Association between C-Reactive Protein and Adiposity in Women

被引:58
|
作者
Bochud, Murielle [1 ]
Marquant, Fabienne [1 ]
Marques-Vidal, Pedro-Manuel [1 ,4 ]
Vollenweider, Peter [2 ]
Beckmann, Jacques S. [3 ]
Mooser, Vincent
Paccaud, Fred [1 ]
Rousson, Valentin [1 ,5 ]
机构
[1] CHU Vaudois, Univ Inst Social & Prevent Med, CH-1005 Lausanne, Switzerland
[2] CHU Vaudois, Dept Med & Internal Med, CH-1005 Lausanne, Switzerland
[3] CHU Vaudois, Dept Med Genet, CH-1005 Lausanne, Switzerland
[4] CHU Vaudois, Dept Cardiomet, CH-1005 Lausanne, Switzerland
[5] GlaxoSmithKline, King Of Prussia, PA 19406 USA
来源
关键词
CARDIOVASCULAR RISK-FACTORS; METABOLIC-SYNDROME; MENDELIAN RANDOMIZATION; LEPTIN RECEPTOR; GENETIC-VARIATION; CAUSAL INFERENCE; CRP LEVELS; OBESITY; POLYMORPHISMS; EPIDEMIOLOGY;
D O I
10.1210/jc.2008-2428
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: The link between C-reactive protein (CRP) and adiposity deserves to be further explored, considering the controversial diabetogenic role of CRP. Objective: We explored the potential causal role of CRP on measures of adiposity. Design: We used a Mendelian randomization approach with the CRP and LEPR genes as instrumental variables in a cross-sectional Caucasian population-based study comprising 2526 men and 2836 women. Adiposity was measured using body mass index (BMI), fat and lean mass estimated by bioelectrical impedance, and waist circumference. Results: Log-transformed CRP explained by the rs7553007 single-nucleotide polymorphism tagging the CRP gene was significantly associated with BMI [regression coefficient: 1.22 (0.18; 2.25), P = 0.02] and fat mass [2.67 (0.65; 4.68), P = 0.01] but not with lean mass in women, whereas no association was found in men. Log-transformed CRP explained by the rs1805096 LEPR single-nucleotide polymorphism was also positively associated, although not significantly, with BMI or fat mass. The combined CRP-LEPR instrument explained 2.24 and 0.77% of CRP variance in women and men, respectively. Log-transformed CRP explained by this combined instrument was significantly associated with BMI [0.98 (0.32; 1.63), P = 0.004], fat mass [2.07 (0.79; 3.34), P = 0.001], and waist [2.09 (0.39; 3.78), P = 0.01] in women but not men. Conclusion: Our data suggest that CRP is causally and positively related to BMI in women and that this is mainly due to fat mass. Results on the combined CRP-LEPR instrument suggest that leptin may play a role in the causal association between CRP and adiposity in women. Results in men were not significant. (J Clin Endocrinol Metab 94: 3969-3977, 2009)
引用
收藏
页码:3969 / 3977
页数:9
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