A critical review and classification of dementia risk assessment tools to inform dementia risk reduction.

IF 7.8 Q2 BUSINESS
Md Hamidul Huque, Ranmalee Eramudugolla, Meiwei Li, Kim M Kiely, Ruth Peters, Kaarin J Anstey
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引用次数: 0

Abstract

Addressing modifiable dementia risk factors requires reliable risk assessment methods. We aimed to synthesise knowledge on risk scores for all cause dementia, Alzheimer's disease (AD) and vascular dementia, classify them according to target population, evaluate their content, cost, appropriateness of validation studies, and suitability for implementing risk reduction guidelines. A systematic search was conducted of PubMed, Cochrane Collaboration, ProQuest, Scopus, Embase, and PsycINFO databases using a pre-registered protocol. Data on risk factors, target population, predictive validity, cost, and alignment with WHO guidelines were extracted. Random-effects meta-analysis was performed. Of 45 risk scores identified, 29 were for all-cause dementia, including 11 based on late-life cohorts, 6 on midlife, and 7 covering mid to late-life. The pooled C-statistic across development and validation studies of dementia risk scores was 0.69 (95 % CI: 0.67, 0.71). Development study AUCs were higher than validation study AUCs and dropped from 0.74 to 0.66 for risk scores developed for clinical samples and from 0.79 to 0.71 for AD specific scores (which include functional indicators non-independent of disease). There were no validated risk scores for vascular dementia. Dem-NCD, CogDrisk, ANU-ADRI and LIBRA risk scores incorporated most WHO-recommended risk factors and demonstrated accuracy comparable to the overall pooled C-statistic. We conclude that across the field, there are methodological limitations relating to validation, and inappropriate comparison of tools designed for different purposes or target populations. However, there are now several validated, risk scores for all-cause dementia and AD that assess modifiable factors and offer cost-effective dementia risk assessment and risk reduction advice.

对痴呆风险评估工具的重要回顾和分类,为降低痴呆风险提供信息。
解决可改变的痴呆风险因素需要可靠的风险评估方法。我们的目的是综合全因痴呆、阿尔茨海默病(AD)和血管性痴呆的风险评分知识,根据目标人群对其进行分类,评估其内容、成本、验证研究的适当性以及实施风险降低指南的适用性。系统检索PubMed、Cochrane Collaboration、ProQuest、Scopus、Embase和PsycINFO数据库,采用预注册协议。提取了有关风险因素、目标人群、预测效度、成本和与世卫组织指南一致性的数据。进行随机效应荟萃分析。在确定的45个风险评分中,29个是针对全因痴呆的,其中11个基于晚年队列,6个基于中年队列,7个涵盖中老年队列。痴呆风险评分的开发和验证研究的合并c统计量为0.69 (95% CI: 0.67, 0.71)。发展研究的auc高于验证研究的auc,临床样本的风险评分从0.74降至0.66,AD特异性评分(包括非独立于疾病的功能指标)从0.79降至0.71。目前还没有有效的血管性痴呆风险评分。Dem-NCD、cogrisk、ANU-ADRI和LIBRA风险评分纳入了大多数世卫组织推荐的风险因素,并显示出与总体合并c统计量相当的准确性。我们得出结论,在整个领域中,存在与验证相关的方法局限性,以及针对不同目的或目标人群设计的工具的不适当比较。然而,现在有几个经过验证的全因痴呆和阿尔茨海默病的风险评分,可以评估可改变的因素,并提供具有成本效益的痴呆风险评估和风险降低建议。
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来源期刊
The Journal of Prevention of Alzheimer's Disease
The Journal of Prevention of Alzheimer's Disease Medicine-Psychiatry and Mental Health
CiteScore
9.20
自引率
0.00%
发文量
0
期刊介绍: The JPAD Journal of Prevention of Alzheimer’Disease will publish reviews, original research articles and short reports to improve our knowledge in the field of Alzheimer prevention including: neurosciences, biomarkers, imaging, epidemiology, public health, physical cognitive exercise, nutrition, risk and protective factors, drug development, trials design, and heath economic outcomes.JPAD will publish also the meeting abstracts from Clinical Trial on Alzheimer Disease (CTAD) and will be distributed both in paper and online version worldwide.We hope that JPAD with your contribution will play a role in the development of Alzheimer prevention.
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