The Association of Endothelin-1 with Markers of Arterial Stiffness in Black South African Women: The SABPA Study
Author(s) -
Christine Susara du Plooy,
Catharina M. C. Mels,
Hugo W. Huisman,
Ruan Kruger
Publication year - 2015
Publication title -
journal of amino acids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.188
H-Index - 5
eISSN - 2090-0112
pISSN - 2090-0104
DOI - 10.1155/2015/481517
Subject(s) - arterial stiffness , algorithm , pulse wave velocity , medicine , population , database , blood pressure , mathematics , computer science , environmental health
Background . Limited data exist regarding endothelin-1 (ET-1), a vasoactive contributor in vascular tone, in a population subjected to early vascular deterioration. We compared ET-1 levels and explored its association with markers of arterial stiffness in black and white South Africans. Methodology . This cross-sectional substudy included 195 black (men: n = 99; women: n = 95) and 197 white (men: n = 99; women: n = 98) South Africans. Serum ET-1 levels were measured as well as markers of arterial stiffness (blood pressure, pulse wave velocity, and arterial compliance). ET-1 levels were higher in black men and white women compared to their counterparts after adjusting for C-reactive protein. In both single and partial (adjusting for body mass index and gamma glutamyl transferase) regression analyses ET-1 correlated with age, interleukin-6, high density lipoprotein cholesterol, systolic blood pressure, pulse pressure, and pulse wave velocity in black women. In multivariate regression analyses the independent association of ET-1 with systolic blood pressure (Adj. R 2 = 0.13; β = 0.28, p < 0.01) and pulse pressure (Adj. R 2 = 0.11; β = 0.27, p < 0.01) was confirmed in black women only. ET-1 additionally associated with interleukin-6 in black women ( p < 0.01). Conclusion . Our result suggests that ET-1 and its link with subclinical arteriosclerosis are potentially driven by low-grade inflammation as depicted by the association with interleukin-6 in the black female cohort.
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