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Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial

BACKGROUND: This randomized controlled trial aimed to investigate the effect of everolimus (EVL) with low-dose tacrolimus (Tac) on the development of post-transplantation diabetes mellitus (PTDM) in kidney transplantation (KT). MATERIAL/METHODS: Seventy-seven kidney transplant patients from 4 transp...

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Autores principales: Kim, Hyung Duk, Chang, Ji-Yeun, Chung, Byung Ha, Kim, Chan-Duck, Lee, Sang-Ho, Kim, Yeong Hoon, Yang, Chul Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836319/
https://www.ncbi.nlm.nih.gov/pubmed/33479188
http://dx.doi.org/10.12659/AOT.927984
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author Kim, Hyung Duk
Chang, Ji-Yeun
Chung, Byung Ha
Kim, Chan-Duck
Lee, Sang-Ho
Kim, Yeong Hoon
Yang, Chul Woo
author_facet Kim, Hyung Duk
Chang, Ji-Yeun
Chung, Byung Ha
Kim, Chan-Duck
Lee, Sang-Ho
Kim, Yeong Hoon
Yang, Chul Woo
author_sort Kim, Hyung Duk
collection PubMed
description BACKGROUND: This randomized controlled trial aimed to investigate the effect of everolimus (EVL) with low-dose tacrolimus (Tac) on the development of post-transplantation diabetes mellitus (PTDM) in kidney transplantation (KT). MATERIAL/METHODS: Seventy-seven kidney transplant patients from 4 transplant centers were included. Patients were randomized to the “EVL group” (n=38) and the “TAC group” (n=39). The target Tac trough level was 2 to 5 ng/mL in the EVL group and 5 to 10 ng/mL in the TAC group. RESULTS: The 1-year cumulative incidence of PTDM in all patients was 7.8%, and no difference was found between the 2 groups (P=0.0819). Insulin resistance measured with the homeostatic model assessment for insulin resistance showed a significant increase only in the TAC group (1.11 to 1.30, P=0.0492). Allograft rejection rate and estimated glomerular filtration rate (eGFR) follow-ups every 3 months were not significantly different between the 2 groups. However, the EVL group showed a significant increase in the mean eGFR at 9 months and 12 months after KT compared to the baseline value (P=0.0242 and 0.0491, respectively). The EVL group showed lower insulin resistance and higher allograft function in comparison to the TAC group. CONCLUSIONS: EVL-based immunosuppressive therapy with lower Tac exposure could be a safer alternative for maintenance treatment.
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spelling pubmed-78363192021-01-26 Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial Kim, Hyung Duk Chang, Ji-Yeun Chung, Byung Ha Kim, Chan-Duck Lee, Sang-Ho Kim, Yeong Hoon Yang, Chul Woo Ann Transplant Original Paper BACKGROUND: This randomized controlled trial aimed to investigate the effect of everolimus (EVL) with low-dose tacrolimus (Tac) on the development of post-transplantation diabetes mellitus (PTDM) in kidney transplantation (KT). MATERIAL/METHODS: Seventy-seven kidney transplant patients from 4 transplant centers were included. Patients were randomized to the “EVL group” (n=38) and the “TAC group” (n=39). The target Tac trough level was 2 to 5 ng/mL in the EVL group and 5 to 10 ng/mL in the TAC group. RESULTS: The 1-year cumulative incidence of PTDM in all patients was 7.8%, and no difference was found between the 2 groups (P=0.0819). Insulin resistance measured with the homeostatic model assessment for insulin resistance showed a significant increase only in the TAC group (1.11 to 1.30, P=0.0492). Allograft rejection rate and estimated glomerular filtration rate (eGFR) follow-ups every 3 months were not significantly different between the 2 groups. However, the EVL group showed a significant increase in the mean eGFR at 9 months and 12 months after KT compared to the baseline value (P=0.0242 and 0.0491, respectively). The EVL group showed lower insulin resistance and higher allograft function in comparison to the TAC group. CONCLUSIONS: EVL-based immunosuppressive therapy with lower Tac exposure could be a safer alternative for maintenance treatment. International Scientific Literature, Inc. 2021-01-22 /pmc/articles/PMC7836319/ /pubmed/33479188 http://dx.doi.org/10.12659/AOT.927984 Text en © Ann Transplant, 2021 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Original Paper
Kim, Hyung Duk
Chang, Ji-Yeun
Chung, Byung Ha
Kim, Chan-Duck
Lee, Sang-Ho
Kim, Yeong Hoon
Yang, Chul Woo
Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial
title Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial
title_full Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial
title_fullStr Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial
title_full_unstemmed Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial
title_short Effect of Everolimus with Low-Dose Tacrolimus on Development of New-Onset Diabetes After Transplantation and Allograft Function in Kidney Transplantation: A Multicenter, Open-Label, Randomized Trial
title_sort effect of everolimus with low-dose tacrolimus on development of new-onset diabetes after transplantation and allograft function in kidney transplantation: a multicenter, open-label, randomized trial
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836319/
https://www.ncbi.nlm.nih.gov/pubmed/33479188
http://dx.doi.org/10.12659/AOT.927984
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