dc.contributor.author
Bellmann-Strobl, Judith
dc.contributor.author
Paul, Friedemann
dc.contributor.author
Wuerfel, Jens
dc.contributor.author
Dörr, Jan
dc.contributor.author
Infante-Duarte, Carmen
dc.contributor.author
Heidrich, Elmira
dc.contributor.author
Körtgen, Benedict
dc.contributor.author
Brandt, Alexander
dc.contributor.author
Pfüller, Caspar
dc.contributor.author
Radbruch, Helena
dc.contributor.author
Rust, Rebekka
dc.contributor.author
Siffrin, Volker
dc.contributor.author
Aktas, Orhan
dc.contributor.author
Heesen, Christoph
dc.contributor.author
Faiss, Jürgen
dc.contributor.author
Hoffmann, Frank
dc.contributor.author
Lorenz, Mario
dc.contributor.author
Zimmermann, Benno
dc.contributor.author
Groppa, Sergiu
dc.contributor.author
Wernecke, Klaus-Dieter
dc.contributor.author
Zipp, Frauke
dc.date.accessioned
2021-10-19T12:19:46Z
dc.date.available
2021-10-19T12:19:46Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/32367
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-32092
dc.description.abstract
Objective: To assess the safety and efficacy of epigallocatechin-3-gallate (EGCG) add-on to glatiramer acetate (GA) in patients with relapsing-remitting multiple sclerosis (RRMS).
Methods: We enrolled patients with RRMS (aged 18-60 years, Expanded Disability Status Scale [EDSS] score 0-6.5), receiving stable GA treatment in a multicenter, prospective, double-blind, phase II, randomized controlled trial. Participants received up to 800 mg oral EGCG daily over a period of 18 months. The primary outcome was the proportion of patients without new hyperintense lesions on T2-weighted (T2w) brain MRI within 18 months. Secondary end points included additional MRI and clinical parameters. Immunologic effects of EGCG were investigated in exploratory experiments.
Results: A total of 122 patients on GA were randomly assigned to EGCG treatment (n = 62) or placebo (n = 60). We could not demonstrate a difference between groups after 18 months for the primary outcome or other radiologic (T2w lesion volume, T1w hypointense lesion number or volume, number of cumulative contrast-enhancing lesions, percent brain volume change), or clinical (EDSS, MS functional composite, and annualized relapse rate) parameter. EGCG treatment did not affect immune response to GA. Pharmacologic analysis revealed wide ranging EGCG plasma levels. The treatment was well tolerated with a similar incidence of mostly mild adverse events similar in both groups.
Conclusion: In RRMS, oral EGCG add-on to GA was not superior to placebo in influencing MRI and clinical disease activity over 18 months. The treatment was safe at a daily dosage up to 800 mg EGCG. It did not influence immune parameters, despite indication of EGCG being bioavailable in patients. Classification of Evidence This study provides Class II evidence that for patients with RRMS, EGCG added to GA did not significantly affect the development of new hyperintense lesions on T2-weighted brain MRI.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
multiple sclerosis
en
dc.subject
epigallocatechin-3-gallate
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Epigallocatechin Gallate in Relapsing-Remitting Multiple Sclerosis
dc.type
Wissenschaftlicher Artikel
dc.title.subtitle
A Randomized, Placebo-Controlled Trial
dcterms.bibliographicCitation.articlenumber
e981
dcterms.bibliographicCitation.doi
10.1212/nxi.0000000000000981
dcterms.bibliographicCitation.journaltitle
Neurology: Neuroimmunology & Neuroinflammation
dcterms.bibliographicCitation.number
3
dcterms.bibliographicCitation.originalpublishername
Wolters Kluwer
dcterms.bibliographicCitation.volume
8
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33762428
dcterms.isPartOf.eissn
2332-7812