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Moderate Obesity and Endothelial Dysfunction in Humans: Influence of Gender and Systemic Inflammation.

Authors :
Suboc TM
Dharmashankar K
Wang J
Ying R
Couillard A
Tanner MJ
Widlansky ME
Source :
Physiological reports [Physiol Rep] 2013 Aug 01; Vol. 1 (3).
Publication Year :
2013

Abstract

Objective: To determine whether moderate obesity (BMI ≥ 30 kg/m <superscript>2</superscript> ) is associated with impaired conduit and microvascular endothelial function, and whether men or women are more susceptible to impairment of endothelial function related to moderate obesity.<br />Design and Methods: 41 middle aged, non-diabetic moderately obese (BMI 34.7±4.0 kg/m <superscript>2</superscript> ) and non obese (BMI 24.3±2.6 kg/m <superscript>2</superscript> ) subjects of both sexes underwent noninvasive studies of endothelial function (brachial reactivity) and measurements of endothelial dependent vasodilation of gluteal subcutaneous arterioles to acetylcholine (Ach).<br />Results: Endothelium dependent vasodilation to Ach was decreased in the moderately obese compared to the non-obese (P<0.001). Stratified analysis based on sex showed impairment of arteriolar endothelial function in women BMI ≥ 30 kg/m <superscript>2</superscript> (P=0.02), but not men. There was no difference between in vivo endothelial function (FMD%, FMD mm) by BMI category. Sex specific analysis showed FMD% was lower in women with BMI ≥ 30 kg/m <superscript>2</superscript> compared to those with BMI < 30 kg/m <superscript>2</superscript> (P=0.02). No differences were seen in men based on BMI category (P=0.18). In women, high sensitivity C-reactive protein (hsCRP) correlated with BMI (ρ=0.68, P=0.006).<br />Conclusion: Moderate obesity is associated with impaired resistance arteriolar endothelial function. This is more prominent in women than men and is associated with systemic inflammation.

Details

Language :
English
ISSN :
2051-817X
Volume :
1
Issue :
3
Database :
MEDLINE
Journal :
Physiological reports
Publication Type :
Academic Journal
Accession number :
24187612
Full Text :
https://doi.org/10.1002/phy2.58