Change in Mycophenolate and Tacrolimus Exposure by Transplant Vintage and Race

被引:1
作者
Soliman, Karim M. [1 ,4 ]
Salas, Aurora C. Posadas [1 ]
Taber, David J. [2 ,3 ]
机构
[1] Med Univ South Carolina, Div Nephrol & Hypertens, Dept Med, Charleston, SC 29425 USA
[2] Med Univ South Carolina, Div Transplant Surg, Dept Surg, Charleston, SC 29425 USA
[3] Ralph H Johnson VA Med Ctr, Med Serv, Charleston, SC USA
[4] Cairo Univ, Dept Med, Div Nephrol, Cairo, Egypt
关键词
Disparity; Drug exposure; Ethnicity; Kidney transplant; Outcoines; AFRICAN-AMERICAN; KIDNEY-TRANSPLANTATION; RENAL-TRANSPLANTATION; ACUTE REJECTION; LONG-TERM; CALCINEURIN INHIBITORS; ACID PHARMACOKINETICS; RACIAL-DIFFERENCES; MOFETIL; IMMUNOSUPPRESSION;
D O I
10.6002/ect.2018.0055
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Objectives: Although both tacrolimus and mycophenolate have improved outcomes after kidney transplant, studies regarding effects of exposure on outcomes, specifically related to racial disparities, are sparse. Materials and Methods: In this 8-year longitudinal cohort study of adult kidney transplant recipients, mycophenolate and tacrolimus levels were compared across transplant vintage stratified by non-African Americans versus African Americans. Data were analyzed with standard univariate tests and multivariable regression models. Results:Our study included 1217 patients (transplanted from 2005-2013) who had tacrolimus and mycophenolate exposure data, with follow-up through 2015 (53.7% were African Americans). Mean mycophenolate dose was 1672 +/- 463 mg/day during the first 3 years posttransplant. Although transplant vintage did not appreciably impact mycophenolate dosing in non African Americans (0.7 mg/day/y; P = .903), doses significantly decreased in African Americans across transplant vintage (-20.5 mg/day/y; P < .001). Rate of mycophenolate being held or discontinued based on transplant vintage significantly increased in African Americans but did not change in non-African Americans. At the beginning of the study, mean tacrolimus levels were lower in African Americans; however, levels then slightly decreased in non-African Americans (-0.03 ng/mL/y;P = .279) and slightly increased in African Americans (+0.03 ng/mL/y; P = .247), with similar levels by 2013. Higher tacrolimus levels were protective against rejection in African Americans only but were protective against death-censored graft loss in both race/ethnicity groups. Mycophenolate dosing had no appreciable impact on outcomes in African Americans, but higher mycophenolate dosing was a significant risk factor for death-censored graft loss in non-African Americans. Conclusions:Tacrolimus and mycophenolate exposure levels have significantly changed over time and differed by race/ethnicity. In non-African Americans, those transplanted more recently tended to have lower tacrolimus but similar mycophenolate exposure. Although mycophenolate exposure in African Americans has recently decreased, tacrolimus has increased. Differences in outcomes likely reflect improved understanding of immunosuppressant tolerability by recipient race/ethnicity.
引用
收藏
页码:707 / 713
页数:7
相关论文
共 42 条
  • [1] Allison A C, 1991, Br J Rheumatol, V30 Suppl 2, P57
  • [2] Tacrolimus Predose Concentrations Do Not Predict the Risk of Acute Rejection After Renal Transplantation: A Pooled Analysis From Three Randomized-Controlled Clinical Trials
    Bouamar, R.
    Shuker, N.
    Hesselink, D. A.
    Weimar, W.
    Ekberg, H.
    Kaplan, B.
    Bernasconi, C.
    van Gelder, T.
    [J]. AMERICAN JOURNAL OF TRANSPLANTATION, 2013, 13 (05) : 1253 - 1261
  • [3] Buell C, 2008, J DRUGS DERMATOL, V7, P741
  • [4] Pharmacokinetics and bioavailability of mycophenolate mofetil in healthy subjects after single-dose oral and intravenous administration
    Bullingham, R
    Monroe, S
    Nicholls, A
    Hale, M
    [J]. JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 36 (04) : 315 - 324
  • [5] Cecka J M, 1996, Clin Transpl, P1
  • [6] Chan Y. H., 2003, SMJ Singapore Medical Journal, V44, P391
  • [7] Chan Y. H., 2003, SMJ Singapore Medical Journal, V44, P498
  • [8] United States Renal Data System public health surveillance of chronic kidney disease and end-stage renal disease
    Collins, Allan J.
    Foley, Robert N.
    Gilbertson, David T.
    Chen, Shu-Cheng
    [J]. KIDNEY INTERNATIONAL SUPPLEMENTS, 2015, 5 (01) : 2 - 7
  • [9] Characterizing the role of enterohepatic recycling in the interactions between mycophenolate mofetil and calcineurin inhibitors in renal transplant patients by pharmacokinetic modelling
    Cremers, S
    Schoemaker, R
    Scholten, E
    den Hartigh, J
    König-Quartel, J
    van Kan, E
    Paul, L
    de Fijter, J
    [J]. BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 60 (03) : 249 - 256
  • [10] New Insights Into the Pharmacokinetics and Pharmacodynamics of the Calcineurin Inhibitors and Mycophenolic Acid: Possible Consequences for Therapeutic Drug Monitoring in Solid Organ Transplantation
    de Jonge, Hylke
    Naesens, Maarten
    Kuypers, Dirk R. J.
    [J]. THERAPEUTIC DRUG MONITORING, 2009, 31 (04) : 416 - 435