Back to Search Start Over

Faster cognitive decline in dementia due to Alzheimer disease with clinically undiagnosed Lewy body disease

Authors :
Charles H. Adler
Bryan M. Spann
Brett Cutler
Sandra A. Jacobson
Bryan K. Woodruff
Javon Oliver
Lisa R. Nicholson
Geoffrey L. Ahern
Eric M. Reiman
Michael Malek-Ahmadi
Steven Z. Rapscak
Richard J. Caselli
Jiong Shi
Kewei Chen
Christine Belden
Edward Zamrini
John N. Caviness
Marwan N. Sabbagh
Jasmine Curry
Michael J. Glass
David Shprecher
Lucia I. Sue
Richard Arce
Douglas G. Walker
Anthony Intorcia
Lih-Fen Lue
Geidy E. Serrano
Kathy E. Long
Holly A. Shill
Michael Callan
Erika Driver-Dunckley
Pierre N. Tariot
Shyamal H. Mehta
Thomas G. Beach
Kathryn J. Davis
Jessica E. Walker
Source :
PLoS ONE, PLoS ONE, Vol 14, Iss 6, p e0217566 (2019)
Publication Year :
2019
Publisher :
Public Library of Science (PLoS), 2019.

Abstract

BackgroundNeuropathology has demonstrated a high rate of comorbid pathology in dementia due to Alzheimer's disease (ADD). The most common major comorbidity is Lewy body disease (LBD), either as dementia with Lewy bodies (AD-DLB) or Alzheimer's disease with Lewy bodies (AD-LB), the latter representing subjects with ADD and LBD not meeting neuropathological distribution and density thresholds for DLB. Although it has been established that ADD subjects with undifferentiated LBD have a more rapid cognitive decline than those with ADD alone, it is still unknown whether AD-LB subjects, who represent the majority of LBD and approximately one-third of all those with ADD, have a different clinical course.MethodsSubjects with dementia included those with "pure" ADD (n = 137), AD-DLB (n = 64) and AD-LB (n = 114), all with two or more complete Mini Mental State Examinations (MMSE) and a full neuropathological examination.ResultsLinear mixed models assessing MMSE change showed that the AD-LB group had significantly greater decline compared to the ADD group (β = -0.69, 95% CI: -1.05, -0.33, pConclusionsThe probable cause of LBD clinical detection failure is the lack of a sufficient set of characteristic core clinical features. Core DLB clinical features were not more common in AD-LB as compared to ADD. Clinical identification of ADD with LBD would allow stratified analyses of ADD clinical trials, potentially improving the probability of trial success.

Details

ISSN :
19326203
Volume :
14
Database :
OpenAIRE
Journal :
PLOS ONE
Accession number :
edsair.doi.dedup.....e14c83c20509eac08a2e4fc356399797
Full Text :
https://doi.org/10.1371/journal.pone.0217566