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中国汉族男性性激素结合球蛋白(SHBG)基因多态性与血清SHBG水平及代谢综合征的关系

The relationship of sex hormone-binding globulin (SHBG) gene polymorphisms with serum SHBG level and metabolic syndrome in Chinese Han males.

作者信息

Pang Xiao-Na, Yuan Ying, Sun Yan, Shen Ji-Ping, Zha Xiao-Yun, Hu Yu

机构信息

Department of Geriatrics, Zhongshan Hospital, Fudan University, 180 Fenglin Road, Shanghai, 200032, China.

出版信息

Aging Clin Exp Res. 2014 Dec;26(6):583-9. doi: 10.1007/s40520-014-0215-1. Epub 2014 Mar 27.

Abstract

OBJECTIVE

Epidemiological studies have shown that circulating sex hormone-binding globulin (SHBG) levels are lower in metabolic syndrome (MetS) patients than in non-MetS individuals. In this study, we investigated the relationship of polymorphisms in the SHBG gene with the serum SHBG levels and MetS in Han Chinese.

METHODS

We performed a cross-sectional study of 316 subjects who were recruited from a health checkup population at Zhongshan Hospital, Fudan University. Anthropometric measurements, blood pressure, fasting plasma glucose, lipid levels, total testosterone, and SHBG levels were obtained in addition to the seven SHBG single-nucleotide polymorphisms (SNPs).

RESULTS

The variant allele (AG or AA) carriers in rs6259, compared to the wild-type allele carriers (GG), have a lower risk for MetS [OR 0.56, 95% confidence interval (CI) 0.33-0.96] and higher serum SHBG and TT levels (P = 0.016, 0.004). CT or TT allele carriers in rs3760213, compared to CC allele carriers, also have a lower risk for MetS (OR 0.59, 95 % CI 0.34-1.00) and significantly higher SHBG and TT levels (P = 0.029, 0.009). Carriers having both of the variant alleles had the lowest risk of MetS (OR 0.51, 95 % CI 0.275-0.950) and the highest SHBG levels. The risk of MetS rose with the decrease in serum SHBG levels for rs6259 and rs376021 carriers.

CONCLUSION

rs6259 and rs3760213 SNPs are associated with the risk of MetS and lower serum SHBG level in Chinese Han males.

摘要

目的

流行病学研究表明,代谢综合征(MetS)患者的循环性激素结合球蛋白(SHBG)水平低于非MetS个体。在本研究中,我们调查了汉族人群中SHBG基因多态性与血清SHBG水平及MetS的关系。

方法

我们对从复旦大学附属中山医院健康体检人群中招募的316名受试者进行了横断面研究。除了七个SHBG单核苷酸多态性(SNP)外,还获得了人体测量数据、血压、空腹血糖、血脂水平、总睾酮和SHBG水平。

结果

与野生型等位基因携带者(GG)相比,rs6259中的变异等位基因(AG或AA)携带者患MetS的风险较低[比值比(OR)0.56,95%置信区间(CI)0.33 - 0.96],血清SHBG和总睾酮(TT)水平较高(P = 0.016,0.004)。与CC等位基因携带者相比,rs3760213中的CT或TT等位基因携带者患MetS的风险也较低(OR 0.59,95% CI 0.34 - 1.00),SHBG和TT水平显著较高(P = 0.029,0.009)。同时携带两个变异等位基因的携带者患MetS的风险最低(OR 0.51,95% CI 0.275 - 0.950),SHBG水平最高。对于rs6259和rs376021携带者,MetS的风险随着血清SHBG水平的降低而升高。

结论

rs6259和rs3760213单核苷酸多态性与中国汉族男性患MetS的风险及较低的血清SHBG水平相关。

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