| dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
| dc.contributor.author | Rotstein, Dalia |
| dc.contributor.author | Solomon, Jacqueline |
| dc.contributor.author | Sormani, Maria Pia |
| dc.contributor.author | Montalban, Xavier |
| dc.contributor.author | Ye, Xiang Y. |
| dc.contributor.author | Dababneh, Dina |
| dc.date.accessioned | 2022-11-18T13:18:58Z |
| dc.date.available | 2022-11-18T13:18:58Z |
| dc.date.issued | 2022-11 |
| dc.identifier.citation | Rotstein D, Solomon JM, Sormani MP, Montalban X, Ye XY, Dababneh D, et al. Association of NEDA-4 With No Long-term Disability Progression in Multiple Sclerosis and Comparison With NEDA-3: A Systematic Review and Meta-analysis. Neurol Neuroimmunol Neuroinflamm. 2022 Nov;9(6):e200032. |
| dc.identifier.issn | 2332-7812 |
| dc.identifier.uri | https://hdl.handle.net/11351/8502 |
| dc.description | Multiple sclerosis; Disability; NEDA-4 |
| dc.description.abstract | Background and Objectives No evidence of disease activity (NEDA)-4 has been suggested as a treatment target for disease-modifying therapy (DMT) in relapsing-remitting multiple sclerosis (RRMS). However, the ability of NEDA-4 to discriminate long-term outcomes in MS and how its performance compares with NEDA-3 remain uncertain. We conducted a systematic review and meta-analysis to evaluate (1) the association between NEDA-4 and no long-term disability progression in MS and (2) the comparative performance of NEDA-3 and NEDA-4 in predicting no long-term disability progression.
Methods English-language abstracts and manuscripts were systematically searched in MEDLINE, Embase, and the Cochrane databases from January 2006 to November 2021 and reviewed independently by 2 investigators. We selected studies that assessed NEDA-4 at 1 or 2 years after DMT start and had at least 4 years of follow-up for determination of no confirmed disability progression. We conducted a meta-analysis using random-effects model to determine the pooled odds ratio (OR) for no disability progression with NEDA-4 vs EDA-4. For the comparative analysis, we selected studies that evaluated both NEDA-3 and NEDA-4 with at least 4 years of follow-up and examined the difference in the association of NEDA-3 and NEDA-4 with no disability progression.
Results Five studies of 1,000 patients (3 interferon beta and 2 fingolimod) met inclusion criteria for both objectives. The median duration of follow-up was 6 years (interquartile range: 4–6 years). The prevalence of NEDA-4 ranged from 4.2% to 13.9% on interferon beta therapy and 24.9% to 25.1% on fingolimod therapy. The pooled OR for no long-term confirmed disability progression with NEDA-4 vs EDA-4 was 2.14 (95% confidence interval: 1.36–3.37; I2 = 0). We did not observe any significant difference between NEDA-4 and NEDA-3 in the comparative analyses.
Discussion In patients with RRMS, NEDA-4 at 1–2 years was associated with 2 times higher odds of no long-term disability progression, at 6 years compared with EDA-4, but offered no advantage over NEDA-3. |
| dc.language.iso | eng |
| dc.publisher | Wolters Kluwer Health |
| dc.relation.ispartofseries | Neurology, Neuroimmunology and Neuroinflammation;9(6) |
| dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.source | Scientia |
| dc.subject | Esclerosi múltiple - Tractament |
| dc.subject | Esclerosi múltiple - Prognosi |
| dc.subject.mesh | Multiple Sclerosis |
| dc.subject.mesh | /drug therapy |
| dc.subject.mesh | Disease Progression |
| dc.title | Association of NEDA-4 With No Long-term Disability Progression in Multiple Sclerosis and Comparison With NEDA-3: A Systematic Review and Meta-analysis |
| dc.type | info:eu-repo/semantics/article |
| dc.identifier.doi | 10.1212/NXI.0000000000200032 |
| dc.subject.decs | esclerosis múltiple |
| dc.subject.decs | /farmacoterapia |
| dc.subject.decs | progresión de la enfermedad |
| dc.relation.publishversion | https://doi.org/10.1212/NXI.0000000000200032 |
| dc.type.version | info:eu-repo/semantics/publishedVersion |
| dc.audience | Professionals |
| dc.contributor.organismes | Institut Català de la Salut |
| dc.contributor.authoraffiliation | [Rotstein D] Department of Medicine, University of Toronto, Ontario, Canada; St. Michael’s Hospital, Toronto, Ontario, Canada. [Solomon JM] Department of Medicine, McMaster University, Hamilton, Ontario, Canada. [Sormani MP] Department of Health Sciences, Section of Biostatistics, University of Genova, Italy; IRCCS Ospedale Policlinico San Martino, Genova, Italy. [Montalban X] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya, Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Ye XY] Department of Pediatrics, Mount Sinai Hospital, Toronto, Canada. [Dababneh D] Columbia University Irving Medical Center, Department of Neurology, New York City; New York Presbyterian Hospital (NYP), New York City |
| dc.identifier.pmid | 36224046 |
| dc.identifier.wos | 000874687300005 |
| dc.rights.accessrights | info:eu-repo/semantics/openAccess |