Impact of Kidney Function on Effects of the Dietary Approaches to Stop Hypertension (Dash) Diet.

Published

Journal Article

OBJECTIVES: Although the Dietary Approaches to Stop Hypertension (DASH) diet lowers blood pressure in adults with hypertension, how kidney function impacts this effect is not known. We evaluated whether Estimated Glomerular Filtration Rate (eGFR) modifies the effect of the DASH diet on blood pressure, markers of mineral metabolism, and markers of kidney function. METHODS: Secondary analysis of the DASH-Sodium trial, a multicenter, randomized, controlled human feeding study that evaluated the blood pressure lowering effect of the DASH diet at three levels of sodium intake. Data from 92 participants with pre-hypertension or stage 1 hypertension during the 3450 mg /day sodium diet assignment contributed to this analysis. Stored frozen plasma and urine specimens were used to measure kidney related laboratory outcomes. RESULTS: Effects of the DASH diet on blood pressure, phosphorus, intact parathyroid hormone, creatinine, and albuminuria were not modified by baseline eGFR (mean 84.5 ± 18.0 ml/min/1.73 m2, range 44.1 to 138.6 ml/min/1.73 m2) or the presence of chronic kidney disease (N=13%). CONCLUSIONS: The impact of the DASH diet on blood pressure, markers of mineral metabolism, and markers of kidney function does not appear to be modified by eGFR in this small subset of DASH-Sodium trial participants with relatively preserved kidney function. Whether greater reduction in eGFR modifies the effects of DASH on kidney related measures is yet to be determined. A larger study in individuals with more advanced kidney disease is needed to establish the efficacy and safety of the DASH diet in this patient population.

Full Text

Duke Authors

Cited Authors

  • Tyson, CC; Kuchibhatla, M; Patel, UD; Pun, PH; Chang, A; Nwankwo, C; Joseph, MA; Svetkey, LP

Published Date

  • 2014

Published In

Volume / Issue

  • 3 /

PubMed ID

  • 26380159

Pubmed Central ID

  • 26380159

International Standard Serial Number (ISSN)

  • 2167-1095

Digital Object Identifier (DOI)

  • 10.4172/2167-1095.1000168

Language

  • eng

Conference Location

  • United States