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African‐American Race Modifies the Influence of Tacrolimus Concentrations on Acute Rejection and Toxicity in Kidney Transplant Recipients
Author(s) -
Taber David J.,
Gebregziabher Mulugeta G.,
Srinivas Titte R.,
Chavin Kenneth D.,
Baliga Prabhakar K.,
Egede Leonard E.
Publication year - 2015
Publication title -
pharmacotherapy: the journal of human pharmacology and drug therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.227
H-Index - 109
eISSN - 1875-9114
pISSN - 0277-0008
DOI - 10.1002/phar.1591
Subject(s) - tacrolimus , medicine , hazard ratio , trough level , confidence interval , urology , trough concentration , kidney transplantation , gastroenterology , toxicity , kidney , kidney transplant , transplantation , pharmacokinetics
Study Objective To determine the effect of tacrolimus trough concentrations on clinical outcomes in kidney transplantation, while assessing if African‐American ( AA ) race modifies these associations. Design Retrospective longitudinal cohort study of solitary adult kidney transplants. Setting Large tertiary care transplant center. Patients Adult solitary kidney transplant recipients (n=1078) who were AA (n=567) or non‐ AA (n=511). Exposure Mean and regressed slope of tacrolimus trough concentrations. Subtherapeutic concentrations were lower than 8 ng/ml. Measurements and Main Results AA patients were 1.7 times less likely than non‐ AA patients to achieve therapeutic tacrolimus concentrations (8 ng/ml or higher) during the first year after kidney transplant (35% vs 21%, respectively, p<0.001). AA s not achieving therapeutic concentrations were 2.4 times more likely to have acute cellular rejection ( ACR ) as compared with AAs achieving therapeutic concentrations (20.8% vs 8.5%, respectively, p<0.01) and 2.5 times more likely to have antibody‐mediated rejection ( AMR; 8.9% vs 3.6%, respectively, p<0.01). Rates of ACR (8.3% vs 6.7%) and AMR (2.0% vs 0.9% p=0.131) were similar in non‐ AA s compared across tacrolimus concentration groups. Multivariate modeling confirmed these findings and demonstrated that AA s with low tacrolimus exposure experienced a mild protective effect for the development of interstitial fibrosis/tubular atrophy ( IF / TA; hazard ratio [ HR] 0.78, 95% confidence interval [ CI] 0.47–1.32) with the opposite demonstrated in non‐ AA s ( HR 2.2, 95% CI 0.90–5.1). Conclusion In contradistinction to non‐ AA s, AA s who achieve therapeutic tacrolimus concentrations have substantially lower acute rejection rates but are at risk of developing IF / TA . These findings may reflect modifiable time‐dependent racial differences in the concentration‐effect relationship of tacrolimus. Achievement of therapeutic tacrolimus trough concentrations, potentially through genotyping and more aggressive dosing and monitoring, is essential to minimize the risk of acute rejection in AA kidney transplant recipients.