N-3 Polyunsaturated Fatty Acids to Prevent and Treat Diabetic Neuropathy
- Conditions
- Diabetic Neuropathies
- Interventions
- Dietary Supplement: Fish-oil derived n-3 polyunsaturated fatty acids
- Registration Number
- NCT05145452
- Lead Sponsor
- University of Missouri-Columbia
- Brief Summary
Sensorimotor neuropathy (SMN) and cardiovascular autonomic neuropathy (CAN) are the most common complications of type 2 diabetes (T2D). SMN affects \~30% of people with T2D and CAN \~20%. SMN causes pain, impairs and limits physical activity, and increases the risk for physical disability, complications (such as foot ulcerations), and premature mortality. Moreover, both motor and sensory nerve function are important regulators of muscle function; impaired myofiber innervation causes myofiber loss, muscle fat infiltration, and increases the risk of age-associated sarcopenia and falls. CAN often goes unrecognized because it presents with non-specific symptoms, such as resting tachycardia and fixed heart rate, exercise intolerance, and orthostatic hypotension. However, CAN is a serious problem because it increases the risk for cardiovascular events and mortality several-fold. Both SMN and CAN have long been considered a consequence of T2D, but it is now becoming clear that they precede the diagnosis of T2D and are already detectable in people with prediabetes, especially those with impaired glucose tolerance. Treatments for both SMN and CAN focus on symptom management because there are no effective therapeutics that target the underlying neuropathy. The results from studies conducted in animal models suggest fish oil-derived n-3 polyunsaturated fatty acids (n-3 PUFA) may have therapeutic effects for people with SMN and CAN. The purpose of this proposal is to conduct a randomized controlled trial to test the hypothesis that dietary supplementation with fish oil-derived n-3 PUFA improves sensorimotor and cardiovascular autonomic functions in people with impaired glucose tolerance. Forty 55-80 year old men and women with impaired glucose tolerance (plasma glucose 2 h after a 75 g glucose challenge ≥140 mg/dl) and evidence of SMN (assessed as epidermal nerve fiber density) will be randomized to either receive fish oil-derived n-3 PUFA (4.2 g per day; n=20) or placebo (n=20) for six months. Sensorimotor and cardiovascular autonomic function will be evaluated after three and 6 months of the interventions.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- SUSPENDED
- Sex
- All
- Target Recruitment
- 60
- age: ≥55 and ≤80 years
- BMI: ≥25.0 and ≤39.9 kg/m2;
- normal plasma glucose (fasting plasma glucose <100 mg/dl and plasma glucose 2 h after a 75 g glucose challenge <140 mg/dl) for the control group and impaired fasting plasma glucose (≥100 mg/dl) or impaired glucose tolerance (plasma glucose 2 h after a 75 g glucose challenge ≥140 mg/dl) or both for the intervention groups
- age: <55 and >80 years
- BMI: <25.0 and >39.9 kg/m2
- fasting plasma glucose ≥100 mg/dl or plasma glucose 2 h after a 75 g glucose challenge ≥140 mg/dl for the control group and normal plasma glucose (fasting plasma glucose <100 mg/dl, plasma glucose at 2 h after 75 g glucose ingestion <140 mg/dl) for the intervention groups
- treatment for T2D, except for metformin
- regular structured high-intensity exercise >150 min total per week
- significant neurological or other organ system dysfunction (e.g., progressive neuromuscular disease, unstable angina, vasculitis, certain cardiopulmonary diseases, cancer that has been in remission for <5 years, dementia, allergies to the dietary supplement) or significant ambulatory impairments (e.g., limb amputations, being wheelchair-bound)
- use of certain medications that are incompatible with the study procedures (e.g., certain anticoagulants) or could confound the study outcomes (e.g., anabolic steroids, metronidazole, etc) alcohol use disorder as defined by the NIAAA or use of controlled substances or smoking >20 cigarettes per week
- regular consumption of fish oil supplements or >2 servings of fatty fish per week
- x) prisoners, and persons who are unable to grant voluntary informed consent.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Placebo Group Fish-oil derived n-3 polyunsaturated fatty acids Subjects randomized to placebo will receive 4.2 g/d sunflower oil. Intervention Group Fish-oil derived n-3 polyunsaturated fatty acids Subjects randomized to n-3 PUFA will receive a total of 4.2 g/d of fish oil.
- Primary Outcome Measures
Name Time Method Sensorimotor function Change from baseline to 6 months Nerve conduction velocity
Cardiovascular autonomic function Change from baseline to 6 months Heart rate variability
Muscle endurance Change from baseline to 6 months Decline in torque during repeat muscle contraction
- Secondary Outcome Measures
Name Time Method Glucose tolerance Change from baseline to 6 months Glucose tolerance (plasma glucose concentration during a 75 gram glucose tolerance test)
Beta cell function Change from baseline to 6 months Insulin secretion rate
Insulin sensitivity Change from baseline to 6 months Oral insulin sensitivity index
Plasma triglyceride concentration Change from baseline to 6 months Plasma triglyceride concentration
Physical performance Change from baseline to 6 months Physical performance test
Muscle strength Change from baseline to 6 months Muscle strength
Trial Locations
- Locations (2)
Washington University
🇺🇸Saint Louis, Missouri, United States
Washington University School of Medicine
🇺🇸St. Louis, Missouri, United States