First clinical inflammatory demyelinating events of the central nervous system in a population aged over 70 years: A multicentre study

• Published in: Multiple sclerosis and related disorders 2019-02, Vol.28, p.309-312
• Main Authors: Lavandier, Noëlle, Bonnan, Mickaël, Carra-Dallière, Clarisse, Charif, Mahmoud, Labauge, Pierre, Camdessanche, Jean-Philippe, Edan, Gilles, Naudin, Aurore, Brassat, David, Ciron, Jonathan, Clavelou, Pierre, Dulau, Cécile, Moroso, Amandine, Brochet, Bruno, Ouallet, Jean-Christophe
• Format: Article
• Language: English
• Subjects: Brain / diagnostic imaging; Central Nervous System Diseases / epidemiology; Demyelinating Diseases / epidemiology; Life Sciences; Neurons and Cognition
• ISSN: 2211-0348; 2211-0356; 2211-0356; 2211-0348
• DOI: 10.1016/j.msard.2018.12.016

Few data are available regarding patients with very late-onset inflammatory demyelinating events. (VLO-IDE). The aim of this study was to describe the clinical, biological, and radiological characteristics and aetiological diagnosis of very late first inflammatory demyelinating events of the central nervous system. We conducted a national descriptive retrospective multicentre study on a case series of patients aged >70 years at the time of VLO-IDE. Patients were recruited from a national call on behalf of the 'Société Francophone de la Sclérose en Plaques' (French Multiple Sclerosis Society). Twenty-five patients were referred (F:M sex ratio 2.1:1). The most frequent clinical impairment was a spinal cord deficit (23/25), usually severe (disability score, median EDSS 4.5 [2-9.5]). Spinal cord lesions were usually extensive, spanning at least three segments (11/25), and large brain lesions were also observed (lesions >20 mm in 6/25). The final aetiological diagnoses comprised multiple sclerosis (9/25), neuromyelitis optica spectrum disorders (7/25), neurosystemic lupus erythematosus (2/25), transverse myelitis without aetiological diagnosis (6/25) and optic neuritis (1/25). This study highlights a particular phenotype of first clinical inflammatory demyelinating events in predominantly female patients aged >70 years who have severe motor impairment with common longitudinal extensive myelitis and large and common very active radiological inflammatory lesions. Neuromyelitis optica spectrum disorders seem overrepresented.