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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2743506232</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_13524585221136036</sage_id><sourcerecordid>2743506232</sourcerecordid><originalsourceid>FETCH-LOGICAL-c320t-f4e9e91d67e88a53f49972e94e419f1f28c41f9266ae1e7859f86323db5f98953</originalsourceid><addsrcrecordid>eNp1kEtLAzEUhYMotlZ_gBsZcONmap6TyVJKtULBja6HNHMjKZmHkxnRf2_GVgXF1b1wvnMu9yB0TvCcECmvCROUi1xQSgjLMMsO0JRwKVOsJD6Me9TTEZigkxC2GGMpmThGE5Zxnksqp2i1fOuhq7VPXrV3pe5dUyeNTXRivKudiULbQenMp1A1JfjExWXwvWs9JMF46Jrgwik6stoHONvPGXq6XT4uVun64e5-cbNODaO4Ty0HBYqUmYQ814JZrpSkoDhwoiyxNDecWEWzTAMBmQtl84xRVm6EVbkSbIaudrlt17wMEPqicsGA97qGZggFlZwJnNHomaHLX-i2GcZfR0qKWBohOFJkR5n4R-jAFm3nKt29FwQXY83Fn5qj52KfPGwqKL8dX71GYL4Dgn6Gn7P_J34A0LiDCw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2775211110</pqid></control><display><type>article</type><title>External validation of a clinical prediction model in multiple sclerosis</title><source>SAGE Complete A-Z List</source><source>MEDLINE</source><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</creator><creatorcontrib>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</creatorcontrib><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 < 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).
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 < 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><subject>Accuracy</subject><subject>Disease Progression</subject><subject>Humans</subject><subject>Models, Statistical</subject><subject>Multiple sclerosis</subject><subject>Multiple Sclerosis - drug therapy</subject><subject>Multiple Sclerosis, Chronic Progressive - drug therapy</subject><subject>Multiple Sclerosis, Relapsing-Remitting - drug therapy</subject><subject>Patients</subject><subject>Prediction models</subject><subject>Prognosis</subject><subject>Recurrence</subject><issn>1352-4585</issn><issn>1477-0970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtLAzEUhYMotlZ_gBsZcONmap6TyVJKtULBja6HNHMjKZmHkxnRf2_GVgXF1b1wvnMu9yB0TvCcECmvCROUi1xQSgjLMMsO0JRwKVOsJD6Me9TTEZigkxC2GGMpmThGE5Zxnksqp2i1fOuhq7VPXrV3pe5dUyeNTXRivKudiULbQenMp1A1JfjExWXwvWs9JMF46Jrgwik6stoHONvPGXq6XT4uVun64e5-cbNODaO4Ty0HBYqUmYQ814JZrpSkoDhwoiyxNDecWEWzTAMBmQtl84xRVm6EVbkSbIaudrlt17wMEPqicsGA97qGZggFlZwJnNHomaHLX-i2GcZfR0qKWBohOFJkR5n4R-jAFm3nKt29FwQXY83Fn5qj52KfPGwqKL8dX71GYL4Dgn6Gn7P_J34A0LiDCw</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Moradi, Nahid</creator><creator>Sharmin, Sifat</creator><creator>Malpas, Charles B</creator><creator>Shaygannejad, Vahid</creator><creator>Terzi, Murat</creator><creator>Boz, Cavit</creator><creator>Yamout, Bassem</creator><creator>Khoury, Samia J</creator><creator>Turkoglu, Recai</creator><creator>Karabudak, Rana</creator><creator>Shalaby, Nevin</creator><creator>Soysal, Aysun</creator><creator>Altıntaş, Ayşe</creator><creator>Inshasi, Jihad</creator><creator>Al-Harbi, Talal</creator><creator>Alroughani, Raed</creator><creator>Kalincik, Tomas</creator><general>SAGE Publications</general><general>Sage Publications Ltd</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>7T5</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><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></search><sort><creationdate>202302</creationdate><title>External validation of a clinical prediction model in multiple sclerosis</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c320t-f4e9e91d67e88a53f49972e94e419f1f28c41f9266ae1e7859f86323db5f98953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Accuracy</topic><topic>Disease Progression</topic><topic>Humans</topic><topic>Models, Statistical</topic><topic>Multiple sclerosis</topic><topic>Multiple Sclerosis - drug therapy</topic><topic>Multiple Sclerosis, Chronic Progressive - drug therapy</topic><topic>Multiple Sclerosis, Relapsing-Remitting - drug therapy</topic><topic>Patients</topic><topic>Prediction models</topic><topic>Prognosis</topic><topic>Recurrence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & 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 < 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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issn | 1352-4585 1477-0970 |
language | eng |
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source | SAGE Complete A-Z List; MEDLINE |
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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