Genome-wide analysis identifies 66 variants underlying anatomical variation in human neuroendocrine structures and reveals links to testosterone

Hannah Currant, Christopher Arthofer, Teresa Ferreira, Gwenaelle Douaud, Barney Hill, Samvida S Venkatesh, Nikolas A Baya, Duncan S Palmer, Saskia Reibe, Anje Moltke-Prehn, Tune H Pers, Andreas Bartsch, Jesper Andersson, Margaret F Lippincott, Yee-Ming Chan, Stephanie B Seminara, Thomas E Nichols, Christoffer Nellaker, Stephen M Smith, Soren Brunak, Frederik J Lange, Cecilia M Lindgren
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Abstract

The hypothalamus, pituitary gland and olfactory bulbs are neuro-anatomical structures key to the regulation of the endocrine system. Variation in their anatomy can affect the function of the reproductive system. To investigate this relationship, we extracted four largely unexplored phenotypes from 34,834 individuals within UK Biobank by quantifying the volume of the hypothalamus, pituitary gland and olfactory bulbs using multi-modal magnetic resonance imaging. Genome-wide association studies of these phenotypes identified 66 independent common genetic associations with endocrine-related neurological volumes (P < 5 × 10−8), five of which had a prior association to testosterone levels, representing enrichment of testosterone-associated SNPs over random chance (P-value = 9.89 × 10−12). Exome-wide rare variant burden analysis identified STAB1 as being significantly associated with hypothalamus volume (P = 3.78 × 10−7), with known associations to brain iron levels. Common variants associated with hypothalamic grey matter volume were also found to be associated with iron metabolism, in which testosterone plays a key role. These results provide initial evidence of common and rare genetic effects on both anatomical variation in neuroendocrine structures and their function in hormone production and regulation. Variants associated with pituitary gland volume were enriched for gene expression specific to theca cells, responsible for testosterone production in ovaries, suggesting shared underlying genetic variation affecting both neurological and gonadal endocrine tissues. Cell-type expression enrichment analysis across hypothalamic cell types identified tanycytes to be associated (P = 1.69 × 10−3) with olfactory bulb volume associated genetic variants, a cell type involved in release of gonadotropin-releasing hormone into the bloodstream. Voxel-wise analysis highlighted associations between the variants associated with pituitary gland volume and regions of the brain involved in the drainage of hormones into the bloodstream. Together, our results suggest a shared role of genetics impacting both the anatomy and function of neuroendocrine structures within the reproductive system in their production and release of reproductive hormones.
全基因组分析确定了人类神经内分泌结构解剖变异的 66 个变体,并揭示了它们与睾酮的联系
下丘脑、脑垂体和嗅球是调节内分泌系统的关键神经解剖结构。它们解剖结构的变化会影响生殖系统的功能。为了研究这种关系,我们利用多模态磁共振成像对下丘脑、垂体和嗅球的体积进行了量化,从而从英国生物库中的 34,834 人中提取了四种在很大程度上未被研究的表型。对这些表型进行的全基因组关联研究发现了 66 个与内分泌相关神经系统体积有关的独立常见遗传关联(P < 5 × 10-8),其中 5 个事先与睾酮水平有关,表明与睾酮相关的 SNPs 比随机机会更丰富(P 值 = 9.89 × 10-12)。全外显子罕见变异负荷分析发现,STAB1 与下丘脑体积显著相关(P = 3.78 × 10-7),已知与脑铁水平有关。还发现与下丘脑灰质体积有关的常见变异与铁代谢有关,而睾酮在铁代谢中起着关键作用。这些结果初步证明了常见和罕见基因对神经内分泌结构的解剖变异及其激素分泌和调节功能的影响。与垂体体积相关的变异富集了卵巢中负责产生睾酮的theca细胞的特异基因表达,这表明影响神经和性腺内分泌组织的潜在遗传变异是共同的。跨下丘脑细胞类型的细胞类型表达富集分析发现,澹红细胞与嗅球体积相关遗传变异有关(P = 1.69 × 10-3),而嗅球体积相关遗传变异是一种参与向血液释放促性腺激素释放激素的细胞类型。体素分析强调了与垂体体积相关的变异与大脑中参与将激素排入血液的区域之间的关联。总之,我们的研究结果表明,遗传因素对生殖系统内神经内分泌结构的解剖结构和功能都有影响,从而共同作用于生殖激素的产生和释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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