Is there a genetic predisposition to new-onset diabetes after kidney transplantation ?

Kidney transplant recipients may develop new-onset diabetes after transplantation (NODAT) and transplant-associated hyperglycemia (TAH) (NODAT or new-onset impaired glucose tolerance-IGT). We studied 251 consecutive renal transplant South Asian recipients for incidence of NODAT and its risk factors...

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Veröffentlicht in:Saudi journal of kidney diseases and transplantation 2015-11, Vol.26 (6), p.1113-1120
Hauptverfasser: Mehra, Nikita, Ramachandran A., Ali, Asik Ali Muhammad, Reddy, Yuvaram N. V., Sundaram, Varun, Reddy, Pooja P., Abraham, Georgi, Reddy, Yogesh N. V., Nagarajan, Prethivee, Mathew, Milly
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Sprache:eng
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Zusammenfassung:Kidney transplant recipients may develop new-onset diabetes after transplantation (NODAT) and transplant-associated hyperglycemia (TAH) (NODAT or new-onset impaired glucose tolerance-IGT). We studied 251 consecutive renal transplant South Asian recipients for incidence of NODAT and its risk factors between June 2004 and January 2009. Pre-transplant glucose tolerance test (GTT) identified non-diabetics (n = 102, IGT-24, NGT-78) for analysis. Baseline immunosuppression along with either cyclosporine (CsA) (n = 70) or tacrolimus (Tac) (n = 32) was given. Patients underwent GTT 20 days (mean) post-transplant to identify NODAT, normal (N) or IGT. TAH was observed in 40.2% of the patients (40 % in CsA and 40.6 % in Tac) (P = 0.5). NODAT developed in 13.7 % of the patients (12.9 % in CsA and 15.6% in Tac) (P = 0.5). Overall, Hepatitis C (P = 0.007), human leukocyte antigen (HLA) B52 (P = 0.03) and lack of HLA A28 (A68/69) (P = 0.03) were associated with TAH. In the Tac group, higher Day 1 dosage (P
ISSN:1319-2442
2320-3838
DOI:10.4103/1319-2442.168558