TY - JOUR
T1 - Application of the international criteria for optic neuritis in the Acute Optic Neuritis Network
AU - Klyscz, Philipp
AU - Asseyer, Susanna
AU - Alonso, Ricardo
AU - Bereuter, Charlotte
AU - Bialer, Omer
AU - Bick, Atira
AU - Carta, Sara
AU - Chen, John J.
AU - Cohen, Leila
AU - Cohen-Tayar, Yamit
AU - Contentti, Edgar Carnero
AU - Dale, Russell C.
AU - Flanagan, Eoin P.
AU - Gernert, Jonathan A.
AU - Haas, Julian
AU - Havla, Joachim
AU - Heesen, Christoph
AU - Hellmann, Mark
AU - Levin, Netta
AU - Lopez, Pablo
AU - Lotan, Itay
AU - Luis, Maria Belen
AU - Mariotto, Sara
AU - Mayer, Christina
AU - Vergara, Alvaro Jose Mejia
AU - Ocampo, Cassandra
AU - Ochoa, Susana
AU - Oertel, Frederike C.
AU - Olszewska, Maja
AU - Uribe, José Luis Peralta
AU - Sastre-Garriga, Jaume
AU - Scocco, Dario
AU - Ramanathan, Sudarshini
AU - Rattanathamsakul, Natthapon
AU - Shi, Fu Dong
AU - Shifa, Jemal
AU - Simantov, Ilya
AU - Siritho, Sasitorn
AU - Tiosano, Alon
AU - Tisavipat, Nanthaya
AU - Torres, Isabel
AU - Dembinsky, Adi Vaknin
AU - Vidal-Jordana, Angela
AU - Wilf-Yarkoni, Adi
AU - Wu, Ti
AU - Zamir, Sol
AU - Zarco, Luis Alfonso
AU - Zimmermann, Hanna G.
AU - Petzold, Axel
AU - Paul, Friedemann
AU - Stiebel-Kalish, Hadas
N1 - Publisher Copyright:
© 2024 The Author(s). Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.
PY - 2024
Y1 - 2024
N2 - Objective: The first international consensus criteria for optic neuritis (ICON) were published in 2022. We applied these criteria to a prospective, global observational study of acute optic neuritis (ON). Methods: We included 160 patients with a first-ever acute ON suggestive of a demyelinating CNS disease from the Acute Optic Neuritis Network (ACON). We applied the 2022 ICON to all participants and subsequently adjusted the ICON by replacing a missing relative afferent pupillary defect (RAPD) or dyschromatopsia if magnetic resonance imaging pathology of the optical nerve plus optical coherence tomography abnormalities or certain biomarkers are present. Results: According to the 2022 ICON, 80 (50%) patients were classified as definite ON, 12 (7%) patients were classified as possible ON, and 68 (43%) as not ON (NON). The main reasons for classification as NON were absent RAPD (52 patients, 76%) or dyschromatopsia (49 patients, 72%). Distribution of underlying ON etiologies was as follows: 78 (49%) patients had a single isolated ON, 41 (26%) patients were diagnosed with multiple sclerosis, 25 (16%) patients with myelin oligodendrocyte glycoprotein antibody-associated disease, and 15 (9%) with neuromyelitis optica spectrum disorder. The application of the adjusted ON criteria yielded a higher proportion of patients classified as ON (126 patients, 79%). Interpretation: According to the 2022 ICON, almost half of the included patients in ACON did not fulfill the requirements for classification of definite or possible ON, particularly due to missing RAPD and dyschromatopsia. Thorough RAPD examination and formal color vision testing are critical to the application of the 2022 ICON.
AB - Objective: The first international consensus criteria for optic neuritis (ICON) were published in 2022. We applied these criteria to a prospective, global observational study of acute optic neuritis (ON). Methods: We included 160 patients with a first-ever acute ON suggestive of a demyelinating CNS disease from the Acute Optic Neuritis Network (ACON). We applied the 2022 ICON to all participants and subsequently adjusted the ICON by replacing a missing relative afferent pupillary defect (RAPD) or dyschromatopsia if magnetic resonance imaging pathology of the optical nerve plus optical coherence tomography abnormalities or certain biomarkers are present. Results: According to the 2022 ICON, 80 (50%) patients were classified as definite ON, 12 (7%) patients were classified as possible ON, and 68 (43%) as not ON (NON). The main reasons for classification as NON were absent RAPD (52 patients, 76%) or dyschromatopsia (49 patients, 72%). Distribution of underlying ON etiologies was as follows: 78 (49%) patients had a single isolated ON, 41 (26%) patients were diagnosed with multiple sclerosis, 25 (16%) patients with myelin oligodendrocyte glycoprotein antibody-associated disease, and 15 (9%) with neuromyelitis optica spectrum disorder. The application of the adjusted ON criteria yielded a higher proportion of patients classified as ON (126 patients, 79%). Interpretation: According to the 2022 ICON, almost half of the included patients in ACON did not fulfill the requirements for classification of definite or possible ON, particularly due to missing RAPD and dyschromatopsia. Thorough RAPD examination and formal color vision testing are critical to the application of the 2022 ICON.
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U2 - 10.1002/acn3.52166
DO - 10.1002/acn3.52166
M3 - Article
AN - SCOPUS:85200408420
SN - 2328-9503
JO - Annals of Clinical and Translational Neurology
JF - Annals of Clinical and Translational Neurology
ER -