Sitagliptin Prophylaxis for Glucocorticoid-Induced Impairment of Glucose Metabolism in Males With the Metabolic Syndrome (SPHINX)

Amsterdam UMC, location VUmc

Status: Completed

Conditions: Diabetes Mellitus; Glucocorticoid-induced Diabetes; Steroid Diabetes; Beta-cell Function

Treatments: Drug: Sitagliptin-placebo; Drug: Sitagliptin 100 mg; Drug: Prednisolone-placebo; Drug: Prednisolone 30 mg

Study type: Interventional

Funder types: Other

Identifiers

NCT00721552

DC2008Pred002

Eudract 2008-004985-25

Details and patient eligibility

About

The investigators will assess whether the DPP-inhibitor sitagliptin will ameliorate glucocorticoid-induced impairment of glucose metabolism and beta-cell dysfunction and thus could be used as a prophylaxis for glucocorticoid-induced diabetes. Therefore the investigators will administer in males with the metabolic syndrome 30 mg prednisolone daily for two weeks and give simultaneously sitagliptin 100 mg daily. Subjects will undergo at baseline and after two weeks of treatment several tests to assess changes in glucose metabolism.

Full description

The investigators will conduct a randomized, placebo-controlled, double-blind, 2x2 factorial-designed intervention trial. The pharmacological intervention for prednisolone/prednisolone-placebo is 14 days and for sitagliptin/sitagliptin-placebo 28 days. Subjects fulfilling the IDF criteria26 for the metabolic syndrome (aged 35-65; n=60) will be randomized to one of four groups: I) prednisolone 30 mg and sitagliptin 100 mg daily; II) prednisolone 30 mg and sitagliptin-placebo daily; III) prednisolone-placebo and sitagliptin 100 mg daily; IV) prednisolone-placebo and sitagliptin-placebo daily. Before and at day 14 of treatment subjects will undergo a standardized mixed-meal test in order to assess glucose disposal and beta-cell function (by modeling analysis). During these meal tests, plasma concentrations of (total and active) GLP-1, GIP, glucagon and additional biomarkers will be assessed. A combined hyperglycemic-euglycemic clamp will be performed at baseline and at day 13 of treatment to assess insulin sensitivity and insulin secretion. During the euglycemic clamp adipose tissue and muscle biopsies will be obtained, both in fasting and under hyperinsulinemic conditions. At baseline and at day 28 of treatment, a 7-point OGTT will be performed to assess time to restoration of glycemic control. Body composition, body fat distribution and liver fat content, measured by respectively bio-impedance analysis and magnetic resonance imaging/spectroscopy (MRI/MRS), will be assessed at baseline and after 28 days of treatment. Blood pressure will be assessed at baseline and after two weeks of treatment. Microvascular function will be assessed with capillary videomicroscopy both at baseline and after two weeks of treatment.

Enrollment: 82 patients

Sex: Male

Ages: 35 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Caucasian males

• Modified from IDF criteria for the metabolic syndrome:

  • Waist circumference ≥ 94 cm

• And at least 2 or more of the following criteria:

  • TG ≥ 1.7 mmol/L
  • HDL cholesterol < 1.03 mmol/L
  • Blood pressure >130/85 mmHg (average of three measurements) or treatment of previously diagnosed hypertension
  • Fasting plasma glucose level (FPG) ≥ 5.6 mmol/L (but no diabetes)

Exclusion criteria

• An allergic or anaphylactic reaction to prednisolone treatment in the past
• Clinically relevant history or presence of any medical disorder, which are mentioned in the Summary of Product Characteristics (SPC) as contraindication for the use of prednisolone
• Glucocorticosteroid use during the last three months prior to the first dose
• Participation in an investigational drug trial within 90 days prior to the first dose
• Donation of blood ( > 100 mL) within 90 days prior to the first dose
• History of or current abuse of drugs or alcohol (>14 U/week)
• Use of grapefruit products during the study period
• Recent changes in weight and/or physical activity
• Serious mental impairment or language problems i.e. preventing to understand the study protocol/aim
• Diabetes mellitus (defined as FPG ≥ 7.0 mmol/l and/or 2hPG ≥ 11.1 mmol/l)
• Serious pulmonary, cardiovascular, hepatic (ALT, AST more than 3x ULN) or renal disease (serum creatinine > 135 micromol/L)
• History of cardiovascular disease, such as myocardial infarction, cerebrovascular accident.
• Major psychiatric disorder, depression
• All diseases that induce changes in the hypothalamic-pituitary-adrenal (HPA) axis
• Malignant disease
• All other relevant medical disorders that potentially interfere with this trial.
• All medication interfering with study drug or interfering with study endpoints/hypotheses

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Factorial Assignment

Masking: Triple Blind

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82 participants in 6 patient groups, including a placebo group

I

Experimental group

Description:

prednisolone + sitagliptin

Treatment:

Drug: Prednisolone 30 mg

Drug: Sitagliptin 100 mg

II

Experimental group

Description:

prednisolone + sitagliptin-placebo

Treatment:

Drug: Prednisolone 30 mg

Drug: Sitagliptin-placebo

III

Experimental group

Description:

prednisolone-placebo + sitagliptin

Treatment:

Drug: Sitagliptin 100 mg

Drug: Prednisolone-placebo

IV

Placebo Comparator group

Description:

prednisolone-placebo + sitagliptin-placebo

Treatment:

Drug: Sitagliptin-placebo

Drug: Prednisolone-placebo

Healthy controls

No Intervention group

Description:

12 healthy men will be included to assess postprandial microvascular function.

Type 2 diabetic subjects

No Intervention group

Description:

12 men with type 2 diabetes will be included in order to assess postprandial microvascular function.