Optimizing Subjective Cognitive Decline to Detect Early Cognitive Dysfunction

Author:

Chapman Silvia12,Sunderaraman Preeti1324,Joyce Jillian L.13,Azar Martina56,Colvin Leigh E.6,Barker Megan S.12,McKeague Ian7,Kreisl William C.1324,Cosentino Stephanie1324

Affiliation:

1. Cognitive Neuroscience Division, Columbia University Medical Center, New York, NY, USA

2. Taub Institute for Research on Alzheimer’s Disease and the Aging Brain, Columbia University Medical Center, New York, NY, USA

3. Gertrude H. Sergievsky Center, Columbia University Medical Center, New York, NY, USA

4. Department of Neurology, Columbia University Medical Center, New York, NY, USA

5. Department of Psychology, Drexel University, Philadelphia, PA, USA

6. VA Boston Health Care System, Boston, MA, USA

7. Department of Biostatistics, Mailman School of Public Health, Columbia University Medical Center, New York, NY, USA

Abstract

Background: The utility of subjective cognitive decline (SCD) as an indicator of preclinical AD is overshadowed by its inconsistent association with objective cognition. Objective: This study examines if manipulations of SCD measurement affect its association with early cognitive dysfunction characteristic of preclinical AD. Methods: Cognitively healthy older adults (n = 110) completed SCD questionnaires that elicited complaints in general, compared to 5 years ago (retrospective SCD) and compared to their peers (age-anchored SCD) in binary and Likert scales. Outcome cognitive tasks included an associative memory task (Face-Name Test), a visual short-term memory binding task (STMB test), and a clinical neuropsychological list learning test (Selective Reminder Test). Results: SCD complaints, when compared to age-matched peers (age-anchored SCD) were endorsed less frequently than complaints compared to 5 years ago (retrospective SCD) (p < 0.01). In demographically adjusted regressions, age-anchored ordinal-rated SCD was associated with short term memory binding (β= –0.22, p = 0.040, CI = –0.45, –0.01), associative memory (β= –0.26, p = 0.018, CI = –0.45, –0.06), and list learning (β= –0.31, p = 0.002, CI = –0.51, –0.12). Retrospective and general ordinal-rated SCD was associated with associative memory (β= –0.25, p = 0.012, CI = –0.44, –0.06; β= –0.29, p = 0.003, CI = –0.47, –0.10) and list learning only (β= –0.25, p = 0.014, CI = –0.45, –0.05; β= –0.28, p = 0.004, CI = –0.48, –0.09). Conclusion: Ordinal age-anchored SCD appears better suited than other SCD measurements to detect early cognitive dysfunction characteristic of preclinical AD.

Publisher

IOS Press

Subject

Psychiatry and Mental health,Geriatrics and Gerontology,Clinical Psychology,General Medicine,General Neuroscience

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