Dow Rachel, DeLong Cindy, Jiang Guihua, Attili Durga, Creech Jeffery, Kraan Rachel, Campbell Katherine, Saraithong Prakaimuk, O'Shea Sue, Monteiro da Rocha Andre, McInnis Melvin G, Herron Todd J
Frankel Cardiovascular Regeneration Core Laboratory, University of Michigan, Ann Arbor, Michigan.
Michigan Medicine, Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan.
Biol Psychiatry Glob Open Sci. 2024 Feb 20;4(3):100296. doi: 10.1016/j.bpsgos.2024.100296. eCollection 2024 May.
A common genetic risk factor for bipolar disorder is , a gene that is also critical for cardiac rhythm. The impact of mutations on bipolar patient cardiac rhythm is unknown. Here, we report the cardiac electrophysiological implications of a bipolar disorder-associated genetic risk factor in using patient induced pluripotent stem cell-derived cardiomyocytes. Results indicate that the 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 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.
双相情感障碍的一个常见遗传风险因素是 ,该基因对心律也至关重要。 突变对双相情感障碍患者心律的影响尚不清楚。在此,我们使用患者诱导多能干细胞衍生的心肌细胞报告了双相情感障碍相关遗传风险因素在 中的心脏电生理意义。结果表明,双相情感障碍相关突变通过连接蛋白43间隙连接受损导致细胞间偶联受损,从而引起心脏电冲动传导减慢。恢复连接蛋白43表达的体外基因治疗增加了心脏电冲动传导速度,并预防了硫利达嗪诱导的QT间期延长。双相情感障碍 遗传风险因素呈阳性的患者,对于减慢传导或延长QT间期的精神药物,发生不良事件的心律失常风险可能会升高。这种体外诊断工具能够对精神疾病患者进行特定的心脏测试,以确定他们对精神药物脱靶效应的敏感性。