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Insulin resistance in amyotrophic lateral sclerosis
Journal of the Neurological Sciences
|March 1, 1984
Summary
Patients with amyotrophic lateral sclerosis (ALS) exhibit impaired insulin sensitivity, indicating a primary carbohydrate metabolism issue. This insulin resistance in ALS is not due to reduced glucose utilization from muscle atrophy.
Area of Science:
- Neurology
- Metabolic Disorders
- Neurodegenerative Diseases
Background:
- Glucose intolerance is frequently observed in patients with amyotrophic lateral sclerosis (ALS).
- A debate exists on whether this carbohydrate abnormality is intrinsic to ALS or a consequence of reduced glucose use from muscle atrophy.
- Previous hypotheses suggested a reduced glucose receptor space in neuromuscular diseases like ALS.
Purpose of the Study:
- To investigate in vivo insulin sensitivity in patients with ALS.
- To determine if insulin resistance in ALS is related to decreased glucose receptor space or represents a primary metabolic defect.
Main Methods:
- The euglycemic insulin clamp technique was employed to assess insulin sensitivity.
- ALS patients and two control groups, matched for ideal body weight, participated in the study.
Main Results:
- The glucose infusion rate, a measure of in vivo insulin sensitivity, was significantly lower in ALS patients compared to both normal and disease controls.
- This finding indicates that insulin resistance in ALS is not explained by a reduction in glucose receptor space.
Conclusions:
- Insulin resistance is a significant finding in amyotrophic lateral sclerosis (ALS).
- The observed insulin resistance in ALS is not attributable to decreased glucose receptor space.
- Evidence suggests a primary carbohydrate metabolism abnormality is involved in the ALS disease process.