Faculty, Staff and Student Publications

Publication Date

4-4-2023

Journal

Journal of the American Heart Association

Abstract

Background

The Dietary Approaches to Stop Hypertension (DASH) diet is recommended for cardiovascular disease prevention. We aimed to identify protein biomarkers of the DASH diet using data from 2 randomized feeding studies and validate them in an observational study, the ARIC (Atherosclerosis Risk in Communities) study.

Methods and Results

Large‐scale proteomic profiling was conducted in serum specimens (SomaLogic) collected at the end of 8‐week and 4‐week DASH diet interventions in multicenter, randomized controlled feeding studies of the DASH trial (N=215) and the DASH‐Sodium trial (N=396), respectively. Multivariable linear regression models were used to compare the relative abundance of 7241 proteins between the DASH and control diet interventions. Estimates from the 2 trials were meta‐analyzed using fixed‐effects models. We validated significant proteins in the ARIC study (N=10 490) using the DASH diet score. At a false discovery rate <0.05, there were 71 proteins that were different between the DASH diet and control diet in the DASH and DASH‐Sodium trials. Nineteen proteins were validated in the ARIC study. The 19 proteins collectively improved the prediction of the DASH diet intervention in the feeding studies (range of difference in C statistics, 0.267–0.313; P<0.001 for both tests) and the DASH diet score in the ARIC study (difference in C statistics, 0.017; P<0.001) beyond participant characteristics.

Conclusions

We identified 19 proteins robustly associated with the DASH diet in 3 studies, which may serve as biomarkers of the DASH diet. These results suggest potential pathways that are impacted by consumption of the DASH diet.

Registration

URL: https://www.clinicaltrials.gov; Unique identifiers: NCT03403166, NCT00000608.

Keywords

Humans, Dietary Approaches To Stop Hypertension, Proteomics, Hypertension, Diet, Sodium, Biomarkers, DASH diet, feeding studies, observational study, protein

DOI

10.1161/JAHA.122.028821

PMID

36974735

PMCID

PMC10122905

PubMedCentral® Posted Date

3-28-2023

PubMedCentral® Full Text Version

Post-print

Published Open-Access

yes

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