Exercise Intolerance in Facioscapulohumeral Muscular Dystrophy

Kathryn A. Vera, Mary McConville, Aline Glazos, William Stokes, Michael Kyba, Manda Keller-Ross

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

VERA, K. A., M. MCCONVILLE, A. GLAZOS, W. STOKES, M. KYBA, and M. KELLER-ROSS. Exercise Intolerance in FacioscapulohumeralMuscular Dystrophy. Med. Sci. Sports Exerc., Vol. 54, No. 6, pp. 887-895, 2022. Purpose: Determine 1) if adults with facioscapulohumeral muscular dystrophy (FSHD) exhibit exercise intolerance and 2) potential contributing mechanisms to exercise intolerance, specific to FSHD. Methods: Eleven people with FSHD (47 ± 13 yr, 4 females) and 11 controls (46 ± 13 yr, 4 females) completed one visit, which included a volitional peak oxygen consumption (V˙O2peak) cycling test. Breath-by-breath gas exchange, ventilation, and cardiovascular responses were measured at rest and during exercise. The test featured 3-min stages (speed, 65-70 rpm)with incremental increases in intensity (FSHD: 20Wper stage; control: 40-60Wper stage). Body lean mass (LM (kg, %)) was collected via dual-energy x-ray absorptiometry. Results: V˙O2peak was 32% lower (24.5 ± 9.7 vs 36.2 ± 9.3 mL·kg-1·min-1, P < 0.01), and wattage was 55% lower in FSHD (112.7 ± 56.1 vs 252.7 ± 67.7 W, P < 0.01). When working at a relative submaximal intensity (40% of V˙O2peak), wattage was 55% lower in FSHD (41.8 ± 30.3 vs 92.7 ± 32.6 W, P = 0.01), although ratings of perceived exertion (FSHD: 11 ± 2 vs control: 10 ± 3, P = 0.61) and dyspnea (FSHD: 3 ± 1 vs control: 3 ± 2, P = 0.78) were similar between groups. At an absolute intensity (60W), the rating of perceived exertion was 63% higher (13 ± 3 vs 8 ± 2, P < 0.01) and dyspnea was 180% higher in FSHD (4 ± 2 vs 2 ± 2, P < 0.01). V˙O2peak was most strongly correlated with resting O2 pulse in controls (P < 0.01, r = 0.90) and percent leg LM in FSHD (P < 0.01, r = 0.88). Among FSHD participants, V˙O2peak was associated with self-reported functionality (FSHD-HI score; activity limitation: P < 0.01, r = -0.78), indicating a strong association between perceived and objective impairments. Conclusions:Disease-driven losses of LMcontribute to exercise intolerance in FSHD, as evidenced by a lower V˙O2peak and elevated symptoms of dyspnea and fatigue during submaximal exercise. Regular exercise participation may preserve LM, thus providing some protection against exercise tolerance in FSHD.

Original languageEnglish (US)
Pages (from-to)887-895
Number of pages9
JournalMedicine and science in sports and exercise
Volume54
Issue number6
DOIs
StatePublished - Jun 1 2022

Bibliographical note

Publisher Copyright:
© 2022 by the American College of Sports Medicine.

Keywords

  • EXERCISE CAPACITY
  • FUNCTIONAL CAPACITY
  • MUSCULAR DYSTROPHY
  • SKELETAL MUSCLE MASS
  • V˙O

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