Metformin, Muscle Energetics, and Vascular Function in Older Adults With Peripheral Artery Disease

Peripheral Artery Disease Clinical Trial

Official title:

Metformin, Muscle Energetics, and Vascular Function in Older Adults With Peripheral Artery Disease

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01901224
• Other study ID #: 2013P001042
• Status: Terminated
• Phase: Phase 4
• Start date: July 2013
• Est. completion date: June 2015

Study information

• Verified date: September 2018
• Source: Brigham and Women's Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators are doing this research study to find out if taking Metformin improves walking ability in patients with peripheral arterial disease (PAD). In PAD the arteries (blood vessels) in the legs are narrowed because of the build up of plaque. The leg muscle can hurt in patients with PAD and this is usually described as a cramp or tiredness. This pain is called intermittent claudication. Metformin is an FDA approved medication for the treatment of diabetes. The investigators believe that Metformin may help your leg muscles work better.

The investigators will enroll up to 100 subjects in order to find 60 subjects with PAD at Brigham and Women's Hospital (BWH).

Description:

Peripheral artery disease (PAD) is a manifestation of atherosclerosis that affects more than 7 million adults in the US. The prevalence of PAD increases with age and is estimated to be 15 20% among individuals 65 years of age and older. Patients with PAD have limited functional capacity; they walk more slowly and have less walking endurance than persons who do not have PAD, irrespective of whether they have classic symptoms of intermittent claudication or critical limb ischemia. This functional impairment adversely affects quality of life. Although flow limitation due to atherosclerotic stenosis is necessary for the development of symptoms in PAD, the lack of correlation between walking capacity and the degree of hemodynamic compromise raises the possibility that alternative mechanisms contribute to functional limitations in these patients. Putative mechanisms include inadequate skeletal muscle glucose uptake, altered skeletal muscle energetics, and impaired vasomotor tone and nutrient delivery mediated by endothelial dysfunction. Metformin, via AMPactivated protein kinase (AMPK)-dependent and independent mechanisms, can favorably affect skeletal muscle metabolic functions including glucose uptake, fatty acid oxidation, mitochondrial function, and consequently cellular energetics, and it also may have a direct salutary effect on vascular function via regulation of nitric oxide synthase. It is intriguing, therefore, to consider the possibility that metformin would improve skeletal muscle metabolic and vascular function in older patients with PAD and translate into functional benefits. Accordingly, the investigators seek to elucidate molecular mechanisms through which metformin affects skeletal muscle energetics and hypothesize that metformin will lead to advantageous metabolic, vascular, and physical functional changes in older patients with PAD.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 2
• Est. completion date: June 2015
• Est. primary completion date: June 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years and older

Eligibility

Inclusion Criteria:

• Age 40 years or greater

• Intermittent claudication for 6 months or greater

• Maximal walk time between 1-20 minutes on all ETTs

• Resting ABI = 0.9 in index leg at baseline

• ABI falls = 20% in index leg 1 minute post baseline ETT

• MWT variability < 20%

Exclusion Criteria:

• Type 1 or Type 2 Diabetes

• Limb-threatening ischemia (rest pain, ulceration, gangrene)

• Peripheral vascular surgery or PCI within 6 months

• MI or CABG within 6 months

• Carotid endarterectomy (CEA) within 6 months

• Cerebrovascular accident or TIA within 6 months

• Uncontrolled hypertension (SBP > 140 mmHg, DBP >90 mmHg)

• Pentoxifylline/Cilostazol added/changed within 3 months

• HMG-CoA reductase inhibitor added/changed within 3 months

• Exercise limitations other than claudication (heart failure, angina, COPD, arthritis, neuropathy, etc.)

• Serum creatinine = 1.5 mg/dL

• Pregnant or plans to become pregnant

• 2 hour Oral Glucose Tolerance Test (OGTT) > 200 mg/dL

Related Conditions & MeSH terms

• Peripheral Arterial Disease
• Peripheral Artery Disease

Intervention

Drug:
• Metformin 1000 mg

• Placebo

Locations

Country	Name	City	State
United States	Brigham and Women's Hospital	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Brigham and Women's Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in Maximal Treadmill Walking Time	Maximal treadmill walking time is measured in minutes or seconds. Higher values indicate a better outcome.	baseline, 12 weeks
Other	Change in Pain-free Treadmill Walking Time	Pain-free treadmill walking time is measured in minutes or seconds. Higher values indicate a better outcome.	baseline, 12 weeks
Other	Change in Oxygen Consumption	Oxygen consumption is measured in ml/kg/min. Higher values indicate better outcomes.	baseline, 12 weeks
Other	Change in Six Minute Walk Test	The 6-min walk test (6 MWT) is a submaximal exercise test that entails measurement of distance walked over a span of 6 minutes.The 6 MWT is measured in meters, and higher values indicate better outcomes.	baseline, 12 weeks
Primary	Change in PCr Recovery Time	PCr recovery time, measured in seconds, is a measure of skeletal muscle metabolic function. PCr is a transport molecule and reservoir of high-energy phosphate bonds, which is important for cellular energetics. Phosphocreatine regeneration depends upon the skeletal muscle mitochondrial cells capacity for oxidative phosphorylation. We will measure PCr recovery time at baseline and after 12 weeks of treatment with metformin or placebo as an in vivo measure of mitochondrial function. Higher Pcr relative to P(i) during recovery is better and shorter recovery times are better.	baseline, 12 weeks
Secondary	Change in Flow-mediated Dilation (FMD)	Flow mediated vasodilation of the brachial artery is a measure of endothelium-dependent vasodilation. Higher flow-mediated dilation (FMD), measured as the diameter of the brachial artery in millimeters, and reported as percent change after a flow stimulus compered to basal measurement, is better, indicative of better endothelial function.	baseline, 12 weeks