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DC Field | Value | Language |
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dc.contributor.author | Chupong Ittiwut | en_US |
dc.contributor.author | Surakameth Mahasirimongkol | en_US |
dc.contributor.author | Smith Srisont | en_US |
dc.contributor.author | Rungnapa Ittiwut | en_US |
dc.contributor.author | Manoch Chockjamsai | en_US |
dc.contributor.author | Piya Durongkadech | en_US |
dc.contributor.author | Waritta Sawaengdee | en_US |
dc.contributor.author | Athiwat Khunphon | en_US |
dc.contributor.author | Kanidsorn Larpadisorn | en_US |
dc.contributor.author | Sukanya Wattanapokayakit | en_US |
dc.contributor.author | Suppachok Wetchaphanphesat | en_US |
dc.contributor.author | Surachet Arunotong | en_US |
dc.contributor.author | Suphot Srimahachota | en_US |
dc.contributor.author | Chakrarat Pittayawonganon | en_US |
dc.contributor.author | Panithee Thammawijaya | en_US |
dc.contributor.author | Derek Sutdan | en_US |
dc.contributor.author | Pawinee Doungngern | en_US |
dc.contributor.author | Apichai Khongphatthanayothin | en_US |
dc.contributor.author | Stephen J. Kerr | en_US |
dc.contributor.author | Vorasuk Shotelersuk | en_US |
dc.date.accessioned | 2022-10-16T07:05:42Z | - |
dc.date.available | 2022-10-16T07:05:42Z | - |
dc.date.issued | 2022-01-01 | en_US |
dc.identifier.issn | 15563871 | en_US |
dc.identifier.issn | 15475271 | en_US |
dc.identifier.other | 2-s2.0-85139237479 | en_US |
dc.identifier.other | 10.1016/j.hrthm.2022.07.019 | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85139237479&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/76105 | - |
dc.description.abstract | Background: 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.subject | Medicine | en_US |
dc.title | Genetic basis of sudden death after COVID-19 vaccination in Thailand | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Heart Rhythm | en_US |
article.stream.affiliations | Ramathibodi Hospital | en_US |
article.stream.affiliations | Faculty of Medicine, Chiang Mai University | en_US |
article.stream.affiliations | King Chulalongkorn Memorial Hospital | en_US |
article.stream.affiliations | Lamphun Hospital | en_US |
article.stream.affiliations | Thailand Ministry of Public Health | en_US |
article.stream.affiliations | Faculty of Medicine, Chulalongkorn University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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