雄激素受体
生物
雄激素
激素
表型
全基因组关联研究
男性型秃发
遗传学
生物信息学
基因
内分泌学
头皮
基因型
癌症
单核苷酸多态性
解剖
前列腺癌
作者
Stefanie Heilmann‐Heimbach,Lara M. Hochfeld,Sabrina K. Henne,Markus M. Nöthen
摘要
Abstract Male‐pattern hair loss, also termed androgenetic alopecia (AGA), is a highly prevalent age‐related condition that is characterized by a distinct pattern of hair loss from the frontotemporal and vertex regions of the scalp. The phenotype is highly heritable and hormone dependent, with androgens being the recognized critical hormonal factor. Numerous molecular genetic studies have focused on genetic variation in and around the gene that encodes the androgen receptor. More recently, however, the availability of high‐throughput molecular genetic methods, novel methods of data analysis and sufficiently large sample sizes have rendered possible the systematic investigation of the contribution of other components of the androgen receptor pathway or hormonal pathways beyond the androgen receptor signalling pathways. Over the past decade, genome‐wide association studies of increasingly large cohorts have enabled the genome‐wide identification of genetic risk factors for AGA, and yielded unprecedented insights into the underlying pathobiology. The present review discusses some of the most intriguing genetic findings on the relevance of (sex)hormonal signalling in AGA.
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