A[Beta] Deposits in Older Non-Demented Individuals with Cognitive Decline Are Indicative of Preclinical Alzheimer's Disease

Saved in:
Bibliographic Details
Title: A[Beta] Deposits in Older Non-Demented Individuals with Cognitive Decline Are Indicative of Preclinical Alzheimer's Disease
Language: English
Authors: Villemagne, V. L., Pike, K. E., Darby, D., Maruff, P., Savage, G., Ng, S., Ackermann, U., Cowie, T. F., Currie, J., Chan, S. G., Jones, G., Tochon-Danguy, H., O'Keefe, G., Masters, C. L., Rowe, C. C.
Source: Neuropsychologia. May 2008 46(6):1688-1697.
Availability: Elsevier. 6277 Sea Harbor Drive, Orlando, FL 32887-4800. Tel: 877-839-7126; Tel: 407-345-4020; Fax: 407-363-1354; e-mail: usjcs@elsevier.com; Web site: http://www.elsevier.com
Peer Reviewed: Y
Page Count: 10
Publication Date: 2008
Document Type: Journal Articles
Reports - Research
Descriptors: Alzheimers Disease, Cognitive Tests, Older Adults, Memory, Neurological Impairments, Predictor Variables, Brain, Diagnostic Tests, Foreign Countries, Aging (Individuals)
Geographic Terms: Australia
DOI: 10.1016/j.neuropsychologia.2008.02.008
ISSN: 0028-3932
Abstract: Approximately 30% of healthy persons aged over 75 years show A[beta] deposition at autopsy. It is postulated that this represents preclinical Alzheimer's disease (AD). We evaluated the relationship between A[beta] burden as assessed by PiB PET and cognitive decline in a well-characterized, non-demented, elderly cohort. PiB PET studies and cognitive tests were performed on 34 elderly participants (age 73 [plus or minus] 6) from the longitudinal Melbourne Healthy Aging Study (MHAS). Subjects were classified as being cognitively "stable" or "declining" by an independent behavioural neurologist based on clinical assessment and serial word-list recall scores from the preceding 6-10 years. Decline was calculated from the slope of the word-list recall scores. A[beta] burden was quantified using Standardized Uptake Value normalized to cerebellar cortex. Ten subjects were clinically classified as declining. At the time of the PET scans, three of the declining subjects had mild cognitive impairment, one had AD, and six were declining but remained within the normal range for age on cognitive tests. Declining subjects were much more likely to show cortical PiB binding than stable subjects (70% vs. 17%, respectively). Neocortical A[beta] burden correlated with word-list recall slopes (r = -0.78) and memory function (r = -0.85) in the declining group. No correlations were observed in the stable group. A[beta] burden correlated with incident memory impairment and the rate of memory decline in the non-demented ageing population. These observations suggest that neither memory decline nor A[beta] deposition are part of normal ageing and likely represent preclinical AD. Further longitudinal observations are required to confirm this hypothesis. (Contains 4 tables and 4 figures.)
Abstractor: As Provided
Entry Date: 2010
Accession Number: EJ906725
Database: ERIC
FullText Text:
  Availability: 0
Header DbId: eric
DbLabel: ERIC
An: EJ906725
AccessLevel: 3
PubType: Academic Journal
PubTypeId: academicJournal
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: A[Beta] Deposits in Older Non-Demented Individuals with Cognitive Decline Are Indicative of Preclinical Alzheimer's Disease
– Name: Language
  Label: Language
  Group: Lang
  Data: English
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Villemagne%2C+V%2E+L%2E%22">Villemagne, V. L.</searchLink><br /><searchLink fieldCode="AR" term="%22Pike%2C+K%2E+E%2E%22">Pike, K. E.</searchLink><br /><searchLink fieldCode="AR" term="%22Darby%2C+D%2E%22">Darby, D.</searchLink><br /><searchLink fieldCode="AR" term="%22Maruff%2C+P%2E%22">Maruff, P.</searchLink><br /><searchLink fieldCode="AR" term="%22Savage%2C+G%2E%22">Savage, G.</searchLink><br /><searchLink fieldCode="AR" term="%22Ng%2C+S%2E%22">Ng, S.</searchLink><br /><searchLink fieldCode="AR" term="%22Ackermann%2C+U%2E%22">Ackermann, U.</searchLink><br /><searchLink fieldCode="AR" term="%22Cowie%2C+T%2E+F%2E%22">Cowie, T. F.</searchLink><br /><searchLink fieldCode="AR" term="%22Currie%2C+J%2E%22">Currie, J.</searchLink><br /><searchLink fieldCode="AR" term="%22Chan%2C+S%2E+G%2E%22">Chan, S. G.</searchLink><br /><searchLink fieldCode="AR" term="%22Jones%2C+G%2E%22">Jones, G.</searchLink><br /><searchLink fieldCode="AR" term="%22Tochon-Danguy%2C+H%2E%22">Tochon-Danguy, H.</searchLink><br /><searchLink fieldCode="AR" term="%22O'Keefe%2C+G%2E%22">O'Keefe, G.</searchLink><br /><searchLink fieldCode="AR" term="%22Masters%2C+C%2E+L%2E%22">Masters, C. L.</searchLink><br /><searchLink fieldCode="AR" term="%22Rowe%2C+C%2E+C%2E%22">Rowe, C. C.</searchLink>
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="SO" term="%22Neuropsychologia%22"><i>Neuropsychologia</i></searchLink>. May 2008 46(6):1688-1697.
– Name: Avail
  Label: Availability
  Group: Avail
  Data: Elsevier. 6277 Sea Harbor Drive, Orlando, FL 32887-4800. Tel: 877-839-7126; Tel: 407-345-4020; Fax: 407-363-1354; e-mail: usjcs@elsevier.com; Web site: http://www.elsevier.com
– Name: PeerReviewed
  Label: Peer Reviewed
  Group: SrcInfo
  Data: Y
– Name: Pages
  Label: Page Count
  Group: Src
  Data: 10
– Name: DatePubCY
  Label: Publication Date
  Group: Date
  Data: 2008
– Name: TypeDocument
  Label: Document Type
  Group: TypDoc
  Data: Journal Articles<br />Reports - Research
– Name: Subject
  Label: Descriptors
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Alzheimers+Disease%22">Alzheimers Disease</searchLink><br /><searchLink fieldCode="DE" term="%22Cognitive+Tests%22">Cognitive Tests</searchLink><br /><searchLink fieldCode="DE" term="%22Older+Adults%22">Older Adults</searchLink><br /><searchLink fieldCode="DE" term="%22Memory%22">Memory</searchLink><br /><searchLink fieldCode="DE" term="%22Neurological+Impairments%22">Neurological Impairments</searchLink><br /><searchLink fieldCode="DE" term="%22Predictor+Variables%22">Predictor Variables</searchLink><br /><searchLink fieldCode="DE" term="%22Brain%22">Brain</searchLink><br /><searchLink fieldCode="DE" term="%22Diagnostic+Tests%22">Diagnostic Tests</searchLink><br /><searchLink fieldCode="DE" term="%22Foreign+Countries%22">Foreign Countries</searchLink><br /><searchLink fieldCode="DE" term="%22Aging+%28Individuals%29%22">Aging (Individuals)</searchLink>
– Name: Subject
  Label: Geographic Terms
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Australia%22">Australia</searchLink>
– Name: DOI
  Label: DOI
  Group: ID
  Data: 10.1016/j.neuropsychologia.2008.02.008
– Name: ISSN
  Label: ISSN
  Group: ISSN
  Data: 0028-3932
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: Approximately 30% of healthy persons aged over 75 years show A[beta] deposition at autopsy. It is postulated that this represents preclinical Alzheimer's disease (AD). We evaluated the relationship between A[beta] burden as assessed by PiB PET and cognitive decline in a well-characterized, non-demented, elderly cohort. PiB PET studies and cognitive tests were performed on 34 elderly participants (age 73 [plus or minus] 6) from the longitudinal Melbourne Healthy Aging Study (MHAS). Subjects were classified as being cognitively "stable" or "declining" by an independent behavioural neurologist based on clinical assessment and serial word-list recall scores from the preceding 6-10 years. Decline was calculated from the slope of the word-list recall scores. A[beta] burden was quantified using Standardized Uptake Value normalized to cerebellar cortex. Ten subjects were clinically classified as declining. At the time of the PET scans, three of the declining subjects had mild cognitive impairment, one had AD, and six were declining but remained within the normal range for age on cognitive tests. Declining subjects were much more likely to show cortical PiB binding than stable subjects (70% vs. 17%, respectively). Neocortical A[beta] burden correlated with word-list recall slopes (r = -0.78) and memory function (r = -0.85) in the declining group. No correlations were observed in the stable group. A[beta] burden correlated with incident memory impairment and the rate of memory decline in the non-demented ageing population. These observations suggest that neither memory decline nor A[beta] deposition are part of normal ageing and likely represent preclinical AD. Further longitudinal observations are required to confirm this hypothesis. (Contains 4 tables and 4 figures.)
– Name: AbstractInfo
  Label: Abstractor
  Group: Ab
  Data: As Provided
– Name: DateEntry
  Label: Entry Date
  Group: Date
  Data: 2010
– Name: AN
  Label: Accession Number
  Group: ID
  Data: EJ906725
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=eric&AN=EJ906725
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1016/j.neuropsychologia.2008.02.008
    Languages:
      – Text: English
    PhysicalDescription:
      Pagination:
        PageCount: 10
        StartPage: 1688
    Subjects:
      – SubjectFull: Alzheimers Disease
        Type: general
      – SubjectFull: Cognitive Tests
        Type: general
      – SubjectFull: Older Adults
        Type: general
      – SubjectFull: Memory
        Type: general
      – SubjectFull: Neurological Impairments
        Type: general
      – SubjectFull: Predictor Variables
        Type: general
      – SubjectFull: Brain
        Type: general
      – SubjectFull: Diagnostic Tests
        Type: general
      – SubjectFull: Foreign Countries
        Type: general
      – SubjectFull: Aging (Individuals)
        Type: general
      – SubjectFull: Australia
        Type: general
    Titles:
      – TitleFull: A[Beta] Deposits in Older Non-Demented Individuals with Cognitive Decline Are Indicative of Preclinical Alzheimer's Disease
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Villemagne, V. L.
      – PersonEntity:
          Name:
            NameFull: Pike, K. E.
      – PersonEntity:
          Name:
            NameFull: Darby, D.
      – PersonEntity:
          Name:
            NameFull: Maruff, P.
      – PersonEntity:
          Name:
            NameFull: Savage, G.
      – PersonEntity:
          Name:
            NameFull: Ng, S.
      – PersonEntity:
          Name:
            NameFull: Ackermann, U.
      – PersonEntity:
          Name:
            NameFull: Cowie, T. F.
      – PersonEntity:
          Name:
            NameFull: Currie, J.
      – PersonEntity:
          Name:
            NameFull: Chan, S. G.
      – PersonEntity:
          Name:
            NameFull: Jones, G.
      – PersonEntity:
          Name:
            NameFull: Tochon-Danguy, H.
      – PersonEntity:
          Name:
            NameFull: O'Keefe, G.
      – PersonEntity:
          Name:
            NameFull: Masters, C. L.
      – PersonEntity:
          Name:
            NameFull: Rowe, C. C.
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 01
              M: 05
              Type: published
              Y: 2008
          Identifiers:
            – Type: issn-print
              Value: 0028-3932
          Numbering:
            – Type: volume
              Value: 46
            – Type: issue
              Value: 6
          Titles:
            – TitleFull: Neuropsychologia
              Type: main
ResultId 1