Role of titin in cardiomyopathy: from DNA variants to patient stratification

被引:120
作者
Ware, James S. [1 ,2 ]
Cook, Stuart A. [1 ,3 ,4 ]
机构
[1] Imperial Coll London, Royal Brompton Hosp, Natl Heart & Lung Inst, Sydney St, London SW3 6NP, England
[2] London Inst Med Sci, MRC, Cane Rd, London W12 0NN, England
[3] Duke NUS, Med Sch, 8 Coll Rd, Singapore 169857, Singapore
[4] Natl Heart Ctr Singapore, 8 Coll Rd, Singapore 169857, Singapore
基金
英国惠康基金; 英国医学研究理事会;
关键词
FAMILIAL DILATED CARDIOMYOPATHY; CAUSE HYPERTROPHIC CARDIOMYOPATHY; EARLY RESPIRATORY-FAILURE; CARDIOLOGY WORKING GROUP; NONSENSE-MEDIATED DECAY; MUSCLE FILAMENT TITIN; PROTEIN-C GENE; EUROPEAN-SOCIETY; HEART-FAILURE; FAILING HEART;
D O I
10.1038/nrcardio.2017.190
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dilated cardiomyopathy (DCM) affects approximately 1 in 250 individuals and is the leading indication for heart transplantation. DCM is often familial, and the most common genetic predisposition is a truncating variation in the giant sarcomeric protein, titin, which occurs in up to 15% of ambulant patients with DCM and 25% of end-stage or familial cases. In this article, we review the evidence for the role of titin truncation in the pathogenesis of DCM and our understanding of the molecular mechanisms and pathophysiological consequences of variation in the gene encoding titin (TTN). Such variation is common in the general population (up to 1% of individuals), and we consider key features that discriminate variants with disease-causing potential from those that are benign. We summarize strategies for clinical interpretation of genetic variants for use in the diagnosis of patients and the evaluation of their relatives. Finally, we consider the contemporary and potential future role for genetic stratification in cardiomyopathy and in the general population, evaluating titin variation as a predictor of outcome and treatment response for precision medicine.
引用
收藏
页码:241 / 252
页数:12
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