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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...
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Published in: | Brain & development (Tokyo. 1979) 2016-10, Vol.38 (9), p.785-791 |
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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. |
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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 & 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 & 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 & 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 & 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> |
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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 |
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