Distinct patterns of genetic overlap among multimorbidities revealed with trivariate MiXeR.

IF 10.4 1区 生物学 Q1 GENETICS & HEREDITY
Alexey A Shadrin, Guy Hindley, Espen Hagen, Nadine Parker, Markos Tesfaye, Piotr Jaholkowski, Zillur Rahman, Gleda Kutrolli, Vera Fominykh, Srdjan Djurovic, Olav B Smeland, Kevin S O'Connell, Dennis van der Meer, Oleksandr Frei, Ole A Andreassen, Anders M Dale
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引用次数: 0

Abstract

Background: Multimorbidities are a global health challenge. Accumulating evidence indicates that overlapping genetic architectures underlie comorbid complex human traits and disorders. This can be quantified for a pair of phenotypes using various techniques. Still, the pattern of genetic overlap between three distinct complex phenotypes, which is important for understanding multimorbidities, has not been possible to quantify.

Methods: Here, we present and validate the novel trivariate MiXeR tool, which disentangles the pattern of genetic overlap between three complex phenotypes using summary statistics from genome-wide association studies. Our simulations show that trivariate MiXeR can reliably reconstruct different patterns of genetic overlap and estimate the proportions of genetic overlap between three phenotypes.

Results: We found substantial genetic overlap between gastro-intestinal and brain diseases supporting a genetic basis of the gut-brain axis-the pattern consistent with pairwise analysis. However, the pattern of genetic overlap between three diverse cardiometabolic and renal health indicators and three immune-linked disorders revealed a much larger genomic component shared between all phenotypes than expected from separate pairwise analyses. This suggests the existence of core pathways underlying distinct but related chronic conditions.

Conclusions: Overall, trivariate MiXeR offers a novel and efficient tool for investigating patterns of genetic overlap among three complex phenotypes. This contributes to a better understanding of genetic relationships between complex traits and disorders, potentially providing new insights into the mechanisms underlying common multimorbidities. Trivariate MiXeR is freely available at https://github.com/precimed/mix3r .

不同模式的遗传重叠在多病之间揭示了三重混合器。
背景:多病是一项全球性的健康挑战。越来越多的证据表明,重叠的遗传结构是复杂的人类特征和疾病共病的基础。这可以使用各种技术对一对表型进行量化。尽管如此,三种不同的复杂表型之间的遗传重叠模式,这对理解多病很重要,还不可能量化。方法:在这里,我们提出并验证了新的三变量MiXeR工具,该工具使用全基因组关联研究的汇总统计数据来解开三种复杂表型之间的遗传重叠模式。我们的模拟表明,三变量MiXeR可以可靠地重建不同的遗传重叠模式,并估计三种表型之间的遗传重叠比例。结果:我们发现胃肠道和脑部疾病之间存在大量的遗传重叠,支持肠-脑轴的遗传基础,这种模式与两两分析一致。然而,三种不同的心脏代谢和肾脏健康指标以及三种免疫相关疾病之间的遗传重叠模式显示,所有表型之间共享的基因组成分比单独的两两分析所预期的要大得多。这表明存在不同但相关的慢性疾病的核心途径。结论:总的来说,三变量MiXeR为研究三种复杂表型之间的遗传重叠模式提供了一种新颖而有效的工具。这有助于更好地理解复杂性状和疾病之间的遗传关系,可能为常见多病的潜在机制提供新的见解。Trivariate MiXeR可在https://github.com/precimed/mix3r免费获得。
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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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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