9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The Combined Efficacy of a Two-Year Period of Cybernic Treatment With a Wearable Cyborg Hybrid-Assistive Limb and Leuprorelin Therapy in a Patient With Spinal and Bulbar Muscular Atrophy: A Case Report

      case-report

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Spinal and bulbar muscular atrophy (SBMA), also known as Kennedy's disease, is a rare, slowly progressive, incurable, and hereditary neurodegenerative disease caused by the testosterone-dependent accumulation of pathogenic polyglutamine-expanded androgen receptor protein. After extensive review, two treatments for SBMA have recently been approved in Japan; this decision was based on the results of randomized controlled trials: First, anti-androgen therapy using leuprorelin acetate (leuprorelin), a disease-modifying drug that can inhibit the progression of dysphagia but has not yet been proved to improve gait function; second, cybernic treatment with a wearable cyborg hybrid assistive limb (HAL®) (Cyberdyne Inc. Tsukuba, Japan). The HAL is an innovative walking exercise system that has been shown to significantly improve gait function in eight neuromuscular diseases without reduction in muscle function, including SBMA. It is possible that the combination of these two approaches might yield better outcomes. However, the long-term effects of such a combined approach have yet to be clinically evaluated. Here, we describe the case of a 39-year-old male with SBMA who commenced anti-androgen therapy with leuprorelin 1 year previously; this was followed by cybernic treatment with HAL. The duration of walking exercise with HAL was 20–30 min a day in one session. Over 2 weeks, the patient underwent nine sessions (one course). The efficacy of HAL was evaluated by gait function tests before and after one course of cybernic treatment. Then, leuprorelin treatment was combined with cybernic sessions every 2 months for 2 years (13 courses in total). Walking ability, as evaluated by the 2-min walk test, improved by 20.3% in the first course and peaked 10 months after the commencement of combined therapy (a 59.0% improvement). Walking function was maintained throughout the period. Generally, SBMA is characterized by moderately increased serum levels of creatine kinase (CK), reflecting neuromuscular damage; interestingly, the patient's CK levels decreased dramatically with combined therapy, indicating remarkable functional improvement. Long-term combined therapy improved the patient's gait function with a steady reduction in CK levels. The combination of leuprorelin with cybernic treatment can, therefore, improve and maintain gait function without damaging the motor unit and may also suppress disease progression.

          Related collections

          Most cited references28

          • Record: found
          • Abstract: found
          • Article: not found

          Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy

          Nusinersen is an antisense oligonucleotide drug that modulates pre-messenger RNA splicing of the survival motor neuron 2 ( SMN2) gene. It has been developed for the treatment of spinal muscular atrophy (SMA).
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

            X-linked spinal and bulbar muscular atrophy (Kennedy's disease) is an adult-onset form of motorneuron disease which may be associated with signs of androgen insensitivity. We have now investigated whether the androgen receptor gene on the proximal long arm of the X chromosome is a candidate gene for this disease. In patient samples we found androgen receptor gene mutations with increased size of a polymorphic tandem CAG repeat in the coding region. These amplified repeats were absolutely associated with the disease, being present in 35 unrelated patients and none of 75 controls. They segregated with the disease in 15 families, with no recombination in 61 meioses (the maximum log likelihood ratio (lod score) is 13.2 at a recombination rate of 0). The association is unlikely to be due to linkage disequilibrium, because 11 different disease alleles were observed. We conclude that enlargement of the CAG repeat in the androgen receptor gene is probably the cause of this disorder.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait.

                Bookmark

                Author and article information

                Contributors
                Journal
                Front Neurol
                Front Neurol
                Front. Neurol.
                Frontiers in Neurology
                Frontiers Media S.A.
                1664-2295
                24 June 2022
                2022
                : 13
                : 905613
                Affiliations
                [1] 1Department of Clinical Research, National Hospital Organization Niigata National Hospital , Kashiwazaki, Japan
                [2] 2Department of Neurology, Nagoya University Graduate School of Medicine , Nagoya, Japan
                [3] 3Department of Neurology, National Hospital Organization Niigata National Hospital , Kashiwazaki, Japan
                [4] 4Brain and Mind Research Center, Nagoya University , Nagoya, Japan
                [5] 5Aichi Medical University , Nagakute, Japan
                Author notes

                Edited by: Giovanni Meola, University of Milan, Italy

                Reviewed by: Yuishin Izumi, Tokushima University, Japan; Maria Pennuto, University of Padua, Italy; Davide Pareyson, Fondazione IRCCS, Istituto Neurologico Carlo Besta, Italy; Gianni Sorarù, University of Padua, Italy; Valeria Crippa, University of Milan, Italy

                *Correspondence: Takashi Nakajima nakajima-md@ 123456mqb.biglobe.ne.jp

                This article was submitted to Neuromuscular Disorders and Peripheral Neuropathies, a section of the journal Frontiers in Neurology

                Article
                10.3389/fneur.2022.905613
                9263275
                35812096
                2b24fc56-cbd0-4636-ad7d-dd439fd4940f
                Copyright © 2022 Nakatsuji, Ikeda, Hashizume, Katsuno, Sobue and Nakajima.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 27 March 2022
                : 25 May 2022
                Page count
                Figures: 3, Tables: 0, Equations: 0, References: 30, Pages: 7, Words: 5291
                Funding
                Funded by: Ministry of Health, Labour and Welfare, doi 10.13039/501100003478;
                Award ID: 20FC1049
                Award ID: 21FC1006
                Categories
                Neurology
                Case Report

                Neurology
                spinal and bulbar muscular atrophy,hybrid assistive limb,cybernic treatment,leuprorelin acetate,anti-androgen therapy,creatine kinase,case report

                Comments

                Comment on this article