4.7 Article

Extreme Variations in Muscle Fiber Composition Enable Detection of Insulin Resistance and Excessive Insulin Secretion

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 107, Issue 7, Pages E2729-E2737

Publisher

ENDOCRINE SOC
DOI: 10.1210/clinem/dgac221

Keywords

insulin; insulin resistance; insulin secretion; intravenous glucose tolerance test; mitochondrial respiration; muscle fiber type

Funding

  1. Ake Wibergs Stiftelse [M20-0230]

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Muscle fiber composition differences are associated with alterations in peripheral insulin action and secretion, which can be used to predict insulin resistance and glucose-stimulated insulin secretion.
Context: Muscle fiber composition is associated with peripheral insulin action. Objective: We investigated whether extreme differences in muscle fiber composition are associated with alterations in peripheral insulin action and secretion in young, healthy subjects who exhibit normal fasting glycemia and insulinemia. Methods: Relaxation time following a tetanic contraction was used to identify subjects with a high or low expression of type I muscle fibers: group 1 (n = 11), area occupied by type I muscle fibers = 61.0 +/- 11.8%, and group 2 (n = 8), type I area = 36.0 +/- 4.9% (P < 0.001). Biopsies were obtained from the vastus lateralis muscle and analyzed for mitochondrial respiration on permeabilized fibers, muscle fiber composition, and capillary density. An intravenous glucose tolerance test was performed and indices of glucose tolerance, insulin sensitivity, and secretion were determined. Results: Glucose tolerance was similar between groups, whereas whole-body insulin sensitivity was decreased by similar to 50% in group 2 vs group 1 (P = 0.019). First-phase insulin release (area under the insulin curve during 10 minutes after glucose infusion) was increased by almost 4-fold in group 2 vs group 1 (P = 0.01). Whole-body insulin sensitivity was correlated with percentage area occupied by type I fibers (r = 0.54; P= 0.018) and capillary density in muscle (r = 0.61; P = 0.005) but not with mitochondrial respiration. Insulin release was strongly related to percentage area occupied by type II fibers (r = 0.93; P < 0.001). Conclusions: Assessment of muscle contractile function in young healthy subjects may prove useful in identifying individuals with insulin resistance and enhanced glucose-stimulated insulin secretion prior to onset of clinical manifestations.

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