捷克共和国心源性猝死(SCD)病因和亲属心脏骤停一级预防的多中心研究结果

Q4 Medicine
Soudni Lekarstvi Pub Date : 2022-01-01
Kučerová Pohlová Štěpánka, Krebsová Alice, Votýpka Pavel, Peldová Petra, Kulvajtová Markéta, Dohnalová Petra, Bílek Matěj, Stufka Veronika, Rücklová Kristina, Grossová Iva, Wünschová Hanka, Tavačová Terezia, Hašková Jana, Segeťová Markéta, Gřegořová Andrea, Zoubková Veronika, Petřková Jana, Dobiáš Martin, Makuša Michal, Blanková Alžběta, Veitr David, Řehulka Hynek, Šubrt Ivan, Pilin Alexander, Tomášek Petr, Janoušek Jan, Kautzner Josef, Macek Milan
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引用次数: 0

摘要

年龄小于40岁的心脏性猝死(SCD)在很大一部分病例中有遗传原因。SCD的鉴定、死后遗传分析以及一级心脏病筛查检查是受害者亲属心脏骤停一级预防的重要诊断工具,需要多中心和多学科合作。在2016年至2021年期间,对115例尸检诊断为心肌病、急性主动脉夹层和未发现形态学解释死因(突发性心律失常死亡或不明原因猝死)的死亡病例进行了复杂的心脏遗传学分析。从死后收集的组织样本或亲属的血液中分离DNA,并进行大规模平行测序(Illumina,美国),测序范围为100至20,000个基因。测序结果使用SOPHiA GENETICS DDM生物信息学平台(瑞士)进行分析。对328名家庭成员进行了遗传咨询和心脏病检查。在分析的RYR2、KCNH2、KCNQ1、SCN5A、FLNC (stop)、GLA、TTN、TNNT2、RBM 20、MYBPC3、MYPN、FHL1、TGFBR1和COL3A1基因的病例中,有19.8%的病例揭示了高度可能或某些分子病因(即基于ACMG.net 4至5类变异的存在)。通过心脏遗传学筛查,我们确定了25%有危及生命的心律失常风险的亲属,并为他们提供个性化护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcomes of a multicenter study of the causes of sudden cardiac death (SCD) in the Czech Republic and primary prevention of cardiac arrest in relatives.

Sudden cardiac death (SCD) in individuals younger than 40 years has a heritable cause in a significant part of the cases. Identification of SCD, post mortem genetic analysis along with the cardiological screening examination in first degree represents an important diagnostic tool for the primary prevention of cardiac arrest in victim´s relatives and requires multicentric and multidisciplinary collaboration. Between 2016 and 2021 the complex cardiogenetic analysis was performed in 115 deaths with post mortem diagnosis of cardiomyopathy, acute aortic dissection and cases without morphological finding explaining the cause of death (sudden arrhythmic death or sudden unexplained death). DNA was isolated from post mortem collected tissue samples or relative´s blood and subjected to massively parallel sequencing (Illumina, USA) in extent of 100 to 20 000 genes. Sequencing results were analysed using the SOPHiA GENETICS DDM bioinformatics platform (Switzerland). Genetic counselling and cardiological examinations were carried out in 328 family members. Highly likely or certain molecular aetiology (i.e. based on presence of ACMG.net Class 4 to 5 variants) was disclosed in 19,8 % of analysed cases in RYR2, KCNH2, KCNQ1, SCN5A, FLNC (stop), GLA, TTN, TNNT2, RBM 20, MYBPC3, MYPN, FHL1, TGFBR1, and COL3A1 genes. With cardiogenetic screening we identified 25 % relatives at risk of life threating arrhythmias and offered them an individualised care.

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Soudni Lekarstvi
Soudni Lekarstvi Medicine-Medicine (all)
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