Sudden cardiac death and its diagnostics
Authors:
M. Sepši 1; M. Zeman 2; I. Synková 3; R. Gaillyová 3; I. Valášková 3; T. Novotný 1; M. Šindler 2; D. Pospíšil 1
Authors place of work:
Interní kardiologická klinika LF MU a FN Brno
1; Ústav soudního lékařství, FN u sv. Anny v Brně
2; Oddělení lékařské genetiky, Pracoviště dětské medicíny, FN Brno
3
Published in the journal:
Kardiol Rev Int Med 2017, 19(4): 247-250
Summary
Sudden death is defined as death that has occurred suddenly, unexpectedly and within one hour of symptoms. According to aetiology, we distinguish between non-cardiac death and sudden cardiac death. The aetiology of sudden cardiac death is difficult to determine. Despite the extended possibilities of autopsy, 40% of sudden deaths remain unexplained. In these cases, we assume malignant arrhythmia to be the aetiology of death and we perform post-mortem genetic examination, primarily targeted at Long QT syndrome, Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia. The list of examined genes is expanding. For the practical diagnosis, it is recommended to test four major genes: KCNQ1, KCNH2, SCN5A, RYR2. The examination of sudden cardiac death involves the collaboration of a forensic pathologist, geneticist, and cardiologist. During the autopsy, the samples for histopathological, microbiological and toxicological examinations are taken together with a sample of myocardium for genetic examination. Relatives are informed about the possibilities for their own clinical examination. Genetic examination helps determine the diagnosis and is followed by a cascade screening of the particular gene in the survivors in the case of a pathogenic mutation in the deceased. Cardiac examination of relatives (personal history with a focus on sudden death in the family, ECG, ergometry, and echocardiography) together with genetic testing helps diagnose and clarify the risk of sudden cardiac death for survivors. This comprehensive approach has been applied in the South-Moravian region for over 10 years. For more information, please visit www.nahlasmrt.cz.
Key words:
sudden cardiac death – post-mortem examination – molecular autopsy – genetic counseling – family – multidisciplinary approach
Zdroje
1. Puranik R, Chow CK, Duflou JA et al. Sudden death in the young. Heart Rhythm 2005; 2(12): 1277– 1282. doi: 10.1016/ j.hrthm.2005.09.008.
2. Ackerman MJ, Tester DJ, Driscoll DJ. Molecular autopsy of sudden unexplained death in the young. Am J Forensic Med Pathol 2001; 22(2): 105– 111.
3. Behr ER, Casey A, Sheppard M et al. Sudden arrhythmic death syndrome: a national survey of sudden unexplained cardiac death. Heart 2007; 93(5): 601– 605. doi: 10.1136/ hrt.2006.099598.
4. Myerburg RJ, Castellanos A. Cardiac arrest and sudden cardiac death. In: Libby P, Bonow RO, Mann DL et al. (eds.) Braunwald’s Heart Disease: A Textbook on Cardiovascular Medicine. Philadelphia: WB Saunders 2007: 933– 973.
5. van Der Werf C, van Langen IM, Wilde AA. Sudden death in the young: ehat do we know about it and how to prevent? Circ Arrhythmia Electrophysiol 2010; 3(1): 96– 104. doi: 10.1161/ CIRCEP.109.877142.
6. Semsarian C, Ingles J, Wilde AA. Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives. Eur Heart J 2015; 36(21): 1290– 1296. doi: 10.1093/ eurheartj/ ehv063.
7. Fishman GI, Chugh SS, Dimarco JP et al. Sudden cardiac death prediction and prevention: Report from a national heart, lung, and blood institute and heart rhythm society workshop. Circulation 2010; 122(22): 2335– 2348. doi: 10.1161/ CIRCULATIONAHA.110.976092.
8. Bagnall RD, Weintraub RG, Ingles J et al. A prospective study of sudden cardiac death among children and young adults. N Engl J Med 2016; 374(25): 2441– 2452. doi: 10.1056/ NEJMoa1510687.
9. Ackerman MJ, Priori SG, Willems S et al. HRS/ EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Europace 2011; 13(8): 1077– 1109. doi: 10.1093/ europace/ eur245.
10. Davies MJ. The investigation of sudden cardiac death. Histopathology 1999; 34(2): 93– 98.
11. Behr E, Wood DA, Wright M et al. Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome. Lancet 2003; 362(9394): 1457– 1459.
12. Hertz CL, Christiansen SL, Ferrero-Miliani L et al. Next-generation sequencing of 100 candidate genes in young victims of suspected sudden cardiac death with structural abnormalities of the heart. Int J Legal Med 2016; 130(1): 91– 102.
13. Richards S, Aziz N, Bale S et al. Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 2015; 17(5): 405– 424. doi: 10.1038/ gim.2015.30.
14. Lahrouchi N, Raju H, Lodder EM et al. Utility of post-mortem genetic testing in cases of sudden arrhythmic death syndrome. J Am Coll Cardiol 2017; 69(17): 2134– 2145. doi: 10.1016/ j.jacc.2017.02.046.
15. Methner DN, Scherer SE, Welch K et al. Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young. Genome Res 2016; 26(9): 1170– 1177. doi: 10.1101/ gr.195800.115.
16. Wang D, Shah KR, Um SY et al. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths. Forensic Sci Int 2014; 237: 90– 99. doi: 10.1016/ j.forsciint.2014.01.014.
17. Jouven X, Desnos M, Guerot C et al. Predicting sudden death in the population: the Paris Prospective Study I. Circulation 1999; 99(15): 1978– 1983.
18. Priori SG, Wilde AA, Horie M et al. HRS/ EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes. Heart Rhythm 2013; 10(12): 1932– 1963. doi: 10.1016/ j.hrthm.2013.05.014.
19. Tan HL, Hofman N, van Langen IM et al. Sudden unexplained death: heritability and diagnostic yield of cardiological and genetic examination in surviving relatives. Circulation 2005; 112(2): 207– 213. doi: 10.1161/ CIRCULATIONAHA.104.522581.
20. Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci 1977; 74(12): 5463– 5467.
21. Ronaghi M, Uhlén M, Nyrén P. A sequencing method based on real-time pyrophosphate. Science 1998; 281(5375): 363– 365.
22. Bentley DR, Balasubramanian S, Swerdlow HP et al. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 2008; 456(7218): 53– 59. doi: 10.1038/ nature07517.
23. Schwartz PJ, Ackerman MJ, George AL et al. Impact of genetics on the clinical management of channelopathies. J Am Coll Cardiol 2013; 62(3): 169– 180. doi: 10.1016/ j.jacc.2013.04.044.
Štítky
Paediatric cardiology Internal medicine Cardiac surgery CardiologyČlánok vyšiel v časopise
Cardiology Review
2017 Číslo 4
Najčítanejšie v tomto čísle
- Myocardial ischaemia and infarction in intraventricular conduction malfunctions on ECG
- Current fixed antihypertensive two-drug combinations in Slovakia
- Modern pharmacologic treatment of type 2 diabetes mellitus
- Acute renal failure