Cardiac Autonomic Modulation in Subjects with Amyotrophic Lateral Sclerosis (ALS) during an Upper Limb Virtual Reality Task: A Prospective Control Trial

Author:

Silveira Ana C.1ORCID,Moraes Íbis A. P.2ORCID,Vidigal Giovanna P.2ORCID,Simcsik Amanda O.1ORCID,Rosa Renata M.1ORCID,Favero Francis M.3ORCID,Fernandes Susi M. S.4ORCID,Garner David M.5ORCID,Araújo Luciano V.6ORCID,Massa Marcelo1ORCID,Vanderlei Luiz C. M.7ORCID,Silva Talita D.289ORCID,Monteiro Carlos B. M.12ORCID

Affiliation:

1. Postgraduate Program in Physical Activity Sciences, School of Arts, Science and Humanities of University of São Paulo (EACH-USP), São Paulo, SP 03828-000, Brazil

2. Postgraduate Program in Rehabilitation Sciences, Faculty of Medicine, University of São Paulo (FMUSP), São Paulo, SP 01246-903, Brazil

3. Department of Neurology and Neurosurgery at Paulista School of Medicine, Federal University of São Paulo (EPM/UNIFESP), São Paulo, SP 04021-001, Brazil

4. Department of Physiotherapy, Mackenzie Presbyterian University, São Paulo, SP 01302-907, Brazil

5. Cardiorespiratory Research Group, Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Headington Campus, Gipsy Lane, Oxford OX3 0BP, UK

6. Postgraduate Program in Information Systems, School of Arts, Science and Humanities of University of São Paulo (EACH-USP), São Paulo, SP 03828-000, Brazil

7. Department of Physiotherapy, Paulista State University (UNESP), Presidente Prudente, São Paulo, SP 19060-900, Brazil

8. Postgraduate Program in Medicine (Cardiology) at Escola Paulista de Medicina, Federal University of São Paulo (EPM/UNIFESP), São Paulo, SP 04021-001, Brazil

9. Faculty of Medicine of the City of São Paulo University (UNICID), São Paulo, SP 03071-000, Brazil

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease. As a result of the rapid progression and severity of the disease, people with ALS experience loss of functionality and independence. Furthermore, it has already been described presence of autonomic dysfunction. Despite the increasing use of virtual reality (VR) in the treatment of different diseases, the use of virtual reality environment as an intervention program for ALS patients is innovative. The benefits and limitations have not yet been proven. Our objective was to evaluate the autonomic function of individuals with amyotrophic lateral sclerosis throughout the virtual reality task. The analysis of autonomic function was completed before, during, and after the virtual reality task using the upper limbs; also, all steps lasted ten minutes in a sitting position. Heart rate variability (HRV) was taken via the Polar® RS800CX cardiofrequencymeter. The following questionnaire was enforced: Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS) and Fatigue Severity Scale (FSS). Different types of HRV were revealed for the groups, indicating that the ALS group has reduced HRV, with most of the representative indices of the sympathetic nervous system. Besides, the physiological process of reducing parasympathetic activity from rest to VR activity (vagal withdrawal), with reduction in HF (ms2) and an increase in HR from rest to activity, and a further increase throughout recovery, with withdrawal of sympathetic nervous system, occurs just for the control group (CG), with no alterations between rest, activity, and recovery in individuals with ALS. We could conclude that patients with ALS have the reduction of HRV with the sympathetic predominance when equated to the healthy CG. Besides that, the ALS individuals have no capability to adapt the autonomic nervous system when likened to the CG during therapy based on VR and their recovery.

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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