Acute disseminated encephalomyelitis: clinical features, HLA DRB1*1501, HLA DRB1*1503, HLA DQA1*0102, HLA DQB1*0602, and HLA DPA1*0301 allelic association study

Author:

Alves-Leon Soniza Vieira1,Veluttini-Pimentel Maria Lucia2,Gouveia Maria Emmerick3,Malfetano Fabíola Rachid2,Gaspareto Emerson L.4,Alvarenga Marcos P.,Frugulhetti Izabel4,Quirico-Santos Thereza5

Affiliation:

1. Universidade Federal do Estado do Rio de Janeiro, Brazil; Universidade Federal do Rio de Janeiro, Brazil

2. Universidade Federal do Rio de Janeiro, Brazil; Universidade Federal Fluminense, Brazil

3. Universidade Federal Fluminense, Brazil

4. UFRJ

5. UFF

Abstract

We evaluated the frequency, demographic, clinical, disability evolution and genetic association of HLA DRB1*1501, DRB1*1503, DQA1*0102, DQB1*0602 and DPA1*0301 alleles in patients diagnosed as acute disseminated encephalomyelitis (ADEM) among a population of CNS demyelinating diseases. Fifteen patients (8.4%) of our series were diagnosed as ADEM. The mean age onset was 35.23 years (range 12 to 77), 53.3% were male and follow-up range was 8.5 to 16 years. Two cases (13.3%) had a preceding infection before neurological symptoms, one presented a parainfectious demyelinating, and one case had been submitted to hepatitis B vaccination four weeks before the clinical onset. The EDSS range was 3.0 to 9.5. Eight patients (53.3%) presented MRI with multiple large lesions. CSF was normal in 73.3%. The severe disability observed at EDSS onset improved in 86.66% patients. The genetic susceptibility for ADEM was significantly associated with the HLA DQB1*0602, DRB1*1501 and DRB1*1503 alleles (<0.05) in monophasic ADEM.

Publisher

FapUNIFESP (SciELO)

Subject

Neurology,Neurology (clinical)

Reference35 articles.

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