Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives
| Autor: | S F Tong, P T Tsui, Y K Lo, C L Lau, W M Poon, Chloe Mak, H H C Lee, N C Fong, C B Tso, Wai-Kwan Siu, W L Cheung, K W Lee, Mok Ns, H C Shum, Sammy Pak-Lam Chen, CK Ching, Y K Chong, K C Lee, S F Shum |
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| Rok vydání: | 2019 |
| Předmět: |
Adult
Male Pediatrics medicine.medical_specialty Adolescent Population Context (language use) Autopsy 030204 cardiovascular system & hematology Sudden cardiac death Young Adult 03 medical and health sciences 0302 clinical medicine Cause of Death medicine Humans Genetic Predisposition to Disease Genetic Testing Prospective Studies First-degree relatives Family history Child Medical History Taking education Retrospective Studies Genetic testing Cause of death education.field_of_study medicine.diagnostic_test business.industry High-Throughput Nucleotide Sequencing Arrhythmias Cardiac General Medicine medicine.disease Death Sudden Cardiac Phenotype Mutation Hong Kong Female business 030217 neurology & neurosurgery |
| Zdroj: | Hong Kong Medical Journal. |
| ISSN: | 1024-2708 |
| Popis: | Objective Sudden arrhythmia death syndrome (SADS) accounts for about 30% of causes of sudden cardiac death (SCD) in young people. In Hong Kong, there are scarce data on SADS and a lack of experience in molecular autopsy. We aimed to investigate the value of molecular autopsy techniques for detecting SADS in an East Asian population. Methods This was a two-part study. First, we conducted a retrospective 5-year review of autopsies performed in public mortuaries on young SCD victims. Second, we conducted a prospective 2-year study combining conventional autopsy investigations, molecular autopsy, and cardiac evaluation of the first-degree relatives of SCD victims. A panel of 35 genes implicated in SADS was analysed by next-generation sequencing. Results There were 289 SCD victims included in the 5-year review. Coronary artery disease was the major cause of death (35%); 40% were structural heart diseases and 25% were unexplained. These unexplained cases could include SADS-related conditions. In the 2-year prospective study, 21 SCD victims were examined: 10% had arrhythmogenic right ventricular cardiomyopathy, 5% had hypertrophic cardiomyopathy, and 85% had negative autopsy. Genetic analysis showed 29% with positive heterozygous genetic variants; six variants were novel. One third of victims had history of syncope, and 14% had family history of SCD. More than half of the 11 first-degree relatives who underwent genetic testing carried related genetic variants, and 10% had SADS-related clinical features. Conclusion This pilot feasibility study shows the value of incorporating cardiac evaluation of surviving relatives and next-generation sequencing molecular autopsy into conventional forensic investigations in diagnosing young SCD victims in East Asian populations. The interpretation of genetic variants in the context of SCD is complicated and we recommend its analysis and reporting by qualified pathologists. |
| Databáze: | OpenAIRE |
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