Background: Obesity-related cardiovascular diseases (CVDs) are a major cause of cardiovascular (CV) mortality. Obesity-related reduction in vascular protective adipose-derived proteins, such as adiponectin (APN), has an important role. Methods: We compared brachial artery distensibility (BrachD) with APN, the level of adiposity and other CV risk factors (CVRFs) in 431 post-pubertal subjects (mean 17.9 years). Gender differences in average values were examined by t-tests. Correlations among BrachD, obesity and other CVRFs were examined. Regression analysis was performed to determine whether APN provided an independent contribution to BrachD, while controlling for obesity and other CVRFs. Results: Male subjects had lower BrachD (5.72 +/- 1.37 vs 6.45 +/- 1.60% change per mmHg, P < 0.0001) and lower APN (10.50 +/- 4.65 vs 13.20 +/- 6.53; all P < 0.04) than female subjects. BrachD correlated with APN (r = 0.25, P < 0.0001). Both BrachD and APN correlated with measures of body size, including height, weight and body mass index (BMI). Both correlated with higher systolic blood pressure, glucose, insulin and lower high-density lipoprotein cholesterol ( all P < 0.01). In multivariate analysis, APN, gender, APN*gender and BMI z-score predicted BrachD (r(2) = 0.305). On the basis of gender difference, only BMI z-score was significant for male subjects (r(2) = 0.080), whereas APN and BMI z-score contributed for female subjects (r(2) = 0.242, all P < 0.0001). Conclusions: BrachD is independently influenced by obesity in both male and female subjects. In female subjects, APN exerts an additional independent effect even after adjusting for blood pressure ( BP), lipid levels and insulin. Differences in the effect of the APN-adiposity relationship on obesity-related vascular disease may be one reason for gender differences in the development and progression of atherosclerosis. International Journal of Obesity ( 2009) 33, 1118-1125; doi:10.1038/ijo.2009.164; published online 25 August 2009
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Tilburg Univ, Cross Cultural Psychol, Tilburg, Netherlands
Univ Queensland, Brisbane, Qld, Australia
North West Univ, Potchefstroom, South AfricaUniv Barcelona, Psychometr, Barcelona, Spain
Van de Vijver, Fons J. R.
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Balluerka, Nekane
Caterino, Linda
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Arizona State Univ, Tempe, AZ USAUniv Barcelona, Psychometr, Barcelona, Spain
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Stanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
Prochaska, Judith J.
Fromont, Sebastien C.
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Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
Fromont, Sebastien C.
Ramo, Danielle E.
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Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
Ramo, Danielle E.
Young-Wolff, Kelly C.
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Stanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
Young-Wolff, Kelly C.
Delucchi, Kevin
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Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
Delucchi, Kevin
Brown, Richard A.
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Brown Univ, Dept Psychiat & Human Behav, Alpert Med Sch, Providence, RI 02912 USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA
Brown, Richard A.
Hall, Sharon M.
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Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USAStanford Univ, Dept Med, Stanford Prevent Res Ctr, Stanford, CA 94305 USA