期刊
GENDER MEDICINE
卷 9, 期 5, 页码 335-347出版社
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
DOI: 10.1016/j.genm.2012.07.004
关键词
gender; H-Y; kidney transplant; minor histocompatibility; sex
资金
- Katherine McCormick Faculty Development Award at Stanford University
- NIDDK [K23 DK087937, K24 DK085446]
Background: The lack of reliable human proxies for minor (ie, non-HLA) histocompatibility loci hampers the ability to leverage these factors toward improving transplant outcomes. Despite conflicting reports of the effect of donor recipient sex mismatch on renal allografts, the association between acute rejection of renal allografts and the development of human alloantibodies to the male H-Y antigen suggested to us that donor recipient sex mismatch deserved re-evaluation. Objective: To evaluate whether the relationships between donor sex and allograft failure differed by recipient sex. Methods: We studied recipients of deceased-donor (n = 125,369) and living-donor (n = 63,139) transplants in the United States Renal Data System. Using Cox proportional hazards models stratified by donor type, we estimated the association between donor recipient sex mismatch and death-censored allograft failure with adjustment for known risk factors, with and without the use of multiple imputation methods to account for potential bias and/or loss of efficiency due to missing data. Results: The advantage afforded by male donor kidneys was more pronounced among male than among female recipients (8% vs 2% relative risk reduction; interaction P < 0.01). This difference is of the order of magnitude of several other risk factors affecting donor selection decisions. Conclusions: Donor recipient sex mismatch affects renal allograft survival in a direction consistent with immune responses to sexually determined minor histocompatibility antigens. Our study provides a paradigm for clinical detection of markers for minor histocompatibility loci. (Gend Med. 2012;9:335-347) (c) 2012 Elsevier HS Journals, Inc. All rights reserved.
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