Analysis of hypocretin (orexin) antibodies in patients with narcolepsy

被引:47
作者
Black, JL
Silber, MH
Krahn, LE
Fredrickson, PA
Pankratz, VS
Avula, R
Walker, DL
Slocumb, NL
机构
[1] Mayo Clin, Coll Med, Psychogenom Lab, Rochester, MN USA
[2] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Rochester, MN USA
[3] Mayo Clin, Coll Med, Mayo Sleep Disorders Ctr, Rochester, MN USA
[4] Mayo Clin, Coll Med, Dept Neurol, Rochester, MN USA
[5] Mayo Clin, Coll Med, Dept Psychiat & Psychol, Scottsdale, AZ USA
[6] Mayo Clin, Coll Med, Mayo Sleep Disorders Lab, Scottsdale, AZ USA
[7] Mayo Clin, Coll Med, Mayo Sleep Disorders Lab, Jacksonville, FL 32224 USA
[8] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN USA
关键词
narcolepsy; antibody; preprohypocretin; hypocretin; 1; 2;
D O I
10.1093/sleep/28.4.427
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: We tested the hypothesis that patients with narcolepsy have serum antibodies specific for preprohypocretin and its derivatives. Design: We tested sera from strictly diagnosed HLA DQB1*0602-positive narcoleptic patients with cataplexy for evidence of autoantibodies against human preprohypocretin, hypocretin 1 and 2, N-terminal leader and C-terminal peptides of preprohypocretin using enzyme-linked immunosorbent assays (ELISA). These results were compared to samples from nonnarcoleptic psychiatric and sleep apnea controls. Laboratory personnel were blinded to subject status, Setting: Narcoleptic patients and nonnarcoleptic controls were recruited from the Mayo Clinic facilities in Rochester, Minnesota; Scottsdale, Arizona; and Jacksonville, Florida. Laboratory testing was conducted in the Mayo Psychogenomic Laboratory at the Rochester Mayo Clinic. Participants: A sample of 34 narcoleptic patients and 49 nonnarcoleptic controls. Interventions: None. Measurements and Results: ELISA measurements were in optical density. Primary analyses were of the entire narcoleptic and control groups for each potential antigen, and none of the differences reached P values required for significance after Bonferroni adjustment. Secondary analyses by age and sex yielded P values that were significant after Bonferroni adjustment in only 2 cases, but further statistical analyses cast doubt on the veracity of these differences. In all cases where a significant difference was recorded, the hypothesis was not supported because the control optical density reading was higher than the narcoleptic values. Conclusions: These ELISA assay results do not support the hypothesis that HLA DQB1*0602-positive narcolepsy with cataplexy is associated with serum antibodies against preprohypocretin or its cleavage products.
引用
收藏
页码:427 / 431
页数:5
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