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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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