A[Beta] Deposits in Older Non-Demented Individuals with Cognitive Decline Are Indicative of Preclinical Alzheimer's Disease
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| 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 |
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| Header | DbId: eric DbLabel: ERIC An: EJ906725 AccessLevel: 3 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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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 |
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