Genetic Epidemiology, Queensland Institute of Medical Research, Australia.
Am J Hum Genet. 2010 Apr 9;86(4):519-25. doi: 10.1016/j.ajhg.2010.02.017. Epub 2010 Mar 18.
The ratio of the lengths of an individual's second to fourth digit (2D:4D) is commonly used as a noninvasive retrospective biomarker for prenatal androgen exposure. In order to identify the genetic determinants of 2D:4D, we applied a genome-wide association approach to 1507 11-year-old children from the Avon Longitudinal Study of Parents and Children (ALSPAC) in whom 2D:4D ratio had been measured, as well as a sample of 1382 12- to 16-year-olds from the Brisbane Adolescent Twin Study. A meta-analysis of the two scans identified a single variant in the LIN28B gene that was strongly associated with 2D:4D (rs314277: p = 4.1 x 10(-8)) and was subsequently independently replicated in an additional 3659 children from the ALSPAC cohort (p = 1.53 x 10(-6)). The minor allele of the rs314277 variant has previously been linked to increased height and delayed age at menarche, but in our study it was associated with increased 2D:4D in the direction opposite to that of previous reports on the correlation between 2D:4D and age at menarche. Our findings call into question the validity of 2D:4D as a simplistic retrospective biomarker for prenatal testosterone exposure.
个体第二指到第四指的长度比(2D:4D)通常被用作一种非侵入性的回溯性生物标志物,用于评估胎儿期雄激素暴露。为了确定 2D:4D 的遗传决定因素,我们应用全基因组关联分析方法,对 1507 名 11 岁的阿冯纵向研究父母和儿童(ALSPAC)参与者进行了研究,这些参与者的 2D:4D 比值已经被测量过,同时对来自布里斯班青少年双胞胎研究的 1382 名 12 至 16 岁的参与者进行了研究。对这两次扫描的元分析确定了 LIN28B 基因中的一个单一变异与 2D:4D 强烈相关(rs314277:p = 4.1 x 10(-8)),随后在来自 ALSPAC 队列的另外 3659 名儿童中进行了独立复制(p = 1.53 x 10(-6))。rs314277 变异体的次要等位基因先前与身高增加和月经初潮年龄延迟有关,但在我们的研究中,它与 2D:4D 的增加有关,与之前关于 2D:4D 与月经初潮年龄之间相关性的报告中的方向相反。我们的发现质疑了 2D:4D 作为一种简单的回溯性生物标志物用于评估胎儿期睾酮暴露的有效性。