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Clinically meaningful effect of strontium ranelate on symptoms in knee osteoarthritis: a responder analysis.

Identifieur interne : 003480 ( PubMed/Curation ); précédent : 003479; suivant : 003481

Clinically meaningful effect of strontium ranelate on symptoms in knee osteoarthritis: a responder analysis.

Auteurs : Olivier Bruyère [Royaume-Uni] ; Jean-Yves Reginster [Royaume-Uni] ; Nicholas Bellamy [Royaume-Uni] ; Roland Chapurlat [Royaume-Uni] ; Pascal Richette [Royaume-Uni] ; Cyrus Cooper [Royaume-Uni]

Source :

RBID : pubmed:24667161

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Abstract

The aim of this study was to assess the efficacy of strontium ranelate in improving symptoms in knee OA.

DOI: 10.1093/rheumatology/keu018
PubMed: 24667161

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pubmed:24667161

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<div type="abstract" xml:lang="en">The aim of this study was to assess the efficacy of strontium ranelate in improving symptoms in knee OA.</div>
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<DateCreated>
<Year>2014</Year>
<Month>07</Month>
<Day>19</Day>
</DateCreated>
<DateCompleted>
<Year>2014</Year>
<Month>09</Month>
<Day>12</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>09</Month>
<Day>22</Day>
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<ISSN IssnType="Electronic">1462-0332</ISSN>
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<Volume>53</Volume>
<Issue>8</Issue>
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<Year>2014</Year>
<Month>Aug</Month>
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<Title>Rheumatology (Oxford, England)</Title>
<ISOAbbreviation>Rheumatology (Oxford)</ISOAbbreviation>
</Journal>
<ArticleTitle>Clinically meaningful effect of strontium ranelate on symptoms in knee osteoarthritis: a responder analysis.</ArticleTitle>
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<Abstract>
<AbstractText Label="OBJECTIVES" NlmCategory="OBJECTIVE">The aim of this study was to assess the efficacy of strontium ranelate in improving symptoms in knee OA.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Symptoms were assessed over 3 years in patients with primary knee OA receiving strontium ranelate 2 g/day (n = 454), 1 g/day (n = 445) or placebo (n = 472) in the Strontium Ranelate Efficacy in Knee Osteoarthritis Trial. Clinical response was evaluated using WOMAC subscores, minimal perceptible clinical improvement (MPCI), minimal clinically important improvement (MCII) and a modified OMERACT-Osteoarthritis Research Society International (OARSI) responder definition. Patients who withdrew prematurely from the study were considered non-responders.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">There was no significant effect on symptoms for strontium ranelate 1 g/day. At the dosage of 2 g/day, strontium ranelate was associated with greater response than placebo in terms of ≥20% improvement in WOMAC pain from baseline to the last visit (58% vs 47%, P = 0.002) and ≥50% improvement in WOMAC pain (42% vs 36%, P = 0.083). Significant differences were found in MPCI response for WOMAC pain (52% vs 40%, P < 0.001), stiffness (47% vs 39%, P = 0.009) and physical function (46% vs 37%, P = 0.009) and in MCII response for WOMAC physical function (46% vs 37%, P = 0.013). There were also more OMERACT-OARSI-like responders with strontium ranelate (44% vs 35%, P = 0.004). The treatment-placebo difference in MPCI response for WOMAC pain was significant after 6 months (P = 0.024), while that in MPCI and MCII response for WOMAC physical function reached significance after 12 months (P = 0.027 and P = 0.019, respectively).</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">Treatment with strontium ranelate 2 g/day over 3 years is associated with a clinically meaningful improvement in pain from 6 months as well as physical function and stiffness as assessed by the number of responders above thresholds of clinical relevance.</AbstractText>
<AbstractText Label="TRIAL REGISTRATION" NlmCategory="BACKGROUND">Current Controlled Trials. http://www.controlled-trials.com/ (ISRCTN41323372).</AbstractText>
<CopyrightInformation>© The Author 2014. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oup.com.</CopyrightInformation>
</Abstract>
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<Affiliation>Department of Public Health, Epidemiology and Health Economics, University of Liège, CHU Sart-Tilman, Liège, Belgium, School of Medicine, University of Queensland, Herston, Queensland, Australia, INSERM UMR 1033 and Université de Lyon, Service de Rhumatologie et Pathologie Osseuse, Hôpital Edouard Herriot, Lyon, France, Université Paris 7, UFR médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Fédération de Rhumatologie, Paris Cedex, France and MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, and NIHR Biomedical Research Unit, University of Oxford, Oxford, UK. olivier.bruyere@ulg.ac.be.</Affiliation>
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<Initials>JY</Initials>
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<Affiliation>Department of Public Health, Epidemiology and Health Economics, University of Liège, CHU Sart-Tilman, Liège, Belgium, School of Medicine, University of Queensland, Herston, Queensland, Australia, INSERM UMR 1033 and Université de Lyon, Service de Rhumatologie et Pathologie Osseuse, Hôpital Edouard Herriot, Lyon, France, Université Paris 7, UFR médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Fédération de Rhumatologie, Paris Cedex, France and MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, and NIHR Biomedical Research Unit, University of Oxford, Oxford, UK.</Affiliation>
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<LastName>Bellamy</LastName>
<ForeName>Nicholas</ForeName>
<Initials>N</Initials>
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<Affiliation>Department of Public Health, Epidemiology and Health Economics, University of Liège, CHU Sart-Tilman, Liège, Belgium, School of Medicine, University of Queensland, Herston, Queensland, Australia, INSERM UMR 1033 and Université de Lyon, Service de Rhumatologie et Pathologie Osseuse, Hôpital Edouard Herriot, Lyon, France, Université Paris 7, UFR médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Fédération de Rhumatologie, Paris Cedex, France and MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, and NIHR Biomedical Research Unit, University of Oxford, Oxford, UK.</Affiliation>
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<Affiliation>Department of Public Health, Epidemiology and Health Economics, University of Liège, CHU Sart-Tilman, Liège, Belgium, School of Medicine, University of Queensland, Herston, Queensland, Australia, INSERM UMR 1033 and Université de Lyon, Service de Rhumatologie et Pathologie Osseuse, Hôpital Edouard Herriot, Lyon, France, Université Paris 7, UFR médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Fédération de Rhumatologie, Paris Cedex, France and MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, and NIHR Biomedical Research Unit, University of Oxford, Oxford, UK.</Affiliation>
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<LastName>Richette</LastName>
<ForeName>Pascal</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Department of Public Health, Epidemiology and Health Economics, University of Liège, CHU Sart-Tilman, Liège, Belgium, School of Medicine, University of Queensland, Herston, Queensland, Australia, INSERM UMR 1033 and Université de Lyon, Service de Rhumatologie et Pathologie Osseuse, Hôpital Edouard Herriot, Lyon, France, Université Paris 7, UFR médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Fédération de Rhumatologie, Paris Cedex, France and MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, and NIHR Biomedical Research Unit, University of Oxford, Oxford, UK.</Affiliation>
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<ForeName>Cyrus</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>Department of Public Health, Epidemiology and Health Economics, University of Liège, CHU Sart-Tilman, Liège, Belgium, School of Medicine, University of Queensland, Herston, Queensland, Australia, INSERM UMR 1033 and Université de Lyon, Service de Rhumatologie et Pathologie Osseuse, Hôpital Edouard Herriot, Lyon, France, Université Paris 7, UFR médicale, Assistance Publique-Hôpitaux de Paris, Hôpital Lariboisière, Fédération de Rhumatologie, Paris Cedex, France and MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, and NIHR Biomedical Research Unit, University of Oxford, Oxford, UK.</Affiliation>
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<Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
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<Grant>
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<Agency>Medical Research Council</Agency>
<Country>United Kingdom</Country>
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<Year>2014</Year>
<Month>03</Month>
<Day>25</Day>
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<Country>England</Country>
<MedlineTA>Rheumatology (Oxford)</MedlineTA>
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<ISSNLinking>1462-0324</ISSNLinking>
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<NameOfSubstance UI="D013876">Thiophenes</NameOfSubstance>
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<DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
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<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D008875" MajorTopicYN="N">Middle Aged</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D020370" MajorTopicYN="N">Osteoarthritis, Knee</DescriptorName>
<QualifierName UI="Q000188" MajorTopicYN="Y">drug therapy</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D013876" MajorTopicYN="N">Thiophenes</DescriptorName>
<QualifierName UI="Q000627" MajorTopicYN="Y">therapeutic use</QualifierName>
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<MeshHeading>
<DescriptorName UI="D016896" MajorTopicYN="N">Treatment Outcome</DescriptorName>
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</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">SEKOIA</Keyword>
<Keyword MajorTopicYN="N">osteoarthritis</Keyword>
<Keyword MajorTopicYN="N">pain</Keyword>
<Keyword MajorTopicYN="N">responder criteria</Keyword>
<Keyword MajorTopicYN="N">strontium ranelate</Keyword>
<Keyword MajorTopicYN="N">symptoms</Keyword>
</KeywordList>
</MedlineCitation>
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<Year>2014</Year>
<Month>3</Month>
<Day>27</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<Year>2014</Year>
<Month>3</Month>
<Day>29</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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<PubMedPubDate PubStatus="medline">
<Year>2014</Year>
<Month>9</Month>
<Day>13</Day>
<Hour>6</Hour>
<Minute>0</Minute>
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</History>
<PublicationStatus>ppublish</PublicationStatus>
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<ArticleId IdType="pubmed">24667161</ArticleId>
<ArticleId IdType="pii">keu018</ArticleId>
<ArticleId IdType="doi">10.1093/rheumatology/keu018</ArticleId>
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