躁狂症患者专用体外诊断测试揭示钙通道遗传风险因素导致的潜在心律失常表型

Rachel Dow , Cindy DeLong , Guihua Jiang , Durga Attili , Jeffery Creech , Rachel Kraan , Katherine Campbell , Prakaimuk Saraithong , Sue O’Shea , Andre Monteiro da Rocha , Melvin G. McInnis , Todd J. Herron
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引用次数: 0

摘要

双相情感障碍的一个常见遗传风险因素是 CACNA1C,该基因对心律也至关重要。CACNA1C 基因突变对双相情感障碍患者心律的影响尚不清楚。在此,我们利用患者诱导多能干细胞衍生的心肌细胞,报告了与双相情感障碍相关的 CACNA1C 遗传风险因子对心脏电生理学的影响。研究结果表明,CACNA1C双相情感障碍相关基因突变会导致心脏电脉冲传导减慢,其原因是通过连接蛋白43间隙连接的细胞间耦合受损。体外基因疗法可恢复连接蛋白 43 的表达,从而提高心脏电脉冲传导速度,并防止硫利达嗪引起的 QT 延长。双相情感障碍 CACNA1C 遗传风险因子呈阳性的患者,在服用会减慢传导速度或延长 QT 间期的精神药物后,可能会增加发生不良事件的前心律失常风险。这种体外诊断工具可对精神病患者进行专门的心脏测试,以确定他们对精神科药物脱靶效应的敏感性。
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Bipolar Patient–Specific In Vitro Diagnostic Test Reveals Underlying Cardiac Arrhythmia Phenotype Caused by Calcium Channel Genetic Risk Factor

A common genetic risk factor for bipolar disorder is CACNA1C, a gene that is also critical for cardiac rhythm. The impact of CACNA1C mutations on bipolar patient cardiac rhythm is unknown. Here, we report the cardiac electrophysiological implications of a bipolar disorder–associated genetic risk factor in CACNA1C using patient induced pluripotent stem cell-derived cardiomyocytes. Results indicate that the CACNA1C bipolar disorder–related mutation causes cardiac electrical impulse conduction slowing mediated by impaired intercellular coupling via connexin 43 gap junctions. In vitro gene therapy to restore connexin 43 expression increased cardiac electrical impulse conduction velocity and protected against thioridazine-induced QT prolongation. Patients positive for bipolar disorder CACNA1C genetic risk factors may have elevated proarrhythmic risk for adverse events in response to psychiatric medications that slow conduction or prolong the QT interval. This in vitro diagnostic tool enables cardiac testing specific to patients with psychiatric disorders to determine their sensitivity to off-target effects of psychiatric medications.

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Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
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