Brain microstructural damage through serial diffusion tensor imaging and outcomes in Susac syndrome: A prospective cohort study
Background Susac syndrome (SuS) is a rare immune‐mediated microangiopathy with potential disabling evolution. We aimed to analyze brain microstructural damage through diffusion tensor imaging (DTI) in SuS and determine its association with poor outcomes. Method CarESS study is a prospective multicen...
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Veröffentlicht in: | European journal of neurology 2025-01, Vol.32 (1), p.e70002-n/a |
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Sprache: | eng |
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Zusammenfassung: | Background
Susac syndrome (SuS) is a rare immune‐mediated microangiopathy with potential disabling evolution. We aimed to analyze brain microstructural damage through diffusion tensor imaging (DTI) in SuS and determine its association with poor outcomes.
Method
CarESS study is a prospective multicenter national cohort study of patients with SuS. Patients included at the principal investigator's center with at least two available brain magnetic resonance imaging (MRI) with DTI were analyzed. Mean diffusivity (MD) and fractional anisotropy (FA) were measured in fibers crossing three regions of interest (ROIs): the corpus callosum as a whole, the genu of the corpus callosum, and the splenium of the corpus callosum. The primary outcome was work resumption.
Results
Twenty‐two patients (36 (25;42) years, 16 (73%) females) were studied. The triad (i.e., brain, eye, and ear involvement) was complete in 21 (95%) patients. All but one patients received steroids alone or in combination with immunosuppressive drugs (n = 11) and/or IVIg (n = 7). Over a median follow‐up of 6 (5;8) years, 15 (68%) patients went back to work. FA and MD were longitudinally measured in 123 DTI MRI accounting for a median of 5.6 [4.2; 7] MRI per patient. Microstructural damages in the corpus callosum as a whole, the genu of the corpus callosum, and the splenium of the corpus callosum increased during follow‐up and were significantly associated with the inability to return to work.
Conclusion
Brain DTI identified microstructural damage in fibers crossing the corpus callosum that are associated with long‐term disability in SuS.
Trial Registration
ClinicalTrials.gov portal identifier: NCT01481662 (https://clinicaltrials.gov/ct2/show/NCT01481662?term=caress&draw=2&rank=5). |
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ISSN: | 1351-5101 1468-1331 1468-1331 |
DOI: | 10.1111/ene.70002 |