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全基因组关联研究鉴定出 2D:4D 手指比率的九个新位点,这是一种推测的胎儿期睾酮暴露的回溯生物标志物。

Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero.

机构信息

The University of Queensland Diamantina Institute, Translational Research Institute, University of Queensland, Brisbane, QLD 4102, Australia.

Queensland Institute of Medical Research, Brisbane, QLD 4006, Australia.

出版信息

Hum Mol Genet. 2018 Jun 1;27(11):2025-2038. doi: 10.1093/hmg/ddy121.

Abstract

The ratio of the length of the index finger to that of the ring finger (2D:4D) is sexually dimorphic and is commonly used as a non-invasive biomarker of prenatal androgen exposure. Most association studies of 2D:4D ratio with a diverse range of sex-specific traits have typically involved small sample sizes and have been difficult to replicate, raising questions around the utility and precise meaning of the measure. In the largest genome-wide association meta-analysis of 2D:4D ratio to date (N = 15 661, with replication N = 75 821), we identified 11 loci (9 novel) explaining 3.8% of the variance in mean 2D:4D ratio. We also found weak evidence for association (β = 0.06; P = 0.02) between 2D:4D ratio and sensitivity to testosterone [length of the CAG microsatellite repeat in the androgen receptor (AR) gene] in females only. Furthermore, genetic variants associated with (adult) testosterone levels and/or sex hormone-binding globulin were not associated with 2D:4D ratio in our sample. Although we were unable to find strong evidence from our genetic study to support the hypothesis that 2D:4D ratio is a direct biomarker of prenatal exposure to androgens in healthy individuals, our findings do not explicitly exclude this possibility, and pathways involving testosterone may become apparent as the size of the discovery sample increases further. Our findings provide new insight into the underlying biology shaping 2D:4D variation in the general population.

摘要

食指与无名指长度的比例(2D:4D)存在性别二态性,通常被用作产前雄激素暴露的非侵入性生物标志物。大多数 2D:4D 比率与各种性别特异性特征相关的关联研究通常涉及小样本量,并且难以复制,这引发了对该测量的实用性和精确含义的质疑。在迄今为止最大的 2D:4D 比率全基因组关联荟萃分析(N = 15661,复制 N = 75821)中,我们确定了 11 个位点(9 个新位点),解释了平均 2D:4D 比率变异的 3.8%。我们还发现,仅在女性中,2D:4D 比率与雄激素(雄激素受体基因中的 CAG 微卫星重复序列长度)敏感性之间存在微弱关联(β = 0.06;P = 0.02)。此外,与(成人)睾酮水平和/或性激素结合球蛋白相关的遗传变异与我们样本中的 2D:4D 比率无关。尽管我们无法从我们的遗传研究中找到强有力的证据来支持 2D:4D 比率是健康个体产前暴露于雄激素的直接生物标志物的假设,但我们的研究结果并没有明确排除这种可能性,并且随着发现样本的进一步扩大,涉及睾酮的途径可能会变得明显。我们的研究结果为理解普通人群中 2D:4D 变异的潜在生物学机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4101/5961159/888deea8af98/ddy121f1.jpg

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