Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Article type: Research Article
Authors: Devlin, Kathryn N.a | Brennan, Laurab | Saad, Laurac | Giovannetti, Taniad | Hamilton, Roy H.e; f | Wolk, David A.e; f | Xie, Sharon X.e; g | Mechanic-Hamilton, Dawne; f; *
Affiliations: [a] Department of Psychological and Brain Sciences, Drexel University, Philadelphia, PA, USA | [b] Department of Neurology, Thomas Jefferson University Hospital, Philadelphia, PA, USA | [c] Department of Psychology, Rutgers University, New Brunswick, NJ, USA | [d] Department of Psychology, Temple University, Philadelphia, PA, USA | [e] Alzheimer’s Disease Research Center, University of Pennsylvania, Philadelphia, PA, USA | [f] Department of Neurology, University of Pennsylvania, Philadelphia, PA, USA | [g] Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, PA, USA
Correspondence: [*] Correspondence to: Dawn Mechanic-Hamilton, Penn Memory Center, 3400 Civic Center Boulevard, Philadelphia, PA 19104, USA. Tel.: +215 662 4516; E-mail: dawn.mechanic@pennmedicine.upenn.edu.
Abstract: Background:Actuarial and statistical methods have been proposed as alternatives to conventional methods of diagnosing mild cognitive impairment (MCI), with the aim of enhancing diagnostic and prognostic validity, but have not been compared in racially diverse samples. Objective:We compared the agreement of consensus, actuarial, and statistical MCI diagnostic methods, and their relationship to race and prognostic indicators, among diverse older adults. Methods:Participants (N = 354; M age = 71; 68% White, 29% Black) were diagnosed with MCI or normal cognition (NC) according to clinical consensus, actuarial neuropsychological criteria (Jak/Bondi), and latent class analysis (LCA). We examined associations with race/ethnicity, longitudinal cognitive and functional change, and incident dementia. Results:MCI rates by consensus, actuarial criteria, and LCA were 44%, 53%, and 41%, respectively. LCA identified three MCI subtypes (memory; memory/language; memory/executive) and two NC classes (low normal; high normal). Diagnostic agreement was substantial, but agreement of the actuarial method with consensus and LCA was weaker than the agreement between consensus and LCA. Among cases classified as MCI by actuarial criteria only, Black participants were over-represented, and outcomes were generally similar to those of NC participants. Consensus diagnoses best predicted longitudinal outcomes overall, whereas actuarial diagnoses best predicted longitudinal functional change among Black participants. Conclusion:Consensus diagnoses optimize specificity in predicting dementia, but among Black older adults, actuarial diagnoses may be more sensitive to early signs of decline. Results highlight the need for cross-cultural validity in MCI diagnosis and should be explored in community- and population-based samples.
Keywords: Actuarial analysis, Alzheimer’s disease, cognitive aging, early diagnosis, latent class analysis, memory disorders, mild cognitive impairment, minority health, race factors, statistical models
DOI: 10.3233/JAD-210455
Journal: Journal of Alzheimer's Disease, vol. 85, no. 2, pp. 627-644, 2022
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl