Published in

American Physiological Society, Journal of Applied Physiology, 1(90), p. 280-286

DOI: 10.1152/jappl.2001.90.1.280

Links

Tools

Export citation

Search in Google Scholar

Differences in skeletal muscle between men and women with chronic heart failure

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Men with chronic heart failure (CHF) have alterations in their skeletal muscle that are partially responsible for a decreased exercise tolerance. The purpose of this study was to investigate whether skeletal muscle alterations in women with CHF are similar to those observed in men and if these alterations are related to exercise intolerance. Twenty-five men and thirteen women with CHF performed a maximal exercise test for evaluation of peak oxygen consumption (V˙o 2) and resting left ventricular ejection fraction, after which a biopsy of the vastus lateralis was performed. Twenty-one normal subjects (11 women, 10 men) were also studied. The relationship between muscle markers and peakV˙o 2 was consistent for CHF men and women. When controlling for gender, analysis showed that oxidative enzymes and capillary density are the best predictors of peakV˙o 2 . These results indicate that aerobically matched CHF men and women have no differences in skeletal muscle biochemistry and histology. However, when CHF groups were separated by peak exercise capacity of 4.5 metabolic equivalents (METs), CHF men with peak V˙o 2 >4.5 METs had increased citrate synthase and 3-hydroxyacyl-CoA dehydrogenase compared with CHF men with peak V˙o 2 <4.5 METs. CHF men with a lower peak V˙o 2 had increased capillary density compared with men with higher peakV˙o 2. These observations were not reproduced in CHF women. This suggests that differences may exist in how skeletal muscle adapts to decreasing peakV˙o 2 in patients with CHF.