Aquaporin-4 Immunoglobulin G–seropositive Neuromyelitis Optica Spectrum Disorder MRI Characteristics: Data Analysis from the International Real-World PAMRINO Study Cohort

Authors: Claudia Chien, Vera Cruz e Silva, Emanuel Geiter, Dominik Meier, Hanna Zimmermann, Denis B. Bichuetti, Marcos I. Idagawa, Ayse Altintas, Uygur Tanriverdi, Sasitorn Siritho, Lehka Pandit, Anitha Dcunha, Maria J. Sá, Rita Figueiredo, Peiqing Qian, Caryl Tongco, Itay Lotan, Vadim Khasminsky, Mark A. Hellmann, Hadas Stiebel-Kalish, Dalia L. Rotstein, Lindsay Waxman, Daniel Ontaneda, Kunio Nakamura, Hesham Abboud, M. Omar Subei, Yang Mao-Draayer, Joachim Havla, Nasrin Asgari, Pernille B. Skejø, Ilya Kister, Marius Ringelstein, Simon Broadley, Simon Arnett, Brie Marron, Anna M. Jolley, Michael Wunderlich, Sean Green, Lawrence J. Cook, Michael R. Yeaman, Terry J. Smith, Alexander U. Brandt, Jens Wuerfel, Friedemann Paul,

Published: 2024-11-12

DOI: 10.1148/radiol.233099

Source: Full article


Abstract

Large, international, real-world MRI assessments showed high heterogeneity in the data collected from patients with aquaporin-4 immunoglobulin G–seropositive neuromyelitis optica spectrum disorder and frequent cerebral and lower spinal cord abnormalities.