HLA-DQA, -DQB and -DRB allele contribution to narcolepsy susceptibility.

Autores de IIS La Fe

• Dolores Planelles Silvestre

  Autor

• Antonio Beneto Pascual

  Autor

• Encarna Gomez Gonzalez

  Autor

• Pedro Rubio Aparicio

  Autor

• Vicente Mirabet Lis

  Autor

• Santiago Bonanad Boix

  Autor

Participantes ajenos a IIS La Fe

• Puig N
• Blasco I
• Montoro JA

Abstract

The association of narcolepsy with HLA class I antigens and HLA class II alleles was studies in a series of Spanish narcoleptic patients. The haplotype DRB1*1501-DRB5*0101-DQA1*0102-DQB1*0602 was found to be significantly associated with the disease, while the haplotype DRB1*0701-DRB4*01-DQA1*0201-DQB1*02 might confer a slight protective effect against narcolepsy. Gene dose-effect was not seen in any of the involved alleles, and linkage disequilibrium between the positively associated alleles was found to be stronger in patients than in controls. Statistical analysis applied to identify the HLA allele truly responsible for the association did not clearly discriminate between the contribution of DRB1*1501 and that of DQB1*0602, but it proved that the association with DQA1*0102 is secondary to that with DRB1*1501/DQB1*0602. Analysis of the diagnostic value of typing for the narcolepsy-associated alleles demonstrated a very high negative predictive value and revealed that this test can be convenient for exclusion of narcolepsy in cases when the diagnosis is not evident after clinical evaluation and the marker haplotype is absent. Finally, a family study indicated that narcolepsy is a multifactorial disorder that involves HLA genes under an incomplete penetrance model, with possible influences from environmental factors or other genes different to HLA genes.