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Article type: Research Article
Authors: Haneuse, Sebastiena; b; * | Larson, Erica | Walker, Roda | Montine, Thomasc | Sonnen, Joshuac
Affiliations: [a] Group Health Center for Health Studies, Seattle, WA, USA | [b] Department of Biostatistics, University of Washington, Seattle, WA, USA | [c] Department of Pathology, University of Washington, Seattle, WA, USA
Correspondence: [*] Corresponding author: Sebastien J.P.A. Haneuse, PhD, Group Health Center for Health Studies, 1730 Minor Avenue, Suite 1600, Seattle, WA 98101, USA. Tel.: +1 206 287 2005; Fax: +1 206 287 2871; E-mail: haneuse.s@ghc.org.
Note: [] Communicated by Sara Debanne
Abstract: Current neuropathologic consensus criteria for diagnosis of dementia yield a classification of processes that likely contributed to dementia in that individual. While dementia diagnosis currently relies on clinical criteria, practicing neuropathologists and researchers might benefit from a simple, accurate risk scoring protocol for the neuropathologic diagnosis of dementia. Using 232 consecutive autopsies from the population-based Adult Changes in Thought study, we developed two logistic regression-based risk scoring systems; one solely using neuropathologic measures and a second additionally including demographic information. Inverse-probability weighting was used to adjust for inherent selection bias in autopsy-based studies of dementing illnesses. Both systems displayed high levels of predictive accuracy; bias-adjusted area-under-the-curve statistics were 0.78 (95% CI 0.71, 0.85) and 0.87 (95% CI 0.83, 0.92), indicating improved performance with the inclusion of demographic characteristics, specifically age and birth cohort information. Application of the combined neuropathlogy/demographic model yielded bias-adjusted sensitivity and specificity of 81% each. In contrast, application of NIA-Reagan criteria yielded sensitivity and specificity of 53% and 84%. Our proposed scoring systems provide neuropathologists with tools to make a diagnosis, and interpret their diagnosis in the light of known sensitivity and specificity estimates. Evaluation in independent samples will be important to verify our findings.
Keywords: Alzheimer's disease, autopsy, dementia, microinfarcts, neuropathology, prediction, selection bias
DOI: 10.3233/JAD-2009-1105
Journal: Journal of Alzheimer's Disease, vol. 17, no. 4, pp. 875-885, 2009
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