"TAKE TIME" Pioglitazone Reverses Defects in Mitochondrial Biogenesis in Patients With T2DM

Pennington Biomedical Research Center

Status and phase

Completed

Phase 4

Conditions

Diabetes Mellitus, Type 2

Treatments

Drug: Pioglitazone

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00402012

PBRC 26027

Details and patient eligibility

About

This study is designed to look at the effect of Pioglitazone treatment on the body's ability to burn food in order to produce energy.

Full description

Skeletal muscle mitochondrial defects are a sine qua non of insulin resistance in patients with T2DM. Pioglitazone decreases free fatty acid levels and restores mitochondria number in adipose tissue whereas high fat diet and lipid infusion decreases genes involved in mitochondrial biogenesis. Increased lipid flux from diet or adipose tissue into skeletal muscle might be the cause of decreased mitochondrial biogenesis. The purpose of this study is to determine if 22 weeks treatment with Pioglitazone can increase mitochondrial biogenesis in muscle in 30 uncomplicated T2DM patients that were previously not taking TZD's. This Phase IV, randomized, double-blind, placebo controlled, clinical trial will consist of 3 phases: a screening, a placebo / Pioglitazone phase (12 weeks) and a weight loss period (6-10 weeks). The primary endpoint is to identify the changes in skeletal muscle mitochondria number and gene expression. Secondary endpoints include MRS measured mitochondrial capacity, insulin sensitivity for glucose disposal and insulin suppression of free fatty acids, electron transport chain activity, mitochondrial content and intra hepatic and intra myocellular lipid. Metformin and Sulfonylurea will be used as standardized oral therapy to maintain HbA1C < 7.0. After completing the protocol, patients will be offered a very low calorie liquid diet (800kcal/d) to assist them in losing weight. During this period they will continue on their previously randomized treatment. When patients lose 10% of their body weight, patients will be switched to a weight maintenance diet (meal replacement with 1 can of glucerna at breakfast and lunch with a "healthy" dinner) for 10 days. MRS measured mitochondrial capacity will again be determined to see if weight loss + pioglitazone has more effect on mitochondrial function than pioglitazone alone.

Enrollment

24 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Men and women aged 18-70 with Type 2 diabetes as defined by:
- Fasting plasma glucose > 126 mg/dL at entry
- Or a two-hour OGTT glucose > 200mg/dL
- Or current treatment with one or two oral anti-diabetic drugs, except TZD
- Or currently using insulin
Fasting plasma glucose < 200mg/dL at entry
BMI >27.0 and <45.0kg/m2
Adequate contraception for women (including, but not limited to: oral contraception, hysterectomy, tubal ligation, or post-menopausal as defined by > 6 months without a menstrual cycle and FSH > 40 mIU/ml).

Exclusion criteria

Significant renal, cardiac, liver, lung, or neurological disease (controlled hypertension is acceptable if baseline bp < 140/90 on medications).
Prior use of other thiazolidinediones (rosiglitazone [AVANDIATM], pioglitazone [ACTOSTM])
Use of drugs known to affect energy metabolism or body weight: including, but not limited to: orlistat, sibutramine, ephedrine, phenylpropanolamine, corticosterone, etc.
Pregnancy
Alcohol or other drug abuse
Unwilling or unable to abstain from caffeine (48h) and tobacco (24h) prior to metabolic rate measurements
Increased liver function tests at baseline (AST/ALT/GGT/or alkaline phosphatase greater than 2.5 times the upper limit of normal)
Metal objects that would interfere with the measurement of body composition /MRS such as implanted rods, surgical clips, etc.
HbA1C of > 10%.
NYHA class III/IV CHF is an exclusionary cardiac condition.
history of deep vein thrombosis (DVT) or pulmonary embolism (PE)
varicose veins
major surgery on the abdomen, pelvis, or lower extremities within previous 3 months
cancer (active malignancy with or without concurrent chemotherapy)
rheumatoid disease
bypass graft in limb
known genetic factor (Factor V Leiden, etc) or hypercoagulable state
diagnosed peripheral arterial or vascular disease, or intermittent claudication
family history of primary DVT or PE (pulmonary embolism)
peripheral neuropathy