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Cited 2 time in webofscience Cited 2 time in scopus
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Tacrolimus trough levels higher than 6 ng/mL might not be required after a year in stable kidney transplant recipientsopen access

Authors
Jung, Hee-YeonSeo, Min YoungJeon, YenaHuh, Kyu HaPark, Jae BermJung, Cheol WoongLee, SikHan, Seung-YeupRo, HanYang, JaeseokAhn, CurieChoi, Ji-YoungCho, Jang-HeePark, Sun-HeeKim, Yong-LimKim, Chan-Duck
Issue Date
Jul-2020
Publisher
Public Library of Science
Citation
PLoS ONE, v.15, no.7
Indexed
SCIE
SCOPUS
Journal Title
PLoS ONE
Volume
15
Number
7
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/33680
DOI
10.1371/journal.pone.0235418
ISSN
1932-6203
Abstract
Background 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. Methods KTRs 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. Results 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 (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. Conclusions 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. 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.
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Jung, Cheol Woong
Anam Hospital (Department of Transplantation and Vascular Surgery, Anam Hospital)
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