The diagnostic value of the central vein sign in radiologically isolated syndrome

Author:

Landes‐Chateau Cassandre1ORCID,Levraut Michael12ORCID,Okuda Darin T.3ORCID,Themelin Albert4,Cohen Mikael15ORCID,Kantarci Orhun H.6ORCID,Siva Aksel7ORCID,Pelletier Daniel8,Mondot Lydiane14ORCID,Lebrun‐Frenay Christine15ORCID,

Affiliation:

1. Université Cote d'Azur, UMR2CA (URRIS) Nice France

2. Service de Médecine Interne Centre Hospitalier Universitaire de Nice Hôpital l'Archet 1 Nice France

3. The University of Texas Southwestern Medical Center Dallas Texas USA

4. Service de Radiologie Centre Hospitalier Universitaire de Nice Hôpital Pasteur 2 Nice France

5. Service de Neurologie, Centre de Ressource et de Compétence Sclérose en Plaques (CRC‐SEP) Centre Hospitalier Universitaire de Nice Hôpital Pasteur 2 Nice France

6. Mayo Clinic Rochester Minnesota USA

7. Istanbul University, Cerrahpasa School of Medicine Istanbul Turkey

8. University of South California San Francisco California USA

Abstract

AbstractObjectiveThe radiologically isolated syndrome (RIS) represents the earliest detectable preclinical phase of multiple sclerosis (MS). Increasing evidence suggests that the central vein sign (CVS) enhances lesion specificity, allowing for greater MS diagnostic accuracy. This study evaluated the diagnostic performance of the CVS in RIS.MethodsPatients were prospectively recruited in a single tertiary center for MS care. Participants with RIS were included and compared to a control group of sex and age‐matched subjects. All participants underwent 3 Tesla magnetic resonance imaging, including postcontrast susceptibility‐based sequences, and the presence of CVS was analyzed. Sensitivity and specificity were assessed for different CVS lesion criteria, defined by proportions of lesions positive for CVS (CVS+) or by the absolute number of CVS+ lesions.Results180 participants (45 RIS, 45 MS, 90 non‐MS) were included, representing 5285 white matter lesions. Among them, 4608 were eligible for the CVS assessment (970 in RIS, 1378 in MS, and 2260 in non‐MS). According to independent ROC comparisons, the proportion of CVS+ lesions performed similarly in diagnosing RIS from non‐MS than MS from non‐MS (p = 0.837). When a 6‐lesion CVS+ threshold was applied, RIS lesions could be diagnosed with an accuracy of 87%. MS could be diagnosed with a sensitivity of 98% and a specificity of 83%. Adding OCBs or Kappa index to CVS biomarker increased the specificity to 100% for RIS diagnosis.InterpretationThis study shows evidence that CVS is an effective imaging biomarker in differentiating RIS from non‐MS, with similar performances to those in MS.

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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