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Sensitivity to perioperative ischemia/reperfusion injury in male and female donor myocardium
M. Smetana, J. Besik, I. Netuka, J. Maly, J. Maluskova, A. Lodererova, L. Hoskova, J. Franeková, E. Pokorna, J. Pirk, O. Szarszoi
Language English Country Czech Republic
Document type Comparative Study, Journal Article
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- MeSH
- Allografts MeSH
- Apoptosis MeSH
- Time Factors MeSH
- Tissue Donors * MeSH
- Caspase 3 metabolism MeSH
- Middle Aged MeSH
- Humans MeSH
- Myocardium metabolism pathology MeSH
- Necrosis MeSH
- Prospective Studies MeSH
- Proto-Oncogene Proteins c-bcl-2 metabolism MeSH
- Myocardial Reperfusion Injury etiology metabolism pathology MeSH
- Risk Factors MeSH
- Sex Factors MeSH
- Heart Transplantation adverse effects MeSH
- Troponin T metabolism MeSH
- Treatment Outcome MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
Many functions of the cardiovascular apparatus are affected by gender. The aim of our study was find out whether markers of cell death present in the donor myocardium differ in male and female hearts. The study involved 81 patients undergoing heart transplantation from September 2010 to January 2013. Patients were divided into two groups: male allograft (n=49), and female allograft (n=32). Two types of myocardial cell death were analyzed. High-sensitive cardiac troponin T as a necrosis marker and protein bcl-2, caspase 3 and TUNEL as apoptosis markers were measured. We observed a significantly higher level of high-sensitive cardiac troponin T after correcting for predicted ventricular mass in female donors before transplantation as well as in the female allograft group after transplantation throughout the monitored period (P=0.011). There were no differences in apoptosis markers (bcl-2, caspase 3, TUNEL) between male and female hearts before transplantation. Both genders showed a significant increase of TUNEL-positive myocytes one week after transplantation without differences between the groups. Moreover, there were no differences in caspase 3 and bcl-2 expression between the two groups. Our results demonstrated the presence of necrotic and apoptotic cell death in human heart allografts. High-sensitive cardiac troponin T adjusted for predicted ventricular mass as a marker of myocardial necrosis was higher in female donors, and this gender difference was even more pronounced after transplantation.
Department of Cardiology Institute for Clinical and Expe rimental Medicine Prague Czech Republic
Department of Pathology Institute for Clinical and Experimental Medicine Prague Czech Republic
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- $a Many functions of the cardiovascular apparatus are affected by gender. The aim of our study was find out whether markers of cell death present in the donor myocardium differ in male and female hearts. The study involved 81 patients undergoing heart transplantation from September 2010 to January 2013. Patients were divided into two groups: male allograft (n=49), and female allograft (n=32). Two types of myocardial cell death were analyzed. High-sensitive cardiac troponin T as a necrosis marker and protein bcl-2, caspase 3 and TUNEL as apoptosis markers were measured. We observed a significantly higher level of high-sensitive cardiac troponin T after correcting for predicted ventricular mass in female donors before transplantation as well as in the female allograft group after transplantation throughout the monitored period (P=0.011). There were no differences in apoptosis markers (bcl-2, caspase 3, TUNEL) between male and female hearts before transplantation. Both genders showed a significant increase of TUNEL-positive myocytes one week after transplantation without differences between the groups. Moreover, there were no differences in caspase 3 and bcl-2 expression between the two groups. Our results demonstrated the presence of necrotic and apoptotic cell death in human heart allografts. High-sensitive cardiac troponin T adjusted for predicted ventricular mass as a marker of myocardial necrosis was higher in female donors, and this gender difference was even more pronounced after transplantation.
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