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Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study

BACKGROUND: Human Immunodeficiency Virus positive subjects present impairment in muscle function, neural activation, balance, and gait. In other populations, all of these factors have been associated with muscle strength asymmetry. OBJECTIVE: To investigate the existence of muscle strength asymmetry...

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Autores principales: Oliveira, Vitor H.F., Wiechmann, Susana L., Narciso, Argéria M.S., Deminice, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Departamento de Fisioterapia da Universidade Federal de Sao Carlos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693428/
https://www.ncbi.nlm.nih.gov/pubmed/28720481
http://dx.doi.org/10.1016/j.bjpt.2017.06.010
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author Oliveira, Vitor H.F.
Wiechmann, Susana L.
Narciso, Argéria M.S.
Deminice, Rafael
author_facet Oliveira, Vitor H.F.
Wiechmann, Susana L.
Narciso, Argéria M.S.
Deminice, Rafael
author_sort Oliveira, Vitor H.F.
collection PubMed
description BACKGROUND: Human Immunodeficiency Virus positive subjects present impairment in muscle function, neural activation, balance, and gait. In other populations, all of these factors have been associated with muscle strength asymmetry. OBJECTIVE: To investigate the existence of muscle strength asymmetry between dominant and non-dominant lower limbs and to determine the hamstrings-to-quadriceps strength ratio in Human Immunodeficiency Virus positive subjects. METHODS: In this cross-sectional study, 48 subjects were included (22 men and 26 women; mean age 44.6 years), all of them under highly active antiretroviral therapy. They performed isokinetic strength efforts at speeds of 60°/s and 180°/s for knee extension and flexion in concentric-concentric mode. RESULTS: Peak torque was higher (p < 0.01) at 60°/s for quadriceps (193, SD = 57 vs. 173, SD = 55% body mass) and hamstrings (97, SD = 36 vs. 90, SD = 37% body mass) in dominant compared to non-dominant. Similarly, peak torque was higher at 180°/s (quadriceps 128, SD = 44 vs. 112, SD = 42; hamstrings 64, SD = 24 vs. 57, SD = 26% body mass) in dominant. Average power was also higher for all muscle groups and speeds, comparing dominant with non-dominant. The hamstrings-to-quadriceps ratio at 60°/s was 0.50 for dominant and 0.52 for non-dominant, and at 180°/s, it was 0.51 for both limbs, with no significant difference between them. The percentage of subjects with strength asymmetry ranged from 46 to 58%, depending upon muscle group and speed analyzed. CONCLUSION: Human Immunodeficiency Virus positive subjects present muscle strength asymmetry between lower limbs, assessed through isokinetic dynamometry.
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spelling pubmed-56934282017-11-21 Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study Oliveira, Vitor H.F. Wiechmann, Susana L. Narciso, Argéria M.S. Deminice, Rafael Braz J Phys Ther Original Research BACKGROUND: Human Immunodeficiency Virus positive subjects present impairment in muscle function, neural activation, balance, and gait. In other populations, all of these factors have been associated with muscle strength asymmetry. OBJECTIVE: To investigate the existence of muscle strength asymmetry between dominant and non-dominant lower limbs and to determine the hamstrings-to-quadriceps strength ratio in Human Immunodeficiency Virus positive subjects. METHODS: In this cross-sectional study, 48 subjects were included (22 men and 26 women; mean age 44.6 years), all of them under highly active antiretroviral therapy. They performed isokinetic strength efforts at speeds of 60°/s and 180°/s for knee extension and flexion in concentric-concentric mode. RESULTS: Peak torque was higher (p < 0.01) at 60°/s for quadriceps (193, SD = 57 vs. 173, SD = 55% body mass) and hamstrings (97, SD = 36 vs. 90, SD = 37% body mass) in dominant compared to non-dominant. Similarly, peak torque was higher at 180°/s (quadriceps 128, SD = 44 vs. 112, SD = 42; hamstrings 64, SD = 24 vs. 57, SD = 26% body mass) in dominant. Average power was also higher for all muscle groups and speeds, comparing dominant with non-dominant. The hamstrings-to-quadriceps ratio at 60°/s was 0.50 for dominant and 0.52 for non-dominant, and at 180°/s, it was 0.51 for both limbs, with no significant difference between them. The percentage of subjects with strength asymmetry ranged from 46 to 58%, depending upon muscle group and speed analyzed. CONCLUSION: Human Immunodeficiency Virus positive subjects present muscle strength asymmetry between lower limbs, assessed through isokinetic dynamometry. Departamento de Fisioterapia da Universidade Federal de Sao Carlos 2017 2017-07-03 /pmc/articles/PMC5693428/ /pubmed/28720481 http://dx.doi.org/10.1016/j.bjpt.2017.06.010 Text en © 2017 Associaç˜ao Brasileira de Pesquisa e Pós-Graduaç˜ao em Fisioterapia. Published by Elsevier Editora Ltda. All rights reserved.
spellingShingle Original Research
Oliveira, Vitor H.F.
Wiechmann, Susana L.
Narciso, Argéria M.S.
Deminice, Rafael
Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study
title Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study
title_full Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study
title_fullStr Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study
title_full_unstemmed Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study
title_short Knee extension and flexion strength asymmetry in Human Immunodeficiency Virus positive subjects: a cross-sectional study
title_sort knee extension and flexion strength asymmetry in human immunodeficiency virus positive subjects: a cross-sectional study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693428/
https://www.ncbi.nlm.nih.gov/pubmed/28720481
http://dx.doi.org/10.1016/j.bjpt.2017.06.010
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