ArticleEnvironmental science and pollution research international2021
Histone deacetylase 2 polymorphisms associated with noise-induced hearing loss in Chinese workers.
Article in Environmental science and pollution research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed, 6 citations in OpenAlex.
- Association of FAS gene polymorphisms with the risk of noise-induced hearing loss in Chinese occupational workers.Frontiers in public health · 2026Article
- The chromatin accessibility and transcriptomic landscape of the aging mice cochlea and the identification of potential functional super-enhancers in age-related hearing loss.Clinical epigenetics · 2024Article
- In silico transcriptome screens identify epidermal growth factor receptor inhibitors as therapeutics for noise-induced hearing loss.Science advances · 2024Article
- [Research progress in genetics of noise-induced hearing loss].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2024Review
- The Role of Genetic Variants in the Susceptibility of Noise-Induced Hearing Loss.Frontiers in cellular neuroscience · 2022Review
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
Abstract
Noise-induced hearing loss (NIHL) is one of these hazards which has been the second most common sensorineural hearing loss. Single-nucleotide polymorphisms (SNPs) mainly refer to the polymorphism of DNA sequence caused by the variation at the genomic nucleotide level. The influence of histone deacetylase 2 (HDAC2) variants on the risk of NIHL has not been studied. This research explored the association between HDAC2 and the development of NIHL. A total of 1146 industrial workers from one textile factory in east China were recruited to perform a case-control study. Basic clinical data such sex, age, smoking, and drinking was obtained by questionnaires; pure-toneaudiometry (PTA) tests were conducted by specialist physicians. Then, we performed genotyping of five selected SNPs (rs10499080, rs2475631, rs2499618, rs6568819, and rs3757016) in the HDAC2 gene in 600 NIHL patients and 546 controls. Finally, the main influences of the SNPs and their interactions with NIHL were assessed. Under the recessive model, there were statistically significant differences in the genotype frequencies of rs10499080 between two groups, and the results showed that individuals with rs10499080 CC+CT had a lower risk of NIHL (OR = 0.597, 95%CI = 0.357-0.998). Meanwhile, the significant difference in the genotype distributions between cases and controls was found in rs10499080 in the group with noise exposure of ≤ 16 years. But the following haplotype analysis showed that no association between all haplotypes in the HDAC2 gene and NIHL was been found. The genetic polymorphisms rs10499080 and rs6568819 within HDAC2 gene have an association with risk of NIHL. Workers exposed to noise with HDAC2 have a lower risk of NIHL.
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