Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/51246
Title: Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes
Authors: Yılmaz, Ü.
Gücüyener, K.
Yavuz, M.
Öncel, İ.
Canpolat, M.
Saltık, S.
Ünver, O.
Çıtak Kurt, Ayşegül Neşe
Tosun, Ayşe
Yılmaz, Sanem
Özgör, Bilge
Haspolat, Şenay
İncecik, Faruk
Kutluk, Gültekin
Dilber, Cengiz
Dundar, Nihal Olgac
Tan, Hüseyin
Dursun, Büşra Daşlı
Dilek, Tuğçe Damla
Türkdoğan, Dilşad
Yalnızoğlu, Dilek
Yılmaz, Deniz
Akbaş, Salih
Güleç, Ayten
İpek, Rojan
Ayanoğlu, Müge
Kanmaz, Seda
Güngör, Serdal
Öztürk, Gülten
Beşen, Şeyda
Haliloğlu, Göknur
Karaca, Nazlı Balcan
Öztürk, Selcan
Yüksel, Deniz
Oktay, Seçil
Gürkaş, Esra
Karaoğlu, Pakize
Serin, Hepsen Mine
Karadağ, Meral
Hakkı Akbeyaz, İsmail
Yiş, Uluç
Polat, Burçin Gönüllü
Okan, Mehmet Sait
Bektaş, Ömer
Orgun, Leman Tekin
Günbey, Ceren
Per, Hüseyin
Keskin, Filiz
Gültutan, Pembe
Öztürk, Semra Büyükkorkmaz
Aksoy, Erhan
Aksoy, Erhan
Akyüz, Gülcan
Tekgül, Hasan
Kürekçi, Fulya
Kurul, A. Semra Hız
Asadova, Nargis
Çarman, Kürşat Bora
Alikılıç, Defne
Duman, Özgür
Kömür, Mustafa
Yıldırım, Miraç
Alıcı, Nurettin
Gümüş, Hakan
Polat, Muzaffer
Kamaşak, Tülay
Konuşkan, Bahadır
Güngör, Olcay
Mert, Gülen Gül
Edizer, Selvinaz
Mıhçı, Filiz
Öztürk, Sedef Terzioğlu
Toker, Rabia Tütüncü
Şenoğlu, Mine Çiğdem
Arslan, Mutluay
Şahin, Sevim
Gencpinar, Pinar
Yıldırım, Elif
Yüksel, Ersin
Ekici, Arzu
Kayılıoğlu, Hülya
Deniz, Adnan
Yayici Köken, Özlem
Okuyaz, Çetin
Süt, Nurşah Yeniay
Atasoy, Ergin
Ayça, Senem
Solmaz, İsmail
Yetkin, Mehmet Fatih
Bilgin, Neslihan
Atasever, Aslı Kübra
Sarıtaş, Serdar
Tekin, Hande Gazeteci
Dokurel, İpek
Özçelik, Aysima
Sarıgeçili, Esra
Aksoy, Ayşe
Türköz, Ayşe Nur
Koç, Habibe
Cavusoglu, Dilek
Ünalp, Aycan
Şahin, Türkan Uygur
Erol, İlknur
Öztoprak, Ülkühan
Elitez, Duygu Aykol
Direk, Meltem Çobanoğulları
Bodur, Muhittin
Teber, Serap
Anlar, Banu
Aykol, Duygu
Yıldız, Edibe Pembegül
Yarar, Coşkun
Kara, Bülent
Acer, Hamit
Keywords: Anti-AQP4-IgG
Anti-MOG-IgG
Antibody
Demyelinating
Pediatric multiple sclerosis
autoantibody
immunoglobulin G
myelin oligodendrocyte glycoprotein
acute disseminated encephalomyelitis
diagnostic imaging
female
human
male
multiple sclerosis
myelooptic neuropathy
nuclear magnetic resonance imaging
Autoantibodies
Encephalomyelitis, Acute Disseminated
Female
Humans
Immunoglobulin G
Magnetic Resonance Imaging
Male
Multiple Sclerosis
Myelin-Oligodendrocyte Glycoprotein
Neuromyelitis Optica
Publisher: W.B. Saunders Ltd
Abstract: Background: The discovery of anti-myelin oligodendrocyte glycoprotein (MOG)-IgG and anti-aquaporin 4 (AQP4)-IgG and the observation on certain patients previously diagnosed with multiple sclerosis (MS) actually have an antibody-mediated disease mandated re-evaluation of pediatric MS series. Aim: To describe the characteristics of recent pediatric MS cases by age groups and compare with the cohort established before 2015. Method: Data of pediatric MS patients diagnosed between 2015 and 2021 were collected from 44 pediatric neurology centers across Türkiye. Clinical and paraclinical features were compared between patients with disease onset before 12 years (earlier onset) and ≥12 years (later onset) as well as between our current (2015–2021) and previous (<2015) cohorts. Results: A total of 634 children (456 girls) were enrolled, 89 (14%) were of earlier onset. The earlier-onset group had lower female/male ratio, more frequent initial diagnosis of acute disseminated encephalomyelitis (ADEM), more frequent brainstem symptoms, longer interval between the first two attacks, less frequent spinal cord involvement on magnetic resonance imaging (MRI), and lower prevalence of cerebrospinal fluid (CSF)-restricted oligoclonal bands (OCBs). The earlier-onset group was less likely to respond to initial disease-modifying treatments. Compared to our previous cohort, the current series had fewer patients with onset <12 years, initial presentation with ADEM-like features, brainstem or cerebellar symptoms, seizures, and spinal lesions on MRI. The female/male ratio, the frequency of sensorial symptoms, and CSF-restricted OCBs were higher than reported in our previous cohort. Conclusion: Pediatric MS starting before 12 years was less common than reported previously, likely due to exclusion of patients with antibody-mediated diseases. The results underline the importance of antibody testing and indicate pediatric MS may be a more homogeneous disorder and more similar to adult-onset MS than previously thought. © 2022 European Paediatric Neurology Society
URI: https://doi.org/10.1016/j.ejpn.2022.08.006
https://hdl.handle.net/11499/51246
ISSN: 1090-3798
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu

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