Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/76105
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dc.contributor.authorChupong Ittiwuten_US
dc.contributor.authorSurakameth Mahasirimongkolen_US
dc.contributor.authorSmith Srisonten_US
dc.contributor.authorRungnapa Ittiwuten_US
dc.contributor.authorManoch Chockjamsaien_US
dc.contributor.authorPiya Durongkadechen_US
dc.contributor.authorWaritta Sawaengdeeen_US
dc.contributor.authorAthiwat Khunphonen_US
dc.contributor.authorKanidsorn Larpadisornen_US
dc.contributor.authorSukanya Wattanapokayakiten_US
dc.contributor.authorSuppachok Wetchaphanphesaten_US
dc.contributor.authorSurachet Arunotongen_US
dc.contributor.authorSuphot Srimahachotaen_US
dc.contributor.authorChakrarat Pittayawonganonen_US
dc.contributor.authorPanithee Thammawijayaen_US
dc.contributor.authorDerek Sutdanen_US
dc.contributor.authorPawinee Doungngernen_US
dc.contributor.authorApichai Khongphatthanayothinen_US
dc.contributor.authorStephen J. Kerren_US
dc.contributor.authorVorasuk Shotelersuken_US
dc.date.accessioned2022-10-16T07:05:42Z-
dc.date.available2022-10-16T07:05:42Z-
dc.date.issued2022-01-01en_US
dc.identifier.issn15563871en_US
dc.identifier.issn15475271en_US
dc.identifier.other2-s2.0-85139237479en_US
dc.identifier.other10.1016/j.hrthm.2022.07.019en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85139237479&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/76105-
dc.description.abstractBackground: Severe acute respiratory syndrome coronavirus 2 vaccination reduces morbidity and mortality associated with coronavirus disease 2019 (COVID-19); unfortunately, it is associated with serious adverse events, including sudden unexplained death (SUD). Objective: We aimed to study the genetic basis of SUD after COVID-19 vaccination in Thailand. Methods: From April to December 2021, cases with natural but unexplained death within 7 days of COVID-19 vaccination were enrolled for whole exome sequencing. Results: Thirteen were recruited, aged between 23 and 72 years; 10 (77%) were men, 12 were Thai; and 1 was Australian. Eight (61%) died after receiving the first dose of vaccine, and 7 (54%) died after receiving ChAdOx1 nCoV-19; however, there were no significant correlations between SUD and either the number or the type of vaccine. Fever was self-reported in 3 cases. Ten (77%) and 11 (85%) died within 24 hours and 3 days of vaccination, respectively. Whole exome sequencing analysis revealed that 5 cases harbored SCN5A variants that had previously been identified in patients with Brugada syndrome, giving an SCN5A variant frequency of 38% (5 of 13). This is a significantly higher rate than that observed in Thai SUD cases occurring 8–30 days after COVID-19 vaccination during the same period (10% [1 of 10]), in a Thai SUD cohort studied before the COVID-19 pandemic (12% [3 of 25]), and in our in-house exome database (12% [386 of 3231]). Conclusion: These findings suggest that SCN5A variants may be associated with SUD within 7 days of COVID-19 vaccination, regardless of vaccine type, number of vaccine dose, and presence of underlying diseases or postvaccine fever.en_US
dc.subjectMedicineen_US
dc.titleGenetic basis of sudden death after COVID-19 vaccination in Thailanden_US
dc.typeJournalen_US
article.title.sourcetitleHeart Rhythmen_US
article.stream.affiliationsRamathibodi Hospitalen_US
article.stream.affiliationsFaculty of Medicine, Chiang Mai Universityen_US
article.stream.affiliationsKing Chulalongkorn Memorial Hospitalen_US
article.stream.affiliationsLamphun Hospitalen_US
article.stream.affiliationsThailand Ministry of Public Healthen_US
article.stream.affiliationsFaculty of Medicine, Chulalongkorn Universityen_US
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