Associations between HLA-C alleles and definite Meniere's disease

Mohammad-Taghi Khorsandi1, Mahsa M Amoli, Hebatodin Borghei

  • 1Tehran University of Medical Sciences, Tehran, Iran.

Insights

Genetic factors, including Human Leukocyte Antigens (HLA), may influence Meniere

Area of Science:

  • Genetics
  • Immunology
  • Otolaryngology

Background:

  • Meniere's disease (MD) etiology involves both genetic and environmental factors.
  • Human Leukocyte Antigens (HLA) are among the genes potentially linked to MD susceptibility.
  • Previous studies suggest certain HLA alleles are predisposing factors for MD in various populations.

Purpose of the Study:

  • To investigate the association between HLA-C allele frequencies and definite Meniere's disease (MD).
  • To analyze HLA-C allele frequencies in patients with definite MD at Amir-Alam otolaryngology tertiary referral center, Tehran.

Main Methods:

  • A case-control study involving 22 patients with definite MD based on AAO-HNS criteria.
  • Exclusion of patients with suspected MD, focusing on those with vertigo, tinnitus, and low-frequency sensorineural hearing loss.
  • HLA-Cw allele frequencies determined using PCR-SSP in patients and 91 unrelated healthy controls.

Main Results:

  • The frequency of the HLA-Cw*04 allele was significantly higher in definite MD patients compared to controls.
  • A strong association was observed: P = 0.0015, Odds Ratio (OR) = 20, 95% Confidence Interval (CI) (3.7-196.9).
  • This finding indicates a significant genetic predisposition conferred by HLA-C in this patient cohort.

Conclusions:

  • HLA-C acts as a genetic predisposing factor for definite Meniere's disease.
  • The HLA-Cw*04 allele is significantly associated with MD in the studied Iranian population.
  • Further research into HLA-C's role could elucidate MD pathogenesis and inform targeted therapies.