Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy

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Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy. / Rue, Nana; Vissing, John; Galbo, Henrik.

In: Journal of Clinical Endocrinology and Metabolism, Vol. 99, No. 10, 2014, p. 3757-3765.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rue, N, Vissing, J & Galbo, H 2014, 'Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy', Journal of Clinical Endocrinology and Metabolism, vol. 99, no. 10, pp. 3757-3765. https://doi.org/10.1210/jc.2014-1831

APA

Rue, N., Vissing, J., & Galbo, H. (2014). Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy. Journal of Clinical Endocrinology and Metabolism, 99(10), 3757-3765. https://doi.org/10.1210/jc.2014-1831

Vancouver

Rue N, Vissing J, Galbo H. Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy. Journal of Clinical Endocrinology and Metabolism. 2014;99(10):3757-3765. https://doi.org/10.1210/jc.2014-1831

Author

Rue, Nana ; Vissing, John ; Galbo, Henrik. / Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy. In: Journal of Clinical Endocrinology and Metabolism. 2014 ; Vol. 99, No. 10. pp. 3757-3765.

Bibtex

@article{3c79a3b1dbf0489ea9d466b4dbbde4db,
title = "Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy",
abstract = "CONTEXT: Mitochondrial dysfunction has been proposed to cause insulin resistance and that might stimulate cytokine production.OBJECTIVE: The objective of the study was to elucidate the association between mitochondrial myopathy, insulin sensitivity, and cytokine levels in muscle.DESIGN AND SETTING: This was an experimental, controlled study in outpatients.PARTICIPANTS: Eight overnight-fasted patients (P) with various inherited mitochondrial myopathies and eight healthy subjects (C) matched for sex, age, weight, height, and physical activity participated in the study.INTERVENTIONS: The intervention included a 120-minute hyperinsulinemic, euglycemic clamp. Another morning, microdialysis of both vastus lateralis muscles for 4 hours, including one-legged, knee extension exercise for 30 minutes, was performed.MAIN OUTCOME MEASURES: Glucose infusion rate during 90-120 minutes of insulin infusion was measured. Cytokine concentrations in dialysate were also measured.RESULTS: Muscle strength, percentage fat mass, and creatine kinase in plasma did not differ between groups. The maximal oxygen uptake was 21 ± 3 (SE) (P) and 36 ± 3(C) mL/kg·min (2P < .05). Basal insulin, C-peptide, and glucagon were higher in P (55 ± 10, 980 ± 92, and 102 ± 13 pM) than in C (36 ± 12, 712 ± 98, and 44 ± 10 pM) (two-sided significance testing [2P ]< .05). The homeostasis model assessment insulin sensitivity index and glucose infusion rate (6.8 ± 1.0 vs 9.4 ± 1.3 mg/min·kg) were lower, and free fatty acids and glycerol at 120 minutes were higher in P vs C (2P < .05). Dialysate concentrations of TNF-α, IL-6, IL-8, IL-10, and monocyte chemoattractant protein-1 were higher in P vs C (2P < .05). Dialysate concentrations of these cytokines and of IL-1 receptor antagonist increased during exercise (2P < .05), identically in P and C. No differences existed in plasma cytokine concentrations.CONCLUSIONS: In patients with a variety of mitochondrial myopathies, insulin sensitivity of muscle, adipose tissue, and pancreatic A cells is reduced, supporting that mitochondrial function influences insulin action. Furthermore, a local, low-grade inflammation of potential clinical importance exists in the muscle of these patients.",
keywords = "Adipose Tissue, Adult, Chemokine CCL2, Cytokines, Exercise, Female, Glucagon-Secreting Cells, Glucose Clamp Technique, Humans, Hyperinsulinism, Insulin Resistance, Interleukin-10, Interleukin-6, Interleukin-8, Male, Middle Aged, Mitochondria, Mitochondrial Myopathies, Muscle, Skeletal, Outpatients, Tumor Necrosis Factor-alpha",
author = "Nana Rue and John Vissing and Henrik Galbo",
year = "2014",
doi = "10.1210/jc.2014-1831",
language = "English",
volume = "99",
pages = "3757--3765",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "10",

}

RIS

TY - JOUR

T1 - Insulin Resistance and Increased Muscle Cytokine Levels in Patients With Mitochondrial Myopathy

AU - Rue, Nana

AU - Vissing, John

AU - Galbo, Henrik

PY - 2014

Y1 - 2014

N2 - CONTEXT: Mitochondrial dysfunction has been proposed to cause insulin resistance and that might stimulate cytokine production.OBJECTIVE: The objective of the study was to elucidate the association between mitochondrial myopathy, insulin sensitivity, and cytokine levels in muscle.DESIGN AND SETTING: This was an experimental, controlled study in outpatients.PARTICIPANTS: Eight overnight-fasted patients (P) with various inherited mitochondrial myopathies and eight healthy subjects (C) matched for sex, age, weight, height, and physical activity participated in the study.INTERVENTIONS: The intervention included a 120-minute hyperinsulinemic, euglycemic clamp. Another morning, microdialysis of both vastus lateralis muscles for 4 hours, including one-legged, knee extension exercise for 30 minutes, was performed.MAIN OUTCOME MEASURES: Glucose infusion rate during 90-120 minutes of insulin infusion was measured. Cytokine concentrations in dialysate were also measured.RESULTS: Muscle strength, percentage fat mass, and creatine kinase in plasma did not differ between groups. The maximal oxygen uptake was 21 ± 3 (SE) (P) and 36 ± 3(C) mL/kg·min (2P < .05). Basal insulin, C-peptide, and glucagon were higher in P (55 ± 10, 980 ± 92, and 102 ± 13 pM) than in C (36 ± 12, 712 ± 98, and 44 ± 10 pM) (two-sided significance testing [2P ]< .05). The homeostasis model assessment insulin sensitivity index and glucose infusion rate (6.8 ± 1.0 vs 9.4 ± 1.3 mg/min·kg) were lower, and free fatty acids and glycerol at 120 minutes were higher in P vs C (2P < .05). Dialysate concentrations of TNF-α, IL-6, IL-8, IL-10, and monocyte chemoattractant protein-1 were higher in P vs C (2P < .05). Dialysate concentrations of these cytokines and of IL-1 receptor antagonist increased during exercise (2P < .05), identically in P and C. No differences existed in plasma cytokine concentrations.CONCLUSIONS: In patients with a variety of mitochondrial myopathies, insulin sensitivity of muscle, adipose tissue, and pancreatic A cells is reduced, supporting that mitochondrial function influences insulin action. Furthermore, a local, low-grade inflammation of potential clinical importance exists in the muscle of these patients.

AB - CONTEXT: Mitochondrial dysfunction has been proposed to cause insulin resistance and that might stimulate cytokine production.OBJECTIVE: The objective of the study was to elucidate the association between mitochondrial myopathy, insulin sensitivity, and cytokine levels in muscle.DESIGN AND SETTING: This was an experimental, controlled study in outpatients.PARTICIPANTS: Eight overnight-fasted patients (P) with various inherited mitochondrial myopathies and eight healthy subjects (C) matched for sex, age, weight, height, and physical activity participated in the study.INTERVENTIONS: The intervention included a 120-minute hyperinsulinemic, euglycemic clamp. Another morning, microdialysis of both vastus lateralis muscles for 4 hours, including one-legged, knee extension exercise for 30 minutes, was performed.MAIN OUTCOME MEASURES: Glucose infusion rate during 90-120 minutes of insulin infusion was measured. Cytokine concentrations in dialysate were also measured.RESULTS: Muscle strength, percentage fat mass, and creatine kinase in plasma did not differ between groups. The maximal oxygen uptake was 21 ± 3 (SE) (P) and 36 ± 3(C) mL/kg·min (2P < .05). Basal insulin, C-peptide, and glucagon were higher in P (55 ± 10, 980 ± 92, and 102 ± 13 pM) than in C (36 ± 12, 712 ± 98, and 44 ± 10 pM) (two-sided significance testing [2P ]< .05). The homeostasis model assessment insulin sensitivity index and glucose infusion rate (6.8 ± 1.0 vs 9.4 ± 1.3 mg/min·kg) were lower, and free fatty acids and glycerol at 120 minutes were higher in P vs C (2P < .05). Dialysate concentrations of TNF-α, IL-6, IL-8, IL-10, and monocyte chemoattractant protein-1 were higher in P vs C (2P < .05). Dialysate concentrations of these cytokines and of IL-1 receptor antagonist increased during exercise (2P < .05), identically in P and C. No differences existed in plasma cytokine concentrations.CONCLUSIONS: In patients with a variety of mitochondrial myopathies, insulin sensitivity of muscle, adipose tissue, and pancreatic A cells is reduced, supporting that mitochondrial function influences insulin action. Furthermore, a local, low-grade inflammation of potential clinical importance exists in the muscle of these patients.

KW - Adipose Tissue

KW - Adult

KW - Chemokine CCL2

KW - Cytokines

KW - Exercise

KW - Female

KW - Glucagon-Secreting Cells

KW - Glucose Clamp Technique

KW - Humans

KW - Hyperinsulinism

KW - Insulin Resistance

KW - Interleukin-10

KW - Interleukin-6

KW - Interleukin-8

KW - Male

KW - Middle Aged

KW - Mitochondria

KW - Mitochondrial Myopathies

KW - Muscle, Skeletal

KW - Outpatients

KW - Tumor Necrosis Factor-alpha

U2 - 10.1210/jc.2014-1831

DO - 10.1210/jc.2014-1831

M3 - Journal article

C2 - 25057876

VL - 99

SP - 3757

EP - 3765

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 10

ER -

ID: 137748847