The Efficacy of Connexin 43 Expression in the Myocardium as an Early Ischemic Marker in Forensic Autopsy.
- Author:
Jae Woo AHN
1
;
Gi Yeong HUH
Author Information
- Publication Type:Original Article
- Keywords: Connexin 43; Immunohistochemistry; Myocardial ischemia; Forensic pathology; Autopsy
- MeSH: Anoxia; Autopsy*; Cause of Death; Connexin 43*; Connexins; Coronary Artery Disease; Death, Sudden; Diagnosis; Forensic Pathology; Humans; Immunohistochemistry; Ischemia; Myocardial Ischemia; Myocardium*; Pathology
- From:Korean Journal of Legal Medicine 2015;39(1):6-11
- CountryRepublic of Korea
- Language:English
- Abstract: The postmortem diagnosis of ischemic heart disease is sometimes difficult for forensic pathologists especially when microscopic ischemic change in the myocardium is not detected at the early stages of ischemic injury by conventional staining techniques. Connexin 43 (Cx43) is a gap junction protein in human myocardium, which is phosphorylated and localized to the intercalated discs in the normal cardiac muscles. However, during ischemia and hypoxia, total Cx43 (tCx43) undergoes progressive dephosphorylation and concomitant accumulation of non-phosphorylated Cx43 (npCx43) at the lateral cell borders. This study was aimed to evaluate the efficacy of the immunohistochemical expression of Cx43 in the myocardium as an early ischemic marker in forensic autopsy. The study group consisted of 24 cases listing patients who died of ischemic heart disease (IHD) with severe coronary atherosclerosis that showed no myocardial pathology. Cases of sudden death of individuals from non-IHD (n=16) were used as controls. The survival times in both IHD and non-IHD groups were within 24 hours of the onset of angina symptoms, related injury, or the event for the cause of death. There was a statistically significant difference in tCx43 and npCX43 immunopositivity in the IHD group due to their expression patterns. In the IHD group, the redistribution of Cx43 expression from the intercalated discs to the lateral cell borders occurred more frequently than in the non-IHD group. In conclusion, the different expression patterns of tCx43 and npCx43 in the myocardium in IHD could be used as adjunctive ischemic markers.
