Publication: Long-Term Disability Trajectories in Primary Progressive MS Patients: A Latent Class Growth Analysis
| dc.authorscopusid | 36545349100 | |
| dc.authorscopusid | 7005179252 | |
| dc.authorscopusid | 7004836896 | |
| dc.authorscopusid | 57190082411 | |
| dc.authorscopusid | 6602085940 | |
| dc.authorscopusid | 57202571257 | |
| dc.authorscopusid | 7005617741 | |
| dc.contributor.author | Signori, A. | |
| dc.contributor.author | Izquierdo, G. | |
| dc.contributor.author | Lugaresi, A. | |
| dc.contributor.author | Hupperts, R. | |
| dc.contributor.author | Grand'Maison, F. | |
| dc.contributor.author | Sola, P. | |
| dc.contributor.author | Horáková, D. | |
| dc.date.accessioned | 2020-06-21T13:11:24Z | |
| dc.date.available | 2020-06-21T13:11:24Z | |
| dc.date.issued | 2018 | |
| dc.department | Ondokuz Mayıs Üniversitesi | en_US |
| dc.department-temp | [Signori] A., Department of Health Sciences (DISSAL), Università degli Studi di Genova, Genoa, Italy; [Izquierdo] Guillermo Ayuso, Hospital Universitario Virgen Macarena, Sevilla, Spain; [Lugaresi] Alessandra, Università degli Studi di Bologna, Facoltà di Medicina e Chirurgia, Bologna, BO, Italy, Istituto delle Scienze Neurologiche di Bologna, Bologna, Italy; [Hupperts] Raymond M.M., Zuyderland, Sittard-Geleen, Limburg, Netherlands; [Grand'Maison] François, Neuro Rive-Sud, Greenfield Park, QC, Canada; [Sola] Patrizia, Nuovo Ospedale Civile Sant'Agostino Estense, Modena, MO, Italy; [Horáková] Dana, Department of Neurology and Center of Clinical Neuroscience, Všeobecná Fakultní Nemocnice v Praze, Prague, Czech Republic; [Kubala Havrdová] Eva Kubala, Department of Neurology and Center of Clinical Neuroscience, Všeobecná Fakultní Nemocnice v Praze, Prague, Czech Republic; [Prat] Alexandre, Hôpital Notre-Dame, Montreal, QC, Canada; [Girard] Marc, Hôpital Notre-Dame, Montreal, QC, Canada; [Duquette] Pierre Pascal, Hôpital Notre-Dame, Montreal, QC, Canada; [Boz] Cavit, Karadeniz Teknik Üniversitesi Tip Fakültesi, Trabzon, Turkey; [Grammond] Pierre, Centre de réadaptation en déficience physique Chaudière-Appalaches, QC, Canada; [Terzi] Murat, Faculty of Medicine, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Singhal] Bhim Sen, Bombay Hospital and Medical Research Centre, Mumbai, MH, India; [Alroughani] Raed A., Al-Amiri Hospital, Safat, Kuwait; [Petersen] Thor K., Aarhus Universitetshospital, Aarhus, Midtjylland, Denmark; [Ramo-Tello] Cristina M., Hospital Universitari Germans Trias i Pujol, Badalona, Spain; [Oreja-Guevara] Celia, Hospital Clínico San Carlos, Madrid, Madrid, Spain; [Spitaleri] Daniele Litterio A., Azienda Ospedaliera di Rilievo Nazionale San Giuseppe Moscati Avellino, Avellino, AV, Italy; [Shaygannejad] Vahid, Isfahan University of Medical Sciences, Isfahan, Isfahan, Iran; [Butzkueven] Helmut, Box Hill Hospital, Sydney, VIC, Australia, Department of Medicine, Melbourne, VIC, Australia; [Kalincik] Tomas, Department of Medicine, Melbourne, VIC, Australia; [Jokubaitis] Vilija G., Department of Medicine, Melbourne, VIC, Australia; [Slee] Mark, Flinders University, Adelaide, SA, Australia; [Fernández-Bolaños] Ricardo, Hospital Universitario de Valme, Sevilla, Seville, Spain; [Sánchez-Menoyo] José Luis, Hospital de Galdakao, Galdakao, Biscay, Spain; [Pucci] Eugenio, UOC Neurologia, Macerata, Italy; [Granella] Franco, Università di Parma, Parma, PR, Italy; [Lechner-Scott] Jeannette S., The University of Newcastle, Australia, Callaghan, NSW, Australia; [Iuliano] Gerardo, Ospedali Riuniti di Salerno, Salerno, Italy; [Hughes] Stella E., Craigavon Area Hospital, Portadown, Armagh, Northern Ireland, United Kingdom; [Bergamaschi] Roberto, IRCCS Fondazione Mondino, Pavia, PV, Italy; [Taylor] Bruce V.M., Royal Hobart Hospital, Hobart, TS, Australia; [Verheul] Freek A.M., Groene Hart Hospital, Gouda, Netherlands; [Edite Rio] Maria, Sao Joao Hospital, Porto, Porto, Portugal; [Amato] Maria Pia, Department of NEUROFARBA, Università degli Studi di Firenze, Florence, FI, Italy; [Sajedi] Seyed Aidin, Department of Neurology, Golestan University of Medical Sciences, Gorgan, Golestan, Iran; [Majdinasab] Nastaran, Golestan Hospital (AJUMS), Ahvaz, Khuzestan, Iran; [van Pesch] Vincent, Cliniques Universitaires Saint-Luc, Brussels, BRU, Belgium; [Sormani] Maria Pia, Department of Health Sciences (DISSAL), Università degli Studi di Genova, Genoa, Italy; [Trojano] Maria, Department of Basic Medical Sciences, Università degli studi di Bari Aldo Moro, Bari, BA, Italy | en_US |
| dc.description.abstract | Background: Several natural history studies on primary progressive multiple sclerosis (PPMS) patients detected a consistent heterogeneity in the rate of disability accumulation. Objectives: To identify subgroups of PPMS patients with similar longitudinal trajectories of Expanded Disability Status Scale (EDSS) over time. Methods: All PPMS patients collected within the MSBase registry, who had their first EDSS assessment within 5 years from onset, were included in the analysis. Longitudinal EDSS scores were modeled by a latent class mixed model (LCMM), using a nonlinear function of time from onset. LCMM is an advanced statistical approach that models heterogeneity between patients by classifying them into unobserved groups showing similar characteristics. Results: A total of 853 PPMS (51.7% females) from 24 countries with a mean age at onset of 42.4 years (standard deviation (SD): 10.8 years), a median baseline EDSS of 4 (interquartile range (IQR): 2.5–5.5), and 2.4 years of disease duration (SD: 1.5 years) were included. LCMM detected three different subgroups of patients with a mild (n = 143; 16.8%), moderate (n = 378; 44.3%), or severe (n = 332; 38.9%) disability trajectory. The probability of reaching EDSS 6 at 10 years was 0%, 46.4%, and 81.9% respectively. Conclusion: Applying an LCMM modeling approach to long-term EDSS data, it is possible to identify groups of PPMS patients with different prognosis. © 2017, © The Author(s), 2017. | en_US |
| dc.identifier.doi | 10.1177/1352458517703800 | |
| dc.identifier.endpage | 652 | en_US |
| dc.identifier.issn | 1352-4585 | |
| dc.identifier.issn | 1477-0970 | |
| dc.identifier.issue | 5 | en_US |
| dc.identifier.pmid | 28382837 | |
| dc.identifier.scopus | 2-s2.0-85032873925 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 642 | en_US |
| dc.identifier.uri | https://doi.org/10.1177/1352458517703800 | |
| dc.identifier.volume | 24 | en_US |
| dc.identifier.wos | WOS:000432098100013 | |
| dc.identifier.wosquality | Q1 | |
| dc.language.iso | en | en_US |
| dc.publisher | SAGE Publications Ltd info@sagepub.co.uk | en_US |
| dc.relation.ispartof | Multiple Sclerosis Journal | en_US |
| dc.relation.journal | Multiple Sclerosis Journal | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.subject | Clinical Trials | en_US |
| dc.subject | Disability | en_US |
| dc.subject | Heterogeneity | en_US |
| dc.subject | Long-Term | en_US |
| dc.subject | Primary Progressive Multiple Sclerosis | en_US |
| dc.subject | Trajectories | en_US |
| dc.title | Long-Term Disability Trajectories in Primary Progressive MS Patients: A Latent Class Growth Analysis | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication |
