Effectiveness of Disease-Modifying Treatment on Spinal Cord Lesion Formation in Relapse-Onset Multiple Sclerosis: an Msbase Registry Study
| dc.contributor.author | Kreiter, D. | |
| dc.contributor.author | Kalincik, T. | |
| dc.contributor.author | Hupperts, R. | |
| dc.contributor.author | Patti, F. | |
| dc.contributor.author | Spitaleri, D. | |
| dc.contributor.author | Foschi, M. | |
| dc.contributor.author | Surcinelli, A. | |
| dc.date.accessioned | 2024-09-22T13:31:49Z | |
| dc.date.available | 2024-09-22T13:31:49Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | Background: Spinal cord lesions in multiple sclerosis (MS) have considerable impact on disability. High-efficacy disease-modifying treatments (hDMTs) are associated with greater reduction of relapses and new brain lesions compared to low-efficacy treatments (lDMTs). Knowledge on the impact of DMTs on cord lesion formation is limited as these outcome measures were not included in MS treatment trials. This study aims to investigate whether hDMTs reduce the formation of cord lesions more effectively than lDMTs. Methods: Patients with relapse-onset MS, a cord magnetic resonance imaging (MRI) within 6 months before/after initiation of their first DMT and ≥1 cord MRI at follow-up (interval > 6 months) were extracted from the MSBase registry (ACTRN12605000455662). Patients treated with hDMTs ≥90% or lDMTs ≥90% of follow-up duration were considered the hDMT and lDMT groups, respectively. Matching was performed using propensity scores. Cox proportional hazards models were used to estimate the hazards of new cord lesions, brain lesions and relapses. Results: Ninety-four and 783 satisfied hDMT and lDMT group criteria, respectively. Seventy-seven hDMT patients were matched to 184 lDMT patients. In the hDMT group there was no evidence of reduction of new cord lesions (hazard ratio [HR] 0.99 [95% CI 0.51, 1.92], p = 0.97), while there were fewer new brain lesions (HR 0.22 [95% CI 0.10, 0.49], p < 0.001) and fewer relapses (HR 0.45 [95% CI 0.28, 0.72], p = 0.004). Conclusion: A potential discrepancy exists in the effect of hDMTs over lDMTs in preventing spinal cord lesions versus brain lesions and relapses. While hDMTs provided a significant reduction for the latter when compared to lDMTs, there was no significant reduction in new spinal cord lesions. © The Author(s) 2024. | en_US |
| dc.identifier.doi | 10.1007/s40263-024-01115-x | |
| dc.identifier.issn | 1172-7047 | |
| dc.identifier.issn | 1179-1934 | |
| dc.identifier.scopus | 2-s2.0-85203272561 | |
| dc.identifier.uri | https://doi.org/10.1007/s40263-024-01115-x | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14365/5538 | |
| dc.language.iso | en | en_US |
| dc.publisher | Adis | en_US |
| dc.relation.ispartof | CNS Drugs | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.title | Effectiveness of Disease-Modifying Treatment on Spinal Cord Lesion Formation in Relapse-Onset Multiple Sclerosis: an Msbase Registry Study | en_US |
| dc.type | Article | en_US |
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| gdc.description.department | İzmir Ekonomi Üniversitesi | en_US |
| gdc.description.departmenttemp | Kreiter D., Department of Neurology, Academic MS Center Zuyd, Zuyderland MC, Sittard-Geleen, Netherlands, School for Mental Health and Neuroscience, Department of Neurology, Maastricht University Medical Center, Maastricht, Netherlands; Kalincik T., Department of Neurology, Neuroimmunology Centre, Royal Melbourne Hospital, Melbourne, Australia, Department of Medicine, CORe, University of Melbourne, Melbourne, Australia; Hupperts R., Department of Neurology, Academic MS Center Zuyd, Zuyderland MC, Sittard-Geleen, Netherlands, School for Mental Health and Neuroscience, Department of Neurology, Maastricht University Medical Center, Maastricht, Netherlands; Patti F., Department of Medical and Surgical Sciences and Advanced Technologies, GF Ingrassia, Catania, Italy, Multiple Sclerosis Unit, AOU Policlinico G Rodolico-San Marco, University of Catania, Catania, Italy; Spitaleri D., Azienda Ospedaliera di Rilievo Nazionale San Giuseppe Moscati Avellino, Avellino, Italy; Foschi M., Department of Neuroscience, MS Center, Neurology Unit, S. Maria delle Croci Hospital, AUSL Romagna, Ravenna, Italy, Department of Biotechnological and Applied Clinical Sciences (DISCAB), University of L’Aquila, L’Aquila, Italy; Surcinelli A., Department of Neur | en_US |
| gdc.description.endpage | 930 | |
| gdc.description.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
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| gdc.description.startpage | 921 | |
| gdc.description.volume | 38 | |
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| gdc.identifier.pmid | 39242483 | |
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| gdc.oaire.keywords | Male | |
| gdc.oaire.keywords | Adult | |
| gdc.oaire.keywords | spinal cord | |
| gdc.oaire.keywords | 610 | |
| gdc.oaire.keywords | Middle Aged | |
| gdc.oaire.keywords | Magnetic Resonance Imaging | |
| gdc.oaire.keywords | high-efficacy disease- modifying treatments (hDMTs) | |
| gdc.oaire.keywords | multiple sclerosis (MS) | |
| gdc.oaire.keywords | Multiple Sclerosis, Relapsing-Remitting | |
| gdc.oaire.keywords | Treatment Outcome | |
| gdc.oaire.keywords | Spinal Cord | |
| gdc.oaire.keywords | Recurrence | |
| gdc.oaire.keywords | low- efficacy treatments (lDMTs) | |
| gdc.oaire.keywords | Humans | |
| gdc.oaire.keywords | Female | |
| gdc.oaire.keywords | Original Research Article | |
| gdc.oaire.keywords | Registries | |
| gdc.oaire.keywords | Follow-Up Studies | |
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