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不明原因猝死:存活亲属的心脏病学和基因检查的遗传度及诊断率

Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives.

作者信息

Tan Hanno L, Hofman Nynke, van Langen Irene M, van der Wal Allard C, Wilde Arthur A M

机构信息

Department of Cardiology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

出版信息

Circulation. 2005 Jul 12;112(2):207-13. doi: 10.1161/CIRCULATIONAHA.104.522581. Epub 2005 Jul 5.

Abstract

BACKGROUND

Sudden death mostly follows from cardiac disorders that elicit lethal ventricular arrhythmias. In young individuals, it often remains unexplained because history and/or postmortem analysis are absent or provide no clue. Because such sudden unexplained deaths (SUDs) may have heritable causes, cardiological and genetic assessment of surviving relatives of SUD victims may reveal the underlying disease and unmask presymptomatic carriers. We aimed to establish the diagnostic yield of such assessments.

METHODS AND RESULTS

We investigated 43 consecutive families with > or =1 SUD victim who died at < or =40 years of age. All studied relatives underwent resting/exercise ECG and Doppler echocardiography. Molecular genetic analysis was conducted to confirm the diagnosis. We identified an inherited disease and likely cause of death in 17 of 43 families (40%). Twelve families had primary electrical disease: catecholaminergic polymorphic ventricular tachycardia (5 families), long-QT syndrome (4 families), Brugada syndrome (2 families), and long-QT/Brugada syndrome (1 family). Furthermore, we found arrhythmogenic right ventricular cardiomyopathy (3 families), hypertrophic cardiomyopathy (1 family), and familial hypercholesterolemia (1 family). Molecular genetic analysis provided confirmation in 10 families. Finding the diagnosis was more likely when more relatives were examined and in families with > or =2 SUD victims < or =40 years of age. The resting/exercise ECG had a high diagnostic yield. These efforts unmasked 151 presymptomatic disease carriers (8.9 per family).

CONCLUSIONS

Examination of relatives of young SUD victims has a high diagnostic yield, with identification of the disease in 40% of families and 8.9 presymptomatic carriers per family. Simple procedures (examining many relatives) and routine tests (resting/exercise ECG) constitute excellent diagnostic strategies. Molecular genetics provide strong supportive information.

摘要

背景

猝死大多源于引发致命性室性心律失常的心脏疾病。在年轻人中,猝死原因常常不明,因为缺乏病史和/或尸检分析,或者这些分析无法提供线索。由于此类不明原因的猝死(SUDs)可能存在遗传因素,对SUD受害者的在世亲属进行心脏和基因评估可能会揭示潜在疾病,并发现症状前携带者。我们旨在确定此类评估的诊断率。

方法与结果

我们调查了43个连续的家庭,每个家庭至少有1名40岁及以下死于SUD的受害者。所有参与研究的亲属均接受了静息/运动心电图和多普勒超声心动图检查。进行分子遗传学分析以确诊。我们在43个家庭中的17个(40%)确定了一种遗传性疾病及可能的死亡原因。12个家庭患有原发性心电疾病:儿茶酚胺能多形性室性心动过速(5个家庭)、长QT综合征(4个家庭)、Brugada综合征(2个家庭)以及长QT/Brugada综合征(1个家庭)。此外,我们还发现了致心律失常性右室心肌病(3个家庭)、肥厚型心肌病(1个家庭)和家族性高胆固醇血症(1个家庭)。分子遗传学分析在10个家庭中得到了确诊。检查的亲属越多,以及在有2名及以上40岁及以下SUD受害者的家庭中,越有可能做出诊断。静息/运动心电图具有较高的诊断率。这些检查发现了151名症状前疾病携带者(每个家庭8.9名)。

结论

对年轻SUD受害者的亲属进行检查具有较高的诊断率,在40%的家庭中确定了疾病,每个家庭发现8.9名症状前携带者。简单的程序(检查众多亲属)和常规检查(静息/运动心电图)构成了出色的诊断策略。分子遗传学提供了有力的支持信息。

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