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Beneficial Effect of Salicylates: Insulin Action, Secretion or Clearance?

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Stanford University

Status

Completed

Conditions

Insulin Resistant
Pre Diabetes

Treatments

Drug: salsalate
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The possibility that obesity-associated inflammatory changes may play a role in the pathogenesis of type 2 diabetes (2DM) has led to increased interest in the possibility that salicylates might represent a useful treatment to improve glucose tolerance. Several studies, performed in patients with 2DM, as well as in nondiabetic, obese individuals, have demonstrated that salicylates have beneficial effects on glucose and insulin metabolism, but have not led to a coherent view as to the mechanism(s) involved.

In this research proposal we will use specific methods to quantify insulin mediated glucose uptake (IMGU), glucose-stimulated insulin secretion rate (GS-ISR), and insulin clearance (I-Cl) in overweight/obese, nondiabetic, insulin resistant individuals. We will use the insulin suppression test (IST) to quantify IMGU in nondiabetic, overweight/obese volunteers to identify those individuals who are sufficiently insulin resistant to be enrolled in this study. We will then use the graded glucose infusion technique in these insulin resistant subjects to generate specific measures of both GS-IS and I-Cl. Following these baseline measurements, salsalate or placebo will be administered for one month to the participants, after which time the IST and the graded glucose infusion will be repeated to quantify and compare the changes in IMGU, GS-ISR, and I-Cl that have resulted from salsalate versus placebo. These results will provide for the first time quantitative data of the effect of salicylates on IMGU, GS-ISR, and I-Cl in overweight/obese, insulin resistant, nondiabetic individuals.

Enrollment

41 patients

Sex

All

Ages

30 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy volunteers,
  • BMI 25-35kg/m2,
  • Without severe anemia, kidney, liver disease or any current GI ulcers or bleeding
  • Or on any medication contraindicated with salsalate

Exclusion criteria

  • Recent history of GI bleed or ulcers,
  • CVD or on anticoagulants
  • Severe kidney or liver disease
  • Allergies to aspirin
  • Taking aspirin or anti inflammatory medication on a regular basis and cannot be taken off for the duration of the study

Trial design

41 participants in 2 patient groups, including a placebo group

salsalate 3500mg in 2 divided doses a day
Active Comparator group
Description:
Participants will take 3, 500 mg tablets with breakfast and 4, 500 mg tablets with dinner
Treatment:
Drug: salsalate
placebo
Placebo Comparator group
Description:
Participants will take 3 placebo tablets with breakfast and 4 placebo tablets with dinner
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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