Progression of regional grey matter atrophy in multiple sclerosis

Autor: Massimo Filippi, Viktor Wottschel, Lukas Pirpamer, Jeroen J. G. Geurts, Alan J. Thompson, Hugo Vrenken, Christian Enzinger, Niamh Cawley, Daniel C. Alexander, Sebastien Ourselin, M. Laura Stromillo, Razvan V. Marinescu, Jaume Sastre-Garriga, Serena Ruggieri, M. Jorge Cardoso, Marco Battaglini, Ferran Prados, Arman Eshaghi, Floriana De Angelis, Claudio Gasperini, Carmen Tur, Olga Ciccarelli, Alex Rovira, Frederik Barkhof, Wallace Brownlee, Maria A. Rocca, Cyra E. Leurs, Bernard M. J. Uitdehaag, Declan T. Chard, Alexandra L. Young, Nicholas C. Firth, Claudia Am Gandini Wheeler-Kingshott, Nicola De Stefano
Přispěvatelé: Eshaghi, Arman, Marinescu, Razvan V., Young, Alexandra L., Firth, Nicholas C., Prados, Ferran, Jorge Cardoso, M., Tur, Carmen, De Angelis, Floriana, Cawley, Niamh, Brownlee, Wallace J, De Stefano, Nicola, Laura Stromillo, M., Battaglini, Marco, Ruggieri, Serena, Gasperini, Claudio, Filippi, Massimo, Rocca, Maria A, Rovira, Alex, Sastre-Garriga, Jaume, Geurts, Jeroen J G, Vrenken, Hugo, Wottschel, Viktor, Leurs, Cyra E, Uitdehaag, Bernard, Pirpamer, Luka, Enzinger, Christian, Ourselin, Sebastien, Gandini Wheeler-Kingshott, Claudia A, Chard, Declan, Thompson, Alan J, Barkhof, Frederik, Alexander, Daniel C, Ciccarelli, Olga, Anatomy and neurosciences, Amsterdam Neuroscience - Neuroinfection & -inflammation, Radiology and nuclear medicine, Neurology
Předmět:
Zdroj: Publons
Eshaghi, A, Marinescu, R V, Young, A L, Firth, N C, Prados, F, Jorge Cardoso, M, Tur, C, De Angelis, F, Cawley, N, Brownlee, W J, De Stefano, N, Laura Stromillo, M, Battaglini, M, Ruggieri, S, Gasperini, C, Filippi, M, Rocca, M A, Rovira, A, Sastre-Garriga, J, Geurts, J J G, Vrenken, H, Wottschel, V, Leurs, C E, Uitdehaag, B, Pirpamer, L, Enzinger, C, Ourselin, S, Gandini Wheeler-Kingshott, C A, Chard, D, Thompson, A J, Barkhof, F, Alexander, D C & Ciccarelli, O 2018, ' Progression of regional grey matter atrophy in multiple sclerosis ', Brain, vol. 141, no. 6, pp. 1665-1677 . https://doi.org/10.1093/brain/awy088
Brain, 141(6), 1665-1677
Web of Science
ISSN: 1665-1677
0006-8950
DOI: 10.1093/brain/awy088
Popis: SummaryGrey matter atrophy is present from the earliest clinical stages of multiple sclerosis (MS), but the temporal ordering is poorly understood. We aimed to determine the sequence in which grey matter regions become atrophic in MS, and its association with disability accumulation.In this longitudinal study, we included 1,417 subjects: 253 with clinically-isolated syndrome (CIS), 708 relapsing-remitting MS (RRMS), 128 secondary-progressive MS (SPMS), 125 primary-progressive MS (PPMS), and 203 healthy controls from 7 European centres. Subjects underwent repeated MRI scanning (total number of scans 3,604); the mean follow-up for patients was 2.41yrs (SD±1.97). Disability was scored using the Expanded Disability Status Scale (EDSS). We calculated the volume of brain grey matter regions and brainstem using an unbiased within-subject template. We used an established data-driven event-based model (EBM) to determine the sequence of occurrence of atrophy and its uncertainty. We assigned each subject to a specific EBM stage, based on the number of their atrophic regions. We used nested linear mixed-effects regression models to explore the associations between the rate of increase in the EBM stages over time, disease duration and annual rate of EDSS gain.The first regions to become atrophic in CIS and relapse-onset MS patients (RRMS and SPMS) were the posterior cingulate cortex and precuneus, followed by the middle cingulate cortex, brainstem and thalamus. The sequence of atrophy in PPMS showed a similar involvement of the thalamus, cuneus, precuneus, and pallidum, followed by the brainstem and posterior cingulate cortex. The cerebellum, caudate and putamen showed early atrophy in relapse-onset MS and late atrophy in PPMS. Patients with SPMS showed the highest EBM stages (highest number of atrophic regions, all ppThis data-driven staging of atrophy progression in a large MS sample demonstrates that grey matter atrophy spreads to involve more regions over time. The sequence in which regions become atrophic is reasonably consistent across MS phenotypes. The spread of atrophy was associated with disease duration, and disability accumulation in RRMS.AbbreviationsMSmultiple sclerosisGMgrey matterFLAIRFluid Attenuated Inversion RecoveryPPMSprimary progressive multiple sclerosis; primary-progressive MS
Databáze: OpenAIRE