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Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function

PURPOSE: Dipeptidyl peptidase-4 (DPP-4) inhibitors lower blood glucose levels and enhance the function of pancreatic β cells. Yet, it is unknown whether posttransplant administration of DPP4 inhibitors is beneficial for pancreas transplant recipients. METHODS: We thus retrospectively analyzed the re...

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Autores principales: Jang, Hye-Won, Jung, Chang Hee, Ko, Youngmin, Lim, Seong Jun, Kwon, Hye Eun, Jung, Joo Hee, Kwon, Hyunwook, Kim, Young Hoon, Shin, Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424438/
https://www.ncbi.nlm.nih.gov/pubmed/34549042
http://dx.doi.org/10.4174/astr.2021.101.3.187
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author Jang, Hye-Won
Jung, Chang Hee
Ko, Youngmin
Lim, Seong Jun
Kwon, Hye Eun
Jung, Joo Hee
Kwon, Hyunwook
Kim, Young Hoon
Shin, Sung
author_facet Jang, Hye-Won
Jung, Chang Hee
Ko, Youngmin
Lim, Seong Jun
Kwon, Hye Eun
Jung, Joo Hee
Kwon, Hyunwook
Kim, Young Hoon
Shin, Sung
author_sort Jang, Hye-Won
collection PubMed
description PURPOSE: Dipeptidyl peptidase-4 (DPP-4) inhibitors lower blood glucose levels and enhance the function of pancreatic β cells. Yet, it is unknown whether posttransplant administration of DPP4 inhibitors is beneficial for pancreas transplant recipients. METHODS: We thus retrospectively analyzed the records of 312 patients who underwent pancreas transplantation between 2000 and 2018 at Asan Medical Center (Seoul, Korea) and compared the metabolic and survival outcomes according to DPP-4 inhibitor treatment. RESULTS: The patients were divided into the no DPP-4 inhibitor group (n = 165; no treatment with DPP-4 inhibitors or treated for <1 month) and the DPP-4 inhibitor group (n = 147; treated with DPP-4 inhibitors for ≥1 month). There were no significant differences in levels of glucose, hemoglobin A1c, and insulin between the 2 groups during 36 months of follow-up. However, the level of C-peptide was significantly higher in the DPP-4 inhibitor group at 1, 6, and 24 months posttransplant (all P < 0.05). Moreover, the DPP-4 inhibitor group had significantly higher rates of overall (log-rank test, P = 0.009) and death-censored (log-rank test, P = 0.036) graft survival during a 15-year follow-up. CONCLUSION: Posttransplant DPP-4 inhibitor administration may help improve the clinical outcomes including β cell function after pancreas transplantation.
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spelling pubmed-84244382021-09-20 Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function Jang, Hye-Won Jung, Chang Hee Ko, Youngmin Lim, Seong Jun Kwon, Hye Eun Jung, Joo Hee Kwon, Hyunwook Kim, Young Hoon Shin, Sung Ann Surg Treat Res Original Article PURPOSE: Dipeptidyl peptidase-4 (DPP-4) inhibitors lower blood glucose levels and enhance the function of pancreatic β cells. Yet, it is unknown whether posttransplant administration of DPP4 inhibitors is beneficial for pancreas transplant recipients. METHODS: We thus retrospectively analyzed the records of 312 patients who underwent pancreas transplantation between 2000 and 2018 at Asan Medical Center (Seoul, Korea) and compared the metabolic and survival outcomes according to DPP-4 inhibitor treatment. RESULTS: The patients were divided into the no DPP-4 inhibitor group (n = 165; no treatment with DPP-4 inhibitors or treated for <1 month) and the DPP-4 inhibitor group (n = 147; treated with DPP-4 inhibitors for ≥1 month). There were no significant differences in levels of glucose, hemoglobin A1c, and insulin between the 2 groups during 36 months of follow-up. However, the level of C-peptide was significantly higher in the DPP-4 inhibitor group at 1, 6, and 24 months posttransplant (all P < 0.05). Moreover, the DPP-4 inhibitor group had significantly higher rates of overall (log-rank test, P = 0.009) and death-censored (log-rank test, P = 0.036) graft survival during a 15-year follow-up. CONCLUSION: Posttransplant DPP-4 inhibitor administration may help improve the clinical outcomes including β cell function after pancreas transplantation. The Korean Surgical Society 2021-09 2021-08-31 /pmc/articles/PMC8424438/ /pubmed/34549042 http://dx.doi.org/10.4174/astr.2021.101.3.187 Text en Copyright © 2021, the Korean Surgical Society https://creativecommons.org/licenses/by-nc/4.0/Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jang, Hye-Won
Jung, Chang Hee
Ko, Youngmin
Lim, Seong Jun
Kwon, Hye Eun
Jung, Joo Hee
Kwon, Hyunwook
Kim, Young Hoon
Shin, Sung
Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
title Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
title_full Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
title_fullStr Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
title_full_unstemmed Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
title_short Beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
title_sort beneficial effects of posttransplant dipeptidyl peptidase-4 inhibitor administration after pancreas transplantation to improve β cell function
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424438/
https://www.ncbi.nlm.nih.gov/pubmed/34549042
http://dx.doi.org/10.4174/astr.2021.101.3.187
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