Literature DB >> 17592398

HLA-DRB1*1101 allele may be associated with bilateral Méniére's disease in southern European population.

Jose A Lopez-Escamez1, Jose R Vilchez, Andres Soto-Varela, Sofia Santos-Perez, Herminio Perez-Garrigues, Ismael Aran, Miguel A Lopez-Nevot.   

Abstract

OBJECTIVE: To analyze the associations of HLA-DRB1* and DQB1* Class II alleles in patients with bilateral Méniére's disease (MD). PATIENTS AND METHODS: Eighty patients from two ethnically defined groups with definite bilateral MD, according to the diagnostic scale of the American Academy of Otolaryngology-Head and Neck Surgery, were compared with normal controls from the same origin in a prospective multicenter study. We performed an allele-specific amplification for HLA-DRB1* and DQB1* genes of the major histocompatibility complex.
RESULTS: The allele HLA-DRB1*1101 was associated with bilateral MD in the Mediterranean population (odds ratio, 3.65 [95% confidence intervals, 1.5-9.1], corrected p = 0.029); however, this allele was not associated in the group from Galicia (northwest of Spain). No differences were found in the distribution of alleles for the gene HLA-DQB1* between patients and controls.
CONCLUSION: The allele HLA-DRB1*1101 and the allelic group HLA-DRB1*11 may determine an increased susceptibility to develop bilateral MD in a southern European population.

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Year:  2007        PMID: 17592398     DOI: 10.1097/MAO.0b013e3180dca1cc

Source DB:  PubMed          Journal:  Otol Neurotol        ISSN: 1531-7129            Impact factor:   2.311


  15 in total

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Authors:  Teresa Requena; Irene Gazquez; Antonia Moreno; Angel Batuecas; Ismael Aran; Andres Soto-Varela; Sofia Santos-Perez; Nicolas Perez; Herminio Perez-Garrigues; Alicia Lopez-Nevot; Eduardo Martin; Ricardo Sanz; Paz Perez; Gabriel Trinidad; Marta E Alarcon-Riquelme; Roberto Teggi; Laura Zagato; Miguel A Lopez-Nevot; Jose A Lopez-Escamez
Journal:  Immunogenetics       Date:  2013-02-01       Impact factor: 2.846

2.  RNA-sequencing study of peripheral blood mononuclear cells in sporadic Ménière's disease patients: possible contribution of immunologic dysfunction to the development of this disorder.

Authors:  Y Sun; D Zhang; G Sun; Y Lv; Y Li; X Li; Y Song; J Li; Z Fan; H Wang
Journal:  Clin Exp Immunol       Date:  2017-12-11       Impact factor: 4.330

3.  Histopathology of Meniere's disease.

Authors:  Sebahattin Cureoglu; Rafael da Costa Monsanto; Michael M Paparella
Journal:  Oper Tech Otolayngol Head Neck Surg       Date:  2016-12

4.  Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière's disease.

Authors:  Irene Gázquez; Antonia Moreno; Teresa Requena; Jeff Ohmen; Sofia Santos-Perez; Ismael Aran; Andres Soto-Varela; Herminio Pérez-Garrigues; Alicia López-Nevot; Angel Batuecas; Rick A Friedman; Miguel A López-Nevot; Jose A López-Escamez
Journal:  Eur Arch Otorhinolaryngol       Date:  2012-11-21       Impact factor: 2.503

5.  Polymorphisms of CD16A and CD32 Fcγ receptors and circulating immune complexes in Ménière's disease: a case-control study.

Authors:  José A Lopez-Escamez; Pablo Saenz-Lopez; Irene Gazquez; Antonia Moreno; Carlos Gonzalez-Oller; Andrés Soto-Varela; Sofía Santos; Ismael Aran; Herminio Perez-Garrigues; Agueda Ibañez; Miguel A Lopez-Nevot
Journal:  BMC Med Genet       Date:  2011-01-05       Impact factor: 2.103

6.  Genetics of recurrent vertigo and vestibular disorders.

Authors:  Irene Gazquez; Jose A Lopez-Escamez
Journal:  Curr Genomics       Date:  2011-09       Impact factor: 2.236

7.  High prevalence of systemic autoimmune diseases in patients with Menière's disease.

Authors:  Irene Gazquez; Andres Soto-Varela; Ismael Aran; Sofia Santos; Angel Batuecas; Gabriel Trinidad; Herminio Perez-Garrigues; Carlos Gonzalez-Oller; Lourdes Acosta; Jose A Lopez-Escamez
Journal:  PLoS One       Date:  2011-10-28       Impact factor: 3.240

Review 8.  The genetics of Ménière's disease.

Authors:  Giuseppe Chiarella; C Petrolo; E Cassandro
Journal:  Appl Clin Genet       Date:  2015-01-08

9.  Intronic variants in the NFKB1 gene may influence hearing forecast in patients with unilateral sensorineural hearing loss in Meniere's disease.

Authors:  Sonia Cabrera; Elena Sanchez; Teresa Requena; Manuel Martinez-Bueno; Jesus Benitez; Nicolas Perez; Gabriel Trinidad; Andrés Soto-Varela; Sofía Santos-Perez; Eduardo Martin-Sanz; Jesus Fraile; Paz Perez; Marta E Alarcon-Riquelme; Angel Batuecas; Juan M Espinosa-Sanchez; Ismael Aran; Jose A Lopez-Escamez
Journal:  PLoS One       Date:  2014-11-14       Impact factor: 3.240

10.  Autoimmunity as a candidate for the etiopathogenesis of Meniere's disease: detection of autoimmune reactions and diagnostic biomarker candidate.

Authors:  Sung Huhn Kim; Jin Young Kim; Hyun Jin Lee; Mia Gi; Bo Gyung Kim; Jae Young Choi
Journal:  PLoS One       Date:  2014-10-17       Impact factor: 3.240

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