Sex differences in COPD-related quadriceps muscle dysfunction and fibre abnormalities

Author:

Sharanya Adithya1,Ciano Margherita1,Withana Shirmila2,Kemp Paul Richard1,Polkey Michael Iain3,Sathyapala Samantha Amanda1

Affiliation:

1. Molecular Medicine, National Heart and Lung Institute, SAF Building, South Kensington Campus, Imperial College London, London, UK

2. Respiratory Medicine, Royal Brompton and Harefield NHS Foundation Trust, Harefield Hospital, Hill End Road, Harefield, Middlesex, UK

3. Respiratory Medicine, Royal Brompton and Harefield NHS Foundation Trust, Royal Brompton Hospital, First Floor, Fulham Road, London, UK

Abstract

In chronic obstructive pulmonary disease (COPD), lower limb dysfunction is associated with reduced exercise capacity, increased hospitalizations and mortality. We investigated sex differences in the prevalence of quadriceps dysfunction and fibre abnormalities in a large COPD cohort, controlling for the normal sex differences in health. We compared existing data from 76 male and 38 female COPD patients where each variable was expressed as a function of gender-specific normal values (obtained from 16 male and 14 female controls). Female COPD patients had lower quadriceps muscle strength and peak workload on a maximal incremental cycle ergometry protocol compared to male patients. Female patients had a smaller type II fibre cross-sectional area (CSA) compared to male patients, suggesting a greater female preponderance to fibre atrophy, although this result was largely driven by a few male patients with a large type II fibre CSA. Female patients had significantly higher concentrations of a number of plasma pro-inflammatory cytokines including tumour necrosis factor alpha and interleukin 8 (IL8), but not lower levels of physical activity or arterial oxygenation, compared to males. Our data confirm results from a previous small study and suggest that female COPD patients have a greater prevalence of muscle wasting and weakness. Larger studies investigating sex differences in COPD-related muscle atrophy and weakness are needed, as the results will have implications for monitoring in clinical practice and for design of clinical trials evaluating novel muscle anabolic agents.

Funder

GlaxoSmithKline

Publisher

SAGE Publications

Subject

Pulmonary and Respiratory Medicine

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