Gender-incompatible liver transplantation is not a risk factor for patient survival
Article first published online: 30 JUL 2008
© 2009 The Authors. Journal compilation © 2009 Blackwell Publishing Ltd
Volume 29, Issue 2, pages 196–202, February 2009
How to Cite
Lehner, F., Becker, T., Klempnauer, J. and Borlak, J. (2009), Gender-incompatible liver transplantation is not a risk factor for patient survival. Liver International, 29: 196–202. doi: 10.1111/j.1478-3231.2008.01827.x
- Issue published online: 6 JAN 2009
- Article first published online: 30 JUL 2008
- Received 15 March 2008Accepted 27 May 2008
- gender incompatibility;
- liver transplantation;
- steroid metabolism;
Background/Aims: Clinical data may be suggestive for differences in patient survival in gender-incompatible orthotopic liver transplantation (OLT), but findings are inconsistent and are putatively linked to circulating hormones. We therefore investigated patient survival as well as metabolism of steroids to identify possible causes of improved graft survival in gender-mismatched OLT.
Methods: We examined our single-centre database of 1355 recipients of first liver transplants for overall patient survival by non-parametric and parametric analysis of multivariance taking the age of recipient and donor, ischaemia time, underlying liver disease and the time period of transplantation into account. Furthermore, the metabolism of androgens in gender-incompatible OLT was studied in cultures of primary human hepatocytes obtained from male and female patients.
Results: Unlike previous studies we were unable to determine overall significant differences in patient survival in gender-incompatible OLT, even though a statistically significant improved patient survival was observed when male donor livers were transplanted into female recipients in univariant analysis (P=0.047). However, when the overall patient management was taken into account no difference in survival was determined in multivariant analysis. Importantly, the metabolism of testosterone did not differ between male and female hepatocyte cultures, except for the production of 6-α-hydroxy-testosterone (P<0.001).
Conclusions: Taken collectively, clinical observations may tend to suggest a slightly improved patient survival in gender-incompatible OLT but this cannot be explained on the bases of androgen metabolism. Overall, we view gender-incompatible liver transplantation not to be a confounder in patient survival after OLT.