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开发一种用于预测 5 年、9 年和 13 年痴呆风险的临床风险评分预测工具。

Development of a Clinical Risk Score Prediction Tool for 5-, 9-, and 13-Year Risk of Dementia.

机构信息

Shenzhen Mental Health Centre, Shenzhen Kangning Hospital, Shenzhen, China.

Department of Electrical and Computer Engineering, Faculty of Science and Technology, University of Macau, Taipa, Macau, China.

出版信息

JAMA Netw Open. 2022 Nov 1;5(11):e2242596. doi: 10.1001/jamanetworkopen.2022.42596.

DOI:10.1001/jamanetworkopen.2022.42596
PMID:36394871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9672974/
Abstract

IMPORTANCE

Although researchers have devoted substantial efforts, money, and time to studying the causes of dementia and the means to prevent it, no effective treatment exists yet. Identifying preclinical risk factors of dementia could help prevent or delay its progression.

OBJECTIVE

To develop a point risk score prediction model of dementia.

DESIGN, SETTING, AND PARTICIPANTS: This study used a large UK population-based prospective cohort study conducted between March 13, 2006, and October 1, 2010. Data analysis was performed from June 7 to September 15, 2021. Individual analyses of time end points were concluded at the first dementia diagnosis during the follow-up period. The data were split into training and testing data sets to separately establish and validate a prediction model.

MAIN OUTCOMES AND MEASURES

Outcomes of interest included 5-, 9-, and 13-year dementia risk. Least absolute shrinkage and selection operator and multivariate Cox proportional hazards regression models were used to identify available and practical dementia predictors. A point risk score model was developed for the individual prediction of 5-, 9-, and 13-year dementia risk.

RESULTS

A total of 502 505 participants were selected; the population after exclusions for missing data and dementia diagnosis at baseline was 444 695 (205 187 men; mean [SD] age, 56.74 [8.18] years; 239 508 women; mean [SD] age, 56.20 [8.01] years). Dementia occurrence during the 13 years of follow-up was 0.7% for men and 0.5% for women. The C statistic of the final multivariate Cox proportional hazards regression model was 0.86 for men and 0.85 for women in the training data set, and 0.85 for men and 0.87 for women in the testing data set. Men and women shared some modifiable risk and protective factors, but they also presented independent risk factors that accounted for 31.7% of men developing dementia and 53.35% of women developing dementia according to the weighted population-attributable fraction. The total point score of the risk score model ranged from -18 to 30 in men and -17 to 30 in women. The risk score model yielded nearly 100% prediction accuracy of 13-year dementia risk both in men and women.

CONCLUSIONS AND RELEVANCE

In this diagnostic study, a practical risk score tool was developed for individual prediction of dementia risk, which may help individuals identify their potential risk profile and provide guidance on precise and timely actions to promote dementia delay or prevention.

摘要

重要性

尽管研究人员已经投入了大量的精力、资金和时间来研究痴呆症的病因和预防方法,但目前仍没有有效的治疗方法。识别痴呆症的临床前风险因素可能有助于预防或延缓其进展。

目的

开发痴呆症的点风险评分预测模型。

设计、地点和参与者:本研究使用了一项大型的英国基于人群的前瞻性队列研究,该研究于 2006 年 3 月 13 日至 2010 年 10 月 1 日进行。数据分析于 2021 年 6 月 7 日至 9 月 15 日进行。对每个时间终点的个体分析在随访期间首次诊断痴呆症时结束。数据被分为训练和测试数据集,以分别建立和验证预测模型。

主要结果和措施

感兴趣的结果包括 5 年、9 年和 13 年的痴呆风险。最小绝对收缩和选择算子和多变量 Cox 比例风险回归模型被用来识别可用的和实用的痴呆预测因素。为个体预测 5 年、9 年和 13 年的痴呆风险,建立了一个点风险评分模型。

结果

共选择了 502505 名参与者;排除缺失数据和基线时痴呆诊断后,人群为 444695 人(男性 205187 人;平均[SD]年龄 56.74[8.18]岁;女性 239508 人;平均[SD]年龄 56.20[8.01]岁)。在 13 年的随访期间,男性的痴呆发生率为 0.7%,女性为 0.5%。在训练数据集中,最终多变量 Cox 比例风险回归模型的 C 统计量为男性 0.86,女性 0.85,在测试数据集中,男性为 0.85,女性为 0.87。男性和女性有一些可改变的风险和保护因素,但也有独立的风险因素,根据加权人群归因分数,男性有 31.7%的人患痴呆症,女性有 53.35%的人患痴呆症。风险评分模型的总评分范围在男性为-18 到 30,在女性为-17 到 30。该风险评分模型在男性和女性中对 13 年痴呆风险的预测准确率均接近 100%。

结论和相关性

在这项诊断研究中,开发了一种实用的风险评分工具,用于个体预测痴呆风险,这可能有助于个体识别其潜在的风险状况,并为精确和及时的行动提供指导,以促进痴呆症的延迟或预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d84b/9672974/0f9bba45dd26/jamanetwopen-e2242596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d84b/9672974/cba34446df29/jamanetwopen-e2242596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d84b/9672974/0f9bba45dd26/jamanetwopen-e2242596-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d84b/9672974/cba34446df29/jamanetwopen-e2242596-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d84b/9672974/0f9bba45dd26/jamanetwopen-e2242596-g002.jpg

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本文引用的文献

1
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Life Sci. 2021 Jan 1;264:118627. doi: 10.1016/j.lfs.2020.118627. Epub 2020 Oct 22.
2
Dementia prevention, intervention, and care: 2020 report of the Lancet Commission.《痴呆症的预防、干预与照护:柳叶刀委员会2020年报告》
Lancet. 2020 Aug 8;396(10248):413-446. doi: 10.1016/S0140-6736(20)30367-6. Epub 2020 Jul 30.
3
The importance of BDNF and RAGE in diabetes-induced dementia.
中老年抑郁症患者痴呆风险新型预测模型的开发与验证:一项大型纵向机器学习队列研究
Alzheimers Res Ther. 2025 May 13;17(1):103. doi: 10.1186/s13195-025-01750-6.
4
Plasma protein risk scores for mild cognitive impairment and Alzheimer's disease in the Framingham heart study.弗雷明汉心脏研究中轻度认知障碍和阿尔茨海默病的血浆蛋白风险评分
Alzheimers Dement. 2025 Mar;21(3):e70066. doi: 10.1002/alz.70066.
5
Development and internal validation of a risk prediction model for dementia in a rural older population in China.中国农村老年人群痴呆风险预测模型的开发与内部验证
Alzheimers Dement. 2025 Feb;21(2):e14617. doi: 10.1002/alz.14617.
6
A point-based cognitive impairment scoring system for southeast Asian adults.一种针对东南亚成年人的基于点数的认知障碍评分系统。
J Prev Alzheimers Dis. 2025 Apr;12(4):100069. doi: 10.1016/j.tjpad.2025.100069. Epub 2025 Jan 24.
7
Establishing a machine learning dementia progression prediction model with multiple integrated data.建立一个使用多种整合数据的机器学习痴呆进展预测模型。
BMC Med Res Methodol. 2024 Nov 22;24(1):288. doi: 10.1186/s12874-024-02411-2.
8
Individualized, cross-validated prediction of future dementia using cognitive assessments in people with mild cognitive symptoms.使用认知评估对有轻度认知症状的人群进行个体化、交叉验证的未来痴呆症预测。
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9
Significance of plasma p-tau217 in predicting long-term dementia risk in older community residents: Insights from machine learning approaches.血浆 p-tau217 对预测老年社区居民长期痴呆风险的意义:基于机器学习方法的见解。
Alzheimers Dement. 2024 Oct;20(10):7037-7047. doi: 10.1002/alz.14178. Epub 2024 Aug 8.
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Lancet Healthy Longev. 2024 Jun;5(6):e406-e421. doi: 10.1016/S2666-7568(24)00061-8.
脑源性神经营养因子(BDNF)和晚期糖基化终产物(RAGE)在糖尿病性痴呆中的作用。
Pharmacol Res. 2020 Oct;160:105083. doi: 10.1016/j.phrs.2020.105083. Epub 2020 Jul 15.
4
Sex-driven modifiers of Alzheimer risk: A multimodality brain imaging study.性驱动的阿尔茨海默病风险修饰因素:一项多模态脑影像学研究。
Neurology. 2020 Jul 14;95(2):e166-e178. doi: 10.1212/WNL.0000000000009781. Epub 2020 Jun 24.
5
Sleep problems and risk of all-cause cognitive decline or dementia: an updated systematic review and meta-analysis.睡眠问题与全因认知能力下降或痴呆风险:一项更新的系统评价和荟萃分析。
J Neurol Neurosurg Psychiatry. 2020 Mar;91(3):236-244. doi: 10.1136/jnnp-2019-321896. Epub 2019 Dec 26.
6
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JAMA Netw Open. 2019 Dec 2;2(12):e1917257. doi: 10.1001/jamanetworkopen.2019.17257.
7
Sex/gender differences in cognitive trajectories vary as a function of race/ethnicity.性别/认知轨迹的差异因种族/民族而异。
Alzheimers Dement. 2019 Dec;15(12):1516-1523. doi: 10.1016/j.jalz.2019.04.006. Epub 2019 Oct 9.
8
Preventing dementia by preventing stroke: The Berlin Manifesto.预防中风以预防痴呆:柏林宣言。
Alzheimers Dement. 2019 Jul;15(7):961-984. doi: 10.1016/j.jalz.2019.06.001.
9
Antiaging Therapies, Cognitive Impairment, and Dementia.抗衰老疗法、认知障碍与痴呆。
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10
Population attributable fractions for risk factors for dementia in low-income and middle-income countries: an analysis using cross-sectional survey data.低收入和中等收入国家痴呆风险因素的人群归因分数:使用横断面调查数据进行的分析。
Lancet Glob Health. 2019 May;7(5):e596-e603. doi: 10.1016/S2214-109X(19)30074-9.