Literature DB >> 23423268

Outcomes in African American kidney transplant patients receiving tacrolimus and mycophenolic acid immunosuppression.

Mohanram Narayanan1, Oleh Pankewycz, Mohamed El-Ghoroury, Fuad Shihab, Anne Wiland, Kevin McCague, Laurence Chan.   

Abstract

BACKGROUND: Prospective data regarding immunosuppression and rejection in African American patients receiving modern immunosuppressive regimens are sparse.
METHODS: One-year data were analyzed from 901 tacrolimus-treated de novo kidney transplant patients in the prospective Mycophenolic Acid Observational Renal Transplant registry.
RESULTS: Mean tacrolimus dose was significantly higher in African Americans (n=217) versus non-African Americans (n=684), but mean tacrolimus trough concentrations were similar. The proportion of patients receiving mycophenolic acid dose equal to or more than 2000 mg per day (mycophenolate mofetil equivalents) was significantly higher with enteric-coated mycophenolate sodium versus mycophenolate mofetil at month 6 among African Americans and at month 3 in non-African Americans, but rates of acute rejection and adverse events (including gastrointestinal events) were similar. The 1-year incidence of biopsy-proven acute rejection (BPAR) was 14.1% in African Americans versus 7.5% in non-African Americans. On multivariate analysis, African American ethnicity was associated with a higher risk of BPAR (hazard ratio, 1.93; 95% confidence interval, 1.19-3.09; P=0.007). Mean (standard deviation) glomerular filtration rate at month 12 estimated by the Chronic Kidney Disease Epidemiology Collaboration formula was 59.2 (22.2) mL/min/1.73 m in African Americans versus 58.8 (19.9) mL/min/1.73 m in non-African Americans (confidence interval of the difference, -3.4 to 4.3; P=0.83).
CONCLUSION: This observational study confirms that African Americans require higher doses of tacrolimus to achieve target trough concentrations and are more likely to experience BPAR during the first year after kidney transplantation despite modern immunosuppression regimens. In our 1-year study, this was not associated with significantly inferior graft survival.

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Year:  2013        PMID: 23423268     DOI: 10.1097/TP.0b013e318277438f

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  6 in total

1.  Early Steroid Withdrawal in Black Transplant Patients: A Selective Process.

Authors:  Joshua J Augustine
Journal:  Clin J Am Soc Nephrol       Date:  2016-12-15       Impact factor: 8.237

2.  Tacrolimus troughs and genetic determinants of metabolism in kidney transplant recipients: A comparison of four ancestry groups.

Authors:  Moataz E Mohamed; David P Schladt; Weihua Guan; Baolin Wu; Jessica van Setten; Brendan J Keating; David Iklé; Rory P Remmel; Casey R Dorr; Roslyn B Mannon; Arthur J Matas; Ajay K Israni; William S Oetting; Pamala A Jacobson
Journal:  Am J Transplant       Date:  2019-05-13       Impact factor: 8.086

Review 3.  Genomics in CKD: Is This the Path Forward?

Authors:  Girish N Nadkarni; Carol R Horowitz
Journal:  Adv Chronic Kidney Dis       Date:  2016-03       Impact factor: 3.620

4.  Tacrolimus Dose-Conversion Ratios Based on Switching of Formulations for Patients with Solid Organ Transplants.

Authors:  Wen-Yuan Johnson Kuan; Nathalie Châteauvert; Vincent Leclerc; Benoît Drolet
Journal:  Can J Hosp Pharm       Date:  2021

5.  Efficacy and safety of prolonged-release tacrolimus in stable pediatric allograft recipients converted from immediate-release tacrolimus - a Phase 2, open-label, single-arm, one-way crossover study.

Authors:  Jacek Rubik; Dominique Debray; Deirdre Kelly; Franck Iserin; Nicholas J A Webb; Piotr Czubkowski; Karel Vondrak; Anne-Laure Sellier-Leclerc; Christine Rivet; Silvia Riva; Burkhard Tönshoff; Lorenzo D'Antiga; Stephen D Marks; Raymond Reding; Gbenga Kazeem; Nasrullah Undre
Journal:  Transpl Int       Date:  2019-08-27       Impact factor: 3.782

6.  Genotype-guided tacrolimus dosing in African-American kidney transplant recipients.

Authors:  K Sanghavi; R C Brundage; M B Miller; D P Schladt; A K Israni; W Guan; W S Oetting; R B Mannon; R P Remmel; A J Matas; P A Jacobson
Journal:  Pharmacogenomics J       Date:  2015-12-15       Impact factor: 3.550

  6 in total

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