Janivara Rohini, Hazra Ujani, Pfennig Aaron, Harlemon Maxine, Kim Michelle S, Eaaswarkhanth Muthukrishnan, Chen Wenlong C, Ogunbiyi Adebola, Kachambwa Paidamoyo, Petersen Lindsay N, Jalloh Mohamed, Mensah James E, Adjei Andrew A, Adusei Ben, Joffe Maureen, Gueye Serigne M, Aisuodionoe-Shadrach Oseremen I, Fernandez Pedro W, Rohan Thomas E, Andrews Caroline, Rebbeck Timothy R, Adebiyi Akindele O, Agalliu Ilir, Lachance Joseph
School of Biological Sciences, Georgia Institute of Technology, Atlanta, Georgia, USA.
Department of Biology, Morgan State University, Baltimore, Maryland, USA.
bioRxiv. 2024 Jan 15:2024.01.12.575396. doi: 10.1101/2024.01.12.575396.
Androgenetic alopecia is a highly heritable trait. However, much of our understanding about the genetics of male pattern baldness comes from individuals of European descent. Here, we examined a novel dataset comprising 2,136 men from Ghana, Nigeria, Senegal, and South Africa that were genotyped using a custom array. We first tested how genetic predictions of baldness generalize from Europe to Africa, finding that polygenic scores from European GWAS yielded AUC statistics that ranged from 0.513 to 0.546, indicating that genetic predictions of baldness in African populations performed notably worse than in European populations. Subsequently, we conducted the first African GWAS of androgenetic alopecia, focusing on self-reported baldness patterns at age 45. After correcting for present age, population structure, and study site, we identified 266 moderately significant associations, 51 of which were independent (p-value < 10, r < 0.2). Most baldness associations were autosomal, and the X chromosomes does not appear to have a large impact on baldness in African men. Finally, we examined the evolutionary causes of continental differences in genetic architecture. Although Neanderthal alleles have previously been associated with skin and hair phenotypes, we did not find evidence that European-ascertained baldness hits were enriched for signatures of ancient introgression. Most loci that are associated with androgenetic alopecia are evolving neutrally. However, multiple baldness-associated SNPs near the and genes have large allele frequency differences between continents. Collectively, our findings illustrate how evolutionary history contributes to the limited portability of genetic predictions across ancestries.
雄激素性脱发是一种高度可遗传的性状。然而,我们对男性型秃发遗传学的大部分了解都来自欧洲血统的个体。在此,我们研究了一个新的数据集,该数据集包含来自加纳、尼日利亚、塞内加尔和南非的2136名男性,他们使用定制阵列进行了基因分型。我们首先测试了秃发的遗传预测如何从欧洲推广到非洲,发现来自欧洲全基因组关联研究(GWAS)的多基因分数产生的AUC统计值在0.513至0.546之间,这表明非洲人群中秃发的遗传预测表现明显不如欧洲人群。随后,我们进行了首次非洲雄激素性脱发全基因组关联研究,重点关注45岁时自我报告的秃发模式。在校正当前年龄、人群结构和研究地点后,我们确定了266个中度显著的关联,其中51个是独立的(p值<10,r<0.2)。大多数秃发关联是常染色体的,X染色体似乎对非洲男性的秃发没有很大影响。最后,我们研究了遗传结构大陆差异的进化原因。尽管尼安德特人等位基因此前已与皮肤和头发表型相关联,但我们没有发现证据表明欧洲确定的秃发相关位点富集了古代基因渗入的特征。大多数与雄激素性脱发相关的基因座正在中性进化。然而,靠近 和 基因的多个与秃发相关的单核苷酸多态性(SNP)在各大洲之间存在较大的等位基因频率差异。总的来说,我们的研究结果说明了进化历史如何导致遗传预测在不同血统之间的可移植性有限。