Exp Clin Endocrinol Diabetes 2000; Vol. 108(5): 347-352
DOI: 10.1055/s-2000-8127
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© Johann Ambrosius Barth

Diabetes mellitus and islet cell specific autoimmunity as adverse effects of immunsuppressive therapy by FK506/Tacrolimus

T. Lohmann 1 , C. List 1 , P. Lamesch 2 , K. Kohlhaw 2 , M. Wenzke 2 , C. Schwarz 2 , O. Richter 2 , J. Hauss 2 , J. Seissler 3
  • 1 Department of Internal Medicine III, and 2 Department of Surgery II, University of Leipzig, Germany; 3 Diabetes Research Institute, University of Duesseldorf, Germany
Further Information

Publication History

Publication Date:
31 December 2000 (online)

Summary:

The induction of diabetes has been recognised as adverse effect of the immunsuppressive drug FK506/Tacrolimus. The aim of this study was to clarify whether insulinopenia or insulin resistance dominates and whether islet cell autoantibodies are present in patients treated by FK506. We investigated 58 patients 1-3 years after liver transplantation while under therapy with FK506 or CsA and prednisolone (0-7.5 mg) for basal blood glucose levels and islet-cell specific autoantibodies. A subgroup of 20 patients on FK506, 10 patients on cyclosporin and 15 healthy volunteers were metabolically tested by oGTT. Five patients had diabetes pre-transplantation. After transplantation, 9/28 FK506-treated patients developed newly diagnosed diabetes compared to 0/25 cyclosporin-treated patients (p < 0.01). Both patient groups showed significantly higher fasting blood glucose, insulin or C-peptide levels compared to controls. Through the oGTT, FK506-treated patients without diabetes, but not cyclosporin-treated patients, had higher C-peptide levels compared to controls (p < 0.05). Five/32 patients on FK506 compared to 0/26 patients on cyclosporin (p < 0.05) had islet cell specific autoantibodies, mainly ICA without GAD- or IA2-Ab, a feature described for latent autoimmune diabetes in adults. ICA positivity was correlated to the diabetes associated HLA haplotype DR4/DQ*0302 (p < 0.05). Although the interpretation of our metabolic data in patients with concomitant liver disease and prednisolone therapy has limitations, we suggest insulin resistance caused by treatment with FK506. However, manifestation of diabetes was associated with relative insulinopenia rather than insulin resistance in patients on FK506. Immunsuppressive therapy by FK506 was not able to suppress islet cell autoimmunity, and may even induce it in genetically predisposed patients.

Abbreviations: Ab antibodies; CsA Cyclosporine A; ICA islet cell antibodies; IGT impaired glucose tolerance; IRI immunreactive insulin; NGT normal glucose tolerance; oGTT oral glucose tolerance test; Tx transplantation

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Dr. T. Lohmann

Department of Internal Medicine III

University of Leipzig

Philipp-Rosenthal-Str. 27

D-04103 Leipzig

Germany

Phone: +49-3 41-9 71 32 00

Fax: +49-3 41-9 71 33 39

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