Genetic and functional insights into the fractal structure of the heart

IF 48.5 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Nature Pub Date : 2020-08-19 DOI:10.1038/s41586-020-2635-8
Hannah V. Meyer, Timothy J. W. Dawes, Marta Serrani, Wenjia Bai, Paweł Tokarczuk, Jiashen Cai, Antonio de Marvao, Albert Henry, R. Thomas Lumbers, Jakob Gierten, Thomas Thumberger, Joachim Wittbrodt, James S. Ware, Daniel Rueckert, Paul M. Matthews, Sanjay K. Prasad, Maria L. Costantino, Stuart A. Cook, Ewan Birney, Declan P. O’Regan
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引用次数: 69

Abstract

The inner surfaces of the human heart are covered by a complex network of muscular strands that is thought to be a remnant of embryonic development1,2. The function of these trabeculae in adults and their genetic architecture are unknown. Here we performed a genome-wide association study to investigate image-derived phenotypes of trabeculae using the fractal analysis of trabecular morphology in 18,096 participants of the UK Biobank. We identified 16 significant loci that contain genes associated with haemodynamic phenotypes and regulation of cytoskeletal arborization3,4. Using biomechanical simulations and observational data from human participants, we demonstrate that trabecular morphology is an important determinant of cardiac performance. Through genetic association studies with cardiac disease phenotypes and Mendelian randomization, we find a causal relationship between trabecular morphology and risk of cardiovascular disease. These findings suggest a previously unknown role for myocardial trabeculae in the function of the adult heart, identify conserved pathways that regulate structural complexity and reveal the influence of the myocardial trabeculae on susceptibility to cardiovascular disease. A genome-wide association study shows that myocardial trabeculae are an important determinant of cardiac performance in the adult heart, identifies conserved pathways that regulate structural complexity and reveals the influence of trabeculae on the susceptibility to cardiovascular disease.

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对心脏分形结构的遗传和功能见解
人类心脏的内表面覆盖着复杂的肌肉股网络,这被认为是胚胎发育的残留物1,2。这些小梁在成人中的功能及其遗传结构尚不清楚。在此,我们进行了一项全基因组关联研究,利用小梁形态的分形分析,对英国生物库中的 18096 名参与者进行了小梁图像衍生表型的研究。我们确定了 16 个重要基因位点,这些位点包含与血液动力学表型和细胞骨架轴化调控相关的基因3,4。通过生物力学模拟和人类参与者的观察数据,我们证明了小梁形态是心脏性能的重要决定因素。通过与心脏疾病表型和孟德尔随机化的遗传关联研究,我们发现小梁形态与心血管疾病风险之间存在因果关系。这些研究结果表明,心肌小梁在成人心脏功能中发挥着之前未知的作用,确定了调节结构复杂性的保守途径,并揭示了心肌小梁对心血管疾病易感性的影响。一项全基因组关联研究表明,心肌小梁是成人心脏功能的重要决定因素,确定了调节结构复杂性的保守途径,并揭示了心肌小梁对心血管疾病易感性的影响。
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来源期刊
Nature
Nature 综合性期刊-综合性期刊
CiteScore
90.00
自引率
1.20%
发文量
3652
审稿时长
3 months
期刊介绍: Nature is a prestigious international journal that publishes peer-reviewed research in various scientific and technological fields. The selection of articles is based on criteria such as originality, importance, interdisciplinary relevance, timeliness, accessibility, elegance, and surprising conclusions. In addition to showcasing significant scientific advances, Nature delivers rapid, authoritative, insightful news, and interpretation of current and upcoming trends impacting science, scientists, and the broader public. The journal serves a dual purpose: firstly, to promptly share noteworthy scientific advances and foster discussions among scientists, and secondly, to ensure the swift dissemination of scientific results globally, emphasizing their significance for knowledge, culture, and daily life.
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