Xia Kai, Yu Yang, Ahn Mihye, Zhu Hongtu, Zou Fei, Gilmore John H, Knickmeyer Rebecca C
Department of Psychiatry, University of North Carolina at Chapel Hill , Chapel Hill, NC , USA.
Department of Statistics and Operations Research, University of North Carolina at Chapel Hill , Chapel Hill, NC , USA.
Front Endocrinol (Lausanne). 2014 Oct 30;5:187. doi: 10.3389/fendo.2014.00187. eCollection 2014.
Transient activation of the hypothalamic-pituitary-gonadal axis in early infancy plays an important role in male genital development and sexual differentiation of the brain, but factors contributing to individual variation in testosterone levels during this period are poorly understood. We measured salivary testosterone levels in 222 infants (119 males, 103 females, 108 singletons, 114 twins) between 2.70 and 4.80 months of age. We tested 16 major demographic and medical history variables for effects on inter-individual variation in salivary testosterone. Using the subset of twins, we estimated genetic and environmental contributions to salivary testosterone levels. Finally, we tested single nucleotide polymorphisms (SNPs) within ±5 kb of genes involved in testosterone synthesis, transport, signaling, and metabolism for associations with salivary testosterone using univariate tests and random forest (RF) analysis. We report an association between 5 min APGAR scores and salivary testosterone levels in males. Twin modeling indicated that individual variability in testosterone levels was primarily explained by environmental factors. Regarding genetic variation, univariate tests did not reveal any variants significantly associated with salivary testosterone after adjusting for false discovery rate. The top hit in males was rs10923844, an SNP of unknown function located downstream of HSD3B1 and HSD3B2. The top hits in females were two SNPs located upstream of ESR1 (rs3407085 and rs2295190). RF analysis, which reflects joint and conditional effects of multiple variants, indicated that genes involved in regulation of reproductive function, particularly LHCGR, are related to salivary testosterone levels in male infants, as are genes involved in cholesterol production, transport, and removal, while genes involved in estrogen signaling are related to salivary testosterone levels in female infants.
婴儿早期下丘脑 - 垂体 - 性腺轴的短暂激活在男性生殖器发育和大脑性分化中起重要作用,但在此期间导致睾酮水平个体差异的因素却知之甚少。我们测量了222名2.70至4.80月龄婴儿(119名男性、103名女性、108名单胎、114名双胞胎)的唾液睾酮水平。我们测试了16个主要人口统计学和病史变量对唾液睾酮个体间差异的影响。利用双胞胎子集,我们估计了遗传和环境因素对唾液睾酮水平的贡献。最后,我们使用单变量检验和随机森林(RF)分析,测试了睾酮合成、转运、信号传导和代谢相关基因上下游±5 kb范围内的单核苷酸多态性(SNP)与唾液睾酮的关联。我们报告了男性5分钟阿氏评分与唾液睾酮水平之间的关联。双胞胎模型表明,睾酮水平的个体差异主要由环境因素解释。关于遗传变异,在调整错误发现率后,单变量检验未发现任何与唾液睾酮显著相关的变异。男性中最显著的是rs10923844,这是一个位于HSD3B1和HSD3B2下游、功能未知的SNP。女性中最显著的是位于ESR1上游的两个SNP(rs3407085和rs2295190)。反映多个变异联合和条件效应的RF分析表明,参与生殖功能调节的基因,特别是LHCGR,与男婴唾液睾酮水平有关,参与胆固醇产生、转运和清除的基因也有关,而参与雌激素信号传导的基因与女婴唾液睾酮水平有关。