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
{"title":"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","authors":"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","doi":"10.1016/j.bpsgos.2024.100296","DOIUrl":null,"url":null,"abstract":"<div><p>A common genetic risk factor for bipolar disorder is <em>CACNA1C</em>, a gene that is also critical for cardiac rhythm. The impact of <em>CACNA1C</em> mutations on bipolar patient cardiac rhythm is unknown. Here, we report the cardiac electrophysiological implications of a bipolar disorder–associated genetic risk factor in <em>CACNA1C</em> using patient induced pluripotent stem cell-derived cardiomyocytes. Results indicate that the <em>CACNA1C</em> 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 <em>CACNA1C</em> 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.</p></div>","PeriodicalId":72373,"journal":{"name":"Biological psychiatry global open science","volume":"4 3","pages":"Article 100296"},"PeriodicalIF":4.0000,"publicationDate":"2024-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2667174324000090/pdfft?md5=efafaa8f782f1926f04d035280bbeeff&pid=1-s2.0-S2667174324000090-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Bipolar Patient–Specific In Vitro Diagnostic Test Reveals Underlying Cardiac Arrhythmia Phenotype Caused by Calcium Channel Genetic Risk Factor\",\"authors\":\"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\",\"doi\":\"10.1016/j.bpsgos.2024.100296\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A common genetic risk factor for bipolar disorder is <em>CACNA1C</em>, a gene that is also critical for cardiac rhythm. The impact of <em>CACNA1C</em> mutations on bipolar patient cardiac rhythm is unknown. Here, we report the cardiac electrophysiological implications of a bipolar disorder–associated genetic risk factor in <em>CACNA1C</em> using patient induced pluripotent stem cell-derived cardiomyocytes. Results indicate that the <em>CACNA1C</em> 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 <em>CACNA1C</em> 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.</p></div>\",\"PeriodicalId\":72373,\"journal\":{\"name\":\"Biological psychiatry global open science\",\"volume\":\"4 3\",\"pages\":\"Article 100296\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2024-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2667174324000090/pdfft?md5=efafaa8f782f1926f04d035280bbeeff&pid=1-s2.0-S2667174324000090-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biological psychiatry global open science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2667174324000090\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological psychiatry global open science","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667174324000090","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
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.