一般人群的痴呆风险预测:基于人群的生命线队列研究中预测模型的外部验证

JAR life Pub Date : 2025-09-26 eCollection Date: 2025-01-01 DOI:10.1016/j.jarlif.2025.100028
Ingeborg Frentz, Sofia Marcolini, Silvan Licher, Peter Paul De Deyn, Mohammad Arfan Ikram
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引用次数: 0

摘要

背景:在初级保健中,痴呆预测模型对于识别有痴呆风险的个体是必要的,但由于缺乏外部验证或使用高成本变量,它们在临床实践中的实施在一定程度上受到限制。我们从外部验证了一个简单但有前途的痴呆症风险预测模型的预测性能。方法:以年龄、卒中史、主观记忆抱怨和相对复杂任务需要帮助为预测因素,采用95%置信区间的c统计量评估患者的判别能力。这是在10,007个人身上完成的,他们参加了生命线队列研究。在生命线队列研究中,痴呆的评估是在随访问卷中自我报告的。结果:基线时间点1b的平均随访时间为1.5年,基线时间点2a的平均随访时间为3.3年,基线时间点3a的平均随访时间为9.1年。总体而言,36名参与者自我报告了痴呆症的发展。模型总体痴呆发展的判别能力的c统计量为0.62 [95% CI=0.48-0.70],在随访2a时的判别能力略好,为0.67 [95% CI=0.57-0.78]。然而,在这个外部验证队列中,模型的校准很差,系统地高估了预测的风险。结论:在本研究中,基础痴呆风险预测模型高估了痴呆的风险,但在生命线队列中具有合理的判别能力。在这个验证队列中,由于报告的痴呆发病率低,该模型的潜力被低估了。需要进一步验证以确定模型的真实值。还应进行评估其在初级保健中实施可行性的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dementia risk prediction in the general population: external validation of a prediction model in the population-based LifeLines Cohort Study.

Dementia risk prediction in the general population: external validation of a prediction model in the population-based LifeLines Cohort Study.

Background: Models for dementia prediction in primary care are necessary to identify individuals at risk for developing dementia, but their implementation in clinical practice is partly limited due to lack of external validation or use of high-cost variables. We externally validated the predictive performance of a simple yet promising dementia risk prediction model.

Methods: We assessed discriminative ability with a c-statistic with 95 % confidence interval, using age, history of stroke, subjective memory complaints and need for assistance with a relatively complex task as predictors. This was done on 10,007 individuals that participated in the Lifelines-cohort study. Assessment of dementia in the Lifelines Cohort Study is self-reported in the follow-up questionnaires.

Results: Mean follow-up at LifeLines timepoint 1b was 1.5 years, mean follow-up at LifeLines timepoint 2a was 3.3 years and mean follow-up at LifeLines timepoint 3a was 9.1 years. Overall, 36 participants self-reported dementia development. Discriminative ability of the model overall dementia development yielded a c-statistic of 0.62 [95 % CI=0.48-0.70], and performed slightly better at follow-up 2a 0.67 [95 % CI=0.57-0.78]. However, calibration of the model in this external validation cohort was poor, with systematic overestimation of the predicted risk.

Conclusion: In this study the basic dementia risk prediction model overestimated the risk of dementia, but had reasonable discriminative ability in the Lifelines cohort. Within this validation cohort the potential of the model is underestimated due to low incidence of reported dementia. Further validation is required to determine the true value of the model. Studies assessing its implementation feasibility in primary care should also be conducted.

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