Influence of cognitive, neuropsychiatric, and diagnostic factors on financial capacity: A longitudinal analysis of the ADNI cohort.

IF 4 Q1 CLINICAL NEUROLOGY
Milap A Nowrangi, Jeannie Marie Leoutsakos, Haijuan Yan, Arnold Bakker, Kevin J Manning, George W Rebok, Paul B Rosenberg, Vidyulata Kamath
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引用次数: 0

Abstract

Introduction: Financial capacity (FC) is the ability to independently manage finances in a manner consistent with one's self-interest. To investigate the relationship between FC, cognitive domains, neuropsychiatric symptoms, and transitions from normal cognition (cognitive normal [CN]) to mild cognitive impairment (MCI) or Alzheimer's disease (AD), we conducted a secondary analysis of the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort using the Financial Capacity Instrument short form (FCI-SF).

Methods: To examine these longitudinal relationships, we fit two models, a random effects (random intercept) "time-averaged" model and a "time since previous visit" model, where we regressed each of the five component financial scores on each of the cognitive composite scores. To examine the effect of baseline FCI-SF performance on conversion rates from normal to MCI or AD, we computed a survival model.

Results: A total of 874 participants (diagnostic group, N, mean age: CN: 501, 74.4; MCI: 319, 74.6; and AD 54, 74.9) were included in the analyses. In time since previous visit models, we found that lower executive function composite scores were related to decline in the complex checkbook score (ß = 1.35 (0.55), p = 0.016) and total completion time of the FCI-SF (ß = 1.85 (9.36), p = 0.025). In addition, lower composite visuospatial score was significantly related to poorer performance on financial conceptual knowledge, complex checkbook, and total completion time. Lower composite memory score was highly related to decline in financial conceptual knowledge, single checkbook, and bank statement subscale scores. ADNI participants in the lowest tertile of total completion time, at any point in time, were four times more likely to receive a diagnosis of MCI or AD compared to participants in the highest tertile with a hazard ratio of 4.22 ([2.29] p = 008).

Discussion: There is a multifaceted interaction between poorer cognition and everyday financial function where executive function, memory, and visuospatial cognition are related to FC. The strongest predictor of conversion from normal to either MCI or AD, appears to be time to completion.

Highlights: Decline in financial capacity (FC) is observed during transition to dementia and increases the risk of negative outcomes.Executive function, memory, and visuospatial cognition are related to FC.The strongest predictor of conversion from normal to either mild cognitive impairment (MCI) or Alzheimer's disease (AD) is time to completion or processing speed.

认知、神经精神和诊断因素对财务能力的影响:ADNI队列的纵向分析。
财务能力(FC)是指以符合个人利益的方式独立管理财务的能力。为了研究FC、认知领域、神经精神症状和从正常认知(认知正常[CN])到轻度认知障碍(MCI)或阿尔茨海默病(AD)的转变之间的关系,我们使用财务能力工具短格式(FCI-SF)对阿尔茨海默病神经影像学倡议(ADNI)队列进行了二次分析。方法:为了检验这些纵向关系,我们拟合了两个模型,一个是随机效应(随机截距)“时间平均”模型和“上次访问后的时间”模型,其中我们将五个组成部分的财务分数回归到每个认知复合分数上。为了检查基线FCI-SF性能对从正常到MCI或AD的转换率的影响,我们计算了一个生存模型。结果:共有874名参与者(诊断组,N,平均年龄:CN: 501, 74.4;MCI: 319,74.6;和公元54,74.9)被纳入分析。与之前的访问模型相比,我们发现较低的执行功能综合得分与复杂支票簿得分(ß = 1.35 (0.55), p = 0.016)和FCI-SF总完成时间(ß = 1.85 (9.36), p = 0.025)的下降有关。此外,较低的综合视觉空间得分与财务概念知识、复杂支票簿和总完成时间的较差表现显著相关。较低的综合记忆得分与金融概念知识、单支票簿和银行对账单分量表得分的下降高度相关。在任何时间点,总完成时间最低分位数的ADNI参与者被诊断为MCI或AD的可能性是最高分位数参与者的四倍,风险比为4.22 ([2.29]p = 008)。讨论:较差的认知与日常财务功能之间存在多方面的相互作用,其中执行功能、记忆和视觉空间认知与FC有关。从正常到轻度认知障碍或AD转换的最强预测因子,似乎是完成的时间。重点:在向痴呆症过渡期间,观察到经济能力(FC)下降,并增加了负面结果的风险。执行功能、记忆和视觉空间认知与FC有关。从正常到轻度认知障碍(MCI)或阿尔茨海默病(AD)转换的最强预测因子是完成时间或处理速度。
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来源期刊
CiteScore
7.80
自引率
7.50%
发文量
101
审稿时长
8 weeks
期刊介绍: Alzheimer''s & Dementia: Diagnosis, Assessment & Disease Monitoring (DADM) is an open access, peer-reviewed, journal from the Alzheimer''s Association® that will publish new research that reports the discovery, development and validation of instruments, technologies, algorithms, and innovative processes. Papers will cover a range of topics interested in the early and accurate detection of individuals with memory complaints and/or among asymptomatic individuals at elevated risk for various forms of memory disorders. The expectation for published papers will be to translate fundamental knowledge about the neurobiology of the disease into practical reports that describe both the conceptual and methodological aspects of the submitted scientific inquiry. Published topics will explore the development of biomarkers, surrogate markers, and conceptual/methodological challenges. Publication priority will be given to papers that 1) describe putative surrogate markers that accurately track disease progression, 2) biomarkers that fulfill international regulatory requirements, 3) reports from large, well-characterized population-based cohorts that comprise the heterogeneity and diversity of asymptomatic individuals and 4) algorithmic development that considers multi-marker arrays (e.g., integrated-omics, genetics, biofluids, imaging, etc.) and advanced computational analytics and technologies.
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