Epidemiological findings of neuromyelitis optica spectrum disorders in a Venezuelan study.


Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
Jan 2021
Historique:
received: 30 07 2020
revised: 17 11 2020
accepted: 23 11 2020
pubmed: 7 12 2020
medline: 15 5 2021
entrez: 6 12 2020
Statut: ppublish

Résumé

Neuromyelitis optica spectrum disorders (NMOSD), is a rare autoimmune inflammatory disease of the central nervous system. Since the countries of Latin America (LATAM) show contrast in geographic, social, environmental factors, and genetic heterogeneity, the information about NMOSD epidemiology in the region allows a better understanding of the disease and its clinical outcome. To determine the prevalence, relative frequency (RF), and clinical characteristics of NMOSD in a multiethnic Venezuelan cohort of patients with demyelinating disorders. We conducted a retrospective descriptive multicenter study of hospital case records of individuals with an established diagnosis of MS and NMOSD in the National Program for Multiple sclerosis (MS) from 2011 to 2018. We selected those NMOSD cases based on the 2006 Wingerchuck and the 2015 International panel for the diagnosis of Neuromyelitis optica (IPND) criteria. We identified 249 patients with NMOSD. The prevalence was 2.11 per100,000 individuals (95% confidence interval (CI)1.85 2.37), the RF was 23%, and the MS/NMOSD ratio was 3.2:1. The average disease onset occurred by the fourth decade of life (34±14.8 years of age); with a strong female predominance (female to male ratio: 4:1). Mestizos constituted 86,7% of this cohort. Most of the patients presented initially with simultaneous optic neuritis (ON) and acute transverse myelitis (ATM) and a recurrent course was registered in 82.3% of cases. The mean of the expanded disability status scale (EDSS) was 3.5 (IQR 2-7). Abnormal brain and spine MRI were present in 47.8% and 81.1% of patients, respectively. Antibodies against aquaporin-4 (AQP4) which were measured through a cell-based assay were positive in 55.3% of the individuals tested. The most used immunosuppressant agent was Azathioprine (57.4%). NMOSD in Venezuela affects mainly young Mestizo women and shows one of the highest relative frequency in the region. Planning and developing healthcare programs for underserved populations as well as more comprehensive LATAM studies are required to identify the distribution and variations of its epidemiological picture.

Sections du résumé

BACKGROUND BACKGROUND
Neuromyelitis optica spectrum disorders (NMOSD), is a rare autoimmune inflammatory disease of the central nervous system. Since the countries of Latin America (LATAM) show contrast in geographic, social, environmental factors, and genetic heterogeneity, the information about NMOSD epidemiology in the region allows a better understanding of the disease and its clinical outcome.
OBJECTIVES OBJECTIVE
To determine the prevalence, relative frequency (RF), and clinical characteristics of NMOSD in a multiethnic Venezuelan cohort of patients with demyelinating disorders.
METHODS METHODS
We conducted a retrospective descriptive multicenter study of hospital case records of individuals with an established diagnosis of MS and NMOSD in the National Program for Multiple sclerosis (MS) from 2011 to 2018. We selected those NMOSD cases based on the 2006 Wingerchuck and the 2015 International panel for the diagnosis of Neuromyelitis optica (IPND) criteria.
RESULTS RESULTS
We identified 249 patients with NMOSD. The prevalence was 2.11 per100,000 individuals (95% confidence interval (CI)1.85 2.37), the RF was 23%, and the MS/NMOSD ratio was 3.2:1. The average disease onset occurred by the fourth decade of life (34±14.8 years of age); with a strong female predominance (female to male ratio: 4:1). Mestizos constituted 86,7% of this cohort. Most of the patients presented initially with simultaneous optic neuritis (ON) and acute transverse myelitis (ATM) and a recurrent course was registered in 82.3% of cases. The mean of the expanded disability status scale (EDSS) was 3.5 (IQR 2-7). Abnormal brain and spine MRI were present in 47.8% and 81.1% of patients, respectively. Antibodies against aquaporin-4 (AQP4) which were measured through a cell-based assay were positive in 55.3% of the individuals tested. The most used immunosuppressant agent was Azathioprine (57.4%).
CONCLUSION CONCLUSIONS
NMOSD in Venezuela affects mainly young Mestizo women and shows one of the highest relative frequency in the region. Planning and developing healthcare programs for underserved populations as well as more comprehensive LATAM studies are required to identify the distribution and variations of its epidemiological picture.

Identifiants

pubmed: 33279797
pii: S2211-0348(20)30726-4
doi: 10.1016/j.msard.2020.102652
pii:
doi:

Substances chimiques

Aquaporin 4 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

102652

Informations de copyright

Copyright © 2020. Published by Elsevier B.V.

Auteurs

Soto de Castillo Ibis (SC)

Department of Neurology. Hospital Universitario de Maracaibo, Maracaibo, Venezuela. Electronic address: ibissotodecastillo@gmail.com.

Molina Omaira (M)

Department of Neurology. Hospital Universitario de Maracaibo, Maracaibo, Venezuela.

Soto Arnoldo (S)

Department of Neurology. Centro Medico Docente La Trinidad, Caracas, Venezuela.

Armas Elizabeth (A)

Department of Neurology. Hospital Universitario de Caracas, Caracas, Venezuela.

Mendoza Sandra (M)

Department of Neurology. Ciudad Hospitalaria "Dr. Enrique Tejera", Valencia, Venezuela.

Castillo Maria Carlota (CM)

Department of Neurology. Hospital Universitario de Maracaibo, Maracaibo, Venezuela.

Castro Elizabeth (C)

Department of Neurology. Hospital Universitario de Maracaibo, Maracaibo, Venezuela.

Vink Laura (V)

Department of Neurology. Hospital Juan Daza Pereira, Barquisimeto, Venezuela.

Leon Rosalba (L)

Department of Neurology. Hospital Universitario de Caracas, Caracas, Venezuela.

Valbuena Oscar (V)

Department of Pediatric Neurology, Hospital de especialidades pediátricas, Maracaibo, Venezuela.

Del Moral Luisa (DM)

Centro Medico de Cabimas, Cabimas, Venezuela.

Acosta Nahir (A)

Research Center, Instituto Cardiovascular del Cesar, Valledupar, Colombia.

Freda Hernandez (F)

Department of Neurology. Hospital Universitario de Maracaibo, Maracaibo, Venezuela.

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