Resistance Training with Vascular Occlusion in Inclusion Body Myositis: A Case Study


Autoria(s): GUALANO, Bruno; NEVES JR., Manoel; LIMA, Fernanda Rodrigues; PINTO, Ana Lucia De Sa; LAURENTINO, Gilberto; BORGES, Claudia; BAPTISTA, Luciana; ARTIOLI, Guilherme Giannini; AOKI, Marcelo Saldanha; MORISCOT, Anselmo; LANCHA JR., Antonio Herbert; BONFA, Eloisa; UGRINOWITSCH, Carlos
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/10/2012

18/10/2012

2010

Resumo

GUALANO, B., M. NEVES JR, F. R. LIMA, A. L. PINTO, G. LAURENTINO, C. BORGES, L. BAPTISTA, G. G. ARTIOLI, M. S. AOKI, A. MORISCOT, A. H. LANCHA JR, E. BONFA, and C. UGRINOWITSCH. Resistance Training with Vascular Occlusion in Inclusion Body Myositis: A Case Study. Med Sci. Spot-is Exerc., Vol. 42, No. 2, pp. 250-254, 2010. Inclusion body myositis (IBM) is a rare idiopathic inflammatory myopathy that produces remarkable muscle weakness. Resistance training with vascular occlusion has been shown to improve muscle strength and cross-sectional area in other muscle wasting conditions. Purpose: We evaluated the efficacy of a moderate-intensity resistance training program combined with vascular occlusion by examining functional capacity, muscle morphology, and changes in the expression of genes related to muscle protein synthesis and proteolysis in a patient with IBM. Methods: A 65-yr-old man with IBM resistant to all proposed treatments underwent resistance training with vascular occlusion for 12 wk. Leg press one-repetition maximum; thigh cross-sectional area; balance, mobility, and muscle function; quality of life; and blood markers of inflammation and muscle damage were assessed at baseline and after the 12-wk program. The messenger RNA (mRNA) expression levels of mechanogrowth factor, mammalian target of rapamycin, atrogin-1, and muscle RING finger-1 were also quantified. Results: After the 12-wk training program, the patient`s leg press one-repetition maximum, balance and mobility function, and thigh cross-sectional area increased 15.9%, 60%, and 4.7%, respectively. All Short Form-36 Health Survey Questionnaire subscales demonstrated improvements as well, varying from 18% to 600%. mRNA expression of mechanogrowth factor increased 3.97-fold, whereas that of atrogin-1 decreased 0.62-fold. Muscle RING finger-1 and mammalian target of rapamycin mRNA levels were only slightly altered, 1.18- and 1.28-fold, respectively. Importantly, the exercise did not induce disease flare. Conclusions: We describe a novel, and likely the first, nonpharmacological therapeutic tool that might be able to counteract the muscle atrophy and the declining strength that usually occur in IBM.

CNPq Conselho Nacional de Desenvolviniento Cientifico e Tecnologico[305468/2006-5]

Federico Wilhelm Agricola Foundation

FAPESP Fundacao de Amparo a Pesquisa de Sao Paulo[06/52204-5]

Identificador

MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, v.42, n.2, p.250-254, 2010

0195-9131

http://producao.usp.br/handle/BDPI/17200

10.1249/MSS.0b013e3181b18fb8

http://dx.doi.org/10.1249/MSS.0b013e3181b18fb8

Idioma(s)

eng

Publicador

LIPPINCOTT WILLIAMS & WILKINS

Relação

Medicine and Science in Sports and Exercise

Direitos

restrictedAccess

Copyright LIPPINCOTT WILLIAMS & WILKINS

Palavras-Chave #EXERCISE TRAINING #STRENGTH #IDIOPATIC INFLAMMATORY MYOPATHIES #MGF #ATROGIN-1 #HUMAN SKELETAL-MUSCLE #GENE-EXPRESSION #ACUTE EXERCISE #TIME-COURSE #Sport Sciences
Tipo

article

original article

publishedVersion