Age, Lifestyle, Muscle Mechanisms in Insulin Resistance

Not Applicable

Completed

• Conditions: Obesity; Glucose Intolerance; Exercise Capacity
• Interventions: Behavioral: Dietary counseling; Behavioral: AEX

• Registration Number: NCT00971594
• Lead Sponsor: National Institute on Aging (NIA)

Brief Summary

The purpose of this study is to investigate the mechanisms by which physical inactivity and obesity alter skeletal muscle insulin signaling to cause insulin resistance and increase the development of impaired glucose tolerance (IGT).

Detailed Description

Aging is associated with a progressive development of impaired glucose tolerance (IGT), due to an increased peripheral tissue resistance to the action of insulin. Insulin resistance, a common state in both obese and sedentary individuals, eventually leads to the development of glucose intolerance, and type 2 diabetes with aging. Even in the absence of diabetes, insulin resistance is a key feature in various metabolic abnormalities that increase the risk for developing cardiovascular disease (CVD). Previous studies demonstrate improvements in glucose tolerance and glucose utilization following moderate energy restriction coupled with moderate intensity AEX. WL, through behavioral modification of diet and aerobic exercise (AEX), is perhaps the most effective way to treat as well as prevent insulin resistance and its associated metabolic complications of IGT and type 2 diabetes. Although these studies demonstrate the beneficial effect of weight loss (WL) and AEX on glucose tolerance and insulin action, not much is known about the cellular and molecular mechanisms by which these nonpharmacologic treatments improve glucose utilization in high-risk obese older individuals.

This study seeks to determine the cellular mechanisms by which aerobic exercise and weight loss alter skeletal muscle insulin signaling to improve insulin action in older glucose intolerant individuals. A second purpose is to determine whether certain genes (hereditary information) affect the way the body utilizes glucose in response to exercise and weight loss. In addition, adipose tissue is increasingly recognized as more than an inert depot serving not only to accept and store excess energy in the form of triglycerides, but also to secrete hormones and adipokines that have substantial effects on lipid and glucose metabolism. Furthermore, there are depot differences in metabolic function, as well as adipokine content. However, the physiology both underlying and consequential to these observations remains unknown. Thus, a third aim is to examine the effects of obesity on regional adipokine secretion and expression, and the relationship of adipokines to insulin resistance and the metabolic syndrome.

Study Timeline

• Study Start: 2004-06
• Primary Completion: 2008-05
• Study Completion: 2008-05
• Status Verified: 2009-09
• Study First Submitted: 2009-09-02
• Study First Submitted QC: 2009-09-02
• Last Update Submitted: 2009-09-02
• Study First Posted: 2009-09-03
• Last Update Posted: 2009-09-03

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 15

Inclusion Criteria

• Men older than 50 yrs of age
• Non-smoking (more than 5 years)
• BMI greater than 25 kg/m2 and less than 50 kg/m2

Exclusion Criteria

• CAD, CHF, Myocardial infarction within 6 months or other symptomatic heart disease
• History of stroke, peripheral arterial disease
• Currently being treated for active cancer
• On oral agents or insulin therapy for diabetes
• Poorly controlled Dyslipidemia (abnormal concentration of lipids or lipoproteins in the blood)
• Poorly controlled hypertension (BP > 180/95)
• Other systematic disorders that are not medically treated and stable
• Physical impairment limiting normal activity and other contraindications to exercise
• Aerobically conditioned
• Abnormal response to exercise (chest pain, significant arrhythmias, extreme shortness of breath, cyanosis, exercising BP > 240/120)
• Taking warfarin/coumadin
• Taking oral steroids
• Abnormal renal function or liver function
• Chronic pulmonary disease severe enough to require oxygen
• Anemia
• MMSE < 24, dementia

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
WL+AEX	Dietary counseling	Weight loss plus aerobic exercise
WL+AEX	AEX	Weight loss plus aerobic exercise

Primary Outcome Measures

Name	Time	Method
Insulin stimulated glucose disposal	Baseline and 6 months
Content and activity of insulin signaling proteins from muscle biopsies	Baseline and 6 months
Glucose tolerance	Baseline and 6 months

Secondary Outcome Measures

Name	Time	Method
Aerobic capacity	Baseline and 6 months
Body weight/Composition	Baseline and 6 months
Cytokines	Baseline and 6 months
Other biomarkers (such as glucose, insulin etc)	Baseline and 6 months

Trial Locations

Locations (2)

Baltimore VA Medical Center; 🇺🇸 Baltimore, Maryland, United States

University of Maryland; 🇺🇸 Baltimore, Maryland, United States