NeuroImage: Clinical (Jan 2024)

Thalamic atrophy and dysconnectivity are associated with cognitive impairment in a multi-center, clinical routine, real-word study of people with relapsing-remitting multiple sclerosis

  • Robert Zivadinov,
  • Niels Bergsland,
  • Dejan Jakimovski,
  • Bianca Weinstock-Guttman,
  • Lorena Lorefice,
  • Menno M. Schoonheim,
  • Sarah A. Morrow,
  • Mary Ann Picone,
  • Gabriel Pardo,
  • Myassar Zarif,
  • Mark Gudesblatt,
  • Jacqueline A. Nicholas,
  • Andrew Smith,
  • Samuel Hunter,
  • Stephen Newman,
  • Mahmoud A. AbdelRazek,
  • Ina Hoti,
  • Jon Riolo,
  • Diego Silva,
  • Tom A. Fuchs,
  • Michael G. Dwyer,
  • Ralph HB. Benedict

Journal volume & issue
Vol. 42
p. 103609

Abstract

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Background: Prior research has established a link between thalamic pathology and cognitive impairment (CI) in people with multiple sclerosis (pwMS). However, the translation of these findings to pwMS in everyday clinical settings has been insufficient. Objective: To assess which global and/or thalamic imaging biomarkers can be used to identify pwMS at risk for CI and cognitive worsening (CW) in a real-world setting. Methods: This was an international, multi-center (11 centers), longitudinal, retrospective, real-word study of people with relapsing-remitting MS (pwRRMS). Brain MRI exams acquired at baseline and follow-up were collected. Cognitive status was evaluated using the Symbol Digit Modalities Test (SDMT). Thalamic volume (TV) measurement was performed on T2-FLAIR, as well as on T1-WI, when available. Thalamic dysconnectivity, T2-lesion volume (T2-LV), and volumes of gray matter (GM), whole brain (WB) and lateral ventricles (LVV) were also assessed. Results: 332 pwMS were followed for an average of 2.8 years. At baseline, T2-LV, LVV, TV and thalamic dysconnectivity on T2-FLAIR (p < 0.016), and WB, GM and TV volumes on T1-WI (p < 0.039) were significantly worse in 90 (27.1 %) CI vs. 242 (62.9 %) non-CI pwRRMS. Greater SDMT decline over the follow-up was associated with lower baseline TV on T2-FLAIR (standardized β = 0.203, p = 0.002) and greater thalamic dysconnectivity (standardized β = -0.14, p = 0.028) in a linear regression model. Conclusions: PwRRMS with thalamic atrophy and worse thalamic dysconnectivity present more frequently with CI and experience greater CW over mid-term follow-up in a real-world setting.