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Forensic significance of intracardiac heme oxygenase-1 expression in acute myocardial ischemia
- Source :
- Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021), Scientific Reports
- Publication Year :
- 2021
- Publisher :
- Nature Portfolio, 2021.
-
Abstract
- Heme oxygenase-1 (HO-1), an inducible stress-response protein, exerts anti-oxidant and anti-apoptotic effects. However, its significance in forensic diagnosis of acute ischemic heart diseases (AIHD) such as myocardial infarction (MI) is still unknown. We examined the immunohistochemical expression of HO-1 in the heart samples to discuss their forensic significance to determine acute cardiac ischemia. The heart samples were obtained from 23 AIHD cases and 33 non-AIHD cases as controls. HO-1 positive signals in cardiomyocyte nuclear were detected in 78.2% of AIHD cases, however, that were detected in only 24.2% control cases with statistical difference between AIHD and non-AIHD groups. In contrast to HO-1 protein expression, there was no significant difference in the appearance of myoglobin pallor regions and leukocyte infiltration in the hearts between AIHD and non-AIHD groups. From the viewpoints of forensic pathology, intracardiac HO-1 expression would be considered a valuable marker to diagnose AIHD as the cause of death.
- Subjects :
- Adult
Male
Pathology
medicine.medical_specialty
Forensic pathology
Science
Myocardial Ischemia
Intracardiac injection
Pallor
Article
chemistry.chemical_compound
Medical research
Cause of Death
medicine
Leukocytes
Humans
Myocardial infarction
Forensic Pathology
Cause of death
Aged
Aged, 80 and over
Multidisciplinary
business.industry
Myocardium
Diagnostic markers
Middle Aged
medicine.disease
Heme oxygenase
Myoglobin
chemistry
Case-Control Studies
Acute Disease
Immunohistochemistry
Medicine
Female
Autopsy
medicine.symptom
business
Biomarkers
Heme Oxygenase-1
Subjects
Details
- Language :
- English
- ISSN :
- 20452322
- Volume :
- 11
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Scientific Reports
- Accession number :
- edsair.doi.dedup.....2c7435a578db0d1a8a98b6074a220a80