Choroid plexus enlargement correlates with periventricular pathology but not with disease activity in radiologically isolated syndrome

Author:

Landes-Château Cassandre1ORCID,Ricigliano Vito AG2,Mondot Lydiane1,Thouvenot Eric3ORCID,Labauge Pierre4,Louapre Céline2,Zéphir Hélène5,Durand-Dubief Françoise6,Le Page Emmanuelle7,Siva Aksel8ORCID,Cohen Mikael1ORCID,Yazdan Panah Arya9,Azevedo Christina J.10ORCID,Okuda Darin T.11ORCID,Stankoff Bruno2,Lebrun-Frénay Christine1

Affiliation:

1. Université Côte d’Azur, UMR2CA (URRIS), Nice, France

2. Paris Brain Institute-ICM, CNRS, Inserm, Neurology Department, Pitié-Salpêtrière Hospital, Sorbonne Université, AP–HP, Paris, France

3. IGF, University Montpellier, CNRS, INSERM, Montpellier, France

4. Centre hospitalier universitaire de Montpellier, Montpellier, France

5. University of Lille, INSERM U 1172, CHU of Lille, Lille, France

6. Hospices Civils de Lyon, Lyon, France

7. Centre hospitalier universitaire de Rennes, Rennes, France

8. Cerrahpasa School of Medicine, Istanbul University, Istanbul, Turkiye

9. Sorbonne Université, Institut du Cerveau-Paris Brain Institute—ICM, CNRS, Inria, Inserm, AP-HP, Hôpital de la Pitié Salpêtrière, France

10. Keck School of Medicine of University of Southern California, Los Angeles, CA, USA

11. The University of Texas Southwestern Medical Center, Peter O’Donnell Jr. Brain Institute, Dallas, TX, USA

Abstract

Background: Choroid plexus (ChP) enlargement is an emerging radiological biomarker in multiple sclerosis (MS). Objectives: This study aims to assess ChP volume in a large cohort of patients with radiologically isolated syndrome (RIS) versus healthy controls (HC) and explore its relationship with other brain volumes, disease activity, and biological markers. Methods: RIS individuals were included retrospectively and compared with HC. ChPs were automatically segmented using an in-house automated algorithm and manually corrected. Results: A total of 124 patients fulfilled the 2023 RIS criteria, and 55 HCs were included. We confirmed that ChPs are enlarged in RIS versus HC (mean (±SD) normalized ChP volume: 17.24 (±4.95) and 11.61 (±3.58), respectively, p < 0.001). Larger ChPs were associated with more periventricular lesions (ρ = 0.26; r2 = 0.27; p = 0.005 for the correlation with lesion volume, and ρ = 0.2; r2 = 0.21; p = 0.002 for the correlation with lesion number) and lower thalamic volume (ρ = −0.38; r2 = 0.44; p < 0.001), but not with lesions in other brain regions. Conversely, ChP volume did not correlate with biological markers. No significant difference in ChP volume was observed between subjects who presented or did not have a clinical event or between those with or without imaging disease activity. Conclusions: This study provides evidence that ChP volume is higher in RIS and is associated with measures reflecting periventricular pathology but does not correlate with biological, radiological, or clinical markers of disease activity.

Publisher

SAGE Publications

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