Advances in Genomics Research of Blood Pressure Responses to Dietary Sodium and Potassium Intakes

Author:

Razavi Michael A.,Bazzano Lydia A.1,Nierenberg Jovia2,Huang Zhijie1,Fernandez Camilo31ORCID,Razavi Alexander C.31ORCID,Whelton Seamus P.4ORCID,He Jiang31,Kelly Tanika N.1ORCID

Affiliation:

1. Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA (L.A.B., Z.H., C.F., A.C.R., J.H., T.N.K.).

2. Department of Epidemiology and Biostatistics, University of California, San Francisco School of Medicine (J.N.).

3. Department of Medicine, Tulane University School of Medicine, New Orleans, LA (C.F., A.C.R., J.H.).

4. The Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, MD (S.P.W.).

Abstract

More than half of US adults have hypertension by 40 years of age and a subsequent increase in atherosclerotic cardiovascular disease risk. Dietary sodium and potassium are intricately linked to the pathophysiology of hypertension. However, blood pressure responses to dietary sodium and potassium, phenomena known as salt and potassium sensitivity of blood pressure, respectively, are heterogenous and normally distributed in the general population. Like blood pressure, salt and potassium sensitivity are complex phenotypes, and previous research has shown that up to 75% of individuals experience a blood pressure change in response to such dietary minerals. Previous research has also implicated both high salt sensitivity and low salt sensitivity (or salt resistance) of blood pressure to an increased risk of hypertension and potentially atherosclerotic cardiovascular disease risk. Given the clinical challenges required to accurately measure the sodium and potassium response phenotypes, genomic characterization of these traits has become of interest for hypertension prevention initiatives on both the individual and population levels. Here, we review advances in human genomics research of blood pressure responses to dietary sodium and potassium by focusing on 3 main areas, including the phenotypic characterization of salt sensitivity and resistance, clinical challenges in diagnosing such phenotypes, and the genomic mechanisms that may help to explain salt and potassium sensitivity and resistance. Through this process, we hope to further underline the value of leveraging genomics and broader multiomics for characterizing the blood pressure response to sodium and potassium to improve precision in lifestyle approaches for primordial and primary atherosclerotic cardiovascular disease prevention.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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