Disease course after pregnancy in women with progressive multiple sclerosis symptoms
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, pozorovací studie, multicentrická studie
PubMed
40974262
PubMed Central
PMC12547043
DOI
10.1177/13524585251368248
Knihovny.cz E-zdroje
- Klíčová slova
- Multiple sclerosis, clinical outcomes, disability, pregnancy, primary progressive multiple sclerosis, secondary progressive multiple sclerosis,
- MeSH
- chronicko-progresivní roztroušená skleróza * patofyziologie MeSH
- dospělí MeSH
- kohortové studie MeSH
- komplikace těhotenství * patofyziologie epidemiologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- poporodní období MeSH
- posuzování pracovní neschopnosti MeSH
- progrese nemoci * MeSH
- registrace MeSH
- těhotenství MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- pozorovací studie MeSH
BACKGROUND: The impact of pregnancy on disease outcomes has not been characterised in women with progressive multiple sclerosis (MS) phenotypes. This study aimed to describe the clinical characteristics and disease course of women who experienced a pregnancy after a diagnosis of primary progressive MS (PPMS) or secondary progressive MS (SPMS). METHODS: This multicentre observational cohort study utilised data from the international MSBase Registry extracted on 2 June 2024. Expanded Disability Status Scale (EDSS) scores of women with progressive MS were assessed up to 10 years postpartum and compared to those of propensity score-matched women with progressive MS without a pregnancy history. RESULTS: In total, 138 women with 164 pregnancies were included in the study, comprising 75 women with PPMS and 63 with SPMS. Of these, 24 women with PPMS and 47 with SPMS had longitudinal peri-pregnancy EDSS assessments and were included in the analysis of disability scores. A history of pregnancy was not associated with a significant difference in long-term disability trajectories in women with either PPMS (estimate = -0.02; 95% confidence interval (CI) = -0.07 to 0.04) or SPMS (estimate = 0.00; 95% CI = -0.02 to 0.03). CONCLUSION: A history of pregnancy is not associated with a significant difference in long-term disability in women with progressive MS symptoms.
Brain and Mind Centre The University of Sydney Sydney NSW Australia
Centre hospitalier de l'Université de Montréal Université de Montréal Montreal QC Canada
CORe Department of Medicine The University of Melbourne Melbourne VIC Australia
Department of Medical and Surgical Sciences and Advanced Technologies G F Ingrassia Catania Italy
Department of Neurology Alfred Health Melbourne VIC Australia
Department of Neurology Box Hill Hospital Melbourne VIC Australia
Department of Neurology Hospital Universitario Virgen Macarena Seville Spain
Department of Neurology Medical Faculty Karadeniz Technical University Trabzon Turkey
Department of Neurosciences Eastern Health Clinical School Monash University Melbourne VIC Australia
Dipartimento di Scienze Biomedieche e Neuromotorie Università di Bologna Bologna Italia
Division of Neurology Department of Medicine Amiri Hospital Sharq Kuwait
IRCCS Istituto delle Scienze Neurologiche di Bologna Bologna Italia
Izmir University of Economics Medical Point Hospital Izmir Turkey
MS Centre Clinical Neurology SS Annunziata University Hospital Chieti Italy
Multiple Sclerosis Research Association Izmir Turkey
Multiple Sclerosis Unit AOU Policlinico G Rodolico San Marco University of Catania Catania Italy
Neuroimmunology Centre Department of Neurology Royal Melbourne Hospital Melbourne VIC Australia
Zobrazit více v PubMed
Kuhlmann T, Moccia M, Coetzee T, et al. Multiple sclerosis progression: Time for a new mechanism-driven framework. Lancet Neurol 2023; 22(1): 78–88. PubMed PMC
Lublin FD, Reingold SC, Cohen JA, et al. Defining the clinical course of multiple sclerosis. Neurology 2014; 83(3): 278–286. PubMed PMC
Krysko KM, Graves JS, Dobson R, et al. Sex effects across the lifespan in women with multiple sclerosis. Ther Adv Neurol Disord 2020; 13: 936166. PubMed PMC
Portaccio E, Magyari M, Havrdova EK, et al. Multiple sclerosis: Emerging epidemiological trends and redefining the clinical course. Lancet Reg Health Eur 2024; 44: 100977. PubMed PMC
Ziemssen T, Bhan V, Chataway J, et al. Secondary progressive multiple sclerosis: A review of clinical characteristics, definition, prognostic tools, and disease-modifying therapies. Neurol Neuroimmunol Neuroinflamm 2023; 10(1): e200064. PubMed PMC
Andersson PB, Waubant E, Gee L, et al. Multiple sclerosis that is progressive from the time of onset. Arch Neurol 1999; 56(9): 1138–1142. PubMed
Kalincik T, Vivek V, Jokubaitis V, et al. Sex as a determinant of relapse incidence and progressive course of multiple sclerosis. Brain 2013; 136(Pt. 12): 3609–3617. PubMed
Coyle PK. Management of women with multiple sclerosis through pregnancy and after childbirth. Ther Adv Neurol Disord 2016; 9(3): 198–210. PubMed PMC
Dobson R, Jokubaitis VG, Giovannoni G. Change in pregnancy-associated multiple sclerosis relapse rates over time: A meta-analysis. Mult Scler Relat Disord 2020; 44: 102241. PubMed
Schubert C, Steinberg L, Peper J, et al. Postpartum relapse risk in multiple sclerosis: A systematic review and meta-analysis. J Neurol Neurosurg Psychiatry 2023; 94(9): 718–725. PubMed
Vukusic S, Hutchinson M, Hours M, et al. Pregnancy and multiple sclerosis (the PRIMS study): Clinical predictors of post-partum relapse. Brain 2004; 127(Pt6): 1353–1360. PubMed
Anderson A, Krysko KM, Rutatangwa A, et al. Clinical and radiologic disease activity in pregnancy and postpartum in MS. Neurol Neuroimmunol Neuroinflamm 2021; 8(2): e959. PubMed PMC
Gavoille A, Rollot F, Casey R, et al. Investigating the long-term effect of pregnancy on the course of multiple sclerosis using causal inference. Neurology 2023; 100(12): e1296–e1308. PubMed PMC
Hughes SE, Spelman T, Gray OM, et al. Predictors and dynamics of postpartum relapses in women with multiple sclerosis. Mult Scler 2014; 20(6): 739–746. PubMed
D’Amico E, Leone C, Patti F. Offspring number does not influence reaching the disability’s milestones in multiple sclerosis: A seven-year follow-up study. Int J Mol Sci 2016; 17(2): 234. PubMed PMC
Cuello JP, Martínez Ginés ML, Martin Barriga ML, et al. Multiple sclerosis and pregnancy: A single-centre prospective comparative study. Neurologia 2017; 32(2): 92–98. PubMed
Koch M, Uyttenboogaart M, Heersema D, et al. Parity and secondary progression in multiple sclerosis. J Neurol Neurosurg Psychiatry 2009; 80(6): 676–678. PubMed
Achiron A, Ben-David A, Gurevich M, et al. Parity and disability progression in relapsing-remitting multiple sclerosis. J Neurol 2020; 267(12): 3753–3762. PubMed
Jokubaitis VG, Spelman T, Kalincik T, et al. Predictors of long-term disability accrual in relapse-onset multiple sclerosis. Ann Neurol 2016; 80(1): 89–100. PubMed
Keyhanian K, Davoudi V, Etemadifar M, et al. Better prognosis of multiple sclerosis in patients who experienced a full-term pregnancy. Eur Neurol 2012; 68(3): 150–155. PubMed
Zeydan B, Atkinson EJ, Weis DM, et al. Reproductive history and progressive multiple sclerosis risk in women. Brain Commun 2020; 2(2): fcaa185. PubMed PMC
Karp I, Manganas A, Sylvestre MP, et al. Does pregnancy alter the long-term course of multiple sclerosis. Ann Epidemiol 2014; 24(7): 504–508. PubMed
Ostrem BL, Anderson A, Conway S, et al. Peripartum disease activity in moderately and severely disabled women with multiple sclerosis. Mult Scler J Exp Transl Clin 2022; 8(2): 104918. PubMed PMC
D’hooghe MB, Haentjens P, Nagels G, et al. Menarche, oral contraceptives, pregnancy and progression of disability in relapsing onset and progressive onset multiple sclerosis. J Neurol 2012; 259(5): 855–861. PubMed
Ramagopalan S, Yee I, Byrnes J, et al. Term pregnancies and the clinical characteristics of multiple sclerosis: A population based study. J Neurol Neurosurg Psychiatry 2012; 83(8): 793–795. PubMed
Butzkueven H, Chapman J, Cristiano E, et al. MSBase: An international, online registry and platform for collaborative outcomes research in multiple sclerosis. Mult Scler 2006; 12(6): 769–774. PubMed
Montalban X, Hauser SL, Kappos L, et al. Ocrelizumab versus placebo in primary progressive multiple sclerosis. N Engl J Med 2017; 376(3): 209–220. PubMed
Forsberg L, Spelman T, Klyve P, et al. Proportion and characteristics of secondary progressive multiple sclerosis in five European registries using objective classifiers. Mult Scler J Exp Transl Clin 2023; 9(1): 153557. PubMed PMC
Sharmin S, Roos I, Simpson-Yap S, et al. The risk of secondary progressive multiple sclerosis is geographically determined but modifiable. Brain 2023; 146(11): 4633–4644. PubMed PMC
Lublin FD, Häring DA, Ganjgahi H, et al. How patients with multiple sclerosis acquire disability. Brain 2022; 145(9): 3147–3161. PubMed PMC
Müller J, Cagol A, Lorscheider J, et al. Harmonizing definitions for progression independent of relapse activity in multiple sclerosis. JAMA Neurol 2023; 80(11): 1232. PubMed
Yeh WZ, Widyastuti PA, Van der Walt A, et al. Natalizumab, fingolimod, and dimethyl fumarate use and pregnancy-related relapse and disability in women with multiple sclerosis. Neurology 2021; 96(24): e2989–e3002. PubMed PMC
Paz Soldán MM, Novotna M, Abou Zeid N, et al. Relapses and disability accumulation in progressive multiple sclerosis. Neurology 2015; 84(1): 81–88. PubMed PMC
Pitt D, Lo CH, Gauthier SA, et al. Toward precision phenotyping of multiple sclerosis. Neurol Neuroimmunol Neuroinflamm 2022; 9(6): e200025. PubMed PMC
Cree BAC, Arnold DL, Chataway J, et al. Secondary progressive multiple sclerosis: New insights. Neurology 2021; 97(8): 378–388. PubMed PMC