Associations between vision impairment and eye diseases with dementia, dementia subtypes and cognitive impairment: An umbrella review

IF 12.5 1区 医学 Q1 CELL BIOLOGY Ageing Research Reviews Pub Date : 2024-10-05 DOI:10.1016/j.arr.2024.102523
Masoud Rahmati , Lee Smith , Hyeri Lee , Laurent Boyer , Guillaume Fond , Dong Keon Yon , Hayeon Lee , Pinar Soysal , Raphael Udeh , Xenia Dolja-Gore , Mark McEVoy , Mapa Prabhath Piyasena , Shahina Pardhan
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Abstract

Vision impairment (VI) and eye diseases such as age-related macular degeneration (AMD), diabetic retinopathy (DR), glaucoma and cataract have been reported to be associated with cognitive impairment and dementia, however, to date, very little attempt has been made to collate and synthesizes such literature. Therefore, the aim of this umbrella review is to systematically assesses the credibility and certainty of evidence of associations between vision impairment (VI) and eye diseases with cognitive impairment, dementia and dementia subtypes. We conducted an umbrella review of meta-analyses by screening articles in any language in PubMed, MEDLINE (Ovid), EMBASE, Web of Science, Cochrane CENTRAL and CDSR published from database inception up to May 30, 2024. Quality appraisal of each included original meta-analysis was assessed using A Measurement Tool for Assessing Systematic Reviews 2 (AMSTAR2). The certainty of the evidence was based on statistical significance, study size, heterogeneity, small study effects, prediction intervals (PI), and bias. We followed an a-priori protocol registered with PROSPERO (CRD42024564249). We identified 13 meta-analyses (AMSTAR 2; high accuracy of the findings 1, moderate 10, and low 2) that included 232 original articles based on 99,337,354 participants. Overall, no evidence was highly suggestive or convincing. Suggestive evidence was found for associations between cataract and dementia (equivalent odds ratio [eOR] 1.20, 95 %CI, 1.16–1.25), cataract and Alzheimer’s disease (eOR 1.21, 95 %CI, 1.15–1.28), and AMD and Alzheimer’s disease (eOR 1.27, 95 %CI, 1.27–1.27). Weak evidence was found for associations between VI and dementia (eOR 1.50, 95 %CI, 1.23–1.84), DR and dementia (eOR 1.33, 95 %CI, 1.17–1.50), cataract and vascular dementia (eOR 1.26, 95 %CI, 1.09–1.45), VI identified by cross-sectional studies and cognitive impairment (eOR 2.37, 95 %CI, 2.31–2.44), and VI identified by objective measures and cognitive impairment (eOR 1.56, 95 %CI, 1.12–2.18). The observed suggestive level of evidence for the relationship between eye disease and dementia (as well as dementia subtypes) suggests that policy and interventions to aid in the prevention and management of eye disease may also aid in the prevention of dementia syndrome. Where the level of evidence is weak, further studies are needed with stronger methodological approaches.
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视力障碍和眼部疾病与痴呆症、痴呆症亚型和认知障碍之间的关系:综述。
据报道,视力损伤(VI)和老年性黄斑变性(AMD)、糖尿病视网膜病变(DR)、青光眼和白内障等眼部疾病与认知障碍和痴呆症有关,但迄今为止,很少有人尝试对这些文献进行整理和归纳。因此,本综述旨在系统地评估视力损伤(VI)和眼部疾病与认知障碍、痴呆症和痴呆症亚型之间相关性证据的可信度和确定性。我们筛选了自数据库建立至 2024 年 5 月 30 日期间在 PubMed、MEDLINE (Ovid)、EMBASE、Web of Science、Cochrane CENTRAL 和 CDSR 上发表的任何语言的文章,对荟萃分析进行了总体回顾。对每项纳入的原始荟萃分析的质量评估均采用系统综述评估测量工具 2 (AMSTAR2)。证据的确定性基于统计学意义、研究规模、异质性、小规模研究效应、预测区间(PI)和偏倚。我们遵循在 PROSPERO(CRD42024564249)注册的事先协议。我们确定了 13 项元分析(AMSTAR 2;结果准确性高 1,中 10,低 2),其中包括 232 篇原始文章,共有 99,337,354 人参与。总体而言,没有证据具有高度提示性或说服力。白内障与痴呆症(等效比值比 [eOR] 1.20,95%CI,1.16-1.25)、白内障与阿尔茨海默病(等效比值比 1.21,95%CI,1.15-1.28)以及老年性视网膜病变与阿尔茨海默病(等效比值比 1.27,95%CI,1.27-1.27)之间的关系存在提示性证据。VI与痴呆症(eOR 1.50,95%CI,1.23-1.84)、DR与痴呆症(eOR 1.33,95%CI,1.17-1.50)、白内障与血管性痴呆症(eOR 1.26,95%CI,1.09-1.45)、横断面识别的VI(eOR 1.27,95%CI,1.27-1.27)之间的关系证据不足。45)、通过横断面研究确定的 VI 与认知障碍(eOR 2.37,95%CI,2.31-2.44),以及通过客观测量确定的 VI 与认知障碍(eOR 1.56,95%CI,1.12-2.18)。眼部疾病与痴呆症(以及痴呆症亚型)之间关系的提示性证据表明,有助于预防和管理眼部疾病的政策和干预措施也可能有助于预防痴呆综合症。在证据不足的情况下,需要采用更有力的方法开展进一步研究。
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来源期刊
Ageing Research Reviews
Ageing Research Reviews 医学-老年医学
CiteScore
19.80
自引率
2.30%
发文量
216
审稿时长
55 days
期刊介绍: With the rise in average human life expectancy, the impact of ageing and age-related diseases on our society has become increasingly significant. Ageing research is now a focal point for numerous laboratories, encompassing leaders in genetics, molecular and cellular biology, biochemistry, and behavior. Ageing Research Reviews (ARR) serves as a cornerstone in this field, addressing emerging trends. ARR aims to fill a substantial gap by providing critical reviews and viewpoints on evolving discoveries concerning the mechanisms of ageing and age-related diseases. The rapid progress in understanding the mechanisms controlling cellular proliferation, differentiation, and survival is unveiling new insights into the regulation of ageing. From telomerase to stem cells, and from energy to oxyradical metabolism, we are witnessing an exciting era in the multidisciplinary field of ageing research. The journal explores the cellular and molecular foundations of interventions that extend lifespan, such as caloric restriction. It identifies the underpinnings of manipulations that extend lifespan, shedding light on novel approaches for preventing age-related diseases. ARR publishes articles on focused topics selected from the expansive field of ageing research, with a particular emphasis on the cellular and molecular mechanisms of the aging process. This includes age-related diseases like cancer, cardiovascular disease, diabetes, and neurodegenerative disorders. The journal also covers applications of basic ageing research to lifespan extension and disease prevention, offering a comprehensive platform for advancing our understanding of this critical field.
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