Volume 7 Supplement 1
New onset diabetes mellitus after kidney transplant: prevalence and risk factors
- Júlia Cabral Bastos1,
- Monique Lima e Silva1Email author,
- Giovanna Petrilli1,
- Mariana Arruda Leal Pires1,
- Lívia Carla Ribeiro1,
- Guilherme da Rocha Branco1,
- Layra Faria de Oliveira1,
- Natalia Treistman Frota Leitão1,
- Marcos Miranda Santos Oliveira1,
- Lenita Zajdenverg1,
- Joana Rodrigues Dantas1 and
- Melanie Rodacki1
© Bastos et al. 2015
Published: 11 November 2015
New onset diabetes mellitus after transplant (NODAT) has been described in 4-25% of kidney transplant recipients. It is not only a major factor leading to dysfunction and deterioration of the allograft, but also has a significant impact on cardiovascular risk and patient survival. Several risk factors have been linked to this condition such as age, class of immunosupressive drug, obesity and family history of diabetes. However this has been poorly studied in our population.
To identify the prevalence and the major risk factors associated with NODAT after kidney transplantation in our population.
Materials and methods
We performed a retrospective evaluation of patients who underwent kidney transplant from 1994 to 2014 and were not diabetic before the procedure. The prevalence of NODAT was established through the ADA criteria. Clinical and epidemiologic data were retrieved by review of medical charts and analised with SPSS 17.0. A p≤0.05 was considered significant. Results: A total of 109 patients were studied (41,5% female and 58,5% male) Their mean age was 52 (±9.7) yrs. old (range: 27 to 72). Among them, 35 developed NODAT (31,5%). Those who developed NODAT were older than others (mean age 44,9 ±10,1 Vs 40,6 ±10,3; p 0.03). NODAT was more common in those who underwent hemodialysis before the transplant (38,8% Vs 8,3%; p 0.016) and that used imunossupressive therapy with mycophenolate (90,9% vs 73%; p 0.03). BMI before transplantation (p=0.671), gender (p=1.0), ethnicity (p=0,94), type of organ donor (p=0,69), family history of diabetes (p=0,79) and use of other imunossupressive drugs, like tacrolimus (p=0,5), sirolimus (p=0,22), cyclosporine (p=1.0) and corticosteroid (p=0,15), were not associated with NODAT in our patients. The majority of patients using corticosteroids (90,5%) used prednisone dosage ≤ 5 mg/day. In patients who developed NODAT, 2,8% used sulfonylureas alone, 14,3% used metformin alone, 5,7% used DPP4 inhibitors, 2,8% used sulfonylureas and insulin, 17,1% used metformin with insulin and 22,8% used insulin alone.
NODAT occurs in aproximately one third of patients that underwent kidney transplant in our population. The development of diabetes in these individuals is associated with older age at the time of surgery, hemodialysis before transplant and surprisingly with use of mycophenolate. This finding could be explained by the more common use of this drug in our center than in others.
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.