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The Impact of Actos Treatment of Diabetes on Glucose Transporters in Muscle

Phase 4
Completed
Conditions
Diabetes Type 2
Interventions
Drug: placebo
Registration Number
NCT01799850
Lead Sponsor
East Tennessee State University
Brief Summary

Subjects with type 2 diabetes will be treated with Actos or placebo for eight weeks and needle biopsies of muscle will quantify changes in any of seven different glucose transport proteins in muscle.

Detailed Description

Twelve subjects with type 2 diabetes, with fair control on oral medication, will be recruited to participate in a randomized, double-blind, placebo-controlled study of the impact on muscle glucose transporter expression of the addition of the insulin-sensitizing agent, pioglitizone (Takeda Pharmaceuticals). Therapy with the active drug will be at 30 mg daily. The other oral medications will be adjusted downward if hypoglycemia occurs. Glycemic control will be monitored by at least twice daily home blood glucose monitoring, weekly telephone contacts, and follow-up visits to the ETSU/VAMC Clinical Research Unit (CRU) every two weeks. During the eight weeks of therapy, subjects will be instructed to maintain their weight and keep their dietary and exercise regimens unchanged. Muscle biopsies will be obtained before and at the end of eight weeks of therapy. Specimens will be assayed for GLUT1, GLUT3, GLUT4, GLUT5, GLUT8, GLUT11, and GLUT12 mRNA and protein content and the subcellular distribution of these proteins as described below. Peroxisome proliferator-activated receptor gamma (PPARgamma), a member of the ligand-activated nuclear hormone receptor superfamily (14), will be quantified in these specimens by immunoblot as described below.

This study design involving a randomized, double-blinded, placebo-controlled treatment regimen is needed to control for confounding variables causing changes in glucose transporter expression that may be erroneously attributed to the drug. These potential variables include close contact with the diabetes management team resulting in improved compliance with diet, exercise, medication, and monitoring and thus better glycemic control, weight loss, or improved fitness.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria
  • diabetes, type 2
  • HbA1c less than 8.5
Exclusion Criteria
  • insulin therapy
  • renal insufficiency
  • clinically apparent coronary disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
ActosPioglitazoneActos 30 mg daily
placeboplacebodouble blind placebo controlled
Primary Outcome Measures
NameTimeMethod
change in muscle glucose transporter expressionpost eight weeks treatment

immunoblots pre and post, placebo and Actos

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

ETSU Quillen College of Medicine

🇺🇸

Johnson City, Tennessee, United States

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