Day Felix R, Perry John R B, Ong Ken K
MRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
Neuroendocrinology. 2015;102(4):247-255. doi: 10.1159/000431023. Epub 2015 May 7.
Understanding the regulation of puberty timing has relevance to developmental and human biology and to the pathogenesis of various diseases. Recent large-scale genome-wide association studies on puberty timing and adult height, body mass index (BMI) and central body shape provide evidence for shared biological mechanisms that regulate these traits. There is a substantial genetic overlap between age at menarche in women and BMI, with almost invariable directional consistency with the epidemiological associations between earlier menarche and higher BMI. By contrast, the genetic loci identified for age at menarche are largely distinct from those identified for central body shape, while alleles that confer earlier menarche can be associated with taller or shorter adult height. The findings of population-based studies on age at menarche show increasing relevance for other studies of rare monogenic disorders and enrich our understanding of the mechanisms that regulate the timing of puberty and reproductive function.
了解青春期启动时间的调节与发育生物学、人类生物学以及各种疾病的发病机制相关。近期关于青春期启动时间与成人身高、体重指数(BMI)及中心体型的大规模全基因组关联研究,为调控这些性状的共同生物学机制提供了证据。女性初潮年龄与BMI之间存在显著的遗传重叠,且与初潮较早和BMI较高之间的流行病学关联几乎始终保持一致的方向。相比之下,为初潮年龄确定的基因座在很大程度上与为中心体型确定的基因座不同,而导致初潮较早的等位基因可能与成人身高较高或较矮有关。基于人群的初潮年龄研究结果对其他罕见单基因疾病的研究越来越重要,并丰富了我们对调节青春期启动时间和生殖功能机制的理解。