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中老年人群中衰弱与青光眼风险的关系

Relationships between Frailty and the Risk of Glaucoma in Middle-aged and Older Adults.

作者信息

Chen Jianqi, Cao Xu, Zhuo Xiaohua, Chen Xuhao, Ling Yuyao, Wen Yuwen, Ye Guitong, Zhang Yuan, Zhan Jinan, Tan Hongmei, Zhu Yingting, Zhuo Yehong

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Guangdong Provincial Key Laboratory of Ophthalmology and Visual Science, Sun Yat-sen University, Guangzhou, China.

Department of Pathophysiology, School of Medicine, Sun Yat-sen University, Shenzhen, China; Shenzhen Eye Hospital, Jinan University, Shenzhen Eye Institute, Shenzhen, China.

出版信息

Ophthalmol Glaucoma. 2025 Jan-Feb;8(1):73-82. doi: 10.1016/j.ogla.2024.09.006. Epub 2024 Oct 5.

Abstract

PURPOSE

Increased frailty in older individuals increases health risks, but its relationship with glaucoma, the leading cause of irreversible blindness in middle-aged and older adults, is unclear. We investigated the association between frailty and glaucoma in a large-scale representative sample and explored possible causal relationships.

DESIGN

Combined cross-sectional and Mendelian randomization (MR) study.

PARTICIPANTS

In the cross-sectional analysis, we included 5744 participants of the US National Health and Nutrition Examination Surveys 2005 to 2008 ≥ 40 years of age. For the MR analysis, frailty genome-wide association study (GWAS) data were sourced from a UK Biobank and TwinGen meta-analysis, and GWAS data on glaucoma subtypes were derived from FinnGen.

METHODS

According to the 49-item frailty index, we classified participants into nonfrail (≤ 0.10), prefrail (0.10-0.21), and frail (> 0.21) groups. Using survey-weighted logistic regression models adjusted for multiple covariates, we explored the association between frailty and glaucoma. We further assessed causation using MR.

MAIN OUTCOME MEASURES

The associations between different levels of frailty (nonfrail, prefrail, and frail) and glaucoma, as well as causal relationships between genetically predicted frailty and various subtypes of glaucoma (primary open-angle glaucoma [POAG], primary angle-closure glaucoma [PACG], normotensive glaucoma [NTG], exfoliation glaucoma, and suspected glaucoma).

RESULTS

After adjusting for covariates, higher frailty levels were significantly associated with glaucoma in frail individuals (odds ratio [OR] = 1.83, 95% confidence interval [CI] = 1.05-3.19, P = 0.036) but not prefrail (OR = 1.90, 95% CI = 0.99-3.64, P = 0.052). The association was significantly stronger among male participants (P interaction = 0.042). The variation in the association between frailty and glaucoma did not reach statistical significance across age groups (P interaction = 0.575) or race groups (P interaction = 0.092). Mendelian randomization revealed that genetically predicted frailty was linked to greater risks for POAG (OR = 1.67, 95% CI = 1.24-2.25, P = 0.001), PACG (OR = 2.78, 95% CI = 1.48-5.20, P = 0.001), exfoliation glaucoma (OR = 1.70, 95% CI = 1.18-2.43, P = 0.004), and suspected glaucoma (OR = 1.74, 95% CI = 1.30-2.34, P < 0.001) but not for NTG (OR = 1.01, 95% CI = 0.61-1.68, P = 0.956).

CONCLUSIONS

Our study revealed an association between frailty and increased glaucoma risk and emphasized the significance of glaucoma screening in frail individuals. Targeted health-care strategies can help prevent or delay irreversible blindness among middle-aged and older adults.

FINANCIAL DISCLOSURE(S): Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.

摘要

目的

老年个体中衰弱程度增加会增加健康风险,但其与青光眼(中老年人群不可逆失明的主要原因)之间的关系尚不清楚。我们在一个大规模代表性样本中调查了衰弱与青光眼之间的关联,并探讨了可能的因果关系。

设计

横断面研究与孟德尔随机化(MR)研究相结合。

参与者

在横断面分析中,我们纳入了2005年至2008年美国国家健康与营养检查调查中年龄≥40岁的5744名参与者。对于MR分析,衰弱全基因组关联研究(GWAS)数据来自英国生物银行和TwinGen荟萃分析,青光眼亚型的GWAS数据来自芬兰基因研究。

方法

根据49项衰弱指数,我们将参与者分为非衰弱组(≤0.10)、衰弱前期组(0.10 - 0.21)和衰弱组(>0.21)。使用针对多个协变量进行调整的调查加权逻辑回归模型,我们探讨了衰弱与青光眼之间的关联。我们进一步使用MR评估因果关系。

主要观察指标

不同衰弱水平(非衰弱、衰弱前期和衰弱)与青光眼之间的关联,以及基因预测的衰弱与青光眼各亚型(原发性开角型青光眼[POAG]、原发性闭角型青光眼[PACG]、正常眼压性青光眼[NTG]、剥脱性青光眼和疑似青光眼)之间的因果关系。

结果

在调整协变量后,衰弱个体中较高的衰弱水平与青光眼显著相关(优势比[OR]=1.83,95%置信区间[CI]=1.05 - 3.19,P = 0.036),但衰弱前期个体则不然(OR = 1.90,95% CI = 0.99 - 3.64,P = 0.052)。这种关联在男性参与者中显著更强(P交互作用 = 0.042)。衰弱与青光眼之间关联的差异在各年龄组(P交互作用 = 0.575)或种族组(P交互作用 = 0.092)中未达到统计学意义。孟德尔随机化显示,基因预测的衰弱与POAG(OR = 1.67,95% CI = 1.24 - 2.25,P = 0.001)、PACG(OR = 2.78,95% CI = 1.48 - 5.20,P = 0.001)、剥脱性青光眼(OR = 1.70,95% CI = 1.18 - 2.43,P = 0.004)和疑似青光眼(OR = 1.74,95% CI = 1.30 - 2.34,P < 0.001)的风险增加相关,但与NTG无关(OR = 1.01,95% CI = 0.61 - 1.68,P = 0.956)。

结论

我们的研究揭示了衰弱与青光眼风险增加之间的关联,并强调了对衰弱个体进行青光眼筛查的重要性。有针对性的医疗保健策略有助于预防或延缓中老年人群不可逆失明。

财务披露

在本文末尾的脚注和披露中可能会找到专有或商业披露信息。

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