Different patterns of longitudinal brain and spinal cord changes and their associations with disability progression in NMO and MS View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2017-06-30

AUTHORS

Yaou Liu, Yunyun Duan, Jing Huang, Zhuoqiong Ren, Zheng Liu, Huiqing Dong, Florian Weiler, Horst K. Hahn, Fu-Dong Shi, Helmut Butzkueven, Frederik Barkhof, Kuncheng Li

ABSTRACT

ObjectiveTo investigate the longitudinal spinal cord and brain changes in neuromyelitis optica (NMO) and multiple sclerosis (MS) and their associations with disability progression.Patients and methodsWe recruited 28 NMO, 22 MS, and 20 healthy controls (HC), who underwent both spinal cord and brain MRI at baseline. Twenty-five NMO and 20 MS completed 1-year follow-up. Baseline spinal cord and brain lesion loads, mean upper cervical cord area (MUCCA), brain, and thalamus volume and their changes during a 1-year follow-up were measured and compared between groups. All the measurements were also compared between progressive and non-progressive groups in NMO and MS.ResultsMUCCA decreased significantly during the 1-year follow-up in NMO not in MS. Percentage brain volume changes (PBVC) and thalamus volume changes in MS were significantly higher than NMO. MUCCA changes were significantly different between progressive and non-progressive groups in NMO, while baseline brain lesion volume and PBVC were associated with disability progression in MS. MUCCA changes during 1-year follow-up showed association with clinical disability in NMO.ConclusionSpinal cord atrophy changes were associated with disability progression in NMO, while baseline brain lesion load and whole brain atrophy changes were related to disability progression in MS.Key Points• Spinal cord atrophy progression was observed in NMO.• Spinal cord atrophy changes were associated with disability progression in NMO.• Brain lesion and atrophy were related to disability progression in MS. More... »

PAGES

96-103

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00330-017-4921-x

DOI

http://dx.doi.org/10.1007/s00330-017-4921-x

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1090317105

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/28667482


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