Abstract

Background: The effect of 3-month respiratory muscle training (RMT) on pulmonary and autonomic function and functional outcomes has been demonstrated in patients with Parkinson's disease (PD); however, there is a paucity of information on the durability of the training effect. In this study, we monitored the pulmonary and cardiovascular autonomic function and clinical severity scales until 18 months after the cessation of RMT to elucidate the detraining effect after RMT.Methods: All patients with PD receiving RMT were assessed with clinical severity scales as well as pulmonary and autonomic function tests at four different stages (baseline on enrollment, immediately after 3 months of RMT, and 6 and 18 months after cessation of RMT). A control group of PD patients who did not receive RMT was also recruited for comparison. Pulmonary function parameters, including forced vital capacity (FVC), forced expiratory volume in one second (FEV1), maximum inspiratory pressure (MIP), and maximum expiratory pressure (MEP), were assessed. Cardiovascular autonomic function was assessed using measures including heart rate response to deep breathing (HRDB), Valsalva ratio, and baroreflex sensitivity. Clinical severity scores were also measured using the Hoehn and Yahr staging and the Unified Parkinson's Disease Rating Scale (UPDRS).Results: The results showed significant improvements in MIP, MEP, HRDB, and UPDRS immediately after RMT. Despite some decay, the improvements in pulmonary function (MIP and MEP) and functional outcomes (UPDRS) remained significant until 6 months of detraining (9 months after enrollment). However, the improvement in cardiovascular autonomic function (HRDB) was reversed after 6 months of detraining.Conclusions: Based on these findings, we recommend that RMT may be repeated after at least 6 months after previous session (9 months after enrollment) for patients with PD to maintain optimal therapeutic effects.

Highlights

  • Patients with Parkinson’s disease (PD) commonly present with restrictive pulmonary dysfunction

  • We evaluated patients with a definitive diagnosis of idiopathic PD based on the clinical diagnostic criteria as well as the magnetic resonance imaging findings [18, 19] in our previous study [17]

  • There is paucity of information on the detraining effect after respiratory muscle training (RMT), the treatment effects of RMT in patients with PD have been demonstrated in our previous study, as well as several previous reports [4,5,6, 17]

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Summary

Introduction

Patients with Parkinson’s disease (PD) commonly present with restrictive pulmonary dysfunction. Previous studies have shown the effect of respiratory muscle training (RMT) on pulmonary function, swallowing function, and quality of life [4,5,6]. Our previous study showed that there was a simultaneous improvement in pulmonary and cardiovascular autonomic function in patients with PD after RMT [17]. The effect of 3-month respiratory muscle training (RMT) on pulmonary and autonomic function and functional outcomes has been demonstrated in patients with Parkinson’s disease (PD); there is a paucity of information on the durability of the training effect. We monitored the pulmonary and cardiovascular autonomic function and clinical severity scales until 18 months after the cessation of RMT to elucidate the detraining effect after RMT

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