Genetic matching between transplant donor and recipient pairs has traditionally focused on the human leukocyte antigen (HLA) regions of the genome, but recent studies suggest that matching for non-HLA regions may be important as well. We assess four genetic matching scores for use in association analyses of transplant outcomes. These scores describe genetic ancestry distance using identity-by-state, or genetic incompatibility or mismatch of the two genomes and therefore may reflect different underlying biological mechanisms for donor and recipient genes to influence transplant outcomes. Our simulation studies show that jointly testing these scores with the recipient genotype is a powerful method for preliminary screening and discovery of transplant outcome related single nucleotide polymorphisms (SNPs) and gene regions. Following these joint tests with marginal testing of the recipient genotype and matching score separately can lead to further understanding of the biological mechanisms behind transplant outcomes. In addition, we present results of a liver transplant data analysis that shows joint testing can detect SNPs significantly associated with acute rejection in liver transplant.
Bibliographical noteFunding Information:
The research reported in this publication was supported by the National Institutes of Health grants R01-HL138306 (J. C., V. L. A.), R21-ES020811 (J. C.), and R01-ES016626 (J. C.).
The research reported in this publication was supported by the National Institutes of Health grants R01‐HL138306 (J. C., V. L. A.), R21‐ES020811 (J. C.), and R01‐ES016626 (J. C.).
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- genetic matching scores
- joint testing
- transplant genetics
PubMed: MeSH publication types
- Journal Article