Zaman Andrew, Caywood Laura, Prough Michael, Clouse Jason, Harrington Sharlene, Adams Larry, Fuzzell Denise, Fuzzell Sarada, Laux Renee, Hochstetler Sherri D, Ogrocki Paula, Lerner Alan, Vance Jeffery M, Haines Jonathan L, Scott William K, Pericak-Vance Margaret A, Cuccaro Michael L
John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Department of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, Ohio, USA.
Int J Geriatr Psychiatry. 2023 Apr;38(4):e5903. doi: 10.1002/gps.5903.
Memory and cognitive problems are central to the diagnosis of Alzheimer's disease (AD). Psychometric approaches to defining phenotypes can aid in identify genetic variants associated with AD. However, these approaches have mostly been limited to affected individuals. Defining phenotypes of both affected and unaffected individuals may help identify genetic variants associated with both AD and healthy aging. This study compares psychometric methods for developing cognitive phenotypes that are more granular than clinical classifications.
682 older Old Order Amish individuals were included in the analysis. Adjusted Z-scores of cognitive tests were used to create four models including (1) global threshold scores or (2) memory threshold scores, and (3) global clusters and (4) memory clusters. An ordinal regression examined the coherence of the models with clinical classifications (cognitively impaired [CI], mildly impaired [MI], cognitively unimpaired), APOE-e4, sex, and age. An ANOVA examined the best model phenotypes for differences in clinical classification, APOE-e4, domain Z-scores (memory, language, executive function, and processing speed), sex, and age.
The memory cluster identified four phenotypes and had the best fit (χ = 491.66). Individuals in the worse performing phenotypes were more likely to be classified as CI or MI and to have APOE-e4. Additionally, all four phenotypes performed significantly differently from one another on the domains of memory, language, and executive functioning.
Memory cluster stratification identified the cognitive phenotypes that best aligned with clinical classifications, APOE-e4, and cognitive performance We predict these phenotypes will prove useful in searching for protective genetic variants.
记忆和认知问题是阿尔茨海默病(AD)诊断的核心。定义表型的心理测量方法有助于识别与AD相关的基因变异。然而,这些方法大多仅限于受影响个体。定义受影响和未受影响个体的表型可能有助于识别与AD和健康衰老相关的基因变异。本研究比较了用于开发比临床分类更精细的认知表型的心理测量方法。
682名年长的老派阿米什人纳入分析。认知测试的调整后Z分数用于创建四个模型,包括(1)总体阈值分数或(2)记忆阈值分数,以及(3)总体聚类和(4)记忆聚类。有序回归检验模型与临床分类(认知受损[CI]、轻度受损[MI]、认知未受损)、APOE-e4、性别和年龄的一致性。方差分析检验最佳模型表型在临床分类、APOE-e4、领域Z分数(记忆、语言、执行功能和处理速度)、性别和年龄方面的差异。
记忆聚类识别出四种表型,拟合度最佳(χ = 491.66)。表现较差表型的个体更有可能被归类为CI或MI,且携带APOE-e4。此外,所有四种表型在记忆、语言和执行功能领域的表现均存在显著差异。
记忆聚类分层识别出与临床分类、APOE-e4和认知表现最相符的认知表型。我们预测这些表型将有助于寻找保护性基因变异。