Effects of metformin on glucose metabolism and mitochondrial function in patients with obstructive sleep apnea: A pilot randomized trial

Author:

Zunica Elizabeth R. M.1ORCID,Heintz Elizabeth C.1,Dantas Wagner S.1,Hebert R. Caitlin2,Tanksley MaKayla3,Beyl Robbie A.1,Mader Edward C.4,Kirwan John P.1ORCID,Axelrod Christopher L.1,Singh Prachi3ORCID

Affiliation:

1. Integrated Physiology and Molecular Medicine Laboratory Pennington Biomedical Research Center Baton Rouge Louisiana USA

2. Translational Physiology Laboratory Pennington Biomedical Research Center Baton Rouge Louisiana USA

3. Sleep and Cardiometabolic Health Laboratory Pennington Biomedical Research Center Baton Rouge Louisiana USA

4. Louisiana State University Health Science Center New Orleans Louisiana USA

Abstract

AbstractObstructive sleep apnea (OSA) is associated with increased risk for diabetes, and standard treatment with positive airway pressure (PAP) device shows inconsistent effects on glucose metabolism. Metformin is known to treat and prevent diabetes, but its effects on skeletal muscle mitochondrial function are not completely understood. Here, we evaluate the effects of metformin on glucose metabolism and skeletal muscle mitochondrial function in patients with OSA. Sixteen adults with obesity (50.9 ± 6.7 years, BMI: 36.5 ± 2.9 kg/m2) and moderate‐to‐severe OSA were provided with PAP treatment and randomized to 3 months of placebo (n = 8) or metformin (n = 8) treatment in a double‐blind parallel‐group design. Whole body glucose metabolism was determined by oral glucose tolerance test. A skeletal muscle biopsy was obtained to evaluate mitochondrial respiratory capacity and expression of proteins related to mitochondrial dynamics and energy metabolism. Whole body insulin‐sensitivity (Matsuda index) did not change in metformin or placebo treated groups. However, metformin treatment prevented increases in insulin release relative to placebo during follow‐up. Insulin area under the curve (AUC) and insulin to glucose AUC ratio increased in placebo but remained unchanged with metformin. Furthermore, metformin treatment improved skeletal muscle mitochondrial respiratory capacity and dynamics relative to placebo. Metformin treatment prevented the decline in whole body glucose homeostasis and skeletal muscle mitochondrial function in patients with moderate to severe OSA. Patients with OSA may benefit from the addition of metformin to prevent diabetes.

Funder

National Institutes of Health

Publisher

Wiley

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