TY - JOUR
T1 - Post-transplant diabetes mellitus
T2 - incidence, predicting factors and outcomes
AU - Mizrahi, Nadav
AU - Braun, Marius
AU - Ben Gal, Tuvia
AU - Rosengarten, Dror
AU - Kramer, Mordechai Reuven
AU - Grossman, Alon
N1 - Publisher Copyright:
© 2020, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Purpose: To identify predictors and evaluate outcomes of posttransplant diabetes mellitus (PTDM) and to investigate the effect of treatment modalities on outcomes. Methods: The database of a tertiary medical center was searched for all adult patients without prior diabetes who underwent lung, liver, or heart transplantation between January 1, 2012 and June 30, 2018. Patients in whom PTDM (defined as HbA1C ≥ 6.5% at least 3 months post transplantation) developed during follow-up (mean 3.32 years) were identified. Risk factors for PTDM, determined by regression analysis and clinical outcomes [all-cause mortality, severe infections, graft loss, and major adverse cardiovascular events (MACE)], were compared between those who developed PTDM and those who did not; in the former, insulin-based therapy was compared with non-insulin regimen. Results: The cohort included 281 transplant recipients: 158 lung, 109 liver, and 14 heart. PTDM was diagnosed in 60 (21.35%) patients at a mean of 11.3 ± 12.89 months post transplantation. The only significant independent risk factor for PTDM was age (HR 1.028, 95% CI = 1.002–1.054, P = 0.0314). PTDM was associated with higher rates of severe infections (HR 2.565, 95% CI = 1.626–4.050, P < 0.0001), MACE (HR 1.856, 95% CI = 1.013–3.401, P = 0.0454) and death (HR 1.840, 95% CI = 1.024–3.304, P = 0.0413). Recipients treated with insulin-based regimens had a higher risk of severe infections (HR 2.579, 95% CI = 1.640–4.055, P < 0.0001), MACE (1.925, 95% CI = 1.074–3.451, P = 0.0278) and death (HR 1.960, 95% CI = 1.071–3.586, P = 0.0291). Conclusions: PTDM is associated with increased mortality and poor outcomes in lung, liver, and heart transplant recipients. Early identification and aggressive treatment of PTDM and its associated cardiometabolic risk factors may improve outcomes.
AB - Purpose: To identify predictors and evaluate outcomes of posttransplant diabetes mellitus (PTDM) and to investigate the effect of treatment modalities on outcomes. Methods: The database of a tertiary medical center was searched for all adult patients without prior diabetes who underwent lung, liver, or heart transplantation between January 1, 2012 and June 30, 2018. Patients in whom PTDM (defined as HbA1C ≥ 6.5% at least 3 months post transplantation) developed during follow-up (mean 3.32 years) were identified. Risk factors for PTDM, determined by regression analysis and clinical outcomes [all-cause mortality, severe infections, graft loss, and major adverse cardiovascular events (MACE)], were compared between those who developed PTDM and those who did not; in the former, insulin-based therapy was compared with non-insulin regimen. Results: The cohort included 281 transplant recipients: 158 lung, 109 liver, and 14 heart. PTDM was diagnosed in 60 (21.35%) patients at a mean of 11.3 ± 12.89 months post transplantation. The only significant independent risk factor for PTDM was age (HR 1.028, 95% CI = 1.002–1.054, P = 0.0314). PTDM was associated with higher rates of severe infections (HR 2.565, 95% CI = 1.626–4.050, P < 0.0001), MACE (HR 1.856, 95% CI = 1.013–3.401, P = 0.0454) and death (HR 1.840, 95% CI = 1.024–3.304, P = 0.0413). Recipients treated with insulin-based regimens had a higher risk of severe infections (HR 2.579, 95% CI = 1.640–4.055, P < 0.0001), MACE (1.925, 95% CI = 1.074–3.451, P = 0.0278) and death (HR 1.960, 95% CI = 1.071–3.586, P = 0.0291). Conclusions: PTDM is associated with increased mortality and poor outcomes in lung, liver, and heart transplant recipients. Early identification and aggressive treatment of PTDM and its associated cardiometabolic risk factors may improve outcomes.
KW - Outcomes
KW - Post-Transplant Diabetes Mellitus
KW - Predictors
KW - Treatment
UR - http://www.scopus.com/inward/record.url?scp=85085015257&partnerID=8YFLogxK
U2 - 10.1007/s12020-020-02339-9
DO - 10.1007/s12020-020-02339-9
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C2 - 32418071
AN - SCOPUS:85085015257
SN - 1355-008X
VL - 69
SP - 303
EP - 309
JO - Endocrine
JF - Endocrine
IS - 2
ER -