular risk factors such as the concentrations of total and LDL cholesterols. HbA1c and insulin concentrations as well as body weight were also reduced in participants assigned to the dietary intervention group compared to the control group, as demonstrated by an umbrella review of systematic reviews and meta-analyses [61].
It should be noted that the DASH diet given exclusively as a dietary intervention to individuals might promote different health outcomes compared to those that emerged from simply measuring adherence to the DASH diet with the use of specific tools. It is possible for dietary interventions to not enhance compliance with a particular dietary pattern as they also require participants’ adherence. On the contrary, dietary adherence demonstrates the degree of compliance to a diet that is directly related to individuals’ preferences, without corresponding to the consumption of a specified dietary plan. In addition, the level of diet adherence may be affected by various factors, including socioeconomic status, medical history, self-efficacy, level of education, religion, and place of residence, as well as psychological factors and individuals’ attitudes [62].
The DASH diet is not only effective in reducing cardiometabolic outcomes, but there are also published syntheses demonstrating that higher adherence to the DASH diet has a protective role in developing type 2 diabetes mellitus [63] and cardiovascular diseases (CVDs) [64] such as coronary heart disease and stroke [65], and also leads to a significant reduction in all-cause, cancer, and CVD mortality [64]. Lastly, a recently published protocol (PROSPERO 2022 CRD42022344686) of a systematic review and meta-analysis aimed to evaluate adherence to the DASH diet and hypertension risk [66]. The authors found that higher adherence to the DASH diet was associated with a reduced risk of hypertension incidence compared to the lowest adherence to the DASH diet.
To the best of our knowledge, this is the first systematic review and meta-analysis that has investigated the association between adherence to the DASH diet and blood pressure levels. It is also worth noting that our study had certain limitations. Firstly, the study design of the majority of the included studies, i.e., observational studies, limits the confidence in our findings. Furthermore, we are unable to establish causality between adherence to the DASH diet and blood pressure outcomes using observational studies. Secondly, the high heterogeneity observed among the included studies could affect the reliability of the findings; hence, they should be cautiously interpreted. Lastly, we used data from crude models as our outcome of interest was not reported in adjusted analyses.
In conclusion, our findings showed that greater adherence to the DASH diet has a significant effect on blood pressure levels compared to the lowest adherence. Increased compliance with DASH diet recommendations might also have a positive effect on cardiometabolic factors and overall health status. Future studies should aim to standardize the tools of adherence to the DASH diet and utilize rigorous study designs to establish a clearer understanding of the potential benefits of the level of adherence to the DASH diet in blood pressure management and monitoring.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/metabo13080924/s1: Supplementary Figure S1. Subgroup analysis for SBP according to the use of antihypertensive medication. Figure S2. Subgroup analysis for SBP according to the use of antihypertensive medication; Figure S3. Subgroup analysis for SBP based on the study design; Figure S4. Subgroup analysis for DBP based on the study design; Figure S5. Subgroup analysis for SBP based on the different continent; Figure S6. Subgroup analysis for DBP based on the different continents; Figure S7. Leave-one-out analysis for the SBP outcome; Figure S8. Leave-one-out analysis for the DBP outcome; Figure S9. Funnel plot for the SBP outcome; Figure S10. Funnel plot for the DBP outcome; Table S1. PRISMA 2020 checklist; Table S2. MOOSE checklist; Table S3. Search strategy for identifying observational studies on Pubmed; Table S4. Quality appraisal of cohort studies using the JBI Tool; Table S5. Quality appraisal of cross-sectional studies using the JBI Tool; Table S6. Quality appraisal of case-control studies using the JBI Tool; Table S7. Quality appraisal of randomized control trials using the RoB 2.0 Tool; Table S8. Quality appraisal of randomized control trials using the CASP.

Author Contributions

Conceptualization, X.T. and A.T.; methodology, X.T.; formal analysis, X.T.; investigation, L.C. and V.C.; data curation, X.T. and L.C.; writing—original draft preparation, X.T., L.C. and F.M.; writing—review and editing, M.C., K.D., E.G. and A.T.; visualization, X.T.; supervision, M.C. and A.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Collaborators, G.R.F. Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet 2018, 392, 1923–1994. [Google Scholar] [CrossRef] [Green Version]
  2. Mills, K.T.; Stefanescu, A.; He, J. The global epidemiology of hypertension. Nat. Rev. Nephrol. 2020, 16, 223–237. [Google Scholar] [CrossRef] [PubMed]
  3. Law, M.R.; Morris, J.K.; Wald, N.J. Use of blood pressure lowering drugs in the prevention of cardiovascular disease: Meta-analysis of 147 randomised trials in the context of expectations from prospective epidemiological studies. BMJ (Clin. Res. Ed.) 2009, 338, b1665. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Williams, B.; Mancia, G.; Spiering, W.; Agabiti Rosei, E.; Azizi, M.; Burnier, M.; Clement, D.L.; Coca, A.; de Simone, G.; Dominiczak, A.; et al. 2018 ESC/ESH Guidelines for the management of arterial hypertension. Eur. Heart J. 2018, 39, 3021–3104. [Google Scholar] [CrossRef] [Green Version]
  5. Appel, L.J.; Moore, T.J.; Obarzanek, E.; Vollmer, W.M.; Svetkey, L.P.; Sacks, F.M.; Bray, G.A.; Vogt, T.M.; Cutler, J.A.; Windhauser, M.M.; et al. A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group. N. Engl. J. Med. 1997, 336, 1117–1124. [Google Scholar] [CrossRef] [Green Version]
  6. Blumenthal, J.A.; Babyak, M.A.; Hinderliter, A.; Watkins, L.L.; Craighead, L.; Lin, P.H.; Caccia, C.; Johnson, J.; Waugh, R.; Sherwood, A. Effects of the DASH diet alone and in combination with exercise and weight loss on blood pressure and cardiovascular biomarkers in men and women with high blood pressure: The ENCORE study. Arch. Intern. Med. 2010, 170, 126–135. [Google Scholar] [CrossRef]
  7. De Geest, S.; Sabaté, E. Adherence to long-term therapies: Evidence for action. Eur. J. Cardiovasc. Nurs. 2003, 2, 323. [Google Scholar] [CrossRef]
  8. Sacks, F.M.; Svetkey, L.P.; Vollmer, W.M.; Appel, L.J.; Bray, G.A.; Harsha, D.; Obarzanek, E.; Conlin, P.R.; Miller, E.R., 3rd; Simons-Morton, D.G.; et al. Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. DASH-Sodium Collaborative Research Group. N. Engl. J. Med. 2001, 344, 3–10. [Google Scholar] [CrossRef]
  9. Feng, Q.; Fan, S.; Wu, Y.; Zhou, D.; Zhao, R.; Liu, M.; Song, Y. Adherence to the dietary approaches to stop hypertension diet and risk of stroke: A meta-analysis of prospective studies. Medicine 2018, 97, e12450. [Google Scholar] [CrossRef]
  10. Page, M.J.; Moher, D.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. PRISMA 2020 explanation and elaboration: Updated guidance and exemplars for reporting systematic reviews. BMJ 2021, 372, n160. [Google Scholar] [CrossRef]
  11. Brooke, B.S.; Schwartz, T.A.; Pawlik, T.M. MOOSE Reporting Guidelines for Meta-analyses of Observational Studies. JAMA Surg. 2021, 156, 787–788. [Google Scholar] [CrossRef]
  12. Wan, X.; Wang, W.; Liu, J.; Tong, T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med. Res. Methodol. 2014, 14, 135. [Google Scholar] [CrossRef] [Green Version]
  13. Higgins, J.; Thomas, J.; Chandler, J.; Cumpston, M.; Li, T.; Page, M.J.; Welch, V.A. Cochrane Handbook for Systematic Reviews of Interventions Version 6.3; Cochrane: London, UK, 2022. [Google Scholar]
  14. Banerjee, T.; Crews, D.C.; Tuot, D.S.; Pavkov, M.E.; Burrows, N.R.; Stack, A.G.; Saran, R.; Bragg-Gresham, J.; Powe, N.R. Poor accordance to a DASH dietary pattern is associated with higher risk of ESRD among adults with moderate chronic kidney disease and hypertension. Kidney Int. 2019, 95, 1433–1442. [Google Scholar] [CrossRef] [Green Version]
  15. Bendinelli, B.; Masala, G.; Bruno, R.M.; Caini, S.; Saieva, C.; Boninsegni, A.; Ungar, A.; Ghiadoni, L.; Palli, D. A priori dietary patterns and blood pressure in the EPIC Florence cohort: A cross-sectional study. Eur. J. Nutr. 2019, 58, 455–466. [Google Scholar] [CrossRef]
  16. Bonaccio, M.; Di Castelnuovo, A.; Costanzo, S.; De Curtis, A.; Persichillo, M.; Cerletti, C.; Donati, M.B.; de Gaetano, G.; Iacoviello, L. Association of a traditional Mediterranean diet and non-Mediterranean dietary scores with all-cause and cause-specific mortality: Prospective findings from the Moli-sani Study. Eur. J. Nutr. 2021, 60, 729–746. [Google Scholar] [CrossRef] [PubMed]
  17. Chan, Q.; Wren, G.M.; Lau, C.E.; Ebbels, T.M.D.; Gibson, R.; Loo, R.L.; Aljuraiban, G.S.; Posma, J.M.; Dyer, A.R.; Steffen, L.M.; et al. Blood pressure interactions with the DASH dietary pattern, sodium, and potassium: The International Study of Macro-/Micronutrients and Blood Pressure (INTERMAP). Am. J. Clin. Nutr. 2022, 116, 216–229. [Google Scholar] [CrossRef]
  18. Critselis, E.; Kontogianni, M.D.; Georgousopoulou, E.; Chrysohoou, C.; Tousoulis, D.; Pitsavos, C.; Panagiotakos, D.B. Comparison of the Mediterranean diet and the Dietary Approach Stop Hypertension in reducing the risk of 10-year fatal and non-fatal CVD events in healthy adults: The ATTICA Study (2002–2012). Public Health Nutr. 2021, 24, 2746–2757. [Google Scholar] [CrossRef]
  19. Dai, S.; Xiao, X.; Xu, C.; Jiao, Y.; Qin, Z.; Meng, J.; Zuo, H.; Zeng, P.; Tang, D.; Wu, X.; et al. Association of Dietary Approaches to Stop Hypertension diet and Mediterranean diet with blood pressure in less-developed ethnic minority regions. Public Health Nutr. 2022, 25, 1–29. [Google Scholar] [CrossRef]
  20. Daniel, G.D.; Chen, H.; Bertoni, A.G.; Rapp, S.R.; Fitzpatrick, A.L.; Luchsinger, J.A.; Wood, A.C.; Hughes, T.M.; Burke, G.L.; Hayden, K.M. DASH diet adherence and cognitive function: Multi-ethnic study of atherosclerosis. Clin. Nutr. ESPEN 2021, 46, 223–231. [Google Scholar] [CrossRef] [PubMed]
  21. Epstein, D.E.; Sherwood, A.; Smith, P.J.; Craighead, L.; Caccia, C.; Lin, P.H.; Babyak, M.A.; Johnson, J.J.; Hinderliter, A.; Blumenthal, J.A. Determinants and consequences of adherence to the dietary approaches to stop hypertension diet in African-American and white adults with high blood pressure: Results from the ENCORE trial. J. Acad. Nutr. Diet. 2012, 112, 1763–1773. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Francisco, S.C.; Araújo, L.F.; Griep, R.H.; Chor, D.; Molina, M.; Mil, J.G.; Bensenor, I.M.; Matos, S.M.A.; Barreto, S.M.; Giatti, L. Adherence to the Dietary Approaches to Stop Hypertension (DASH) and hypertension risk: Results of the Longitudinal Study of Adult Health (ELSA-Brasil). Br. J. Nutr. 2020, 123, 1068–1077. [Google Scholar] [CrossRef]
  23. Gao, X.; Tian, Z.; Zhao, D.; Li, K.; Zhao, Y.; Xu, L.; Wang, X.; Fan, D.; Ma, X.; Ling, W.; et al. Associations between Adherence to Four A Priori Dietary Indexes and Cardiometabolic Risk Factors among Hyperlipidemic Patients. Nutrients 2021, 13, 2179. [Google Scholar] [CrossRef] [PubMed]
  24. Gao, Y.; Cui, L.F.; Sun, Y.Y.; Yang, W.H.; Wang, J.R.; Wu, S.L.; Gao, X. Adherence to the Dietary Approaches to Stop Hypertension Diet and Hyperuricemia: A Cross-Sectional Study. Arthritis Care Res. 2020, 73, 603–611. [Google Scholar] [CrossRef] [PubMed]
  25. Ghorabi, S.; Salari-Moghaddam, A.; Daneshzad, E.; Sadeghi, O.; Azadbakht, L.; Djafarian, K. Association between the DASH diet and metabolic syndrome components in Iranian adults. Diabetes Metab. Syndr. 2019, 13, 1699–1704. [Google Scholar] [CrossRef] [PubMed]
  26. Glenn, A.J.; Hernández-Alonso, P.; Kendall, C.W.C.; Martínez-González, M.Á.; Corella, D.; Fitó, M.; Martínez, J.A.; Alonso-Gómez, Á.M.; Wärnberg, J.; Vioque, J.; et al. Longitudinal changes in adherence to the portfolio and DASH dietary patterns and cardiometabolic risk factors in the PREDIMED-Plus study. Clin. Nutr. 2021, 40, 2825–2836. [Google Scholar] [CrossRef]
  27. Goyal, P.; Balkan, L.; Ringel, J.B.; Hummel, S.L.; Sterling, M.R.; Kim, S.; Arora, P.; Jackson, E.A.; Brown, T.M.; Shikany, J.M.; et al. The Dietary Approaches to Stop Hypertension (DASH) Diet Pattern and Incident Heart Failure. J. Card. Fail. 2021, 27, 512–521. [Google Scholar] [CrossRef]
  28. Harrington, J.M.; Fitzgerald, A.P.; Kearney, P.M.; McCarthy, V.J.; Madden, J.; Browne, G.; Dolan, E.; Perry, I.J. DASH diet score and distribution of blood pressure in middle-aged men and women. Am. J. Hypertens. 2013, 26, 1311–1320. [Google Scholar] [CrossRef] [Green Version]
  29. Hu, E.A.; Coresh, J.; Anderson, C.A.M.; Appel, L.J.; Grams, M.E.; Crews, D.C.; Mills, K.T.; He, J.; Scialla, J.; Rahman, M.; et al. Adherence to Healthy Dietary Patterns and Risk of CKD Progression and All-Cause Mortality: Findings From the CRIC (Chronic Renal Insufficiency Cohort) Study. Am. J. Kidney Dis. Off. J. Natl. Kidney Found. 2021, 77, 235–244. [Google Scholar] [CrossRef]
  30. Ishikawa, Y.; Laing, E.M.; Anderson, A.K.; Zhang, D.; Kindler, J.M.; Trivedi-Kapoor, R.; Sattler, E.L.P. Adherence to the Dietary Approaches to Stop Hypertension (DASH) diet is associated with low levels of insulin resistance among heart failure patients. Nutr. Metab. Cardiovasc. Dis. NMCD 2022, 32, 1841–1850. [Google Scholar] [CrossRef]
  31. Jalilpiran, Y.; Darooghegi Mofrad, M.; Mozaffari, H.; Bellissimo, N.; Azadbakht, L. Adherence to dietary approaches to stop hypertension (DASH) and Mediterranean dietary patterns in relation to cardiovascular risk factors in older adults. Clin. Nutr. ESPEN 2020, 39, 87–95. [Google Scholar] [CrossRef] [PubMed]
  32. Jayedi, A.; Mirzaei, K.; Rashidy-Pour, A.; Yekaninejad, M.S.; Zargar, M.S.; Akbari Eidgahi, M.R. Dietary approaches to stop hypertension, mediterranean dietary pattern, and diabetic nephropathy in women with type 2 diabetes: A case-control study. Clin. Nutr. ESPEN 2019, 33, 164–170. [Google Scholar] [CrossRef]
  33. Jones, N.R.V.; Forouhi, N.G.; Khaw, K.T.; Wareham, N.J.; Monsivais, P. Accordance to the Dietary Approaches to Stop Hypertension diet pattern and cardiovascular disease in a British, population-based cohort. Eur. J. Epidemiol. 2018, 33, 235–244. [Google Scholar] [CrossRef] [Green Version]
  34. Kang, S.H.; Cho, K.H.; Do, J.Y. Association between the Modified Dietary Approaches to Stop Hypertension and Metabolic Syndrome in Postmenopausal Women without Diabetes. Metab. Syndr. Relat. Disord. 2018, 16, 282–289. [Google Scholar] [CrossRef]
  35. Khodarahmi, M.; Nikniaz, L.; Abbasalizad Farhangi, M. The Interaction between Fatty Acid Desaturase-2 (FADS2) rs174583 Genetic Variant and Dietary Quality Indices (DASH and MDS) Constructs Different Metabolic Phenotypes Among Obese Individuals. Front. Nutr. 2021, 8, 669207. [Google Scholar] [CrossRef] [PubMed]
  36. Kim, Y.; Huan, T.; Joehanes, R.; McKeown, N.M.; Horvath, S.; Levy, D.; Ma, J. Higher diet quality relates to decelerated epigenetic aging. Am. J. Clin. Nutr. 2022, 115, 163–170. [Google Scholar] [CrossRef]
  37. Köroğlu, Ö.; Tel Adıgüzel, K. Cardiometabolic risk parameters of individuals with lower extremity amputation: What is the effect of adherence to DASH diet and Mediterranean diet? Turk. J. Phys. Med. Rehabil. 2020, 66, 291–298. [Google Scholar] [CrossRef]
  38. Lin, J.; Fung, T.T.; Hu, F.B.; Curhan, G.C. Association of dietary patterns with albuminuria and kidney function decline in older white women: A subgroup analysis from the Nurses’ Health Study. Am. J. Kidney Dis. Off. J. Natl. Kidney Found. 2011, 57, 245–254. [Google Scholar] [CrossRef] [Green Version]
  39. Liu, Y.; Kuczmarski, M.F.; Miller, E.R., 3rd; Nava, M.B.; Zonderman, A.B.; Evans, M.K.; Powe, N.R.; Crews, D.C. Dietary Habits and Risk of Kidney Function Decline in an Urban Population. J. Ren. Nutr. Off. J. Counc. Ren. Nutr. Natl. Kidney Found. 2017, 27, 16–25. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  40. Mackenbach, J.D.; Lakerveld, J.; Generaal, E.; Gibson-Smith, D.; Penninx, B.; Beulens, J.W.J. Local fast-food environment, diet and blood pressure: The moderating role of mastery. Eur. J. Nutr. 2019, 58, 3129–3134. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Mattei, J.; Sotos-Prieto, M.; Bigornia, S.J.; Noel, S.E.; Tucker, K.L. The Mediterranean Diet Score Is More Strongly Associated with Favorable Cardiometabolic Risk Factors over 2 Years than Other Diet Quality Indexes in Puerto Rican Adults. J. Nutr. 2017, 147, 661–669. [Google Scholar] [CrossRef] [Green Version]
  42. Mertens, E.; Markey, O.; Geleijnse, J.M.; Lovegrove, J.A.; Givens, D.I. Adherence to a healthy diet in relation to cardiovascular incidence and risk markers: Evidence from the Caerphilly Prospective Study. Eur. J. Nutr. 2018, 57, 1245–1258. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Missikpode, C.; Ricardo, A.C.; Durazo-Arvizu, R.A.; Manoharan, A.; Mattei, J.; Isasi, C.R.; Mossavar-Rahmani, Y.; Talavera, G.A.; Sotres-Alvarez, D.; Daviglus, M.L.; et al. Association of Diet Quality Indices with Longitudinal Changes in Kidney Function in U.S. Hispanics/Latinos: Findings from the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). Kidney360 2021, 2, 50–62. [Google Scholar] [CrossRef] [PubMed]
  44. Mousavi, S.N.; Hassani, F.; Namadian, M. Dietary Patterns and the Intake of Trace Elements in People with Hypertension: A Cross-Sectional Study. J. Adv. Med. Biomed. Res. 2020, 28, 1–10. [Google Scholar] [CrossRef]
  45. Navarro-Prado, S.; Schmidt-RioValle, J.; Montero-Alonso, M.A.; Fernández-Aparicio, Á.; González-Jiménez, E. Stricter Adherence to Dietary Approaches to Stop Hypertension (DASH) and its Association with Lower Blood Pressure, Visceral Fat, and Waist Circumference in University Students. Nutrients 2020, 12, 740. [Google Scholar] [CrossRef] [Green Version]
  46. Nilsson, A.; Halvardsson, P.; Kadi, F. Adherence to DASH-Style Dietary Pattern Impacts on Adiponectin and Clustered Metabolic Risk in Older Women. Nutrients 2019, 11, 805. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  47. Ramezankhani, A.; Hosseini-Esfahani, F.; Mirmiran, P.; Azizi, F.; Hadaegh, F. The association of priori and posteriori dietary patterns with the risk of incident hypertension: Tehran Lipid and Glucose Study. J. Transl. Med. 2021, 19, 44. [Google Scholar] [CrossRef] [PubMed]
  48. Rebholz, C.M.; Crews, D.C.; Grams, M.E.; Steffen, L.M.; Levey, A.S.; Miller, E.R., 3rd; Appel, L.J.; Coresh, J. DASH (Dietary Approaches to Stop Hypertension) Diet and Risk of Subsequent Kidney Disease. Am. J. Kidney Dis. Off. J. Natl. Kidney Found. 2016, 68, 853–861. [Google Scholar] [CrossRef] [Green Version]
  49. Santiago-Torres, M.; Shi, Z.; Tinker, L.F.; Lampe, J.W.; Allison, M.A.; Barrington, W.; Crane, T.E.; Garcia, D.O.; Hayden, K.M.; Isasi, C.R.; et al. Diet quality indices and risk of metabolic syndrome among postmenopausal women of Mexican ethnic descent in the Women’s Health Initiative Observational Study. Nutr. Healthy Aging 2020, 5, 261–272. [Google Scholar] [CrossRef]
  50. Tangney, C.; Sarkar, D.; Staffileno, B.A. Comparison of three DASH scoring paradigms and prevalent hypertension among older Hispanics. J. Hum. Hypertens. 2016, 30, 210–215. [Google Scholar] [CrossRef]
  51. Fung, T.T.; Chiuve, S.E.; McCullough, M.L.; Rexrode, K.M.; Logroscino, G.; Hu, F.B. Adherence to a DASH-style diet and risk of coronary heart disease and stroke in women. Arch. Intern. Med. 2008, 168, 713–720. [Google Scholar] [CrossRef] [Green Version]
  52. Mellen, P.B.; Gao, S.K.; Vitolins, M.Z.; Goff, D.C., Jr. Deteriorating Dietary Habits Among Adults with Hypertension: DASH Dietary Accordance, NHANES 1988–1994 and 1999–2004. Arch. Intern. Med. 2008, 168, 308–314. [Google Scholar] [CrossRef] [PubMed]
  53. Valipour, G.; Esmaillzadeh, A.; Azadbakht, L.; Afshar, H.; Hassanzadeh, A.; Adibi, P. Adherence to the DASH diet in relation to psychological profile of Iranian adults. Eur. J. Nutr. 2017, 56, 309–320. [Google Scholar] [CrossRef]
  54. Lee, H.S.; Lee, K.B.; Hyun, Y.Y.; Chang, Y.; Ryu, S.; Choi, Y. DASH dietary pattern and chronic kidney disease in elderly Korean adults. Eur. J. Clin. Nutr. 2017, 71, 755–761. [Google Scholar] [CrossRef] [Green Version]
  55. Folsom, A.R.; Parker, E.D.; Harnack, L.J. Degree of concordance with DASH diet guidelines and incidence of hypertension and fatal cardiovascular disease. Am. J. Hypertens. 2007, 20, 225–232. [Google Scholar] [CrossRef] [Green Version]
  56. Fransen, H.P.; May, A.M.; Stricker, M.D.; Boer, J.M.; Hennig, C.; Rosseel, Y.; Ocké, M.C.; Peeters, P.H.; Beulens, J.W. A posteriori dietary patterns: How many patterns to retain? J. Nutr. 2014, 144, 1274–1282. [Google Scholar] [CrossRef] [Green Version]
  57. National Heart, Lung, and Blood Institute. Your Guide to Lowering Your Blood Pressure with DASH; National Heart, Lung, and Blood Institute: Bethesda, MD, USA, 2006.
  58. Siervo, M.; Lara, J.; Chowdhury, S.; Ashor, A.; Oggioni, C.; Mathers, J.C. 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, 1–15. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  59. Saneei, P.; Salehi-Abargouei, A.; Esmaillzadeh, A.; Azadbakht, L. Influence of Dietary Approaches to Stop Hypertension (DASH) diet on blood pressure: A systematic review and meta-analysis on randomized controlled trials. Nutr. Metab. Cardiovasc. Dis. NMCD 2014, 24, 1253–1261. [Google Scholar] [CrossRef]
  60. Guo, R.; Li, N.; Yang, R.; Liao, X.Y.; Zhang, Y.; Zhu, B.F.; Zhao, Q.; Chen, L.; Zhang, Y.G.; Lei, Y. 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. [Google Scholar] [CrossRef] [PubMed]
  61. Chiavaroli, L.; Viguiliouk, E.; Nishi, S.K.; Blanco Mejia, S.; Rahelić, D.; Kahleová, H.; Salas-Salvadó, J.; Kendall, C.W.; Sievenpiper, J.L. DASH Dietary Pattern and Cardiometabolic Outcomes: An Umbrella Review of Systematic Reviews and Meta-Analyses. Nutrients 2019, 11, 338. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Al-Salmi, N.; Cook, P.; D’Souza, M.S. Diet Adherence among Adults with Type 2 Diabetes Mellitus: A Concept Analysis. Oman Med. J. 2022, 37, e361. [Google Scholar] [CrossRef]
  63. Jannasch, F.; Kröger, J.; Schulze, M.B. Dietary Patterns and Type 2 Diabetes: A Systematic Literature Review and Meta-Analysis of Prospective Studies. J. Nutr. 2017, 147, 1174–1182. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  64. Schwingshackl, L.; Hoffmann, G. Diet quality as assessed by the Healthy Eating Index, the Alternate Healthy Eating Index, the Dietary Approaches to Stop Hypertension score, and health outcomes: A systematic review and meta-analysis of cohort studies. J. Acad. Nutr. Diet. 2015, 115, 780–800.e785. [Google Scholar] [CrossRef] [PubMed]
  65. Salehi-Abargouei, A.; Maghsoudi, Z.; Shirani, F.; Azadbakht, L. Effects of Dietary Approaches to Stop Hypertension (DASH)-style diet on fatal or nonfatal cardiovascular diseases–incidence: A systematic review and meta-analysis on observational prospective studies. Nutrition 2013, 29, 611–618. [Google Scholar] [CrossRef]
  66. Theodoridis, X.; Triantafyllou, A.; Gkaliagkousi, E.; Mastrogiannis, K. Adherence to DASH Diet and Hypertension Risk: A Systematic Review and Meta-Analysis. Nutrients 2023, 15, 3261. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Flow diagram of the eligibility process.
Figure 1. Flow diagram of the eligibility process.
Metabolites 13 00924 g001
Figure 2. Meta-analysis for SBP (mmHg).
Figure 2. Meta-analysis for SBP (mmHg).
Metabolites 13 00924 g002
Figure 3. Meta-analysis results for DBP (mmHg).
Figure 3. Meta-analysis results for DBP (mmHg).
Metabolites 13 00924 g003
Table 1. Study characteristics included in the systematic review.
Table 1. Study characteristics included in the systematic review.
Study IDCountryStudy DesignPopulationNo. of Participants (Low/High)Mean Age (SD)Exclusion CriteriaDASH Assessment ToolUse of Anti-Hypertensive Medication
Benerjee et al., 2019 [14] U.S.Prospective observational studyAdults with hypertension and CKD enrolled in the National Health and Nutrition Examination Survey (NHANES) III321/197
Total: 1110
70.2 ± 12.9Missing data on dietary intake, eGFR < 30 or >59 mL/min, pregnancyDASH Score by Mellen et al. (2008)ACEI, ARB
Bendinellii et al., 2019 [15]ItalyCross-sectional observational studyResidents of Florence and Prato 843/1959
Total: 10,163
50.4 ± 7.7Diagnosis of hypertension or anti-hypertensive drugs at any time in the pastDASH Score by Fung et al. (2008)No
Bonaccio et al., 2020 [16]ItalyProspective observational studyMen and women from the general population of Moli-sami Study6368/6013
Total: 12,381
55.0 ± 12.0EI < 800 kcal/day in men and <500 kcal/day in women or >4000 kcal/day in men and >3500 kcal/day in women, unreliable medical dietary questionnaires, lost to follow-up, missing data on outcome exposure, missing information on the main covariates of interestDASH Score by Fung et al. (2008)No
Chan et al., 2022 [17]China, Japan, U.K., U.S.Cross-sectional observational studyAdults410/420
Total: 2164
28.9 ± 5.9Incomplete dietary dataDASH Score by Fung et al. (2008)Yes
Critselis et al., 2019 [18]GreeceProspective observational studyGreek male adults, free of CVD965/1054
Total: 2019
45.2 ± 14.0CVD at baselineDASH Score by Fung et al. (2008)No
Dai et al., 2022 [19]ChinaProspective observational studyAdults from Tibetan, Yi, Miao, Bai, Bouyei and Dong ethnic groupsNo info
Total: 81,433
50.5 ± 11.2<30 y or >79 y, missing information on diet-related variables, missing information on outcome-related data, implausible BMI values (BMI < 14 or >45 kg/m2), unusual daily EI (<600 or >3500 kcal/d for females, <800 or >4200 kcal/d for males), self-reported physician-diagnosed hypertension and use of anti-hypertensive medicationDASH Score by Fung et al. (2008)No
Daniel et al., 2021 [20]U.S.Prospective observational studyChinese, Hispanic, non-Hispanic Black or non-Hispanic white4169
Total: 1760
60.4 ± 9.5Extreme EI of < 500 kcal or >5000 kcal, without FFQ, no cognitive data, using Alzheimer’s medicationsDASH Score by Fung et al. (2008)Yes
Epstein et al., 2012 [21]U.S.RCTHealthy, overweight or obese men and women with above-normal BP40/26
Total: 144
51.3 ± 9.0Medication, other comorbidities, too high/low BMI and BP, dietary reasonsDASH Score by Folsom et al. (2007)No
Fransisco et al., 2020 [22] BrazilProspective observational studyActive or retired civil servants of higher education and research institutions4987/645
Total: 5632
49.9 ± 8.3Fulfilled the criteria for hypertension, anti-hypertensive drugs, reported CVD, missing information on BP values, dietary reasons, urinary Na, race/skin colorDASH Score developed based on guidelines by the National Institutes of Health and National Heart Lung and Blood Institute (2018)No
Gao et al., 2021 [23]ChinaRCTChinese adults with hyperilipidemiaNo info
Total: 269
58.0 ± 8.0Known chronic diseases, acute and chronic infectious diseases, trauma or surgery, use of hormonal therapies, use of medications known to influence lipid metabolism within the past six months, use of anti-inflammatory or antibiotic drugs within the past three months, use of vasomotor function drugs within the past three months, taking phytochemicals or other dietary supplements within the past two months and pregnant or lactating womenDASH Score by Fung et al. (2008)No
Gao et al., 2020 [24]ChinaProspective observational studyAdults from Tangshan City18,024/19,503
Total: 71,893
51.4 ± 0.1Previously diagnosed as having gout, reported an implausible EI (<800 kcal/day or >4000 kcal/day for men, and <500 kcal/day or >3500 kcal/day for women), poor results on food frequency questionnaires, incomplete information on demographic dataDASH Score by Fung et al. (2008)No
Ghorabi et al., 2019 [25]IranCross-sectional observational studyIranian adults136/129
Total: 396
38.2 ± 9.5Pregnancy, post-menopausal status, lactation, any kind of cancers, medication for modifying fat, blood sugar and BP, ischemic heart disease, use of sedative or hypnotic drug, use of anti-histamine, use of immune system inhibitors, following any special diet for any reasons under the supervision of a diet therapist, being a professional athlete, use of weight loss drugDASH Score by Valipour et al. (2017)No
Glenn et al., 2021 [26]SpainRCTOlder men and women with BMI 27–40 kg/m2 and fulfilled at least three criteria of the MetS2026/1636
Total: 6874
65.0Implausible EI (<500 or >3500 kcal/d for women and <800 or >4000 kcal/d for men) or missing information on FFQ at baselineDASH Score by Fung et al. (2008)Yes
Goyal et al., 2021 [27]U.S.Prospective observational studyAfrican-American and white adults4203/5764
Total: 18,856
64.0 ± 9.2Missing or incomplete FFQ (≤85%), implausible EI (men <3347 kJ/d or >20,920 kJ/d, and women <2093 kJ/d or >18,841)DASH Score by Fung et al. (2008)No
Harrington et al., 2013 [28]IrelandCross-sectional observational studyMen and women based in a primary care setting in the North Cork Region of the Republic of IrelandNo info
Total: 2047
60.7 Duplicates, deaths and ineligibles, mortality, lost to follow-up, too unwell to participateDASH Score by Fung et al. (2008)No
Hu et al., 2021 [29]U.S.Prospective observational studyMen and women with an estimated eGFR 20–70 mL/min/1.73 m2912/795
Total: 2403
57.3 ± 11.3Unfilled FFQ, extreme self-reported EI (women: <500 or >3500 kcal/d; men: <700 or >4500 kcal/d), not sufficient data to calculate all dietary pattern scores, missing covariates of interestDASH Score by Fung et al. (2008)ACEI, ARB
Ishikawa et al., 2022 [30]U.S.Cross-sectional observational studyAdults with self-reported diagnosis of HF76/81
Total: 348
65.3 ± 0.9Did not attend the mobile examination center morning
session, incomplete data on fasting plasma glucose and insulin to calculate the HOMA-IR, physician diagnosis of DM or used diabetes medications, pregnancy, implausible EI (gender-specific <1st and >99th percentiles of EI per day)
DASH Score by Fung et al. (2008)ACEIs, ARBs, beta-blockers, loop diuretics
Jalilpiran et al., 2020 [31]IranCross-sectional observational studyOlder adult men living in southern Tehran203/154
Total: 357
64.9 ± 6.5Malignant diseases (e.g., cancer), under- or over-reported total EI (<800 kcal/day and >4200 kcal/day), under- and over-reporting of total EIDASH Score by Fung et al. (2008)No info
Jayedi et al., 2019 [32]IranCase–control studyWomen with type 2 DM and diabetic nephropathy at Kowsar Diabetes Clinic in SemnanNo info
Total: 210
55.3 ± 7.0GDM, type 1 DM, medication treatment, previous history of cancer, myocardial infarction, hepatic disease, autoimmune disorders, stroke and coronary angiographyDASH Score by Fung et al. (2008)beta-blockers, ACEIs, ARBs
Jones et al., 2018 [33]U.K.Prospective observational studyMen and women participating in general practices in Norfolk5744/4181
Total: 23,655
59.1Missing FFQ data, missing baseline CVD data, missing covariate data, incorrect date of deathDASH Score by Fung et al. (2008)Yes
Kang et al., 2018 [34]KoreaCross-sectional observational studyPost-menopausal women from South Korean population1606/1623
Total: 6826
58.5 ± 6.3Missing clinical data, DM, extremely low or high EI (<500 kcal or 5000 kcal)DASH Score by Lee et al. (2017)No
Khodarahmi et al., 2021 [35]IranCross-sectional observational studyHealthy obese adults in the city of TabrizNo info
Total: 347
38.0 ± 7.4Pregnancy, lactation, menopausal women, medical history of chronic diseases (CVD, hypertension, hyperlipidemia, DM, renal diseases, hepatic disorders and cancer), recent surgery such as bariatric surgery, any medications and supplements which had effects on weight and variables studied such as loop diuretics, corticosteroids, antidepressants, statins and anti-hypertensive agents, EI outside of the range of 800–4200 kcal/dayDASH Score by Fung et al. (2008)No
Kim et al., 2022 [36]U.S.Prosopective observational studyMen and women of African American, Hispanic, Asian, Indian, Pacific Islander and Native American origins522/410
Total: 1899
67.0 ± 9.0Missing information on diets and covariates, missing mortalityDASH Score by Fung et al. (2008)Yes
Köroğlu et al., 2020 [37]TurkeyCross-sectional observational studyMale patients with at least one year and maximum three years of amputation historyNo info
Total: 35
36.9 ± 9.3DM, hypertension, thyroid dysfunction, amputees due to vascular problemsDASH Score developed based on guidelines by the National Institutes of Health and National Heart Lung and Blood Institute (2018)No
Lin et al., 2011 [38]U.S.Prospective observational study U.S. female nurses780/780
Total: 3121
67.0No cumulative average dietary pattern data available, no measured plasma creatine in sample collectionDASH Score by Fung et al. (2008)ACEI, ARB
Liu et al., 2017 [39]U.S.Prospective observational studyAfrican American and white people from U.S. census tracts in Baltimore City, Maryland648/886
Total: 1534
48.0Did not undergo serum creatinine at baseline, no dietary intake data, eGFR <60 mL/min per 1.73 m2 at baseline, survived but did not undergo a follow-up serum creatinine measurementDASH Score by Mellen et al. (2008)No
Mackenbach et al., 2019 [40]The NetherlandsCross-sectional observational studyAdults (Netherlands Study of Depression and Anxiety)344/347
Total: 1543
52.4 ± 12.9Incomplete FFQ, extreme EI, missing data on their six-digit postcode, hypertensive medicationDASH Score by Fung et al. (2008)No
Mattei et al., 2017 [41]U.S.Propsective observational studySelf-identified Puerto Ricans residing in BostonNo info
Total: 1189
Low: 55.3 ± 7.1
High: 58.8 ± 7.3
Unable to answer questions due to serious health conditions, planned to move away from the area within two years, low MMSE score (≤10)DASH Score by Fung et al. (2008)Yes
Mertens et al., 2017 [42]U.K.Prospective observational studyMiddle-aged men from the town of Caerphilly and adjoining villages, South Wales (U.K.)550/713
Total: 1867
56.6 ± 4.3Men who died, history of myocardial infarction or stroke, DM, missing dietary dataDASH Score by Fung et al. (2008)No
Missikpode et al., 2021 [43]U.S.Prospective observational studyAdults self-identified as Hispanic/Latino2480/2481
Total: 9921
41.0 ± 0.28Missing information on kidney-function measures, incomplete diet data, missing data on covariates, CKD at baselineDASH Score by Fung et al. (2008)ACEI, ARB
Mousavi et al., 2020 [44]IranCross-sectional observational studyAdults with mild
to moderate hypertension
25/25
Total: 101
40.7 ± 4.48Angina pectoris, type 1 DM, renal diseases, pregnancy and lactation, special diet and intake of supplementsDASH Score derived from PCA (Fransen et al., 2014)Yes
Navarro-Prado et al., 2020 [45]SpainCross-sectional observational studyUniversity students during the 2013–2014 academic year73/69
Total: 244
22.4 ± 4.76Accepted and signed an informed consent document, previously diagnosed with an endocrine disease, lacking anthropometric, dietary or demographic data, ≥32 years oldDASH Score by Fung et al. (2008)No
Nilsson et al., 2019 [46]SwedenCross-sectional observational studyCommunity-dwelling womenNo info
Total: 112
67.0 ± 1.6CHD and DM, disability with respect to mobility, using prescribed anti-inflammatory medication, smokers, incomplete data on PA, incomplete data on inflammatory and metabolic biomarkersDASH Score by Fung et al. (2008)Yes
Ramezankhani et al., [47]IranProspective observational studyAdult residents of Tehran participating in Tehran Lipid and Glucose Study (TLGS)1254/1279
Total: 4793
38.9 ± 12.7Under- or over-reporters of EI (<800 or ≥4200 kcal/day), hypertension at baseline, missing data on hypertension status without any follow-up dataDASH Score by Fung et al. (2008)No
Rebholz et al., 2016 [48]U.S.Prospective observational studyParticipants of Atherosclerosis Risk in Communities Study (ARIC), predominantly African American and white with baseline eGFR ≥60 mL/min/1.73 m5759/4840
Total: 14,882
54.1 ± 5.7Missing dietary ΕΙ data, implausibly low caloric intake (<600 kcal for men and <500 kcal for women) and implausibly high caloric EI (>4200 kcal for men and >3600 kcal for women), baseline eGFR <60 mL/min/1.73 m2 or ESRD, identified by linkage to the US Renal Data System registry, neither African American nor white, missing covariatesDASH Score by Mellen et al. (2008)ACEI, ARB
Santiago-Torres et al., 2020 [49]U.S.Prospective observational studyPost-menopausal women of Mexican ethnic descent who participated in the Women’s Health Initiative (WHI)117/106
Total: 334
58.6 ± 6.4Non-Mexican, American or Chicana, metabolic syndrome, diabetes, participated in the intervention group for the Dietary Modification trial, either low or high self-reported EI from the FFQ (<500 or >4000 kcal)DASH Score by Fung et al. (2008)Yes
Tangney et al., 2015 [50]U.S.Cross sectional observational studyOlder Latino adults from CAPACES (who had a score less than 14 on a 21-point Mini-Mental State Examination)Fung: 35/2866.0 ± 9.0Less than 50 years old, score <14 on the shortened MMSE, too young, used a walking assistive
device, not Latino
DASH Score by Fung et al. (2008) Yes
ACEI: angiotensin-converting-enzyme inhibitor; ARB: angiotensin receptor blockers; BMI: body mass index; BP: blood pressure; CHD: coronary heart disease; CKD: chronic kidney disease; CVD: cardiovascular disease; DASH: dietary approaches to stop hypertension; DM: diabetes mellitus; eGFR: estimated glomerular filtration rate; EI: energy intake; ESRD: end-stage renal disease; HOMA-IR: homeostatic model assessment of insulin resistance; FFQ: Food Frequency Question-naire; GDM: gestational diabetes mellitus; HF: heart failure; MetS: metabolic syndrome; MMSE: mini-mental state examination; PCA: principal component analysis; RCT: randomized controlled trial.
Table 2. Patients’ health characteristics of the included studies.
Table 2. Patients’ health characteristics of the included studies.
Study IDComorbidities
(Low/High) *
Percentage (%) of Participants with HTN
(Low/High)
BMI (Low/High) *SBP (Low/High) *DBP (Low/High) *Physical Activity
(Low/High) *
Smoking Status (Low/High)Sodium Intake (mg)Potassium Intake (mg)
Benerjee et al., 2019 [14] CKDNo info26.5 ± 4.9/
28.7 ± 6.0
154.1 ± 1.4/
151.5 ± 1.6
No infoModerate: 96.0%/93.8%
Intense: 4.0%/6.2%
Current: 22.0%/6.3%
Past: 37.4%/53.4
Never: 40.6%/40.3%
1809.9 ± 26.0/
1597.9 ± 48.1
1227.7 ± 15.1/
2249.6 ± 35.4
Bendinellii et al., 2019 [15]NoNo infoUnder/normal weight: 55.9%/53.9%
Overweight: 33.9%/35.6% Obesity: 10.2%/10.6%
124.6 ± 15.7/
123.6 ± 15.7
80.0 ± 9.4/
79.2 ± 9.1
Inactive: 22.5%/16.6% Moderately inactive: 23.4%/23.9% Moderately active: 45.0%/47.7% Active: 9.1%/11.7%Current: 34.2%/24.5% Former: 25.5%/31.3% Never smoked: 40.3%/44.3%2740.0 ± 9.9/2640.0 ± 11.3No info
Bonaccio et al., 2020 [16]Obesity,
DM (3.7%/5.6%),
Hyperlipidemia (5.3%/10.3%)
22.5%/31.5%Obesity:
29.1%/29.3%
140.0 ± 20.0/
140.0 ± 21.0
82.0 ± 9.0/82.0 ± 9.0Leisure-time PA
(MET-h/day): 42.6%/56.5%
Current: 27.2%/19.4%No infoNo info
Chan et al., 2022 [17]CVD
(42.2%/33.8%)
No info30.5 ± 6.3/
26.9 ± 5.0
120.8 ± 13.6/
114.8 ± 13.3
73.7 ± 9.8/
71.5 ± 9.2
Μoderate or heavy (hours/day): 4.0 ± 3.7/3.0 ± 2.9Current: 31.2%/5.5%No infoNo info
Critselis et al., 2019 [18]Hypercholesterolemia (40.6%/44.5%),
DM (7.4%/7.0%),
MetS (18.4%/20.9%)
29.9%/33.0%26.1 ± 4.4/
26.5 ± 4.6
123.0 ± 18.2/
123.0 ± 18.5
78.6 ± 11.2/
79.4 ± 11.9
38.9%/42.7%42.5%/42.6%No infoNo info
Dai et al., 2022 [19]Hypertension, Depression, Insomnia25.7%/20.4%24.2 ± 3.6/
23.9 ± 3.3
125.8 ± 17.6/
123.0 ± 16.5
79.5 ± 11.1/
77.7 ± 10.5
29.1 ± 19.7/
24.4 ± 16.7
(MET hours/day)
Never: 74.7%/76.6% Previous: 21.8%/17.7%
Current: 3.5%/5.7%
No infoNo info
Daniel et al., 2021 [20]DM (9.3%/7.5%)40.3%/41.4%29.3 ± 5.3/
27.4 ± 5.0
124.3 ± 19.7/
125.5 ± 21.4
73.9 ± 10.0/
69.9 ± 10.1
1456.1 ± 2631.8/
1956.6 ± 2641.9
(MET min/week)
Current: 21.2%/4.9%No infoNo info
Epstein et al., 2012 [21]ObesityTotal: 47%No info129.2 ± 1.9/
134.5 ± 2.2
76.6+1.1/
80.9+1.3
No infoNo infoNo infoNo info
Fransisco et al., 2020 [22] DM (8.1%/9.5%)No info25.8 ± 4.2/
24.9 ± 3.8
114.5 ± 11.5/
114.5 ± 11.8
72.7 ± 8.1/
71.4 ± 8.2
Light: 78.6%/62.8% Μoderate: 14.1%/24.9%
Vigorous: 7.3%/12.4%
Non-smoker: 58.8%/65.3%
Former: 25.8%/25.4% Smokers: 15.4%/9.3%
No info3982.0 ± 1607.0/
5260.0 ± 1664.0
Gao et al., 2021 [23]Central obesity
(total 44.2%)
No infoUnderweight (total 12%)
Overweight (total 39.4%)
Obesity (total 11.5%)
No infoNo infoNo infoNo: 93.3%
Yes: 6.7%
No infoNo info
Gao et al., 2020 [24]CHD (1.6%/2.5%)
Hyperuricemia
(18.3%/14.4%)
No info24.7 ± 0.03/
24.8 ± 0.03
132.8 ± 0.1/
131.8 ± 0.1
80.0 ± 0.1/
80.8 ± 0.1
Low: 29.4%/48.1% Μoderate: 21.1%/8.6%
High: 33.0%/26.0%
Unknown: 16.4%/17.2%
No: 51.5%/58.5%
Yes: 48.5%/41.5%
No infoNo info
Ghorabi et al., 2019 [25]Components of MetS:
Abdominal obesity: 30.6%/36.1%,
Elevated BP: 47.3%/22.1%,
High TG: 43.5%/23.2%,
Reduced HDL: 27.7%/40.1%,
Abnormal GL: 41.0%/32.7%
No info28.7 ± 4.9/
28.5 ± 4.9
102.5 ± 35.8/
68.1 ± 52.1
53.7 ± 33.1/
45.8 ± 35.0
No infoCurrent: 35.3%/23.5%No infoNo info
Glenn et al., 2021 [26]DM (29.0%/32.0%), Hypercholesterolemia (76.0%/75.0%)93.0%/94.0%32.8 ± 3.5/
32.1 ± 3.4
No infoNo info2193.0 ± 2154.0/
2856.0 ± 2444.0
(MET min/week)
Never: 41.0%/48.0%
Former: 44.0%/42.0%
Current: 15.0%/32.1%
No infoNo info
Goyal et al., 2021 [27]Atrial fibrilation (7.3%/7.3%),
DM (14.9%/17.3%)
57.4%/53.8%29.0 ± 6.2/
28.0 ± 5.7
128.0 ± 16.0/126.0 ± 16.077.0 ± 9.7/76.0 ± 9.14 or more times/week: 24.4%/32.0%
1 to 3 times/week: 34.7%/39.9%
None: 40.9%/28.2%
Current: 26.0%/9.5%
Past: 36.9%/42.1%
Never: 37.2%/48.4%
No infoNo info
Harrington et al., 2013 [28]Hypertension33.6%/27.3%No info131.3 ± 16.4/
126.8 ± 16.6
80.9 ± 9.9/
79.8 ± 9.6
No infoNo infoNo infoNo info
Hu et al., 2021 [29]CKD, DM (37.0%/49.0%)85.0%/79.0%32.0 ± 8.0/
32.0 ± 8.0
127.0 ± 21.0/
125.0 ± 20.0
73.0 ± 13.0/
69.0 ± 11.0
204.0 ± 135.0/
198.0 ± 118.0
(METs/week)
21.0%/5.0%2922.0 ± 1415.0/
2788.0 ± 1268.0
2723.0 ± 1240.0/
3311.0 ± 1313.0
Ishikawa et al., 2022 [30]No infoNo infoNo info122.4 ± 3.1/
132.3 ± 2.8
70.9 ± 2.2/
62.6 ± 1.9
No info51.3%/4.3%No infoNo info
Jalilpiran et al., 2020 [31]Any disease (dyslipidemia, HTN, abnormal GL levels) 60.9%/39.1%No info25.7 ± 2.8/
25.3 ± 3.4
No infoNo infoNo info51.0%/14.8%No info3710.0 ± 62.5/
4528.8 ± 71.6
Jayedi et al., 2019 [32]Type 2 DM, Diabetic nephropathyNo info27.5 ± 4.6/
28.7 ± 3.8
125.0 ± 15.2/
126.3 ± 13.15
83.5 ± 11.9/
79.0 ± 11.4
Low: 28.4%/32.9% Moderate: 35.8%/36.7%
High: 35.8%/30.4%
No infoNo infoNo info
Jones et al., 2018 [33]DM (4.1%/4.1%)No infoNo info136.8/135.083.4/81.5Inactive: 1953/920
Active: 3791/3261
Current: 19.0%/6.0%No infoNo info
Kang et al., 2018 [34]MetSNo info24.3 ± 3.1/
24.0 ± 2.9
123.9 ± 17.7/
121.4 ± 17.2
77.5 ± 9.9/
76.9 ± 9.8
47.0%/54.7%Non-smoker: 92.3%/94.9% Ex-smoker: 1.6%/2.0% Current smoker: 6.1%/3.1%No infoNo info
Khodarahmi et al., 2021 [35]Obesity, Depression, MetS No infoNo info120** (105.0, 130.0)/110.0** (110.0, 130.0)77.5 ± 12.6/70.4 ± 16.6 Men
Low: 35.3%/35.3%
Moderate: 46.9%/12.5%
High: 26.7%/23.3%
Women
Low: 33.9%/25.0%
Moderate: 45.0%/30.0%
High: 31.3%/18.8%
No infoNo infoNo info
Kim et al., 2022 [36]Type 2 DM (63.0%/46.0%) No info29.0 ± 6.0/
27.0 ± 5.0
129.0 ± 17.0/
128.0 ± 18.0
No infoScore 1: 35.0 ± 6.0/
36.0 ± 5.0
Current: 14.0%/14.0% Former: 36.0%/32.0%No infoNo info
Köroğlu et al., 2020 [37]Traumatic lower limb amputationNo info31.0 ± 7.7/
24.1 ± 2.5
120.0 ± 17.6/112.5 ± 6.380.0 ± 11.7/
77.5 ± 3.1
No infoNo infoNo infoNo info
Lin et al., 2011 [38]DM (24.6%/20.3%), hypercholesterolemia (65.0%/66.4%),
CVD (6.8%/5.3%)
56.5%/48.3%27.3 ± 1.3/
25.1 ± 0.9
130.0 ± 3.2/
125.0 ± 3.2
79.5 ± 2.9/
77.5 ± 1.6
8.8 ± 2.5/
18.9 ± 3.9
(METs/week)
Current: 11.6%/2.2%
Ever: 56.3%/48.4%
2007.5 ± 67.5/
1923.5 ± 60.4
No info
Liu et al., 2017 [39]Obesity (42.4%/41.1%),
DM (15.5%/15.6%)
42.1%/43.0%29.7 ± 7.6/
29.8 ± 7.8
120.0 ± 19.0/
119.0 ± 19.0
No infoNo infoCurrent: 52.3%/41.7%
Former: 20.0%/21.4%
None: 27.8%/36.9%
No infoNo info
Mackenbach et al., 2019 [40]Depression17.6%/12.6%26.7 ± 4.8/
25.2 ± 4.0
139.9 ± 21.4/
137.1 ± 21.7
No infoNo infoCurrent: 38.4%/13.0%No infoNo info
Mattei et al., 2017 [41]DM (36.4%/37.4%),
CVD (19.4%/25.9%),
Obesity (53.4%/57.4%)
68.2%/70.4%31.8 ± 6.9/
31.7 ± 6.3
135.0 ± 21.0/
136.0 ± 19.0
82.1 ± 11.9/
79.4 ± 9.8
Score 2: 31.0 ± 3.8/
32.0 ± 4.6
Current: 31.1%/13.8%No infoNo info
Mertens et al., 2017 [42]CVDNo info25.5 ± 3.5/
27.1 ± 3.4
145.3 ± 19.7/
144.4 ± 19.8
82.6 ± 10.7/
83.1 ± 10.1
Active: 42.4%/44.3%Current: 61.8%/28.9%2575.0 ± 596.7/
2134.8 ± 577.3
No info
Missikpode et al., 2021 [43]DM (12.0%/19.0%),
CVD (21.0%/25.0%)
21.0%/24.0%29.6 ± 9.5/
29.4 ± 8.9
119.6 ± 20.9/119.7 ± 26.472.4 ± 16.9/71.3 ± 16.4Low PA level: 44.0%/42.0%Current: 28.0%/12.0%No infoNo info
Mousavi et al., 2020 [44]Mild to moderate HTNNo info29.7 ± 4.3/
29.1 ± 5.1
144.4 ± 10.9/
143.0 ± 12.7
88.3 ± 10.5/
88.8 ± 7.25
4192.5 ± 6088.1/
4132.3 ± 5508.6
(MET/min/week)
No info3338.7 ± 978.7/
2949.2 ± 320.2
2011.9 ± 694.5/
2030.4 ± 915.6
Navarro-Prado et al., 2020 [45]No infoNo info23.1 ± 4.1/
23.1 ± 3.89
118.2 ± 13.3/
111.6 ± 10.1
69.3 ± 12.1/65.2 ± 9.6PAQ-C summary score: 3.9 ± 0.8/
4.1 ± 0.8
No info2800.0 ± 940.0/2400.0 ± 1130.02400.0 ± 850.0/
2600.0 ± 1140.0
Nilsson et al., 2019 [46]Obesity, DyslipidemiaNo infoNo info134.0 ± 15.0/
139.0 ± 14.0
79.0 ± 9.0/
79.0 ± 7.0
Daily time in moderate to vigorous PA (min):
23.0 ± 16.0/
30.0 ± 24.0
No infoNo infoNo info
Ramezankhani et al., [47]DM (3.3%/7.7%)No info26.0 ± 4.6/
27.5 ± 4.5
109.0 ± 12.0/
107.0 ± 11.7
72.5 ± 8.5/
73.2 ± 8.2
Low PAL: 75.2%/64.3%Current: 32.5%/13.4%No infoNo info
Rebholz et al., 2016 [48]DM (9.2%/13.0%)
Obesity
35.9%/32.7%No info122.3 ± 19.1/
119.6 ± 18.3
No infoPAI: 2.3 ± 0.7/
2.6 ± 0.8
Current: 35.7%/17.2%No infoNo info
Santiago-Torres et al., 2020 [49]MetS (42.0%/25.0%)No infoNo info120.0 ± 10.5/
121.0 ± 13.4
70.6 ± 6.9/
71.0 ± 8.0
No infoNo infoNo infoNo info
Tangney et al., 2015 [50]HypertensionFung DASH Score: 23.0%/36.0% Toledo DASH Score:
29.5 ± 4.4/30.7 ± 2.5
Fung DASH Score:
29.9 ± 5.7/31.0 ± 5.4
Folsom DASH Score:
30.3 ± 3.8/29.6 ± 4.5
Fung DASH Score:
128.0 ± 18.0/132.0 ± 20.0
Fung DASH Score:
70.0 ± 11.0/
69.0 ± 12.0
No infoNo infoNo infoNo info
Refers to low- and high-adherence DASH diet group. * Expressed as median (25th and 75th percentiles). Abbreviations: BMI: body mass index; BP: blood pressure; CHD: coronary heart disease; CKD: chronic kidney disease; CVD: cardio-vascular disease; DASH: dietary approaches to stop hypertension; DBP: diastolic blood pressure; DM: diabetes mellitus; GL: glucose; HDL: high-density lipoprotein; HTN: hypertension; MET: Metabolic Equivalent Task; MetS: metabolic syndrome; PA: physical activity; PAI: physical activity index; PAQ-C: physical activity questionnaire for older children; SBP: systolic blood pressure; TG: triglycerides. 1 Generated using the intensity and time spent performing each type of activity, assessed using a physical activity questionnaire. 2 Assessed using a modified Paffenbarger questionnaire from the Harvard Alumni Activity Survey; the score was defined by multiplying the self-reported hours spent doing heavy, moderate, light or sedentary activities over 24 h by weighing factors that paralleled the rate of oxygen consumption of each activity.
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Theodoridis, X.; Triantafyllou, A.; Chrysoula, L.; Mermigkas, F.; Chroni, V.; Dipla, K.; Gkaliagkousi, E.; Chourdakis, M. Impact of the Level of Adherence to the DASH Diet on Blood Pressure: A Systematic Review and Meta-Analysis. Metabolites 2023, 13, 924. https://doi.org/10.3390/metabo13080924

AMA Style

Theodoridis X, Triantafyllou A, Chrysoula L, Mermigkas F, Chroni V, Dipla K, Gkaliagkousi E, Chourdakis M. Impact of the Level of Adherence to the DASH Diet on Blood Pressure: A Systematic Review and Meta-Analysis. Metabolites. 2023; 13(8):924. https://doi.org/10.3390/metabo13080924

Chicago/Turabian Style

Theodoridis, Xenophon, Areti Triantafyllou, Lydia Chrysoula, Fotios Mermigkas, Violeta Chroni, Konstantina Dipla, Eugenia Gkaliagkousi, and Michail Chourdakis. 2023. "Impact of the Level of Adherence to the DASH Diet on Blood Pressure: A Systematic Review and Meta-Analysis" Metabolites 13, no. 8: 924. https://doi.org/10.3390/metabo13080924

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