Literature DB >> 27193363

Mild Cognitive Impairment in Late Middle Age in the Wisconsin Registry for Alzheimer's Prevention Study: Prevalence and Characteristics Using Robust and Standard Neuropsychological Normative Data.

Lindsay R Clark1,2, Rebecca L Koscik1, Christopher R Nicholas2,3, Ozioma C Okonkwo1,2,3, Corinne D Engelman1,4, Lisa C Bratzke1,5, Kirk J Hogan1,6, Kimberly D Mueller1, Barbara B Bendlin2,3, Cynthia M Carlsson1,2,3, Sanjay Asthana1,2,3, Mark A Sager1, Bruce P Hermann1,7, Sterling C Johnson1,2,3.   

Abstract

OBJECTIVE: Detecting cognitive decline in presymptomatic Alzheimer's disease (AD) and early mild cognitive impairment (MCI) is challenging, but important for treatments targeting AD-related neurodegeneration. The current study aimed to investigate the utility and performance of internally developed robust norms and standard norms in identifying cognitive impairment in late middle-age (baseline age range = 36-68; M = 54).
METHOD: Robust norms were developed for neuropsychological measures based on longitudinally confirmed cognitively normal (CN) participants (n= 476). Seven hundred and seventy-nine participants enriched for AD risk were classified as psychometric MCI (pMCI) or CN based on standard and robust norms and "single-test" versus "multi-test" criteria.
RESULTS: Prevalence of pMCI ranged from 3% to 49% depending on the classification scheme used. Those classified as pMCI using robust norms exhibited greater subjective cognitive complaints, diagnostic stability, and mild clinical symptoms at follow-up.
CONCLUSIONS: Results suggest that identifying early clinically relevant cognitive decline in late middle-age is feasible using robust norms and multi-test criteria.
© The Author 2016. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Alzheimer's disease; Dementia; Elderly/Geriatrics/Aging; Learning and Memory; Mild cognitive impairment; Norms/normative studies

Year:  2016        PMID: 27193363      PMCID: PMC5088607          DOI: 10.1093/arclin/acw024

Source DB:  PubMed          Journal:  Arch Clin Neuropsychol        ISSN: 0887-6177            Impact factor:   2.813


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