Development and validation of a two-step shared parameter model for dementia imputation in the Cardiovascular Health Study Cohort.

Katie M Lynch,Erin E Bennett,Chelsea Liu,Emma K Stapp,Deborah A Levine,M Maria Glymour,Scott C Zimmerman,Michael E Griswold,Michelle C Odden,Oscar L Lopez,Melinda C Power
{"title":"Development and validation of a two-step shared parameter model for dementia imputation in the Cardiovascular Health Study Cohort.","authors":"Katie M Lynch,Erin E Bennett,Chelsea Liu,Emma K Stapp,Deborah A Levine,M Maria Glymour,Scott C Zimmerman,Michael E Griswold,Michelle C Odden,Oscar L Lopez,Melinda C Power","doi":"10.1093/gerona/glag072","DOIUrl":null,"url":null,"abstract":"BACKGROUND\r\nLarge-scale dementia ascertainment for research remains challenging. We demonstrate a method to impute dementia status and onset time using data from the Cardiovascular Health Study (CHS).\r\n\r\nMETHODS\r\nWe used a linear mixed effects model to estimate individual cognitive trajectories and included the estimates as covariates in an accelerated failure time model used to impute time to incident dementia in the CHS Cognition Study, a sub-study with dementia ascertainment. We calibrated the model in a 60% random sample (n = 2,000) of eligible participants with CHS Cognition Study dementia classifications and validated the final model in the remaining 40% sample (n = 1,334). We then imputed dementia onset time and dementia status during follow-up in the full CHS sample, including those without (n = 1,415) CHS Cognition Study dementia classifications.\r\n\r\nRESULTS\r\nIn the validation sample, relative to the CHS Cognition Study dementia classifications used as the \"reference standard\", specificity (98.5%), positive predictive value (81.9%), negative predictive value (92.0%) and accuracy (91.3%) were high, while sensitivity was modest (43.8%), with mean imputed onset time +/-1.5 years of classified. Performance varied by participant characteristics. Ultimately, 227 (16.0%) of participants without CHS Cognition Study classifications, and 472 (9.9%) of all CHS participants were classified as having dementia according to this approach.\r\n\r\nCONCLUSION\r\nThe shared parameter approach can be implemented in samples with existing cognitive data and a validation sample with reference-standard dementia adjudication. We found high overall accuracy and higher specificity than sensitivity, similar to reported performance metrics for algorithmic approaches requiring linkage to administrative data.","PeriodicalId":22892,"journal":{"name":"The Journals of Gerontology Series A: Biological Sciences and Medical Sciences","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2026-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journals of Gerontology Series A: Biological Sciences and Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/gerona/glag072","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND Large-scale dementia ascertainment for research remains challenging. We demonstrate a method to impute dementia status and onset time using data from the Cardiovascular Health Study (CHS). METHODS We used a linear mixed effects model to estimate individual cognitive trajectories and included the estimates as covariates in an accelerated failure time model used to impute time to incident dementia in the CHS Cognition Study, a sub-study with dementia ascertainment. We calibrated the model in a 60% random sample (n = 2,000) of eligible participants with CHS Cognition Study dementia classifications and validated the final model in the remaining 40% sample (n = 1,334). We then imputed dementia onset time and dementia status during follow-up in the full CHS sample, including those without (n = 1,415) CHS Cognition Study dementia classifications. RESULTS In the validation sample, relative to the CHS Cognition Study dementia classifications used as the "reference standard", specificity (98.5%), positive predictive value (81.9%), negative predictive value (92.0%) and accuracy (91.3%) were high, while sensitivity was modest (43.8%), with mean imputed onset time +/-1.5 years of classified. Performance varied by participant characteristics. Ultimately, 227 (16.0%) of participants without CHS Cognition Study classifications, and 472 (9.9%) of all CHS participants were classified as having dementia according to this approach. CONCLUSION The shared parameter approach can be implemented in samples with existing cognitive data and a validation sample with reference-standard dementia adjudication. We found high overall accuracy and higher specificity than sensitivity, similar to reported performance metrics for algorithmic approaches requiring linkage to administrative data.
在心血管健康研究队列中痴呆归因的两步共享参数模型的开发和验证。
背景:大规模痴呆研究的确定仍然具有挑战性。我们展示了一种利用心血管健康研究(CHS)数据推断痴呆状态和发病时间的方法。方法:我们使用线性混合效应模型来估计个体认知轨迹,并将这些估计值作为协变量纳入加速失效时间模型中,该模型用于在CHS认知研究(痴呆症确定的子研究)中计算痴呆发生的时间。我们在60%的随机样本(n = 2000)符合CHS认知研究痴呆分类的参与者中校准了模型,并在剩余的40%样本(n = 1334)中验证了最终模型。然后,我们在整个CHS样本中计算痴呆发病时间和痴呆状态,包括那些没有(n = 1,415) CHS认知研究痴呆分类的样本。结果验证样本中,相对于作为“参考标准”的CHS认知研究痴呆分类,特异性(98.5%)、阳性预测值(81.9%)、阴性预测值(92.0%)和准确性(91.3%)较高,敏感性(43.8%)中等,平均估算发病时间+/-1.5年。表现因参与者的特点而异。最终,根据这种方法,227名(16.0%)没有CHS认知研究分类的参与者和472名(9.9%)所有CHS参与者被归类为痴呆症。结论共享参数方法可应用于已有认知数据的样本和具有参考标准痴呆判定的验证样本。我们发现总体准确性高,特异性高于敏感性,类似于报告的需要与管理数据联系的算法方法的性能指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书