利用三维群体表型分析与心脏形态和功能相关的新基因位点。

IF 5.5 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Chang Lu, Kathryn A McGurk, Sean L Zheng, Antonio de Marvao, Paolo Inglese, Wenjia Bai, James S Ware, Declan P O'Regan
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引用次数: 0

摘要

背景:心脏重塑发生在成熟的心脏,是对应激反应的级联适应,在生命早期就开始了。一个关键的问题仍然是调节心脏的几何形状和运动的过程,以及它如何适应压力。方法:我们使用基于机器学习的心脏磁共振成像分析对47549名英国生物银行参与者进行了空间分辨表型分析。我们分析了16种左心室空间表型,包括区域心肌壁厚度和收缩应变在周向和径向。在多达40,058名参与者中,使用与输入基因型参与者的全基因组关联研究,以及使用全外显子组测序数据的全外显子组关联研究和基于基因的负担测试,评估了整个等位基因频谱的遗传关联。我们整合了来自GTEx项目的转录组学数据,并使用途径富集分析来进一步解释鉴定位点的生物学相关性。为了研究因果关系,我们进行了孟德尔随机化分析,以评估血压对区域心脏特征的影响以及这些特征对心肌病风险的影响。结果:我们发现了42个与心脏结构和收缩力相关的基因座,其中许多基因座揭示了心脏的空间组织模式。全外显子组测序显示了3个未被全基因组关联研究捕获的额外变体,包括CSRP3的错义变体(次要等位基因频率0.5%)。大多数新发现的基因座是在心肌病相关基因中发现的,这表明它们调节着成年人左心室重构的空间不同模式。我们的因果分析还发现,区域调节血压对心脏壁厚度和应变。结论:这些发现为协调心脏发育和心脏重塑的途径提供了全面的描述。这些数据强调了心肌病相关基因在那些没有已知疾病的人的空间适应调节中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Genetic Loci Implicated in Cardiac Morphology and Function Using Three-Dimensional Population Phenotyping.

Background: Cardiac remodeling occurs in the mature heart and is a cascade of adaptations in response to stress, which are primed in early life. A key question remains as to the processes that regulate the geometry and motion of the heart and how it adapts to stress.

Methods: We performed spatially resolved phenotyping using machine learning-based analysis of cardiac magnetic resonance imaging in 47 549 UK Biobank participants. We analyzed 16 left ventricular spatial phenotypes, including regional myocardial wall thickness and systolic strain in both circumferential and radial directions. In up to 40 058 participants, genetic associations across the allele frequency spectrum were assessed using genome-wide association studies with imputed genotype participants, and exome-wide association studies and gene-based burden tests using whole-exome sequencing data. We integrated transcriptomic data from the GTEx project and used pathway enrichment analyses to further interpret the biological relevance of identified loci. To investigate causal relationships, we conducted Mendelian randomization analyses to evaluate the effects of blood pressure on regional cardiac traits and the effects of these traits on cardiomyopathy risk.

Results: We found 42 loci associated with cardiac structure and contractility, many of which reveal patterns of spatial organization in the heart. Whole-exome sequencing revealed 3 additional variants not captured by the genome-wide association study, including a missense variant in CSRP3 (minor allele frequency 0.5%). The majority of newly discovered loci are found in cardiomyopathy-associated genes, suggesting that they regulate spatially distinct patterns of remodeling in the left ventricle in an adult population. Our causal analysis also found regional modulation of blood pressure on cardiac wall thickness and strain.

Conclusions: These findings provide a comprehensive description of the pathways that orchestrate heart development and cardiac remodeling. These data highlight the role that cardiomyopathy-associated genes have on the regulation of spatial adaptations in those without known disease.

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来源期刊
Circulation: Genomic and Precision Medicine
Circulation: Genomic and Precision Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
9.20
自引率
5.40%
发文量
144
期刊介绍: Circulation: Genomic and Precision Medicine is a distinguished journal dedicated to advancing the frontiers of cardiovascular genomics and precision medicine. It publishes a diverse array of original research articles that delve into the genetic and molecular underpinnings of cardiovascular diseases. The journal's scope is broad, encompassing studies from human subjects to laboratory models, and from in vitro experiments to computational simulations. Circulation: Genomic and Precision Medicine is committed to publishing studies that have direct relevance to human cardiovascular biology and disease, with the ultimate goal of improving patient care and outcomes. The journal serves as a platform for researchers to share their groundbreaking work, fostering collaboration and innovation in the field of cardiovascular genomics and precision medicine.
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