精神分裂症与心律失常和心电图特征的关联:对人群样本的遗传学探索

Jorien L. Treur, Anaïs B. Thijssen, Dirk J. A. Smit, Rafik Tadros, Rada R. Veeneman, Damiaan Denys, Jentien M. Vermeulen, Julien Barc, Jacob Bergstedt, Joëlle A. Pasman, Connie R. Bezzina, Karin J. H. Verweij
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引用次数: 0

摘要

背景精神分裂症患者预期寿命缩短的一个重要原因是心脏性猝死。Aims To assess shared genetic liability and potential causal effects between schizophrenia and arrhythmic disorders and electrocardiogram (ECG) traits.方法我们利用精神分裂症(53 386 例,77 258 例对照)、心律失常疾病(心房颤动,55 114 例,482 295 例对照;Brugada 综合征,2820 例,10 001 例对照)和心电图特征(心率(变异性)、PR 间期、QT 间期、JT 间期和 QRS 持续时间,n = 46 952-293 051)的大规模全基因组关联研究的汇总数据。我们通过评估整体和局部遗传相关性以及进行功能注释,研究了共同的遗传责任。结果除精神分裂症与 Brugada 综合征(rg = 0.14,95% CIs = 0.06-0.22,P = 4.0E-04)外,没有证据表明存在整体遗传相关性。相反,在整个基因组中,精神分裂症与所有心脏特征之间都存在很强的正相关和负相关。在关联性最强的区域,与免疫和病毒反应机制相关的基因所占比例较高。孟德尔随机分析表明,精神分裂症易感性会因果性地增加布鲁加达综合征的风险(β=0.14,CIs=0.03-0.25,P=0.009)和活动时的心率(β=0.25,CIs=0.05-0.45,P=0.015)。精神分裂症对 Brugada 综合征的影响可能是因果关系,因此需要加强对精神分裂症患者的心脏监测和早期医疗干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations of schizophrenia with arrhythmic disorders and electrocardiogram traits: genetic exploration of population samples
Background

An important contributor to the decreased life expectancy of individuals with schizophrenia is sudden cardiac death. Arrhythmic disorders may play an important role herein, but the nature of the relationship between schizophrenia and arrhythmia is unclear.

Aims

To assess shared genetic liability and potential causal effects between schizophrenia and arrhythmic disorders and electrocardiogram (ECG) traits.

Method

We leveraged summary-level data of large-scale genome-wide association studies of schizophrenia (53 386 cases, 77 258 controls), arrhythmic disorders (atrial fibrillation, 55 114 cases, 482 295 controls; Brugada syndrome, 2820 cases, 10 001 controls) and ECG traits (heart rate (variability), PR interval, QT interval, JT interval and QRS duration, n = 46 952–293 051). We examined shared genetic liability by assessing global and local genetic correlations and conducting functional annotation. Bidirectional causal relations between schizophrenia and arrhythmic disorders and ECG traits were explored using Mendelian randomisation.

Results

There was no evidence for global genetic correlation, except between schizophrenia and Brugada syndrome (rg = 0.14, 95% CIs = 0.06–0.22, P = 4.0E−04). In contrast, strong positive and negative local correlations between schizophrenia and all cardiac traits were found across the genome. In the most strongly associated regions, genes related to immune and viral response mechanisms were overrepresented. Mendelian randomisation indicated that liability to schizophrenia causally increases Brugada syndrome risk (beta = 0.14, CIs = 0.03–0.25, P = 0.009) and heart rate during activity (beta = 0.25, CIs = 0.05–0.45, P = 0.015).

Conclusions

Despite little evidence for global genetic correlation, specific genomic regions and biological pathways emerged that are important for both schizophrenia and arrhythmia. The putative causal effect of liability to schizophrenia on Brugada syndrome warrants increased cardiac monitoring and early medical intervention in people with schizophrenia.

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