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dc.creatorMavridis T., Papagiannakis N., Breza M., Vavougios G.D., Patas K., Daponte A., Laskaratos A., Archontakis-Barakakis P., Pantazopoulos I., Mitsikostas D.D.en
dc.date.accessioned2023-01-31T08:58:05Z
dc.date.available2023-01-31T08:58:05Z
dc.date.issued2022
dc.identifier10.3390/jpm12091474
dc.identifier.issn20754426
dc.identifier.urihttp://hdl.handle.net/11615/76433
dc.description.abstractBackground: Multiple Sclerosis treatment with B-cell targeted therapies may be associated with an increased incidence of headache. We aimed to find and compare the association of B-cell targeted therapies with the incidence of headache in patients with Multiple Sclerosis. Methods: In a systematic based approach, the following databases were searched from inception until the 6th of June 2020: Pubmed/MEDLINE, ClinicalTrials.gov, EU Clinical Trials Register. Only randomized clinical trials (RCTs) enrolling patients with Multiple Sclerosis comparing B-cell targeted therapies (Rituximab, Ocrelizumab, Ofatumumab, Ublituximab or Cladribine) with placebo were selected for the systematic review and further meta-analysis. PRISMA guidelines were followed at all stages of the systematic review. The primary outcome was an all-cause headache of B-cell targeting therapy in patients with Multiple Sclerosis. Results: Nine RCTs were included. Compared with placebo, treatment with B-cell targeting therapies revealed a trend in headache risk, but it was not statistically significant (Relative Risk 1.12 [95% Confidence Interval 0.96–1.30]; p = 0.15; I2 = 9.32%). Surprisingly, in a sub-group analysis, Cladribine was statistically significant for an increase in headache risk (RR 1.20 [95% CI 1.006–1.42]; p = 0.042; I2 = 0%; 3 studies with 2107 participants). Conclusions: Even though a trend is shown, B-cell targeted therapies do not correlate with an increased incidence of headache as an adverse effect. Sub-analyses revealed a significant association between Cladribine alone and an increased incidence of headache. Whereas a purinergic signaling cascade is proposed as a mechanism of action, further research is needed to unravel the underlying pathogenetic mechanism of headache induction and establish headache prevention strategies. © 2022 by the authors.en
dc.language.isoenen
dc.sourceJournal of Personalized Medicineen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85138654501&doi=10.3390%2fjpm12091474&partnerID=40&md5=9c18ff11625c2026f5279952676b76ca
dc.subjectcalcitonin gene related peptideen
dc.subjectcladribineen
dc.subjectocrelizumaben
dc.subjectofatumumaben
dc.subjectrituximaben
dc.subjectublituximaben
dc.subjectdrug therapyen
dc.subjectheadacheen
dc.subjecthumanen
dc.subjectmeta analysisen
dc.subjectmultiple sclerosisen
dc.subjectnervous system inflammationen
dc.subjectpurinergic signalingen
dc.subjectReviewen
dc.subjectsystematic reviewen
dc.subjectMDPIen
dc.titleB-Cell Targeted Therapies in Patients with Multiple Sclerosis and Incidence of Headache: A Systematic Review and Meta-Analysisen
dc.typeotheren


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