Huang Yikeng, Zhang Xinyu, Liang Li, Jiang Yujin, Li Bo, Zhu Xinyu, Li Chenxin, Gu Chufeng, Zou Wenjun, Zheng Zhi, Zhao Shuzhi
Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
National Clinical Research Centre for Eye Diseases, Shanghai, China.
J Glob Health. 2025 Jan 31;15:04029. doi: 10.7189/jogh.15.04029.
Recreational screen time (RST) has been found to be associated with cognitive decline and neurodegenerative diseases. However, the association between RST and age-related macular degeneration (AMD), an ocular neurodegenerative disease, is still unclear. We aimed to elucidate the association between RST and AMD.
This study consisted of three parts: 1) a prospective cohort study with 482 939 UK Biobank participants and a 12.8-year median follow-up to explore the association between RST and incident AMD; 2) a two-sample Mendelian randomisation (MR) analysis using summary-level genome-wide association analysis data for RST based on 526 725 European individuals to assess causality between RST and AMD; and 3) a cross-sectional study involving 38 478 UK Biobank individuals with optical coherence tomography data to investigate the link between RST and retinal thickness.
Multivariable Cox proportional-hazards models showed that an increase in total daily RST was associated with a greater risk of developing AMD (hazard ratio (HR) per standard deviation (SD) increase = 1.05; 95% confidence interval (CI) = 1.03, 1.07, P < 0.001). With further analysis, we revealed that daily high RST (>4 h/d) significantly increased the risk of AMD compared with low RST (0-3 h/d) (HR = 1.09; 95% CI = 1.04, 1.15, P = 0.001), while moderate RST (3.5-4 h/d) had no significant effect on AMD. Restricted cubic spline plots revealed a linear dose-response association between RST and AMD. With MR analysis we confirmed the potential causal association between RST and AMD (odds ratio per SD = 1.26; 95% CI = 1.01, 1.59, P = 0.042). Multivariable linear models suggested that an increase in RST was associated with thinning of the outer and inner retinal layers and total macular thickness.
Longer RST may be a potential causal risk factor for AMD and may lead to pathological retinal thinning. Reducing RST could be beneficial for preventing AMD, and future research should identify the most effective time points for intervening on RST.
研究发现娱乐性屏幕使用时间(RST)与认知能力下降和神经退行性疾病有关。然而,RST与年龄相关性黄斑变性(AMD,一种眼部神经退行性疾病)之间的关联仍不明确。我们旨在阐明RST与AMD之间的关联。
本研究包括三个部分:1)一项前瞻性队列研究,纳入482939名英国生物银行参与者,中位随访时间为12.8年,以探讨RST与新发AMD之间的关联;2)一项两样本孟德尔随机化(MR)分析,使用基于526725名欧洲个体的RST全基因组关联分析汇总数据,评估RST与AMD之间的因果关系;3)一项横断面研究,纳入38478名有光学相干断层扫描数据的英国生物银行个体,以研究RST与视网膜厚度之间的联系。
多变量Cox比例风险模型显示,每日总RST增加与发生AMD的风险增加相关(每标准差(SD)增加的风险比(HR)=1.05;95%置信区间(CI)=1.03,1.07,P<0.001)。进一步分析显示,与低RST(0 - 3小时/天)相比,每日高RST(>4小时/天)显著增加了AMD风险(HR=1.09;95%CI=1.04,1.15,P=0.001),而中度RST(3.5 - 4小时/天)对AMD无显著影响。受限立方样条图显示RST与AMD之间存在线性剂量反应关联。通过MR分析,我们证实了RST与AMD之间的潜在因果关联(每SD的优势比=1.26;95%CI=1.01,1.59,P=0.042)。多变量线性模型表明,RST增加与视网膜外层和内层变薄以及黄斑总厚度有关。
更长的RST可能是AMD的潜在因果风险因素,并可能导致病理性视网膜变薄。减少RST可能有助于预防AMD,未来的研究应确定干预RST的最有效时间点。