Multitrait analysis to decipher the intertwined genetic architecture of neuroanatomical phenotypes and psychiatric disorders.

Antoine Auvergne, Nicolas Traut, Léo Henches, Lucie Troubat, Arthur Frouin, Christophe Boetto, Sayeh Kazem, Hanna Julienne, Roberto Toro, Hugues Aschard
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Abstract

Background: There is increasing evidence of shared genetic factors between psychiatric disorders and brain magnetic resonance imaging (MRI) phenotypes. However, deciphering the joint genetic architecture of these outcomes has proven challenging, and new approaches are needed to infer potential genetic structure underlying those phenotypes. Multivariate analyses is arising as a meaningful approach to reveal links between MRI phenotypes and psychiatric disorders missed by univariate approaches.

Methods: We first conducted univariate and multivariate genome-wide association studies (GWAS) for nine MRI-derived brain volume phenotypes in 20K UK Biobank participants. We next performed various complementary enrichment analyses to assess whether and how univariate and multitrait approaches can distinguish disorder-associated and non-disorder-associated variants from six psychiatric disorders: bipolarity, attention-deficit/hyperactivity disorder (ADHD), autism, schizophrenia, obsessive-compulsive disorder, and major depressive disorder. Finally, we conducted a clustering analysis of top associated variants based on their MRI multitrait association using an optimized k-medoids approach.

Results: Univariate MRI GWAS displayed only negligible genetic correlation with psychiatric disorders, while multitrait GWAS identified multiple new associations and showed significant enrichment for variants related to both ADHD and schizophrenia. Clustering analyses further detected two clusters displaying not only enrichment for association with ADHD and schizophrenia, but also consistent direction of effects. Functional annotation analyses of those clusters pointed to multiple potential mechanisms, suggesting in particular a role of neurotrophins pathways on both MRI and schizophrenia.

Conclusions: Our results show that multitrait association signature can be used to infer genetically-driven latent MRI variables associated with psychiatric disorders, opening paths for future biomarker development.

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通过多特征分析,破解神经解剖表型和精神疾病相互交织的遗传结构。
背景:越来越多的证据表明,精神疾病和脑磁共振成像(MRI)表型之间存在共同的遗传因素。然而,破译这些结果的共同遗传结构已被证明具有挑战性,需要新的方法来推断这些表型的潜在遗传结构。多变量分析是揭示单变量方法所遗漏的 MRI 表型与精神疾病之间联系的一种有意义的方法:我们首先对 20K 名英国生物库参与者的九种 MRI 衍生脑容量表型进行了单变量和多变量全基因组关联研究(GWAS)。接下来,我们进行了各种互补性富集分析,以评估单变量和多特征方法是否以及如何区分六种精神疾病(双相情感障碍、注意缺陷/多动障碍(ADHD)、自闭症、精神分裂症、强迫症和重度抑郁障碍)中的障碍相关变异和非障碍相关变异。最后,我们使用优化的 k-medoids 方法,根据磁共振成像多特征相关性对顶级相关变异进行了聚类分析:结果:单变量核磁共振成像基因组学分析(Univariate MRI GWAS)显示出与精神疾病的遗传相关性微乎其微,而多特征基因组学分析(multitrait GWAS)则发现了多种新的关联,并显示出与多动症和精神分裂症相关的变异具有显著的富集性。聚类分析进一步发现了两个聚类,它们不仅富集了与多动症和精神分裂症相关的变异,而且效应方向一致。对这些聚类的功能注释分析表明了多种潜在机制,特别是神经营养素通路在核磁共振成像和精神分裂症中的作用:我们的研究结果表明,多特征关联特征可用于推断与精神疾病相关的基因驱动的潜在 MRI 变量,为未来生物标记物的开发开辟了道路。
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