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Inefficient skeletal muscle oxidative function flanks impaired motor neuron recruitment in Amyotrophic Lateral Sclerosis during exercise.

Authors :
Lanfranconi F
Ferri A
Corna G
Bonazzi R
Lunetta C
Silani V
Riva N
Rigamonti A
Maggiani A
Ferrarese C
Tremolizzo L
Source :
Scientific reports [Sci Rep] 2017 Jun 07; Vol. 7 (1), pp. 2951. Date of Electronic Publication: 2017 Jun 07.
Publication Year :
2017

Abstract

This study aimed to evaluate muscle oxidative function during exercise in amyotrophic lateral sclerosis patients (pALS) with non-invasive methods in order to assess if determinants of reduced exercise tolerance might match ALS clinical heterogeneity. 17 pALS, who were followed for 4 months, were compared with 13 healthy controls (CTRL). Exercise tolerance was assessed by an incremental exercise test on cycle ergometer measuring peak O <subscript>2</subscript> uptake ([Formula: see text]O <subscript>2peak</subscript> ), vastus lateralis oxidative function by near infrared spectroscopy (NIRS) and breathing pattern ([Formula: see text]E <subscript>peak</subscript> ). pALS displayed: (1) 44% lower [Formula: see text]O <subscript>2peak</subscript> vs. CTRL (p < 0.0001), paralleled by a 43% decreased peak skeletal muscle oxidative function (p < 0.01), with a linear regression between these two variables (r <superscript>2</superscript>  = 0.64, p < 0.0001); (2) 46% reduced [Formula: see text]E <subscript>peak</subscript> vs. CTRL (p < 0.0001), achieved by using an inefficient breathing pattern (increasing respiratory frequency) from the onset until the end of exercise. Inefficient skeletal muscle O <subscript>2</subscript> function, when flanking the impaired motor units recruitment, is a major determinant of pALS clinical heterogeneity and working capacity exercise tolerance. CPET and NIRS are useful tools for detecting early stages of oxidative deficiency in skeletal muscles, disclosing individual impairments in the O <subscript>2</subscript> transport and utilization chain.

Details

Language :
English
ISSN :
2045-2322
Volume :
7
Issue :
1
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
28592858
Full Text :
https://doi.org/10.1038/s41598-017-02811-z