Analysis of the Group of Pediatric Patients With Relapsing-Remitting Multiple Sclerosis: Data From the Czech National Registry
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
35518208
PubMed Central
PMC9062179
DOI
10.3389/fneur.2022.851426
Knihovny.cz E-zdroje
- Klíčová slova
- disease-modifying drugs, glatiramer acetate, interferon beta-a, pediatric multiple sclerosis, relapsing-remitting form,
- Publikační typ
- časopisecké články MeSH
IMPORTANCE: Multiple sclerosis can also affect children. Approximately 3-10% of patients develop multiple sclerosis before the age of 16. OBJECTIVE: The aim of this analysis is to describe the characteristics of pediatric patients with multiple sclerosis who started their treatment with disease-modifying drugs in 2013-2020, with data obtained from the Czech National Registry of patients with multiple sclerosis. DESIGN AND SETTING: A method of retrospective analysis conducted with 134 pediatric patients with multiple sclerosis was used. RESULTS: The findings reveal that the mean age at the date of the introduction of the first disease-modifying drugs treatment is 15.89 years, and gender does not play any role. In addition, moderate (51.6%) and mild (45.2%) relapses are predominant in these young patients. Seventy five percent of patients will not experience a confirmed progression of the expanded disability status scale within 54.7 months from starting the treatment. Furthermore, the results confirm that the first-choice treatment is interferon beta-a and glatiramer acetate, which is common for adult patients. However, some factors, such as a low efficacy or a lack of tolerance may impact on treatment discontinuation in children. CONCLUSION: More research should be performed on novel disease-modifying drugs for this target group.
Clinic of Neurology University Hospital Ostrava Ostrava Czechia
Department of Neurology 2nd Faculty of Medicine Charles University Prague Czechia
Department of Neurology Hospital of Jihlava Jihlava Czechia
Department of Neurology KZ a s Hospital Teplice Teplice Czechia
Department of Neurology Tomas Bata Regional Hospital Zlín Czechia
Department of Neurology University Hospital Hradec Kralove Hradec Kralove Czechia
Department of Neurology University Hospital Masaryk University Brno Czechia
Zobrazit více v PubMed
Alroughani R, Boyko A. Pediatric multiple sclerosis: a review. BMC Neurol. (2018) 18:27. 10.1186/s12883-018-1026-3 PubMed DOI PMC
Pavelek Z, Sobíšek L, Šarláková J, Potužník P, Peterka M, Štětkárová I, et al. . Comparison of therapies in MS patients after the first demyelinating event in real clinical practice in the czech republic: data from the national registry ReMuS. Front Neurol. (2021) 11:593527. 10.3389/fneur.2020.593527 PubMed DOI PMC
Frahm N, Peters M, Bätzing J, Ellenberger D, Akmatov MK, Haas J, et al. . Prevalence of pediatric multiple sclerosis in Germany: a nationwide populationulationtionwide p Eur J Neurol. (2021) 28:3173. 10.1111/ene.15015 PubMed DOI
Waldman A, Ness J, Pohl D, Simone IL, Anlar B, Amato MP, et al. . Pediatric multiple sclerosis: Clinical features and outcome. Neurology. (2016) 87:S74et al 10.1212/WNL.0000000000003028 PubMed DOI PMC
Ghezzi A, Amato MP, Makhani N, Shreiner T, Gärtner J, Tenembaum S. (2016). Pediatric multiple sclerosis: Conventional first-line treatment and general management. Neurology. 87:S97–S102. 10.1212/WNL.0000000000002823 PubMed DOI
Renoux C, Vukusic S, Mikaeloff Y, Edan G, Clanet M, Dubois B, et al. . Natural history of multiple sclerosis with childhood onset. N Engl J Med. (2007) 356:2603 al. 10.1056/NEJMoa067597 PubMed DOI
Krupp LB, Tardieu M, Amato MP, Banwell B, Chitnis T, Dale RC, et al. . International Pediatric Multiple Sclerosis Study Group criteria for pediatric multiple sclerosis and immune-mediated central nervous system demyelinating disorders: revisions to the 2007 definitions. Mult Scler. (2013) 19:1261. 10.1177/1352458513484547 PubMed DOI
Waldman AT, Gorman MP, Rensel MR, Austin TE, Hertz DP, Kuntz NL. Network of pediatric multiple sclerosis centers of excellence of national multiple sclerosis society. Management of pediatric central nervous system demyelinating disorders: consensus of United States neurologists. J Child Neurol. (2011) 26:675–82. 10.1177/0883073810395141 PubMed DOI PMC
Margoni M, Rinaldi F, Perini P, Gallo P. Therapy of pediatric-onset multiple sclerosis: state of the art, challenges, and opportunities. Front Neurol. (2021) 12:676095. 10.3389/fneur.2021.676095 PubMed DOI PMC
Jakimovski D, Awan S, Eckert SP, Farooq O, Weinstock-Guttman B. Multiple sclerosis in children: differential diagnosis, prognosis, and disease-modifying treatment. CNS Drugs. (2022) 36:45scler 10.1007/s40263-021-00887-w PubMed DOI PMC
Saijo N, Abe Y, Oikawa Y, Okubo Y, Endo W, Numata-Uematsu Y, et al. . Successful treatment with dimethyl fumarate in a child with relapsing-remitting multiple sclerosis. Brain Dev. (2022) 44:353–356. 10.1016/j.braindev.2021.12.010 PubMed DOI
Abdel-mannan OA, Manchoon C, Rossor T, Southin J-C, Tur C, Brownlee W, et al. . Use of Disease-modifying therapies in pediatric relapsing-remitting multiple sclerosis in the United Kingdom. Neurol Neuroimmunol Neuroinflamm. (2021) 8:e1008. 10.1212/NXI.0000000000001008 PubMed DOI PMC
Belman AL, Krupp LB, Olsen CS, Rose JW, Aaen G, Benson L, et al. . Characteristics of children and adolescents with multiple sclerosis. Pediatrics. (2016) 138:e20160120. 10.1542/peds.2016-0120 PubMed DOI PMC
Chitnis T, Glanz B, Jaffin S, Healy B. Demographics of pediatric-onset multiple sclerosis in an MS center population from the Northeastern United States. Mult Scler. (2009) 15:627emogr 10.1177/1352458508101933 PubMed DOI
Boiko A, Vorobeychik G, Paty D, Devonshire V, Sadovnick D. University of british columbia MS clinic neurologists. Early onset multiple sclerosis: a longitudinal study. Neurology. (2002) 59:1006tiple 10.1212/WNL.59.7.1006 PubMed DOI
Gorman MP, Healy BC, Polgar-Turcsanyi M, Chitnis T. Increased relapse rate in pediatric-onset compared with adult-onset multiple sclerosis. Arch Neurol. (2009) 66:54 rel10.1001/archneurol.2008.505 PubMed DOI
Hacohen Y, Banwell B, Ciccarelli O. What does first-line therapy mean for paediatric multiple sclerosis in the current era? Mult Scler. (2020) 27:1970–6. 10.1177/1352458520937644 PubMed DOI
Benson LA, Healy BC, Gorman MP, Baruch NF, Gholipour T, Musallam A, et al. . Elevated relapse rates in pediatric compared to adult MS persist for at least 6 years. Mult Scler Relat Disord. (2014) 3:186.sord10.1016/j.msard.2013.06.004 PubMed DOI
Chitnis T. Role of puberty in multiple sclerosis risk and course. Clin Immunol. (2013) 149:192erty i10.1016/j.clim.2013.03.014 PubMed DOI
Harding KE, Liang K, Cossburn MD, Ingram G, Hirst CL, Pickersgill TP, et al. . Long-term outcome of paediatric-onset multiple sclerosis: a population-based study. J Neurol Neurosurg Psychiatry. (2013) 84:141hh P 10.1136/jnnp-2012-303996 PubMed DOI
Banwell B, Reder AT, Krupp L, Tenembaum S, Eraksoy M, Alexey B, et al. . Safety and tolerability of interferon beta-1b in pediatric multiple sclerosis. Neurology. (2006) 66:472et a 10.1212/01.wnl.0000198257.52512.1a PubMed DOI
Kornek B, Bernert G, Balassy C, Geldner J, Prayer D, Feucht M. Glatiramer acetate treatment in patients with childhood and juvenile onset multiple sclerosis. Neuropediatrics. (2003) 34:120s.nt10.1055/s-2003-41274 PubMed DOI
Dale RC, Brilot F, Duffy LV, Twilt M, Waldman AT, Narula S, et al. . Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease. Neurology. (2014) 83:142lity 10.1212/WNL.0000000000000570 PubMed DOI PMC
Krysko KM, Graves JS, Rensel M, Weinstock-Guttman B, Rutatangwa A, Aaen G, et al. . Real-world effectiveness of initial disease-modifying therapies in pediatric multiple sclerosis. Ann Neurol. (2020) 88:42al-wo 10.1002/ana.25737 PubMed DOI