Pagadala Meghana S, Teerlink Craig C, Jasuja Guneet K, Palnati Madhuri, Anglin-Foote Tori, Chang Nai-Chung N, Deka Rishi, Lee Kyung M, Agiri Fatai Y, Amariuta Tiffany, Seibert Tyler M, Rose Brent S, Pridgen Kathryn M, Lynch Julie A, Carter Hannah K, Panizzon Matthew S, Hauger Richard L
Research Service, VA San Diego Healthcare System, San Diego, CA, USA.
Medical Scientist Training Program, University of California San Diego, La Jolla, CA, USA.
Nat Commun. 2025 May 2;16(1):4104. doi: 10.1038/s41467-025-57372-x.
Given the various roles of testosterone in men's health, we conducted a multi-ancestral genetic analysis of total testosterone, free testosterone, SHBG, and hypogonadism in men within the Million Veteran Program (MVP). Here we identified 157 significant testosterone genetic variants, of which 8 have significant ancestry-specific associations. These variants implicate several genes, including SERPINF2, PRPF8, BAIAP2L1, SHBG, PRMT6, and PPIF, related to liver function. Genetic regulators of testosterone have cell type-specific effects in the testes, liver, and adrenal gland and are associated with disease risk. We conducted a meta-analysis amongst ancestry groups to identify 188 variants significantly associated with testosterone, of which 22 are novel associations. We constructed genetic scores for total testosterone, SHBG levels, and hypogonadism and find that men with higher testosterone genetic scores have lower odds of diabetes, hyperlipidemia, gout, and cardiac disorders. These findings provide insight into androgen regulation and identify novel variants for disease risk stratification.
鉴于睾酮在男性健康中的多种作用,我们在百万退伍军人计划(MVP)中对男性的总睾酮、游离睾酮、性激素结合球蛋白(SHBG)和性腺功能减退进行了多祖先遗传分析。在此,我们鉴定出157个显著的睾酮基因变异,其中8个具有显著的特定祖先关联。这些变异涉及多个基因,包括与肝功能相关的丝氨酸蛋白酶抑制剂F2(SERPINF2)、前体mRNA加工因子8(PRPF8)、脑和肌动蛋白结合蛋白2样蛋白1(BAIAP2L1)、SHBG、蛋白质精氨酸甲基转移酶6(PRMT6)和亲环蛋白F(PPIF)。睾酮的遗传调节因子在睾丸、肝脏和肾上腺中具有细胞类型特异性作用,并与疾病风险相关。我们在不同祖先群体中进行了荟萃分析,以鉴定出188个与睾酮显著相关的变异,其中22个是新的关联。我们构建了总睾酮、SHBG水平和性腺功能减退的遗传评分,发现睾酮遗传评分较高的男性患糖尿病、高脂血症、痛风和心脏疾病的几率较低。这些发现为雄激素调节提供了见解,并确定了用于疾病风险分层的新变异。