Nie Jingwen, Li Qing, Guo Min, Li Jiaqing, Yang Jiahui, Chang Qing, Cai Yaping
Department of Nephrology, The First Affiliated Hospital of Kunming Medical University, Kunming, China.
Department of Otolaryngology, The First Affiliated Hospital of Kunming Medical University, Kunming, China.
PeerJ. 2021 Oct 13;9:e12295. doi: 10.7717/peerj.12295. eCollection 2021.
End-stage renal disease (ESRD) patients often experience hearing impairment, resulting in a high rate of disability and a decline in their quality of life. Fibroblast growth factor-23 (FGF23) is a diagnostic biomarker for chronic kidney disease (CKD) and a pathogenic contributor to CKD progression. However, the correlation between FGF23 level and CKD patients with hearing impairment remains elusive. This study aimed to investigate the relationship between the FGF23 and ESRD accompanied with hearing impairment.
A total of 144 ESRD patients, who were admitted to the First Affiliated Hospital of Kunming Medical University from November to December 2020, were enrolled in this study. Firstly, 144 ESRD patients underwent pure-tone audiometry (PTA). Secondly, it was attempted to randomly select 20 ESRD patients with normal hearing, and 20 ESRD patients with hearing impairment (match ratio, 1:1). Age- and gender-matched healthy people ( = 20) were also recruited as controls group. The expression levels of FGF23 was detected by enzyme-linked immunosorbent assay (ELISA).
The results of pure-tone audiometry showed that the prevalence of hearing impairment in ESRD patients was 80.5%. Male ESRD patients were more likely to develop hearing impairment compared to female patients. The incidence rate of hearing impairment at a high frequency was significantly higher than that at a low frequency ( < 0.01). The serum levels of FGF23, phosphorus, and parathyroid hormone (PTH) in ESRD patients with hearing impairment significantly increased compared with those with normal hearing and healthy controls.
ESRD patients had a higher risk of hearing loss, especially high-frequency hearing impairment. As FGF23 level increased, the risk of hearing loss was also elevated. The hearing impairment in ESRD patients was associated with the degree of kidney injury, and serum FGF23 level.
终末期肾病(ESRD)患者常出现听力障碍,导致残疾率高且生活质量下降。成纤维细胞生长因子23(FGF23)是慢性肾脏病(CKD)的诊断生物标志物,也是CKD进展的致病因素。然而,FGF23水平与CKD听力障碍患者之间的相关性仍不明确。本研究旨在探讨FGF23与伴有听力障碍的ESRD之间的关系。
本研究纳入了2020年11月至12月在昆明医科大学第一附属医院住院的144例ESRD患者。首先,144例ESRD患者接受了纯音听力测试(PTA)。其次,试图随机选择20例听力正常的ESRD患者和20例听力障碍的ESRD患者(匹配比例为1:1)。年龄和性别匹配的健康人(n = 20)也被招募为对照组。采用酶联免疫吸附测定(ELISA)检测FGF23的表达水平。
纯音听力测试结果显示,ESRD患者听力障碍的患病率为80.5%。男性ESRD患者比女性患者更容易出现听力障碍。高频听力障碍的发生率明显高于低频(P < 0.01)。与听力正常的患者和健康对照组相比,伴有听力障碍的ESRD患者的血清FGF23、磷和甲状旁腺激素(PTH)水平显著升高。
ESRD患者听力损失风险较高,尤其是高频听力障碍。随着FGF23水平升高,听力损失风险也升高。ESRD患者的听力障碍与肾损伤程度和血清FGF23水平有关。