You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 60 No. 9, September 2003 TABLE OF CONTENTS
  Archives
  •  Online Features
  Original Contribution
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on ISI (27)
 •Contact me when this article is cited
 Related Content
 •Similar articles in this journal
 Topic Collections
 •Alzheimer Disease
 •Lewy Body Disease
 •Movement Disorders
 •Neuropathology
 •Alert me on articles by topic

Cerebrospinal Fluid Markers in Dementia With Lewy Bodies Compared With Alzheimer Disease

Estrella Gómez-Tortosa, MD, PhD; Isabel Gonzalo, PhD; Samira Fanjul, MD; Maria José Sainz, PhD; Susana Cantarero, MD; Carlos Cemillán, MD; Justo García Yébenes, MD, PhD; Teodoro del Ser, MD, PhD

Arch Neurol. 2003;60:1218-1222.

Background  Most patients with dementia with Lewy bodies (DLB) exhibit diffuse plaque–only pathology with rare neocortical neurofibrillary tangles (NFTs), as opposed to the widespread cortical neurofibrillary-tau involvement in Alzheimer disease (AD). Another pathological difference is the astrocytic and microglial inflammatory responses, including release of interleukins (ILs), around the neuritic plaques and NFTs in AD brains that are absent or much lower in DLB. We analyzed cerebrospinal fluid (CSF) markers that reflect the pathological differences between AD and DLB.

Objective  To determine CSF concentrations of tau, {beta}-amyloid, IL-1{beta}, and IL-6 as potential diagnostic clues to distinguish between AD and DLB.

Methods  We measured total tau, {beta}-amyloid1-42, IL-1{beta}, and IL-6 levels in CSF samples of 33 patients with probable AD without parkinsonism, 25 patients with all the core features of DLB, and 46 age-matched controls.

Results  Patients with AD had significantly higher levels of tau protein than patients with DLB and controls (P<.001). The most efficient cutoff value provided 76% specificity to distinguish AD and DLB cases. Patients with AD and DLB had lower, but not significantly so, {beta}-amyloid levels than controls. The combination of tau and {beta}-amyloid levels provided the best sensitivity (84%) and specificity (79%) to differentiate AD vs controls but was worse than tau values alone in discriminating between AD and DLB. {beta}-Amyloid levels had the best correlation with disease progression in both AD and DLB (P = .01). There were no significant differences in IL-1{beta} levels among patients with AD, patients with DLB, and controls. Patients with AD and DLB showed slightly, but not significantly, higher IL-6 levels than controls.

Conclusions  The tau levels in CSF may contribute to the clinical distinction between AD and DLB. {beta}-Amyloid CSF levels are similar in both dementia disorders and reflect disease progression better than tau levels. Interleukin CSF concentrations do not distinguish between AD and DLB.


From the Department of Neurology, Fundación Jiménez Díaz (Drs Gómez-Tortosa, Fanjul, Sainz, Cantarero, and García Yébenes), the Brain Bank for Neurological Research, Complutense University (Drs Gómez-Tortosa, Gonzalo, and García Yébenes), and the Department of Neurology, Hospital Severo Ochoa (Drs Cemillán and del Ser), Madrid, Spain.







HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2003 American Medical Association. All Rights Reserved.