Shin J, Sung J, Lee K, Song Y-M
Department of Family Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Department of Epidemiology, School of Public Health, Seoul National University, Seoul, South Korea.
Osteoporos Int. 2016 Feb;27(2):643-51. doi: 10.1007/s00198-015-3298-4. Epub 2015 Sep 2.
Low bone mineral density (BMD) leads to an increased risk of osteoporotic fracture. Total testosterone and free testosterone were positively associated with BMD, which was significantly influenced by the additive genetic effects.
This cross-sectional study aimed to evaluate an association between testosterone and BMD and the influence of genetic factors on the association.
Study subjects were 1070 Korean men including 144 pairs of monozygotic twins and their family members. Levels of serum total testosterone and sex hormone binding globulin (SHBG) were measured by chemiluminescence immunoassay. Calculated free testosterone (cFT) was then determined using Vermeulen's method. BMDs of the whole body and specific regions were measured using dual-energy X-ray absorptiometry.
Linear mixed regression analyses showed that total testosterone and cFT were positively associated with BMD at most regions, after considering intra-familial relationship and covariates including fat mass, lean mass, and SHBG. SHBG had an inverse association with BMD at the pelvis but not with the BMD at other regions after adjusting for all covariates and cFT. Co-twin control analysis in monozygotic twins found no association between pairwise difference of testosterone and pairwise difference of BMD. Bivariate variance component analysis showed that both total testosterone and cFT had a significant positive additive genetic correlation with BMD at rib, spine, and arm, whereas SHBG had no significant genetic correlation with BMD. Inverse environmental correlations were seen between total testosterone and BMDs at the lumbar spine and arm.
This Korean twin and family study showed that both total testosterone and free testosterone were positively associated with BMD and that genetic effects were significant on the association between testosterone and BMD.
低骨矿物质密度(BMD)会导致骨质疏松性骨折风险增加。总睾酮和游离睾酮与骨矿物质密度呈正相关,这受到加性遗传效应的显著影响。
本横断面研究旨在评估睾酮与骨矿物质密度之间的关联以及遗传因素对该关联的影响。
研究对象为1070名韩国男性,包括144对同卵双胞胎及其家庭成员。采用化学发光免疫分析法测定血清总睾酮和性激素结合球蛋白(SHBG)水平。然后使用韦尔梅伦方法测定计算游离睾酮(cFT)。使用双能X线吸收法测量全身及特定区域的骨矿物质密度。
线性混合回归分析表明,在考虑家族内关系以及包括脂肪量、瘦体重和SHBG在内的协变量后,总睾酮和cFT与大多数区域的骨矿物质密度呈正相关。在调整所有协变量和cFT后,SHBG与骨盆处的骨矿物质密度呈负相关,但与其他区域的骨矿物质密度无关。对同卵双胞胎进行的共双胞胎对照分析发现,睾酮的成对差异与骨矿物质密度的成对差异之间无关联。双变量方差成分分析表明,总睾酮和cFT在肋骨、脊柱和手臂处与骨矿物质密度均存在显著的正加性遗传相关性,而SHBG与骨矿物质密度无显著遗传相关性。在腰椎和手臂处,总睾酮与骨矿物质密度之间存在反向环境相关性。
这项韩国双胞胎及家族研究表明,总睾酮和游离睾酮均与骨矿物质密度呈正相关,且遗传效应在睾酮与骨矿物质密度之间的关联中具有显著意义。