Evidence map›Paper›PMID 12901784›Full record

Trial reportJournal of the International Neuropsychological Society : JINS2003

Neuropsychological deficits associated with Alzheimer's disease in the very-old: discrepancies in raw vs. standardized scores.

Mark W Bondi, Wes S Houston, David P Salmon, Jody Corey-Bloom, Robert Katzman, Leon J Thal, Dean C Delis

Abstract readClinical TrialComparative Study
In one paragraph

Trial report in Journal of the International Neuropsychological Society : JINS, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Weak Social Networks in Late Life Predict Incident Alzheimer's Disease: The Kuakini Honolulu-Asia Aging Study.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Selection of Normative Group Affects Rates of Mild Cognitive Impairment in Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2018
    Article
  11. Article
  12. Article
  13. APOE interacts with age to modify rate of decline in cognitive and brain changes in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2014
    Article
  14. Article
  15. Article
  16. Emotional working memory in Alzheimer's disease patients.Dementia and geriatric cognitive disorders extra · 2011
    Article
  17. Neuropsychological assessment of dementia.Annual review of psychology · 2009
    Review
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mark W BondiVA San Diego Healthcare System, San Diego, California 92161, USA. mbondi@ucsd.edu
Wes S Houston
David P Salmon
Jody Corey-Bloom
Robert Katzman
Leon J Thal
Dean C Delis

Funding

VIRUS-INDUCED BRAIN PATHOLOGYP50AG005131 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BREWER, JAMES B · 1985 to 2018
$55.4M
Cognitive Abilities of At-Risk Elderly for DementiaR01AG012674 · NIA · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI BONDI, MARK W · 2001 to 2012
$2.7M
Cognitive Abilities of At-Risk Elderly for DementiaR56AG012674 · NIA · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI BONDI, MARK W · 2007 to 2007
$347k
COGNITIVE ABILITIES OF AT RISK ELDERLY FOR DEMENTIAR29AG012674 · NIA · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI BONDI, MARK W · 1994 to 1998
–
NIA NIH HHS AG05131NIA NIH HHS AG12674NIA NIH HHS P50 AG005131NIA NIH HHS R01 AG012674NIA NIH HHS R29 AG012674NIA NIH HHS R56 AG012674
6 · The paper itself

Abstract

The profiles of neuropsychological deficits associated with Alzheimer's disease (AD) in Young-Old (M age and 70) and Very-Old (M age > 80) patients were compared, along with possible modifying effects of apolipoprotein E (APOE) genotype on these profiles. A comprehensive battery of neuropsychological tests was administered to the two AD patient groups (Young-Old: n = 33; Very-Old: n = 48) and their respective age-matched normal control (NC) groups who remained free of dementia on follow-up examinations over a 1 to 10 year period (Young-Old: n = 43; Very-Old: n = 36). AD and NC groups did not differ in education levels or gender distributions. Young-Old AD and Very-Old AD groups were comparable in education, gender, dementia severity, and disease duration. Results showed that both AD groups achieved comparable raw scores on all the neuropsychological measures. However, when scores were standardized on the basis of performance of their respective NC groups (i.e., age-corrected z scores), Very-Old AD patients significantly outperformed Young-Old AD patients on tests of executive functions, visuospatial skills, and delayed memory. Furthermore, the relationship between age and memory and executive function deficits in AD was modified by APOE genotype. These data suggest that the profile of neuropsychological deficits associated with AD in the Very-Old lacks the disproportionate saliency of episodic memory and executive function deficits typical of the Young-Old.

Indexed as

Neuropsychological TestsAgedAged, 80 and overAgingAlzheimer DiseaseApolipoproteins ECognitionEducationFemaleFollow-Up StudiesGenotypeHumansLanguageLearningMaleMemoryApolipoproteins E

Identifiers

PMID12901784
PMCPMC1621043

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.