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The association of plasma resistin with dietary sodium manipulation, the renin‐angiotensin‐aldosterone system, and 25‐Hydroxyvitamin D 3 in human hypertension
Author(s) -
Vaidya Anand,
Pojoga Luminita,
Underwood Patricia C.,
Forman John P.,
Hopkins Paul N.,
Williams Gordon H.,
Williams Jonathan S.
Publication year - 2011
Publication title -
clinical endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.055
H-Index - 147
eISSN - 1365-2265
pISSN - 0300-0664
DOI - 10.1111/j.1365-2265.2010.03922.x
Subject(s) - resistin , medicine , endocrinology , vitamin d and neurology , renin–angiotensin system , aldosterone , plasma renin activity , sodium , adipokine , blood pressure , chemistry , leptin , obesity , organic chemistry
Summary Objective  Both resistin and vitamin D have been associated with the renin‐angiotensin‐aldosterone system (RAAS). We investigated the association between resistin and the RAAS, and resistin and vitamin D under controlled dietary sodium conditions. Design  Retrospective cross‐sectional study of subjects from the HyperPATH Consortium, who were maintained in high dietary sodium (HS) and low dietary sodium (LS) balance for 1 week each. Patients  Caucasian subjects with hypertension ( n  = 177). Measurements  25‐hydroxyvitamin D (25[OH]D) levels were used to assess vitamin D status. Plasma resistin and RAAS measures were evaluated on each dietary intervention. Results  Resistin levels were significantly higher in LS, where RAAS activity was high, when compared with HS balance, where RAAS activity was suppressed (6·36 vs 5·86 μg/l, P  < 0·0001); however, resistin concentrations were not associated with plasma renin activity or serum aldosterone on either diet. 25(OH)D levels were positively and independently associated with resistin in both dietary conditions (HS: β = 0·400, P ‐trend = 0·027; LS: β = 0·540, P ‐trend = 0·014). Conclusions  Dietary sodium loading reduced resistin levels, possibly by suppressing the RAAS; however, circulating RAAS components were not related to resistin concentrations within each specific dietary sodium condition. 25(OH)D was positively associated with resistin and may be involved in resistin regulation through an unknown mechanism. Further studies to understand resistin regulation in human hypertension better are warranted.

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