Epidemiologic association and shared genetic architecture between cataract and hearing difficulties among middle-aged and older adults

Hum Genomics. 2024 Apr 17;18(1):39. doi: 10.1186/s40246-024-00601-z.

Abstract

Age-related cataract and hearing difficulties are major sensory disorders that often co-exist in the global-wide elderly and have a tangible influence on the quality of life. However, the epidemiologic association between cataract and hearing difficulties remains unexplored, while little is known about whether the two share their genetic etiology. We first investigated the clinical association between cataract and hearing difficulties using the UK Biobank covering 502,543 individuals. Both unmatched analysis (adjusted for confounders) and a matched analysis (one control matched for each patient with cataract according to confounding factors) were undertaken and confirmed that cataract was associated with hearing difficulties (OR, 2.12; 95% CI, 1.98-2.27; OR, 2.03; 95% CI, 1.86-2.23, respectively). Furthermore, we explored and quantified the shared genetic architecture of these two complex sensory disorders at the common variant level using the bivariate causal mixture model (MiXeR) and conditional/conjunctional false discovery rate method based on the largest available genome-wide association studies of cataract (N = 585,243) and hearing difficulties (N = 323,978). Despite detecting only a negligible genetic correlation, we observe polygenic overlap between cataract and hearing difficulties and identify 6 shared loci with mixed directions of effects. Follow-up analysis of the shared loci implicates candidate genes QKI, STK17A, TYR, NSF, and TCF4 likely contribute to the pathophysiology of cataracts and hearing difficulties. In conclusion, this study demonstrates the presence of epidemiologic association between cataract and hearing difficulties and provides new insights into the shared genetic architecture of these two disorders at the common variant level.

Keywords: Cataract; Hearing difficulties; Oxidative stress; Sensory traits; Shared genetic architecture.

MeSH terms

  • Aged
  • Apoptosis Regulatory Proteins
  • Cataract*
  • Genetic Loci
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study / methods
  • Hearing
  • Hearing Loss*
  • Humans
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Protein Serine-Threonine Kinases
  • Quality of Life

Substances

  • STK17A protein, human
  • Protein Serine-Threonine Kinases
  • Apoptosis Regulatory Proteins