Literature DB >> 19327849

Reduced knee extensor function in heart failure is not explained by inactivity.

Michael J Toth1, Anthony O Shaw, Mark S Miller, Peter VanBuren, Martin M LeWinter, David W Maughan, Philip A Ades.   

Abstract

BACKGROUND: The goal of this study was to determine if heart failure alters knee extensor muscle torque, power production or contractile velocity.
METHODS: Heart failure patients (n=11; 70.4±4.3 yrs) and controls (n=11; 70.3±3.4 yrs) matched for age and sex were evaluated for knee extensor contractile performance under isometric and isokinetic conditions and body composition by dual energy X-ray absorptiometry. Additionally, we recruited sedentary to minimally active elderly controls to match heart failure patients for habitual physical activity and assessed activity levels using accelerometry.
RESULTS: Groups did not differ for total or regional body composition or average daily physical activity level. Despite similar muscle size and use, heart failure patients exhibited 21-29% lower (P<0.05 to P<0.01) isometric knee extensor torque throughout a range of knee angles, 15-33% lower (P=0.05 to P<0.01) peak concentric torque measured at various isokinetic speeds and corresponding reductions (P=0.05 to P<0.01) in peak power output. Expression of peak isokinetic torque data relative to isometric torque eliminated group differences, suggesting that impaired contractile function under dynamic conditions is explained by deficits in the force generating capacity of muscle. No group differences were found in the time required to reach target velocity during isokinetic contractions, an index of contractile velocity.
CONCLUSION: Because group differences in muscle torque were independent of age, sex, physical activity level and muscle size, our results suggest that muscle contractile dysfunction in these patients is likely attributable to the heart failure syndrome.
Copyright © 2009 Elsevier Ireland Ltd. All rights reserved.

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Year:  2009        PMID: 19327849      PMCID: PMC3411851          DOI: 10.1016/j.ijcard.2009.02.040

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


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