SFEBES2008 Poster Presentations Thyroid (68 abstracts)
1Royal Victoria Infirmary, Newcastle, UK; 2Freeman Hospital, Newcastle, UK.
Thyroid eye disease is the most frequent extrathyroidal manifestation of Graves disease. Severe and active disease is frequently treated with immunosuppressive therapy. IV methylprednisolone (500 mg daily for 3 days) is the treatment of choice with efficacy rates of up to 77%. New onset glucose intolerance/diabetes is the most relevant side effect of this treatment. We investigated the risk of steroid induced diabetes and the risk factors for its development.
Aims: To quantify the risk of developing impaired glucose tolerance/diabetes as a consequence of IV methyl prednisolone therapy.
To look at factors predisposing to an increased risk of developing diabetes.
Methods: Retrospective analysis of case notes of patients attending Thyroid eye clinic (19982007).
Pathology reports used to inform glucose values checked before treatment commencement and after each dose.
Definitions: Impaired glucose tolerance (IGT): >7.8 mmol/l: <11.1 mmol/l.
Diabetes mellitus: >11.1 mmol/l.
Results: Eighty-seven courses of treatment with IV methyl predisolone were received by forty-five patients of whom twenty-four patients (51.1%) had abnormal glucose values. Fourteen patients (31.1%) had values >11.1 mmol/l and 10 patients (22.2%) had values >7.8 but <11.1 mmol/l. Of the thirty-three patients with no family history or prior diagnosis of diabetes, 16 patients showed glucose intolerance with 9 patients (27.2%) showing IGT (>7.8<11.1 mmol/l) and 7 patients (21.2%) demonstrating diabetes (>11.1 mmol/l).
A family history of diabetes in a first-degree relative was identified in seven patients of which three patients (42.8%) developed diabetes during treatment. Four patients already had type 2 diabetes and one patient had type 1 diabetes.
Conclusions: The risk of developing diabetes with Methylprednisolone in a patient cohort with no family history of diabetes is 21.2%. A positive family history of diabetes increases this risk to 42.8% and so this subgroup merits careful follow up during treatment.