Published In

Aging Clinical and Experimental Research

Document Type

Post-Print

Publication Date

9-1-2019

Abstract

Objective: A lack of understanding of the causes of attrition in longitudinal studies of older adults may lead to higher attrition rates and bias longitudinal study results. In longitudinal epidemiological studies of Alzheimer’s disease and related dementias, high rates of attrition may cause a systematic underestimation of dementia prevalence and skew the characterization of the disease. This can compromise the generalizability of the study results and any inferences based on the surviving sample may grossly misrepresent the importance of the risk factors for dementia. The National Institute on Aging outlined a National Strategy for Recruitment and Participation in Alzheimer’s Disease Clinical Research to address this problem, providing evidence of the magnitude of this problem. Method: To explore predictors of attrition, this study examined the National Alzheimer’s Coordinating Center ( NACC ) Uniform Data Set, a repository of observations of older adults spanning 11 years, using survival analysis. Four samples were examined: the full sample ( n = 30,433 ) , the alive subsample excluding those who died ( n = 24,231 ) , the MRI sample [participants with complete MRI data ( n = 1104 ) ] , and the alive MRI subsample [participants with MRI data excluding those who died (n = 947 ) ] . Results: Worsening cognitive impairment, neuropsychiatric symptoms, and difficulty with functional activities predicted attrition, as did lower hippocampal volume in the MRI subsample. Questionable co-participant reliability and an informant other than a spouse also increased risk of attrition. Discussion: Special considerations exist in recruiting and retaining older adults in longitudinal studies, and results of baseline psychological, functional, and cognitive functioning should be used to identify targeted retention strategies.

Description

At the time of publication, Mitra Naseh was employed at Florida International University.

Published in final edited form as: Aging Clin Exp Res. 2019 Sep; 31(9): 1283–1297. Published online 2018 Dec 10. doi: 10.1007/s40520-018-1087-6

DOI

10.1007/s40520-018-1087-6

Persistent Identifier

https://archives.pdx.edu/ds/psu/35618

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