New Onset Diabetes and Non-Alcoholic Fatty Liver Disease after Liver Transplantation

Adult Male 0301 basic medicine Steatosis Time Factors Calcineurin Inhibitors Specialties of internal medicine 03 medical and health sciences Non-alcoholic Fatty Liver Disease Recurrence Risk Factors Diabetes Mellitus Humans Prospective Studies Non-alcoholic steatohepatitis Aged 2. Zero hunger Liver transplantation Diabetes Middle Aged Metabolic syndrome Liver Transplantation 3. Good health Treatment Outcome RC581-951 Female Immunosuppressive Agents
DOI: 10.5604/01.3001.0010.5285 Publication Date: 2017-10-17T07:07:39Z
ABSTRACT
Non-alcoholic fatty liver disease (NAFLD) is an emerging cause of graft dysfunction after liver transplantation (LT) frequently related to the development of new onset diabetes after LT (NODAT). This study was undertaken to evaluate the frequencies of NODAT and NAFLD after LT, to investigate their major risk factors and the impact of de novo or recurrent NAFLD in graft function.119 patients submitted to LT were prospectively evaluated.After 4 ± 1 years, NODAT, recurrent and de novo NAFLD were observed in 31%, 56% and 43% of the subjects, respectively. Only 3 patients had non-alcoholic steatohepatitis (NASH) without fibrosis. Other risk factors for NAFLD such as arterial hypertension (AHT), metabolic syndrome (MS), hypertriglyceridemia and obesity were seen in 51%, 50%, 35% and 24% of the subjects, respectively. In addition, insulin resistance (IR), assessed by HOMA-IR and β-cell dysfunction, determined by HOMA-β, were observed in 16% and 94% of the patients, respectively. Occurrence of NODAT was associated with male gender, higher waist circumference, higher HOMA-IR and lower HOMA-β values. No correlation was found between NAFLD and NODAT, MS, hypertriglyceridemia, obesity and HOMAIR and HOMA-β levels.NODAT, recurrent and de novo NAFLD are common after LT but are not associated with signs of graft dysfunction, possibly due to the low frequency of IR and NASH. No correlation is observed between NAFLD and NODAT, MS, hypertriglyceridemia, obesity and IR. β-cell dysfunction and diabetes, however, are seen in most of the patients, possibly due to calcineurin inhibitor toxicity.
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