Tear analysis in clinically isolated syndrome as new multiple sclerosis criterion

Author:

Calais Gauthier1,Forzy Gerard2,Crinquette Charlotte3,Mackowiak Alexandre3,de Seze Jerome4,Blanc Frederic4,Lebrun Christine5,Heinzlef Olivier6,Clavelou Pierre7,Moreau Thibault8,Hennache Bernadette9,Zephir Helene10,Verier Albert11,Neuville Véronique12,Confavreux Christian13,Vermersch Patrick9,Hautecoeur Patrick3

Affiliation:

1. Groupe Hospitalier de l'Institut Catholique de Lille, Service de Neurologie, Lille, France,

2. Université Catholique de Lille, Faculte Libre de Medecine, Lille, France

3. Groupe Hospitalier de l'Institut Catholique de Lille, Service de Neurologie, Lille, France

4. Hôpitaux Universitaires de Strasbourg, Service de Neurologie, Strasbourg, France

5. Centre Hospitalier et Universitaire de Nice, Service de Neurologie, Nice, France

6. Poissy Hospital, Neurology, Poissy, France

7. Clavelou, Pierre, Centre Hospitalier et Universitaire de Clermand-Ferrand, Service de Neurologie B, Clermont-Ferrand, France

8. Centre Hospitalier Universitaire de Dijon, Service de Neurologie, Dijon, France

9. Centre Hospitalier Universitaire de Lille, Laboratoire de Biologie, Lille, France

10. Centre Hospitalier Universitaire de Lille, Service de Neurologie D, Lille, France

11. Centre Hospitalier de Valenciennes, Service de Neurologie, Valenciennes, France

12. Centre Hospitalier de Sambre Avesnois, Service de Neurologie, Maubeuge, France

13. Hôpital Neurologique Pierre Wertheimer, Neurologie A, Lyon, France

Abstract

In clinically isolated syndrome (CIS), the detection of oligoclonal bands (OCBs) in cerebrospinal fluid (CSF) is critical for space dissemination validation when magnetic resonance imaging (MRI) diagnostic criteria are not fulfilled. However, lumbar puncture for CSF collection is considered relatively invasive. Previous studies have demonstrated applicability of OCB detection in tears to the diagnosis of multiple sclerosis (MS). The objective of the present study was to assess concordance between OCB detection in tears and in CSF. We have prospectively included patients with CIS and compared results of CSF and tear OCB detection by isoelectric focusing (IEF). Tears were collected using a Schirmer strip. We included 82 patients. For 69 of them, samples were analysable. OCBs were detected in CSF for 63.8% and in tears for 42% of patients. All patients with tear OCBs had CSF OCBs. We suggest that tear OCB detection may replace CSF OCB detection as a diagnostic tool in patients with CIS. This would circumvent the practice of invasive lumbar punctures currently used in MS diagnosis.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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