Ding Fan, Pang Zehao, Ji Xiujia, Jiang Yuanfang, Wang Qiulan, Bing Zhitong
Teaching and Experimental Training Center, Gansu University of Chinese Medicine, Lanzhou 730000, China.
Advanced Nuclear Physics Laboratory, Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000, China.
Int J Mol Sci. 2025 Apr 26;26(9):4132. doi: 10.3390/ijms26094132.
Radiotherapy-induced hearing impairment significantly affects patients' quality of life, yet its genetic basis remains poorly understood. This study seeks to identify genetic variants associated with radiotherapy-induced tinnitus and hearing loss and explore their functional implications. A genome-wide association study (GWAS) was conducted to identify single-nucleotide polymorphisms (SNPs) associated with radiotherapy-induced tinnitus and hearing loss. Protein-protein interaction networks and functional enrichment analyses were performed to explore underlying biological pathways. A phenome-wide association study (PheWAS) analysis across five databases examined associations between identified SNPs and various phenotypes. The GWAS identified 97 SNPs significantly associated with radiotherapy-induced tinnitus and 76 SNPs with hearing loss. Tinnitus-associated variants were enriched in pathways involving Wnt signaling and telomerase RNA regulation, while hearing-loss-associated variants were linked to calcium-dependent cell adhesion and neurotransmitter receptor regulation. The PheWAS analysis revealed significant associations between these hearing-impairment-related SNPs and metabolic phenotypes, particularly BMI and metabolic disorders. A chromosomal distribution analysis showed concentrated significant SNPs on chromosomes 1, 2, 5, and 10. This study identified distinct genetic architectures underlying radiotherapy-induced tinnitus and hearing loss, revealing different molecular pathways involved in their pathogenesis. The unexpected association with metabolic phenotypes suggests potential interactions between metabolic status and susceptibility to radiotherapy-induced hearing complications. These findings provide insights for developing genetic screening tools and targeted interventions to prevent or mitigate radiotherapy-related hearing damage.
放射治疗引起的听力损伤显著影响患者的生活质量,但其遗传基础仍知之甚少。本研究旨在识别与放射治疗引起的耳鸣和听力损失相关的基因变异,并探讨其功能意义。开展了一项全基因组关联研究(GWAS),以识别与放射治疗引起的耳鸣和听力损失相关的单核苷酸多态性(SNP)。进行了蛋白质-蛋白质相互作用网络和功能富集分析,以探索潜在的生物学途径。通过对五个数据库进行全表型关联研究(PheWAS)分析,检测已识别的SNP与各种表型之间的关联。GWAS识别出97个与放射治疗引起的耳鸣显著相关的SNP和76个与听力损失相关的SNP。与耳鸣相关的变异在涉及Wnt信号传导和端粒酶RNA调控的途径中富集,而与听力损失相关的变异则与钙依赖性细胞粘附和神经递质受体调控有关。PheWAS分析揭示了这些与听力损伤相关的SNP与代谢表型之间存在显著关联,尤其是体重指数(BMI)和代谢紊乱。染色体分布分析显示,1号、2号、5号和10号染色体上存在集中的显著SNP。本研究识别出了放射治疗引起的耳鸣和听力损失背后不同的遗传结构,揭示了其发病机制中涉及的不同分子途径。与代谢表型的意外关联表明代谢状态与放射治疗引起的听力并发症易感性之间可能存在相互作用。这些发现为开发基因筛查工具和针对性干预措施以预防或减轻放射治疗相关的听力损伤提供了思路。