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靶向新一代测序检测心肌病中新的基因-表型关联并扩展突变谱。

Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies.

作者信息

Forleo Cinzia, D'Erchia Anna Maria, Sorrentino Sandro, Manzari Caterina, Chiara Matteo, Iacoviello Massimo, Guaricci Andrea Igoren, De Santis Delia, Musci Rita Leonarda, La Spada Antonino, Marangelli Vito, Pesole Graziano, Favale Stefano

机构信息

Cardiology Unit, Department of Emergency and Organ Transplantation, University of Bari Aldo Moro, Bari, Italy.

Department of Biosciences, Biotechnology and Biopharmaceutics, University of Bari Aldo Moro, Bari, Italy.

出版信息

PLoS One. 2017 Jul 27;12(7):e0181842. doi: 10.1371/journal.pone.0181842. eCollection 2017.

Abstract

Cardiomyopathies are a heterogeneous group of primary diseases of the myocardium, including hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and arrhythmogenic right ventricular cardiomyopathy (ARVC), with higher morbidity and mortality. These diseases are genetically diverse and associated with rare mutations in a large number of genes, many of which overlap among the phenotypes. To better investigate the genetic overlap between these three phenotypes and to identify new genotype-phenotype correlations, we designed a custom gene panel consisting of 115 genes known to be associated with cardiomyopathic phenotypes and channelopathies. A cohort of 38 unrelated patients, 16 affected by DCM, 14 by HCM and 8 by ARVC, was recruited for the study on the basis of more severe phenotypes and family history of cardiomyopathy and/or sudden death. We detected a total of 142 rare variants in 40 genes, and all patients were found to be carriers of at least one rare variant. Twenty-eight of the 142 rare variants were also predicted as potentially pathogenic variants and found in 26 patients. In 23 out of 38 patients, we found at least one novel potential gene-phenotype association. In particular, we detected three variants in OBSCN gene in ARVC patients, four variants in ANK2 gene and two variants in DLG1, TRPM4, and AKAP9 genes in DCM patients, two variants in PSEN2 gene and four variants in AKAP9 gene in HCM patients. Overall, our results confirmed that cardiomyopathic patients could carry multiple rare gene variants; in addition, our investigation of the genetic overlap among cardiomyopathies revealed new gene-phenotype associations. Furthermore, as our study confirms, data obtained using targeted next-generation sequencing could provide a remarkable contribution to the molecular diagnosis of cardiomyopathies, early identification of patients at risk for arrhythmia development, and better clinical management of cardiomyopathic patients.

摘要

心肌病是一组异质性的心肌原发性疾病,包括肥厚型心肌病(HCM)、扩张型心肌病(DCM)和致心律失常性右室心肌病(ARVC),其发病率和死亡率较高。这些疾病具有遗传多样性,与大量基因中的罕见突变相关,其中许多基因在不同表型之间存在重叠。为了更好地研究这三种表型之间的遗传重叠,并确定新的基因型-表型相关性,我们设计了一个定制基因panel,其中包含115个已知与心肌病表型和离子通道病相关的基因。基于更严重的表型以及心肌病和/或猝死的家族史,招募了一组38名无亲缘关系的患者,其中16名患有DCM,14名患有HCM,8名患有ARVC,用于该研究。我们在40个基因中总共检测到142个罕见变异,并且发现所有患者均为至少一个罕见变异的携带者。142个罕见变异中的28个也被预测为潜在致病性变异,并在26名患者中被发现。在38名患者中的23名中,我们发现了至少一种新的潜在基因-表型关联。具体而言,我们在ARVC患者中检测到OBSCN基因的三个变异,在DCM患者中检测到ANK2基因的四个变异以及DLG1、TRPM4和AKAP9基因的两个变异,在HCM患者中检测到PSEN2基因的两个变异和AKAP9基因的四个变异。总体而言,我们的结果证实心肌病患者可能携带多个罕见基因变异;此外,我们对心肌病之间遗传重叠的研究揭示了新的基因-表型关联。此外,正如我们的研究所证实的,使用靶向二代测序获得的数据可为心肌病的分子诊断、心律失常发生风险患者的早期识别以及心肌病患者的更好临床管理做出显著贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f97/5531468/00d765747d7d/pone.0181842.g001.jpg

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