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Sudden cardiac death of Duchenne muscular dystrophy with NT-proBNP in pericardial fluid as a useful biomarker for diagnosis of the cause of death

A case report

Bibliographic Data

ID13119672
AuthorsMengzhou Zhang (0000-0003-0178-7637, China Medical University), Rui Zhao (0000-0001-6445-3461, China University of Political Science and Law), Tian-Shui Yu (0009-0001-5216-4600, China University of Political Science and Law), Tianshui Yu, Jiao-Yong Li (China Medical University), Jiaoyong Li, Miao Zhang (0009-0008-4320-6232, China Medical University), Shukun Jiang (China Medical University), Linlin Wang (0000-0003-4346-5409, China Medical University), Guohua Zhang (0000-0003-2743-3167, China Medical University), Rubo Li (China Medical University), Bao-Li Zhu (0000-0001-6083-4187, China Medical University), Baoli Zhu (0000-0001-5326-9503), Da-Wei Guan (0000-0002-6048-7119, China University of Political Science and Law, corresponding author), Dawei Guan
Year2017
Volume5
Issue2
Pages165-169
Publication date2017-06-22
Open AccessYes
TypeARTICLE
VenueForensic Sciences Research (JOURNAL)
Journal identifiersISSN: 2471-1411 • E-ISSN: 2096-1790
PublisherTaylor & Francis (PUBLISHER • GB)
DOI10.1080/20961790.2017.1333249
PMID32939432
OpenAlexW2657439694
LanguageEN
References cited25

Duchenne muscular dystrophy (DMD) is one of the most common and severest muscular dystrophies. Although it can be a cause of death when associated with cardiac muscle and/or respiratory muscles, no cases of sudden deaths in the setting of undiagnosed DMD with cardiac involvement have been reported in the literatures. Previous studies showed that N-terminal-proBNP (NT-proBNP) was a robust laboratory biomarker to diagnose and monitor cardiac failure in clinical situations, suggesting that it may be used as an auxiliary indicator for diagnosis on left ventricular dysfunction in sudden cardiac deaths in forensic settings. Here, we reported a case of 29-year-old man who died suddenly. Autopsy revealed that muscles of the body were almost replaced by fatty and fibrotic tissues. The heart was enlarged with disarray and degeneration of cardiomyocytes in cardiac muscle. Total absence of dystrophin was detected by immunohistochemical staining, which confirmed DMD. Postmortem biochemical test of pericardial fluid revealed a high level of NT-proBNP, indicating dysfunction of the left ventricle before death. The cause of death was certified as an early dilated cardiomyopathy (DCM)/dysfunction of the left ventricle secondary to DMD, suggesting that sudden cardiac death with cardiac dysfunction could be identified by immunohistochemical method in combination with pericardial fluid NT-proBNP determination after systemic autopsy

Autopsy · Biomarker · Cardiac muscle · Cardiology · Cardiomyopathy · Cause of death · Dilated cardiomyopathy · Disease · Duchenne muscular dystrophy · Dystrophin · Heart failure · Muscular dystrophy · Pathology · Sudden cardiac death · Sudden death · Ventricle · Cardiomyopathy and Myosin Studies · Cardiovascular Effects of Exercise · Medicine · Muscle Physiology and Disorders · Internal Medicine

Highly citedNo
Open DOISci-HubOpen Access
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