Artigo Revisado por pares

Heterogeneous pathological processes account for thalamic degeneration in multiple sclerosis: Insights from 7 T imaging

2017; SAGE Publishing; Volume: 24; Issue: 11 Linguagem: Inglês

10.1177/1352458517726382

ISSN

1477-0970

Autores

Céline Louapre, Sindhuja Tirumalai Govindarajan, Costanza Giannì, Nancy Madigan, Jacob A. Sloane, Constantina A. Treaba, Elena Herranz, Revere P. Kinkel, Caterina Mainero,

Tópico(s)

Neurogenesis and neuroplasticity mechanisms

Resumo

Background: Thalamic degeneration impacts multiple sclerosis (MS) prognosis. Objective: To investigate heterogeneous thalamic pathology, its correlation with white matter (WM), cortical lesions and thickness, and as function of distance from cerebrospinal fluid (CSF). Methods: In 41 MS subjects and 17 controls, using 3 and 7 T imaging, we tested for (1) differences in thalamic volume and quantitative T 2 * (q-T 2 *) (2) globally and (3) within concentric bands originating from the CSF/thalamus interface; (4) the relation between thalamic, cortical, and WM metrics; and (5) the contribution of magnetic resonance imaging (MRI) metrics to clinical scores. We also assessed MS thalamic lesion distribution as a function of distance from CSF. Results: Thalamic lesions were mainly located next to the ventricles. Thalamic volume was decreased in MS versus controls ( p < 10 −2 ); global q-T 2 * was longer in secondary progressive multiple sclerosis (SPMS) only ( p < 10 −2 ), indicating myelin and/or iron loss. Thalamic atrophy and longer q-T 2 * correlated with WM lesion volume ( p < 0.01). In relapsing-remitting MS, q-T 2 * thalamic abnormalities were located next to the WM ( p < 0.01 (uncorrected), p = 0.09 (corrected)), while they were homogeneously distributed in SPMS. Cortical MRI metrics were the strongest predictors of clinical outcome. Conclusion: Heterogeneous pathological processes affect the thalamus in MS. While focal lesions are likely mainly driven by CSF-mediated factors, overall thalamic degeneration develops in association with WM lesions.

Referência(s)