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dc.contributor.authorYılmaz, Deniz
dc.contributor.authorTeber, Serap
dc.contributor.authorGültutan, Pembe
dc.contributor.authorYıldırım, Miraç
dc.contributor.authorBektaş, Ömer
dc.contributor.authorAlikılıç, Defne
dc.contributor.authorGüngör, Mesut
dc.contributor.authorKara, Bülent
dc.contributor.authorÖncel, İbrahim
dc.contributor.authorDilek, Tuğçe Damla
dc.contributor.authorSaltık, Sema
dc.contributor.authorKanmaz, Seda
dc.contributor.authorYılmaz, Sanem
dc.contributor.authorTekgül, Hasan
dc.contributor.authorÇavuşoğlu, Dilek
dc.contributor.authorKaraoğlu, Pakize
dc.contributor.authorYılmaz, Ünsal
dc.contributor.authorOrak, Sibğatullah Ali
dc.contributor.authorGüngör, Olcay
dc.contributor.authorAnlar, Banu
dc.date.accessioned2023-10-17T11:31:52Z
dc.date.available2023-10-17T11:31:52Z
dc.date.issued2023en_US
dc.identifier.citationYılmaz, D., Teber, S., Gültutan, P., Yıldırım, M., Bektaş, Ö., Alikılıç, D., ... & Anlar, B. (2023). A multicenter study of radiologically isolated syndrome in children and adolescents: Can we predict the course?. Multiple Sclerosis and Related Disorders, 79, 104948.en_US
dc.identifier.issn2211-0356
dc.identifier.urihttps://dx.doi.org/10.1016/j.msard.2023.104948.
dc.identifier.urihttps://hdl.handle.net/20.500.12933/1645
dc.description.abstractObjectives: To evaluate clinical characteristics, imaging features and etiological profile of Radiologically Isolated Syndrome (RIS) along with clinical and radiological follow-up. Methods: Demographic, clinical and radiological data of patients younger than 18 years fulfilling the criteria for RIS were retrospectively analyzed. RIS was defined by the detection of lesions meeting the revised 2010 McDonald Criteria for dissemination in space on magnetic resonance imaging (MRI) in the absence of any symptoms of demyelinating disease or an alternative cause for the MRI findings. Results: There were total 69 patients (38 girls, 31 boys). The median age at index MRI was 15.7 years, and median follow-up time was 28 months. The most common reason for neuroimaging was headache (60.9%). A first clinical event occurred with median 11 months in 14/69 (20%) of cases. Those with oligoclonal bands (OCB) in cerebrospinal fluid (CSF) and follow-up longer than 3 years were more likely to experience a clinical event (p<0.05): 25% of those with OCB manifested clinical symptoms within the first year and 33.3% within the first two years compared to 6.3% and 9.4%, respectively in those without OCB. Radiological evolution was not associated with any variables: age, sex, reason for neuroimaging, serum 25-hydroxyvitamin D level, elevated IgG index, OCB positivity, total number and localization of lesions, presence of gadolinium enhancement, achievement of 2005 criteria for DIS and duration of follow-up. Conclusion: Children and adolescents with RIS and CSF OCB should be followed-up for at least 3 years in order to detect any clinical symptoms suggestive of a demyelinating event. Because disease-modifying treatments are not approved in RIS and no consensus report justifies their use especially in pediatric RIS, close follow-up of OCB-positive patients is needed for early recognition of any clinical event and timely initiation of specific treatment.en_US
dc.language.isoengen_US
dc.publisherElsevier B. V.en_US
dc.relation.isversionof10.1016/j.msard.2023.104948.en_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectMultiple Sclerosisen_US
dc.subjectPediatricen_US
dc.subjectRadiologically Isolated Syndromeen_US
dc.titleA multicenter study of radiologically isolated syndrome in children and adolescents: Can we predict the course?en_US
dc.typearticleen_US
dc.authorid0000-0003-4924-5300en_US
dc.departmentAFSÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.contributor.institutionauthorÇavuşoğlu, Dilek
dc.identifier.volume79en_US
dc.relation.journalMultiple sclerosis and related disordersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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