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Multiple Sclerosis
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research-article

Neuromyelitis optica positive antibodies confer a worse course in relapsing-neuromyelitis optica in Cuba and French West Indies

JA Cabrera-Gómez

Cuban Multiple Sclerosis Society and International Neurological Restoration Center, Havana, Cubacabrera.gomez{at}infomed.sld.cu

M Bonnan

Department of Neurology, Pierre Zobda Quitman Hospital, Fort de France, Martinique, French West Indies

A González-Quevedo

Institute of Neurology and Neurosurgery, Havana, Cuba. Calle 29 y D, Vedado, La Habana, Cuba

A Saiz-Hinarejos

Service of Neurology Hospital Clinic and Institut d’Invesigación Biomèdica August Pi i Sanyer (IAIBAPS), University of Barcelona, Villarroel, Barcelona, Spain

R Marignier

Hôpital Neurologique Pierre Wertheimer, Lyon, France; U842 INSERM, Faculté Laënnec, Lyon Cedex

S Olindo

Department of Neurology, Pierre Zobda Quitman Hospital, Fort de France, Martinique, French West Indies

F Graus

Service of Neurology Hospital Clinic and Institut d’Invesigación Biomèdica August Pi i Sanyer (IAIBAPS), University of Barcelona, Villarroel, Barcelona, Spain

D Smadja

Department of Neurology, Pierre Zobda Quitman Hospital, Fort de France, Martinique, French West Indies

H Merle

Department of Ophthalmology, Pierre Zobda Quitman Hospital, Fort de France, Martinique, French West Indies

L Thomas

Emergency Department, Pierre Zobda Quitman Hospital, Fort de France, Martinique, French West Indies

A Gómez-García

Sancti Spiritus Children Hospital, Sancti Spiritus, Cuba

P Cabre

Department of Neurology, Pierre Zobda Quitman Hospital, Fort de France, Martinique, French West Indies

Background

In Caucasian populations Neuromyelitis Optica (NMO-IgG) antibody has been detected in 27.1% / 78.2% of patients with relapsing-NMO (R-NMO). The prevalence reported for the disease in the Caribbean is 3.1/100,000 in the French West Indies (FWI) and 0.52 /100,000 in Cuba, but the NMO antibody status is unknown.

Objective

To assess the NMO-IgG antibody status of Cuban/FWI RNMO patients, comparing with European cases tested at the same laboratories.

Methods

Serum NMO-IgG antibodies were assayed in 48 R-NMO patients (Wingerchucks 1999 criteria): Cuba (24)/FWI (24), employing Lennon et als method. We compared the demographic, clinical, disability and laboratory data between NMO-IgG +/- patients. All the data were reviewed and collected blinded to the NMO-IgG status.

Results

Seropositivity of the NMO-IgG antibody demonstrated a lower rate in the Caribbean (33.3%), as compared with Caucasian patients from Spain/Italy (62.5%) and France (53.8%). Caribbean patients with NMO-IgG (+) displayed more attacks, more spinal attacks and a higher EDSS than NMO-IgG (-) cases, while brain and spinal cord MRI lesions were more frequent during remission, with more vertebral segments, more gray, white matter and holocord involvement.

Conclusions

NMO IgG positive antibodies in NMO patients had a lower rate in the Caribbean area – where the population has a predominant African ancestry – than in Caucasian Europeans, suggesting the influence of a possible ethnic factor in the pathogenesis of the disease, but they confer a worse course with more attacks, more disability and MRI lesions.

Key Words: aquaporin-4 • Caribbean Basin • Devic’s disease • neuromyelitis IgG antibody • relapsing-neuromyelitis optica

This version was published on July 1, 2009

Multiple Sclerosis, Vol. 15, No. 7, 828-833 (2009)
DOI: 10.1177/1352458509104585


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