Five Year Follow-Up of a Phase 2 Clinical Trial to Induce Tolerance in Mismatched Living Donor Renal Transplant Recipients.

2014 ◽  
Vol 98 ◽  
pp. 231
Author(s):  
J. Leventhal ◽  
M. Abecassis ◽  
J. Miller ◽  
L. Gallon ◽  
J. Galvin ◽  
...  
2018 ◽  
Vol 102 ◽  
pp. S394
Author(s):  
Suzanne Ildstad ◽  
Joseph Leventhal ◽  
John Galvin ◽  
Dianne Stare ◽  
K Kurtenbach ◽  
...  

2020 ◽  
Vol 104 (S3) ◽  
pp. S90-S90
Author(s):  
Joseph R. Leventhal ◽  
James Mathew ◽  
John Galvin ◽  
Lorenzo Gallon ◽  
Dianne Belshe ◽  
...  

2014 ◽  
Vol 8 (2) ◽  
pp. 44-50 ◽  
Author(s):  
Harsh Vardhan ◽  
Narayan Prasad ◽  
Akhilesh Jaiswal ◽  
Brijesh Yadav ◽  
Shashi Kumar ◽  
...  

2020 ◽  
Vol 9 (2) ◽  
pp. 511 ◽  
Author(s):  
Maryse C. J. Osté ◽  
Jose L. Flores-Guerrero ◽  
Eke G. Gruppen ◽  
Lyanne M. Kieneker ◽  
Margery A. Connelly ◽  
...  

Post-transplant diabetes mellitus (PTDM) is a serious complication in renal transplant recipients. Branched-chain amino acids (BCAAs) are involved in the pathogenesis of insulin resistance. We determined the association of plasma BCAAs with PTDM and included adult renal transplant recipients (≥18 y) with a functioning graft for ≥1 year in this cross-sectional cohort study with prospective follow-up. Plasma BCAAs were measured in 518 subjects using nuclear magnetic resonance spectroscopy. We excluded subjects with a history of diabetes, leaving 368 non-diabetic renal transplant recipients eligible for analyses. Cox proportional hazards analyses were used to assess the association of BCAAs with the development of PTDM. Mean age was 51.1 ± 13.6 y (53.6% men) and plasma BCAA was 377.6 ± 82.5 µM. During median follow-up of 5.3 (IQR, 4.2–6.0) y, 38 (9.8%) patients developed PTDM. BCAAs were associated with a higher risk of developing PTDM (HR: 1.43, 95% CI 1.08–1.89) per SD change (p = 0.01), independent of age and sex. Adjustment for other potential confounders did not significantly change this association, although adjustment for HbA1c eliminated it. The association was mediated to a considerable extent (53%) by HbA1c. The association was also modified by HbA1c; BCAAs were only associated with renal transplant recipients without prediabetes (HbA1c < 5.7%). In conclusion, high concentrations of plasma BCAAs are associated with developing PTDM in renal transplant recipients. Alterations in BCAAs may represent an early predictive biomarker for PTDM.


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