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Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management

Post‐transplant diabetes mellitus (PTDM) is a significant contributor to morbidity and mortality in liver transplant recipients (LTRs). With concurrent comorbidities and use of various immunosuppression medications, identifying a safe and personalized regimen for management of PTDM is needed. There...

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Autores principales: Richardson, Brooks, Khan, Mohammad Qasim, Brown, Sara A, Watt, Kymberly D, Izzy, Manhal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134800/
https://www.ncbi.nlm.nih.gov/pubmed/34921530
http://dx.doi.org/10.1002/hep4.1876
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author Richardson, Brooks
Khan, Mohammad Qasim
Brown, Sara A
Watt, Kymberly D
Izzy, Manhal
author_facet Richardson, Brooks
Khan, Mohammad Qasim
Brown, Sara A
Watt, Kymberly D
Izzy, Manhal
author_sort Richardson, Brooks
collection PubMed
description Post‐transplant diabetes mellitus (PTDM) is a significant contributor to morbidity and mortality in liver transplant recipients (LTRs). With concurrent comorbidities and use of various immunosuppression medications, identifying a safe and personalized regimen for management of PTDM is needed. There are many comorbidities associated with the post‐transplant course including chronic kidney disease, cardiovascular disease, allograft steatosis, obesity, and de novo malignancy. Emerging data suggest that available diabetes medications may carry beneficial or, in some cases, harmful effects in the setting of these co‐existing conditions. Sodium‐glucose co‐transporter 2 inhibitors and glucagon‐like peptide 1 receptor agonists have shown the most promising beneficial results. Although there is a deficiency of LTR‐specific data, they appear to be generally safe. Effects of other medications are varied. Metformin may reduce the risk of malignancy. Pioglitazone may be harmful in patients combatting obesity or heart failure. Insulin may exacerbate obesity and increase the risk of developing malignancy. This review thoroughly discusses the roles of these extra‐glycemic effects and safety considerations in LTRs. Through weighing the risks and benefits, we conclude that alternatives to insulin should be strongly considered, when feasible, for personalized long‐term management based on risk factors and co‐morbidities.
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spelling pubmed-91348002022-06-04 Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management Richardson, Brooks Khan, Mohammad Qasim Brown, Sara A Watt, Kymberly D Izzy, Manhal Hepatol Commun Review Post‐transplant diabetes mellitus (PTDM) is a significant contributor to morbidity and mortality in liver transplant recipients (LTRs). With concurrent comorbidities and use of various immunosuppression medications, identifying a safe and personalized regimen for management of PTDM is needed. There are many comorbidities associated with the post‐transplant course including chronic kidney disease, cardiovascular disease, allograft steatosis, obesity, and de novo malignancy. Emerging data suggest that available diabetes medications may carry beneficial or, in some cases, harmful effects in the setting of these co‐existing conditions. Sodium‐glucose co‐transporter 2 inhibitors and glucagon‐like peptide 1 receptor agonists have shown the most promising beneficial results. Although there is a deficiency of LTR‐specific data, they appear to be generally safe. Effects of other medications are varied. Metformin may reduce the risk of malignancy. Pioglitazone may be harmful in patients combatting obesity or heart failure. Insulin may exacerbate obesity and increase the risk of developing malignancy. This review thoroughly discusses the roles of these extra‐glycemic effects and safety considerations in LTRs. Through weighing the risks and benefits, we conclude that alternatives to insulin should be strongly considered, when feasible, for personalized long‐term management based on risk factors and co‐morbidities. John Wiley and Sons Inc. 2021-12-17 /pmc/articles/PMC9134800/ /pubmed/34921530 http://dx.doi.org/10.1002/hep4.1876 Text en © 2021 The Authors. Hepatology Communications published by Wiley Periodicals LLC on behalf of American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Richardson, Brooks
Khan, Mohammad Qasim
Brown, Sara A
Watt, Kymberly D
Izzy, Manhal
Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management
title Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management
title_full Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management
title_fullStr Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management
title_full_unstemmed Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management
title_short Personalizing Diabetes Management in Liver Transplant Recipients: The New Era for Optimizing Risk Management
title_sort personalizing diabetes management in liver transplant recipients: the new era for optimizing risk management
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134800/
https://www.ncbi.nlm.nih.gov/pubmed/34921530
http://dx.doi.org/10.1002/hep4.1876
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