Genetic and phenotypic architecture of human myocardial trabeculation.

IF 9.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Kathryn A McGurk, Mengyun Qiao, Sean L Zheng, Arunashis Sau, Albert Henry, Antonio Luiz P Ribeiro, Antônio H Ribeiro, Fu Siong Ng, R Thomas Lumbers, Wenjia Bai, James S Ware, Declan P O'Regan
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引用次数: 0

Abstract

Cardiac trabeculae form a network of muscular strands that line the inner surfaces of the heart. Their development depends on multiscale morphogenetic processes and, while highly conserved across vertebrate evolution, their role in the pathophysiology of the mature heart is not fully understood. Here we report variant associations across the allele frequency spectrum for trabecular morphology in 47,803 participants of the UK Biobank using fractal dimension analysis of cardiac imaging. We identified an association between trabeculation and rare variants in 56 genes that regulate myocardial contractility and ventricular development. Genome-wide association studies identified 68 loci in pathways that regulate sarcomeric function, differentiation of the conduction system and cell fate determination. We found that trabeculation-associated variants were modifiers of cardiomyopathy phenotypes with opposing effects in hypertrophic and dilated cardiomyopathy. Together, these data provide insights into mechanisms that regulate trabecular development and plasticity, and identify a potential role in modifying monogenic disease expression.

人类心肌小梁的遗传和表型结构。
心脏小梁形成了一个肌肉股网络,排列在心脏的内表面。它们的发育依赖于多尺度的形态发生过程,虽然在脊椎动物的进化过程中高度保守,但它们在成熟心脏的病理生理学中的作用还不完全清楚。在此,我们利用心脏成像的分形维度分析,报告了英国生物库中 47803 名参与者的小梁形态等位基因频率谱的变异关联。我们在 56 个调节心肌收缩力和心室发育的基因中发现了小梁与罕见变异之间的关联。全基因组关联研究在调节肌纤维功能、传导系统分化和细胞命运决定的通路中发现了 68 个基因位点。我们发现,小梁相关变异是心肌病表型的修饰因子,对肥厚型和扩张型心肌病的影响截然相反。这些数据共同揭示了调节小梁发育和可塑性的机制,并确定了其在改变单基因疾病表达中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.70
自引率
0.00%
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