TY - JOUR
T1 - Pick a PACC
T2 - Comparing Domain-Specific and General Cognitive Composites in Alzheimer Disease Research
AU - McKay, Nicole S.
AU - Millar, Peter R.
AU - Nicosia, Jessica
AU - Aschenbrenner, Andrew J.
AU - Gordon, Brian A.
AU - Benzinger, Tammie L.S.
AU - Cruchaga, Carolos C.
AU - Schindler, Suzanne E.
AU - Morris, John C.
AU - Hassenstab, Jason
N1 - Publisher Copyright:
© 2024 American Psychological Association
PY - 2024/4/11
Y1 - 2024/4/11
N2 - Objective: We aimed to illustrate how complex cognitive data can be used to create domain-specific and general cognitive composites relevant to Alzheimer disease research. Method: Using equipercentile equating, we combined data from the Charles F. and Joanne Knight Alzheimer Disease Research Center that spanned multiple iterations of the Uniform Data Set. Exploratory factor analyses revealed four domain-specific composites representing episodic memory, semantic memory, working memory, and attention/processing speed. The previously defined preclinical Alzheimer disease cognitive composite (PACC) and a novel alternative, the Knight-PACC, were also computed alongside a global composite comprising all available tests. These three composites allowed us to compare the usefulness of domain and general composites in the context of predicting common Alzheimer disease biomarkers. Results: General composites slightly outperformed domain-specific metrics in predicting imaging-derived amyloid, tau, and neurodegeneration burden. Power analyses revealed that the global, Knight-PACC, and attention and processing speed composites would require the smallest sample sizes to detect cognitive change in a clinical trial, while the Alzheimer Disease Cooperative Study-PACC required two to three times as many participants. Conclusions: Analyses of cognition with the Knight-PACC and our domain-specific composites offer researchers flexibility by providing validated outcome assessments that can equate across test versions to answer a wide range of questions regarding cognitive decline in normal aging and neurodegenerative disease.
AB - Objective: We aimed to illustrate how complex cognitive data can be used to create domain-specific and general cognitive composites relevant to Alzheimer disease research. Method: Using equipercentile equating, we combined data from the Charles F. and Joanne Knight Alzheimer Disease Research Center that spanned multiple iterations of the Uniform Data Set. Exploratory factor analyses revealed four domain-specific composites representing episodic memory, semantic memory, working memory, and attention/processing speed. The previously defined preclinical Alzheimer disease cognitive composite (PACC) and a novel alternative, the Knight-PACC, were also computed alongside a global composite comprising all available tests. These three composites allowed us to compare the usefulness of domain and general composites in the context of predicting common Alzheimer disease biomarkers. Results: General composites slightly outperformed domain-specific metrics in predicting imaging-derived amyloid, tau, and neurodegeneration burden. Power analyses revealed that the global, Knight-PACC, and attention and processing speed composites would require the smallest sample sizes to detect cognitive change in a clinical trial, while the Alzheimer Disease Cooperative Study-PACC required two to three times as many participants. Conclusions: Analyses of cognition with the Knight-PACC and our domain-specific composites offer researchers flexibility by providing validated outcome assessments that can equate across test versions to answer a wide range of questions regarding cognitive decline in normal aging and neurodegenerative disease.
KW - Alzheimer
KW - factor analysis
KW - magnetic resonance imaging
KW - positron emission tomography
KW - preclinical Alzheimer disease cognitive composite
UR - http://www.scopus.com/inward/record.url?scp=85195572903&partnerID=8YFLogxK
U2 - 10.1037/neu0000949
DO - 10.1037/neu0000949
M3 - Article
C2 - 38602816
AN - SCOPUS:85195572903
SN - 0894-4105
VL - 38
SP - 443
EP - 464
JO - Neuropsychology
JF - Neuropsychology
IS - 5
ER -