Neurobiology of Aging
Volume 29, Issue 5 , Pages 669-675, May 2008

CSF and MRI markers independently contribute to the diagnosis of Alzheimer's disease

  • Niki S.M. Schoonenboom

      Affiliations

    • Department of Neurology, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands
    • Corresponding Author InformationCorresponding author at: Department of Neurology, Alzheimer Center, VU University Medical Center, Postbus 7057, 1081 HV Amsterdam, The Netherlands. Tel.: +31 204440183/646022014; fax: +31 204440715.
  • ,
  • Wiesje M. van der Flier

      Affiliations

    • Department of Neurology, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands
  • ,
  • Marinus A. Blankenstein

      Affiliations

    • Department of Clinical Chemistry, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands
  • ,
  • Femke H. Bouwman

      Affiliations

    • Department of Neurology, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands
  • ,
  • Gerard J. Van Kamp

      Affiliations

    • Department of Neurology, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands
  • ,
  • Frederik Barkhof

      Affiliations

    • Department of Radiology, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands
  • ,
  • Philip Scheltens

      Affiliations

    • Department of Neurology, Alzheimer Center, VU University Medical Center, 1081 HV Amsterdam, The Netherlands

Received 12 May 2006; received in revised form 17 November 2006; accepted 25 November 2006. published online 08 January 2007.

Abstract 

Background

Decreased amyloid β (1-42) (Aβ42) and increased (phosphorylated) tau in cerebrospinal fluid (CSF) are considered to be a reflection of plaques, tangles, and neuronal degeneration in Alzheimer's disease (AD). Atrophy of the medial temporal lobe (MTA) on magnetic resonance imaging (MRI) reflects neuronal loss in this area.

Objective

To compare diagnostic accuracy of CSF biomarkers and MTA in AD versus controls.

Methods

Aβ42, tau and tau phosphorylated at threonine 181 (Ptau-181) were measured in CSF from 61 AD patients and 32 controls by sandwich enzyme-linked immunosorbent assay. A CSF biomarker profile for AD was constructed. MTA was rated visually on MRI.

Results

When AD patients and controls were evaluated separately, no correlations were present between the CSF markers and MTA score. Both MTA and CSF biomarker profile were independently associated with the diagnosis AD (MTA: OR (95% CI)=28 (3–239); CSF biomarker profile: OR (95% CI)=57 (13–262)). Among individuals younger than 65 years old and without MTA 60% suffered AD, and the finding of an abnormal CSF biomarker profile was limited to AD patients only.

Conclusions

MTA and CSF biomarkers seem to be of incremental value for the diagnosis AD. CSF analysis is most sensitive in the absence of MTA, and especially among early-onset AD patients.

Keywords: Alzheimer's disease, CSF and MRI markers, Aβ42, tau and phosphorylated tau

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0197-4580(06)00440-4

doi:10.1016/j.neurobiolaging.2006.11.018

Neurobiology of Aging
Volume 29, Issue 5 , Pages 669-675, May 2008