Abstract

BackgroundLittle is known regarding optimal tacrolimus (TAC) trough levels after 1 year post-transplant in stable kidney transplant recipients (KTRs) who have not experienced renal or cardiovascular outcomes. This study aimed to investigate the effect of 1-year post-transplant TAC trough levels on long-term renal and cardiovascular outcomes and opportunistic infections in stable KTRs.MethodsKTRs receiving TAC with mycophenolate-based immunosuppression who did not experience renal or cardiovascular outcomes within 1 year post-transplant were enrolled from a multicenter observational cohort study. Renal outcome was defined as a composite of biopsy-proven acute rejection, interstitial fibrosis and tubular atrophy, and death-censored graft loss. Cardiovascular outcome was defined as a composite of de novo cardiomegaly, left ventricular hypertrophy, and cardiovascular events. Opportunistic infections were defined as the occurrence of BK virus or cytomegalovirus infections.ResultsA total of 603 eligible KTRs were divided into the low-level TAC (LL-TAC) and high-level TAC (HL-TAC) groups based on a median TAC level of 5.9 ng/mL (range 1.3–14.3) at 1 year post-transplant. The HL-TAC group had significantly higher TAC trough levels at 2, 3, 4, and 5 years compared with the levels of the LL-TAC group. During the mean follow-up of 63.7 ± 13.0 months, there were 121 renal outcomes and 224 cardiovascular outcomes. In multivariate Cox regression analysis, LL-TAC and HL-TAC were not independent risk factors for renal and cardiovascular outcomes, respectively. No significant differences in the development of opportunistic infections and de novo donor-specific anti-human leukocyte antigen antibodies and renal allograft function were observed between the two groups.ConclusionsTAC trough levels after 1 year post-transplant remained at a similar level until the fifth year after kidney transplantation and were not directly associated with long-term outcomes in stable Korean KTRs who did not experience renal or cardiovascular outcomes. Therefore, in Asian KTRs with a stable clinical course, TAC trough levels higher than approximately 6 ng/mL might not be required after a year of kidney transplantation.

Highlights

  • Underdosing of tacrolimus (TAC) in kidney transplant recipients (KTRs) can lead to biopsyproven acute rejection (BPAR) and immunologic sensitization; overdosing of TAC can result in calcineurin inhibitor (CNI) toxicity and opportunistic infections including BK virus and cytomegalovirus (CMV) infections, which have detrimental effects on renal allograft outcomes [1,2,3,4,5]

  • A total of 603 eligible KTRs were divided into the low-level TAC (LL-TAC) and high-level TAC (HL-TAC) groups based on a median TAC level of 5.9 ng/mL at 1

  • TAC trough levels after 1 year post-transplant remained at a similar level until the fifth year after kidney transplantation and were not directly associated with long-term outcomes in stable Korean KTRs who did not experience renal or cardiovascular outcomes

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Summary

Introduction

Underdosing of tacrolimus (TAC) in kidney transplant recipients (KTRs) can lead to biopsyproven acute rejection (BPAR) and immunologic sensitization; overdosing of TAC can result in calcineurin inhibitor (CNI) toxicity and opportunistic infections including BK virus and cytomegalovirus (CMV) infections, which have detrimental effects on renal allograft outcomes [1,2,3,4,5]. The Kidney Disease: Improving Global Outcomes guidelines suggest that 5–15 ng/mL of TAC trough levels should be maintained during the first 2–4 months post-transplant and reduced in stable KTRs to minimize toxicity, with a low quality of evidence [21]. Little is known regarding optimal TAC trough levels after 1 year post-transplant in stable KTRs who have not experienced renal or cardiovascular outcomes. Since ethnicity can affect tacrolimus pharmacokinetics [22], it is crucial to determine the optimal TAC trough levels in Asian KTRs. Little is known regarding optimal tacrolimus (TAC) trough levels after 1 year post-transplant in stable kidney transplant recipients (KTRs) who have not experienced renal or cardiovascular outcomes. This study aimed to investigate the effect of 1-year post-transplant TAC trough levels on long-term renal and cardiovascular outcomes and opportunistic infections in stable KTRs

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