External validation of a clinical prediction model in multiple sclerosis

Background: Timely initiation of disease modifying therapy is crucial for managing multiple sclerosis (MS). Objective: We aimed to validate a previously published predictive model of individual treatment response using a non-overlapping cohort from the Middle East. Methods: We interrogated the MSBas...

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Veröffentlicht in:Multiple sclerosis 2023-02, Vol.29 (2), p.261-269
Hauptverfasser: Moradi, Nahid, Sharmin, Sifat, Malpas, Charles B, Shaygannejad, Vahid, Terzi, Murat, Boz, Cavit, Yamout, Bassem, Khoury, Samia J, Turkoglu, Recai, Karabudak, Rana, Shalaby, Nevin, Soysal, Aysun, Altıntaş, Ayşe, Inshasi, Jihad, Al-Harbi, Talal, Alroughani, Raed, Kalincik, Tomas
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container_end_page 269
container_issue 2
container_start_page 261
container_title Multiple sclerosis
container_volume 29
creator Moradi, Nahid
Sharmin, Sifat
Malpas, Charles B
Shaygannejad, Vahid
Terzi, Murat
Boz, Cavit
Yamout, Bassem
Khoury, Samia J
Turkoglu, Recai
Karabudak, Rana
Shalaby, Nevin
Soysal, Aysun
Altıntaş, Ayşe
Inshasi, Jihad
Al-Harbi, Talal
Alroughani, Raed
Kalincik, Tomas
description Background: Timely initiation of disease modifying therapy is crucial for managing multiple sclerosis (MS). Objective: We aimed to validate a previously published predictive model of individual treatment response using a non-overlapping cohort from the Middle East. Methods: We interrogated the MSBase registry for patients who were not included in the initial model development. These patients had relapsing MS or clinically isolated syndrome, a recorded date of disease onset, disability and dates of disease modifying therapy, with sufficient follow-up pre- and post-baseline. Baseline was the visit at which a new disease modifying therapy was initiated, and which served as the start of the predicted period. The original models were used to translate clinical information into three principal components and to predict probability of relapses, disability worsening or improvement, conversion to secondary progressive MS and treatment discontinuation as well as changes in the area under disability-time curve (ΔAUC). Prediction accuracy was assessed using the criteria published previously. Results: The models performed well for predicting the risk of disability worsening and improvement (accuracy: 81%–96%) and performed moderately well for predicting the risk of relapses (accuracy: 73%–91%). The predictions for ΔAUC and risk of treatment discontinuation were suboptimal (accuracy 
doi_str_mv 10.1177/13524585221136036
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Objective: We aimed to validate a previously published predictive model of individual treatment response using a non-overlapping cohort from the Middle East. Methods: We interrogated the MSBase registry for patients who were not included in the initial model development. These patients had relapsing MS or clinically isolated syndrome, a recorded date of disease onset, disability and dates of disease modifying therapy, with sufficient follow-up pre- and post-baseline. Baseline was the visit at which a new disease modifying therapy was initiated, and which served as the start of the predicted period. The original models were used to translate clinical information into three principal components and to predict probability of relapses, disability worsening or improvement, conversion to secondary progressive MS and treatment discontinuation as well as changes in the area under disability-time curve (ΔAUC). Prediction accuracy was assessed using the criteria published previously. Results: The models performed well for predicting the risk of disability worsening and improvement (accuracy: 81%–96%) and performed moderately well for predicting the risk of relapses (accuracy: 73%–91%). The predictions for ΔAUC and risk of treatment discontinuation were suboptimal (accuracy &lt; 44%). Accuracy for predicting the risk of conversion to secondary progressive MS ranged from 50% to 98%. Conclusion: The previously published models are generalisable to patients with a broad range of baseline characteristics in different geographic regions.</description><identifier>ISSN: 1352-4585</identifier><identifier>EISSN: 1477-0970</identifier><identifier>DOI: 10.1177/13524585221136036</identifier><identifier>PMID: 36448727</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Accuracy ; Disease Progression ; Humans ; Models, Statistical ; Multiple sclerosis ; Multiple Sclerosis - drug therapy ; Multiple Sclerosis, Chronic Progressive - drug therapy ; Multiple Sclerosis, Relapsing-Remitting - drug therapy ; Patients ; Prediction models ; Prognosis ; Recurrence</subject><ispartof>Multiple sclerosis, 2023-02, Vol.29 (2), p.261-269</ispartof><rights>The Author(s), 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c320t-f4e9e91d67e88a53f49972e94e419f1f28c41f9266ae1e7859f86323db5f98953</cites><orcidid>0000-0001-5436-5804 ; 0000-0003-3778-1376 ; 0000-0001-6253-4487 ; 0000-0001-5892-751X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/13524585221136036$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/13524585221136036$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36448727$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moradi, Nahid</creatorcontrib><creatorcontrib>Sharmin, Sifat</creatorcontrib><creatorcontrib>Malpas, Charles B</creatorcontrib><creatorcontrib>Shaygannejad, Vahid</creatorcontrib><creatorcontrib>Terzi, Murat</creatorcontrib><creatorcontrib>Boz, Cavit</creatorcontrib><creatorcontrib>Yamout, Bassem</creatorcontrib><creatorcontrib>Khoury, Samia J</creatorcontrib><creatorcontrib>Turkoglu, Recai</creatorcontrib><creatorcontrib>Karabudak, Rana</creatorcontrib><creatorcontrib>Shalaby, Nevin</creatorcontrib><creatorcontrib>Soysal, Aysun</creatorcontrib><creatorcontrib>Altıntaş, Ayşe</creatorcontrib><creatorcontrib>Inshasi, Jihad</creatorcontrib><creatorcontrib>Al-Harbi, Talal</creatorcontrib><creatorcontrib>Alroughani, Raed</creatorcontrib><creatorcontrib>Kalincik, Tomas</creatorcontrib><title>External validation of a clinical prediction model in multiple sclerosis</title><title>Multiple sclerosis</title><addtitle>Mult Scler</addtitle><description>Background: Timely initiation of disease modifying therapy is crucial for managing multiple sclerosis (MS). 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Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Multiple sclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moradi, Nahid</au><au>Sharmin, Sifat</au><au>Malpas, Charles B</au><au>Shaygannejad, Vahid</au><au>Terzi, Murat</au><au>Boz, Cavit</au><au>Yamout, Bassem</au><au>Khoury, Samia J</au><au>Turkoglu, Recai</au><au>Karabudak, Rana</au><au>Shalaby, Nevin</au><au>Soysal, Aysun</au><au>Altıntaş, Ayşe</au><au>Inshasi, Jihad</au><au>Al-Harbi, Talal</au><au>Alroughani, Raed</au><au>Kalincik, Tomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>External validation of a clinical prediction model in multiple sclerosis</atitle><jtitle>Multiple sclerosis</jtitle><addtitle>Mult Scler</addtitle><date>2023-02</date><risdate>2023</risdate><volume>29</volume><issue>2</issue><spage>261</spage><epage>269</epage><pages>261-269</pages><issn>1352-4585</issn><eissn>1477-0970</eissn><abstract>Background: Timely initiation of disease modifying therapy is crucial for managing multiple sclerosis (MS). Objective: We aimed to validate a previously published predictive model of individual treatment response using a non-overlapping cohort from the Middle East. Methods: We interrogated the MSBase registry for patients who were not included in the initial model development. These patients had relapsing MS or clinically isolated syndrome, a recorded date of disease onset, disability and dates of disease modifying therapy, with sufficient follow-up pre- and post-baseline. Baseline was the visit at which a new disease modifying therapy was initiated, and which served as the start of the predicted period. The original models were used to translate clinical information into three principal components and to predict probability of relapses, disability worsening or improvement, conversion to secondary progressive MS and treatment discontinuation as well as changes in the area under disability-time curve (ΔAUC). Prediction accuracy was assessed using the criteria published previously. Results: The models performed well for predicting the risk of disability worsening and improvement (accuracy: 81%–96%) and performed moderately well for predicting the risk of relapses (accuracy: 73%–91%). The predictions for ΔAUC and risk of treatment discontinuation were suboptimal (accuracy &lt; 44%). Accuracy for predicting the risk of conversion to secondary progressive MS ranged from 50% to 98%. Conclusion: The previously published models are generalisable to patients with a broad range of baseline characteristics in different geographic regions.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>36448727</pmid><doi>10.1177/13524585221136036</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5436-5804</orcidid><orcidid>https://orcid.org/0000-0003-3778-1376</orcidid><orcidid>https://orcid.org/0000-0001-6253-4487</orcidid><orcidid>https://orcid.org/0000-0001-5892-751X</orcidid></addata></record>
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subjects Accuracy
Disease Progression
Humans
Models, Statistical
Multiple sclerosis
Multiple Sclerosis - drug therapy
Multiple Sclerosis, Chronic Progressive - drug therapy
Multiple Sclerosis, Relapsing-Remitting - drug therapy
Patients
Prediction models
Prognosis
Recurrence
title External validation of a clinical prediction model in multiple sclerosis
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