Loading…

Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan

Abstract Introduction Corticosteroids are effective for improving motor function in patients with Duchenne muscular dystrophy (DMD), but there is no consensus on a regimen that balances efficacy and side effects. Methods Data from three groups of DMD patients were retrospectively analyzed: those tre...

Full description

Saved in:
Bibliographic Details
Published in:Brain & development (Tokyo. 1979) 2016-10, Vol.38 (9), p.785-791
Main Authors: Goto, Masahide, Komaki, Hirofumi, Takeshita, Eri, Abe, Yoshiki, Ishiyama, Akihiko, Sugai, Kenji, Sasaki, Masayuki, Goto, Yu-ichi, Nonaka, Ikuya
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23
cites cdi_FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23
container_end_page 791
container_issue 9
container_start_page 785
container_title Brain & development (Tokyo. 1979)
container_volume 38
creator Goto, Masahide
Komaki, Hirofumi
Takeshita, Eri
Abe, Yoshiki
Ishiyama, Akihiko
Sugai, Kenji
Sasaki, Masayuki
Goto, Yu-ichi
Nonaka, Ikuya
description Abstract Introduction Corticosteroids are effective for improving motor function in patients with Duchenne muscular dystrophy (DMD), but there is no consensus on a regimen that balances efficacy and side effects. Methods Data from three groups of DMD patients were retrospectively analyzed: those treated with 0.75 mg/kg/day prednisolone every day (daily group, n = 51); those treated with 1 mg/kg/day prednisolone on alternate days (intermittent group, n = 36), and those not treated with steroids (nontreatment group, n = 42). Results Although the age of ambulation loss did not differ significantly among the groups, the hazard ratios for ambulation loss relative to the nontreatment group were 0.24 (95% confidence interval [CI]: 0.11–0.54) in the daily group and 0.34 (95% CI: 0.19–0.62) in the intermittent group. The percentage of predicted forced vital capacity increased until 9.6 years of age (to 94.1%) in the daily group, until 8.8 years of age (to 96.9%) in the intermittent group, and until 7.2 years of age (to 87.6%) in the nontreatment group. Weight gain was the most frequently observed side effect in the treated groups. Height was significantly lower in the daily than in the nontreatment group. Other side effects were observed, but no patient discontinued therapy. There were no marked differences in benefits and side effects between the two treated groups. Discussion This is the first assessment of long-term outcomes of different steroid therapy regimens in Japanese DMD patients. Benefits and side effects, except height, did not differ significantly between steroid regimens.
doi_str_mv 10.1016/j.braindev.2016.04.001
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1817041867</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0387760416300298</els_id><sourcerecordid>1817041867</sourcerecordid><originalsourceid>FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23</originalsourceid><addsrcrecordid>eNqFkcGO1DAMQCMEYmcXfmGVI5eWOGmT9IJAu8CCRnAAzlGaepgMbTIk7Ur9ezKaXQ5cOFm2nm35mZBrYDUwkK8PdZ-sDwPe17zkNWtqxuAJ2YBWvFIg4CnZMKFVpSRrLshlzgdWCA7sObngCoAL3WzIl20MP6sZ00TjMrs4YaZxR3OpRD_QeY_JHle6i4neLm6PISCdluyW0SY6rHlO8bhfqQ_0sz3a8II829kx48uHeEV-fHj__eau2n79-Onm3bZyLYi50s4paYVlUivVddZx1TMuuQQluraHptdOuZYBY7xtNPadkK1gqrFq6PTAxRV5dZ57TPH3gnk2k88Ox9EGjEs2oEGxBrRUBZVn1KWYc8KdOSY_2bQaYObk0hzMo0tzcmlYY4qp0nj9sGPpJxz-tj3KK8DbM4Dl0nuPyWTnMTgcfEI3myH6_-94888IN_rgnR1_4Yr5EJcUikcDJnPDzLfTR08PBSmKmk6LP8b7nDQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1817041867</pqid></control><display><type>article</type><title>Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan</title><source>ScienceDirect Freedom Collection</source><creator>Goto, Masahide ; Komaki, Hirofumi ; Takeshita, Eri ; Abe, Yoshiki ; Ishiyama, Akihiko ; Sugai, Kenji ; Sasaki, Masayuki ; Goto, Yu-ichi ; Nonaka, Ikuya</creator><creatorcontrib>Goto, Masahide ; Komaki, Hirofumi ; Takeshita, Eri ; Abe, Yoshiki ; Ishiyama, Akihiko ; Sugai, Kenji ; Sasaki, Masayuki ; Goto, Yu-ichi ; Nonaka, Ikuya</creatorcontrib><description>Abstract Introduction Corticosteroids are effective for improving motor function in patients with Duchenne muscular dystrophy (DMD), but there is no consensus on a regimen that balances efficacy and side effects. Methods Data from three groups of DMD patients were retrospectively analyzed: those treated with 0.75 mg/kg/day prednisolone every day (daily group, n = 51); those treated with 1 mg/kg/day prednisolone on alternate days (intermittent group, n = 36), and those not treated with steroids (nontreatment group, n = 42). Results Although the age of ambulation loss did not differ significantly among the groups, the hazard ratios for ambulation loss relative to the nontreatment group were 0.24 (95% confidence interval [CI]: 0.11–0.54) in the daily group and 0.34 (95% CI: 0.19–0.62) in the intermittent group. The percentage of predicted forced vital capacity increased until 9.6 years of age (to 94.1%) in the daily group, until 8.8 years of age (to 96.9%) in the intermittent group, and until 7.2 years of age (to 87.6%) in the nontreatment group. Weight gain was the most frequently observed side effect in the treated groups. Height was significantly lower in the daily than in the nontreatment group. Other side effects were observed, but no patient discontinued therapy. There were no marked differences in benefits and side effects between the two treated groups. Discussion This is the first assessment of long-term outcomes of different steroid therapy regimens in Japanese DMD patients. Benefits and side effects, except height, did not differ significantly between steroid regimens.</description><identifier>ISSN: 0387-7604</identifier><identifier>EISSN: 1872-7131</identifier><identifier>DOI: 10.1016/j.braindev.2016.04.001</identifier><identifier>PMID: 27112384</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adolescent ; Adrenal Cortex Hormones - adverse effects ; Adrenal Cortex Hormones - therapeutic use ; Ambulation ; Body Height - drug effects ; Child ; Child, Preschool ; Corticosteroid treatment ; Disability Evaluation ; Follow-Up Studies ; Height ; Humans ; Japan - epidemiology ; Kaplan-Meier Estimate ; Mixed model ; Motor Activity - drug effects ; Muscular Dystrophy, Duchenne - drug therapy ; Muscular Dystrophy, Duchenne - epidemiology ; Muscular Dystrophy, Duchenne - genetics ; Neurology ; Neuromuscular Agents - adverse effects ; Neuromuscular Agents - therapeutic use ; Prednisolone - adverse effects ; Prednisolone - therapeutic use ; Regression Analysis ; Respiration - drug effects ; Respiratory function ; Retrospective Studies ; Side effect ; Time Factors ; Treatment Outcome ; Vital Capacity - drug effects</subject><ispartof>Brain &amp; development (Tokyo. 1979), 2016-10, Vol.38 (9), p.785-791</ispartof><rights>The Japanese Society of Child Neurology</rights><rights>2016 The Japanese Society of Child Neurology</rights><rights>Copyright © 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23</citedby><cites>FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27112384$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goto, Masahide</creatorcontrib><creatorcontrib>Komaki, Hirofumi</creatorcontrib><creatorcontrib>Takeshita, Eri</creatorcontrib><creatorcontrib>Abe, Yoshiki</creatorcontrib><creatorcontrib>Ishiyama, Akihiko</creatorcontrib><creatorcontrib>Sugai, Kenji</creatorcontrib><creatorcontrib>Sasaki, Masayuki</creatorcontrib><creatorcontrib>Goto, Yu-ichi</creatorcontrib><creatorcontrib>Nonaka, Ikuya</creatorcontrib><title>Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan</title><title>Brain &amp; development (Tokyo. 1979)</title><addtitle>Brain Dev</addtitle><description>Abstract Introduction Corticosteroids are effective for improving motor function in patients with Duchenne muscular dystrophy (DMD), but there is no consensus on a regimen that balances efficacy and side effects. Methods Data from three groups of DMD patients were retrospectively analyzed: those treated with 0.75 mg/kg/day prednisolone every day (daily group, n = 51); those treated with 1 mg/kg/day prednisolone on alternate days (intermittent group, n = 36), and those not treated with steroids (nontreatment group, n = 42). Results Although the age of ambulation loss did not differ significantly among the groups, the hazard ratios for ambulation loss relative to the nontreatment group were 0.24 (95% confidence interval [CI]: 0.11–0.54) in the daily group and 0.34 (95% CI: 0.19–0.62) in the intermittent group. The percentage of predicted forced vital capacity increased until 9.6 years of age (to 94.1%) in the daily group, until 8.8 years of age (to 96.9%) in the intermittent group, and until 7.2 years of age (to 87.6%) in the nontreatment group. Weight gain was the most frequently observed side effect in the treated groups. Height was significantly lower in the daily than in the nontreatment group. Other side effects were observed, but no patient discontinued therapy. There were no marked differences in benefits and side effects between the two treated groups. Discussion This is the first assessment of long-term outcomes of different steroid therapy regimens in Japanese DMD patients. Benefits and side effects, except height, did not differ significantly between steroid regimens.</description><subject>Adolescent</subject><subject>Adrenal Cortex Hormones - adverse effects</subject><subject>Adrenal Cortex Hormones - therapeutic use</subject><subject>Ambulation</subject><subject>Body Height - drug effects</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Corticosteroid treatment</subject><subject>Disability Evaluation</subject><subject>Follow-Up Studies</subject><subject>Height</subject><subject>Humans</subject><subject>Japan - epidemiology</subject><subject>Kaplan-Meier Estimate</subject><subject>Mixed model</subject><subject>Motor Activity - drug effects</subject><subject>Muscular Dystrophy, Duchenne - drug therapy</subject><subject>Muscular Dystrophy, Duchenne - epidemiology</subject><subject>Muscular Dystrophy, Duchenne - genetics</subject><subject>Neurology</subject><subject>Neuromuscular Agents - adverse effects</subject><subject>Neuromuscular Agents - therapeutic use</subject><subject>Prednisolone - adverse effects</subject><subject>Prednisolone - therapeutic use</subject><subject>Regression Analysis</subject><subject>Respiration - drug effects</subject><subject>Respiratory function</subject><subject>Retrospective Studies</subject><subject>Side effect</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Vital Capacity - drug effects</subject><issn>0387-7604</issn><issn>1872-7131</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkcGO1DAMQCMEYmcXfmGVI5eWOGmT9IJAu8CCRnAAzlGaepgMbTIk7Ur9ezKaXQ5cOFm2nm35mZBrYDUwkK8PdZ-sDwPe17zkNWtqxuAJ2YBWvFIg4CnZMKFVpSRrLshlzgdWCA7sObngCoAL3WzIl20MP6sZ00TjMrs4YaZxR3OpRD_QeY_JHle6i4neLm6PISCdluyW0SY6rHlO8bhfqQ_0sz3a8II829kx48uHeEV-fHj__eau2n79-Onm3bZyLYi50s4paYVlUivVddZx1TMuuQQluraHptdOuZYBY7xtNPadkK1gqrFq6PTAxRV5dZ57TPH3gnk2k88Ox9EGjEs2oEGxBrRUBZVn1KWYc8KdOSY_2bQaYObk0hzMo0tzcmlYY4qp0nj9sGPpJxz-tj3KK8DbM4Dl0nuPyWTnMTgcfEI3myH6_-94888IN_rgnR1_4Yr5EJcUikcDJnPDzLfTR08PBSmKmk6LP8b7nDQ</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Goto, Masahide</creator><creator>Komaki, Hirofumi</creator><creator>Takeshita, Eri</creator><creator>Abe, Yoshiki</creator><creator>Ishiyama, Akihiko</creator><creator>Sugai, Kenji</creator><creator>Sasaki, Masayuki</creator><creator>Goto, Yu-ichi</creator><creator>Nonaka, Ikuya</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20161001</creationdate><title>Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan</title><author>Goto, Masahide ; Komaki, Hirofumi ; Takeshita, Eri ; Abe, Yoshiki ; Ishiyama, Akihiko ; Sugai, Kenji ; Sasaki, Masayuki ; Goto, Yu-ichi ; Nonaka, Ikuya</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adrenal Cortex Hormones - adverse effects</topic><topic>Adrenal Cortex Hormones - therapeutic use</topic><topic>Ambulation</topic><topic>Body Height - drug effects</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Corticosteroid treatment</topic><topic>Disability Evaluation</topic><topic>Follow-Up Studies</topic><topic>Height</topic><topic>Humans</topic><topic>Japan - epidemiology</topic><topic>Kaplan-Meier Estimate</topic><topic>Mixed model</topic><topic>Motor Activity - drug effects</topic><topic>Muscular Dystrophy, Duchenne - drug therapy</topic><topic>Muscular Dystrophy, Duchenne - epidemiology</topic><topic>Muscular Dystrophy, Duchenne - genetics</topic><topic>Neurology</topic><topic>Neuromuscular Agents - adverse effects</topic><topic>Neuromuscular Agents - therapeutic use</topic><topic>Prednisolone - adverse effects</topic><topic>Prednisolone - therapeutic use</topic><topic>Regression Analysis</topic><topic>Respiration - drug effects</topic><topic>Respiratory function</topic><topic>Retrospective Studies</topic><topic>Side effect</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Vital Capacity - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goto, Masahide</creatorcontrib><creatorcontrib>Komaki, Hirofumi</creatorcontrib><creatorcontrib>Takeshita, Eri</creatorcontrib><creatorcontrib>Abe, Yoshiki</creatorcontrib><creatorcontrib>Ishiyama, Akihiko</creatorcontrib><creatorcontrib>Sugai, Kenji</creatorcontrib><creatorcontrib>Sasaki, Masayuki</creatorcontrib><creatorcontrib>Goto, Yu-ichi</creatorcontrib><creatorcontrib>Nonaka, Ikuya</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Brain &amp; development (Tokyo. 1979)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goto, Masahide</au><au>Komaki, Hirofumi</au><au>Takeshita, Eri</au><au>Abe, Yoshiki</au><au>Ishiyama, Akihiko</au><au>Sugai, Kenji</au><au>Sasaki, Masayuki</au><au>Goto, Yu-ichi</au><au>Nonaka, Ikuya</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan</atitle><jtitle>Brain &amp; development (Tokyo. 1979)</jtitle><addtitle>Brain Dev</addtitle><date>2016-10-01</date><risdate>2016</risdate><volume>38</volume><issue>9</issue><spage>785</spage><epage>791</epage><pages>785-791</pages><issn>0387-7604</issn><eissn>1872-7131</eissn><abstract>Abstract Introduction Corticosteroids are effective for improving motor function in patients with Duchenne muscular dystrophy (DMD), but there is no consensus on a regimen that balances efficacy and side effects. Methods Data from three groups of DMD patients were retrospectively analyzed: those treated with 0.75 mg/kg/day prednisolone every day (daily group, n = 51); those treated with 1 mg/kg/day prednisolone on alternate days (intermittent group, n = 36), and those not treated with steroids (nontreatment group, n = 42). Results Although the age of ambulation loss did not differ significantly among the groups, the hazard ratios for ambulation loss relative to the nontreatment group were 0.24 (95% confidence interval [CI]: 0.11–0.54) in the daily group and 0.34 (95% CI: 0.19–0.62) in the intermittent group. The percentage of predicted forced vital capacity increased until 9.6 years of age (to 94.1%) in the daily group, until 8.8 years of age (to 96.9%) in the intermittent group, and until 7.2 years of age (to 87.6%) in the nontreatment group. Weight gain was the most frequently observed side effect in the treated groups. Height was significantly lower in the daily than in the nontreatment group. Other side effects were observed, but no patient discontinued therapy. There were no marked differences in benefits and side effects between the two treated groups. Discussion This is the first assessment of long-term outcomes of different steroid therapy regimens in Japanese DMD patients. Benefits and side effects, except height, did not differ significantly between steroid regimens.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27112384</pmid><doi>10.1016/j.braindev.2016.04.001</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0387-7604
ispartof Brain & development (Tokyo. 1979), 2016-10, Vol.38 (9), p.785-791
issn 0387-7604
1872-7131
language eng
recordid cdi_proquest_miscellaneous_1817041867
source ScienceDirect Freedom Collection
subjects Adolescent
Adrenal Cortex Hormones - adverse effects
Adrenal Cortex Hormones - therapeutic use
Ambulation
Body Height - drug effects
Child
Child, Preschool
Corticosteroid treatment
Disability Evaluation
Follow-Up Studies
Height
Humans
Japan - epidemiology
Kaplan-Meier Estimate
Mixed model
Motor Activity - drug effects
Muscular Dystrophy, Duchenne - drug therapy
Muscular Dystrophy, Duchenne - epidemiology
Muscular Dystrophy, Duchenne - genetics
Neurology
Neuromuscular Agents - adverse effects
Neuromuscular Agents - therapeutic use
Prednisolone - adverse effects
Prednisolone - therapeutic use
Regression Analysis
Respiration - drug effects
Respiratory function
Retrospective Studies
Side effect
Time Factors
Treatment Outcome
Vital Capacity - drug effects
title Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T02%3A57%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Long-term%20outcomes%20of%20steroid%20therapy%20for%20Duchenne%20muscular%20dystrophy%20in%20Japan&rft.jtitle=Brain%20&%20development%20(Tokyo.%201979)&rft.au=Goto,%20Masahide&rft.date=2016-10-01&rft.volume=38&rft.issue=9&rft.spage=785&rft.epage=791&rft.pages=785-791&rft.issn=0387-7604&rft.eissn=1872-7131&rft_id=info:doi/10.1016/j.braindev.2016.04.001&rft_dat=%3Cproquest_cross%3E1817041867%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c513t-8cc76a3a0687799ac27b0262617395b14b8c7c501002548eb93653074a7d98d23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1817041867&rft_id=info:pmid/27112384&rfr_iscdi=true