Literature DB >> 9191765

HLA DR15 (DR2) and DQB1*0602 typing studies in 188 narcoleptic patients with cataplexy.

A E Rogers1, J Meehan, C Guilleminault, F C Grumet, E Mignot.   

Abstract

Narcolepsy is considered a homogeneous clinical entity when excessive daytime sleepiness and cataplexy are present. Cataplexy is a polymorphic symptom that can be very mild and is thus subjectively defined. The Multiple Sleep Latency Test (MSLT) is widely used as a diagnostic test for narcolepsy. A short mean sleep latency and multiple sleep onset REM periods (SOREMPs) are typically observed in narcoleptic patients. The discovery of a tight association of narcolepsy with HLA class II antigens offers a unique opportunity to explore the respective value of the MSLT or of the presence of clear-cut cataplexy in defining an etiologically homogeneous group of narcoleptic patients. In this study, we carried out HLA typing for DR15(DR2) and DQB1*0602 in 188 narcoleptic patients with cataplexy in three ethnic groups (24 Asians, 61 Blacks, and 103 Caucasians). These results confirm the importance of DQB1*0602 typing rather than DR15 (DR2) typing in Black narcoleptic patients and demonstrate that the presence of clear-cut cataplexy is a better predictor for DQB1*0602 positivity than the presence of abnormal MSLT results.

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Year:  1997        PMID: 9191765     DOI: 10.1212/wnl.48.6.1550

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  16 in total

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Review 3.  Genetics of narcolepsy and other sleep disorders.

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4.  DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe.

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Journal:  Sleep       Date:  2014-01-01       Impact factor: 5.849

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8.  A real-time polymerase chain reaction assay for the rapid identification of the autoimmune disease-associated allele HLA-DQB1*0602.

Authors:  V H Gersuk; G T Nepom
Journal:  Tissue Antigens       Date:  2009-04

Review 9.  Genetic Ancestry for Sleep Research: Leveraging Health Inequalities to Identify Causal Genetic Variants.

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Review 10.  The autoimmune basis of narcolepsy.

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