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Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant

Diabetes mellitus (DM) arising de novo after transplant is a common complication, sharing many features with type 2 DM but also specific causes, such as administration of steroids and immunosuppressive drugs. Although post-transplant DM (PTDM) is generally assumed to worsen recipients’ outcomes, its...

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Autores principales: Durante-Mangoni, Emanuele, Iossa, Domenico, Iorio, Valeria, Mattucci, Irene, Malgeri, Umberto, Pinto, Daniela, Andini, Roberto, Maiello, Ciro, Zampino, Rosa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687884/
https://www.ncbi.nlm.nih.gov/pubmed/36359224
http://dx.doi.org/10.3390/biomedicines10112704
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author Durante-Mangoni, Emanuele
Iossa, Domenico
Iorio, Valeria
Mattucci, Irene
Malgeri, Umberto
Pinto, Daniela
Andini, Roberto
Maiello, Ciro
Zampino, Rosa
author_facet Durante-Mangoni, Emanuele
Iossa, Domenico
Iorio, Valeria
Mattucci, Irene
Malgeri, Umberto
Pinto, Daniela
Andini, Roberto
Maiello, Ciro
Zampino, Rosa
author_sort Durante-Mangoni, Emanuele
collection PubMed
description Diabetes mellitus (DM) arising de novo after transplant is a common complication, sharing many features with type 2 DM but also specific causes, such as administration of steroids and immunosuppressive drugs. Although post-transplant DM (PTDM) is generally assumed to worsen recipients’ outcomes, its impact on renal function, cardiac allograft vasculopathy and mortality remains understudied in heart transplant (HT). We evaluated incidence and risk factors of PTDM and studied glucose metabolic alterations in relation to major HT outcomes. 119 subjects were included in this retrospective, single centre, observational study. A comprehensive assessment of glucose metabolic state was done pre-transplant and a median of 60 months [IQR 30–72] after transplant. Most patients were males (75.6%), with prior non-ischemic cardiomyopathy (64.7%) and median age of 58 years [IQR 48–63]. 14 patients developed PTDM, an incidence of 3.2 cases/100 patient-years. Patients with worsening glucose metabolic pattern were the only who showed a significant increase of BMI and metabolic syndrome prevalence after transplant. 23 (19.3%) patients died during follow up. Early mortality was lower in those with stably normal glucose metabolism, whereas improvement of glucose metabolic state favorably affected mid-term mortality (log-rank p = 0.028). No differences were observed regarding risk of infections and cancer. PTDM is common, but glucose metabolism may also improve after HT. PTDM is strictly related with BMI increase and metabolic syndrome development and may impact recipient survival.
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spelling pubmed-96878842022-11-25 Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant Durante-Mangoni, Emanuele Iossa, Domenico Iorio, Valeria Mattucci, Irene Malgeri, Umberto Pinto, Daniela Andini, Roberto Maiello, Ciro Zampino, Rosa Biomedicines Article Diabetes mellitus (DM) arising de novo after transplant is a common complication, sharing many features with type 2 DM but also specific causes, such as administration of steroids and immunosuppressive drugs. Although post-transplant DM (PTDM) is generally assumed to worsen recipients’ outcomes, its impact on renal function, cardiac allograft vasculopathy and mortality remains understudied in heart transplant (HT). We evaluated incidence and risk factors of PTDM and studied glucose metabolic alterations in relation to major HT outcomes. 119 subjects were included in this retrospective, single centre, observational study. A comprehensive assessment of glucose metabolic state was done pre-transplant and a median of 60 months [IQR 30–72] after transplant. Most patients were males (75.6%), with prior non-ischemic cardiomyopathy (64.7%) and median age of 58 years [IQR 48–63]. 14 patients developed PTDM, an incidence of 3.2 cases/100 patient-years. Patients with worsening glucose metabolic pattern were the only who showed a significant increase of BMI and metabolic syndrome prevalence after transplant. 23 (19.3%) patients died during follow up. Early mortality was lower in those with stably normal glucose metabolism, whereas improvement of glucose metabolic state favorably affected mid-term mortality (log-rank p = 0.028). No differences were observed regarding risk of infections and cancer. PTDM is common, but glucose metabolism may also improve after HT. PTDM is strictly related with BMI increase and metabolic syndrome development and may impact recipient survival. MDPI 2022-10-26 /pmc/articles/PMC9687884/ /pubmed/36359224 http://dx.doi.org/10.3390/biomedicines10112704 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Durante-Mangoni, Emanuele
Iossa, Domenico
Iorio, Valeria
Mattucci, Irene
Malgeri, Umberto
Pinto, Daniela
Andini, Roberto
Maiello, Ciro
Zampino, Rosa
Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant
title Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant
title_full Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant
title_fullStr Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant
title_full_unstemmed Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant
title_short Incidence, Risk Factors and Clinical Implications of Glucose Metabolic Changes after Heart Transplant
title_sort incidence, risk factors and clinical implications of glucose metabolic changes after heart transplant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687884/
https://www.ncbi.nlm.nih.gov/pubmed/36359224
http://dx.doi.org/10.3390/biomedicines10112704
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