Low Dose Fat-Induced Insulin Resistance

Korábbi kezelés

• Use of tobacco within the previous year
• Receiving treatment for a medical condition requiring chronic use of systemic steroids, except for the use of ≤ 5 mg prednisone daily, or an equivalent physiological dose of hydrocortisone
• Use of any investigational agents within 4 weeks of enrollment

Más betegség

• History of diabetes
• History of diabetes in more than one first-degree relative
• Presence of soy or egg allergies (due to possible reactions with fat infusate)
• Presence of a seizure disorder
• Any medical condition, which in the opinion of the investigator, will interfere with the safe completion of the study
• History of pancreatitis
• Presence of a metal allergy (aluminum)

Laborértékek

• HbA1c \>5.7%
• Baseline hemoglobin concentration \< 11 g/dl in women and \< 12 g/dl in men
• Estimated glomerular filtration rate \< 55 ml/min/1.73 m2 (calculated using the subject's measured serum creatinine and the Modification of Diet in Renal Disease \[MDRD\] study estimation formula).
• Severe co-existing cardiac disease, characterized by any one of these conditions:
  • history of myocardial infarction within past 6 months;
  • history of ischemia on functional cardiac exam within the last year;
  • history of left ventricular ejection fraction \< 30%.
• Hyperlipidemia (fasting LDL cholesterol \> 130 mg/dl, treated or untreated; and/or fasting triglycerides \> 200 mg/dl)

Egyéb

• Body mass index (BMI) \<19 or \>27 kg/m2
• Blood Pressure: systolic \>160 mmHg or diastolic \> 100 mmHg
• For female participants: Positive pregnancy test, presently breast-feeding, or unwillingness to use effective contraceptive measures for the duration of the study. Oral contraceptives, Norplant®, Depo-Provera®, and barrier devices with spermicide are acceptable contraceptive methods; condoms used alone are not acceptable.
• Known active alcohol or substance abuse
• Persistent elevation of liver function tests \> 1.5 times normal upper limits

• Subjects who are able to provide written informed consent and to comply with the procedures of the study protocol