Evidence map›Paper›PMID 30339707›Full record

ArticlePloS one2018

Apolipoprotein E, cognitive function, and cognitive decline among older Taiwanese adults.

Megan Todd, Lisa Schneper, Sarinnapha M Vasunilashorn, Daniel Notterman, Michael T Ullman, Noreen Goldman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

6 authors at 5 institutions in 1 country.

Megan ToddColumbia Aging Center, Columbia University, New York, New York, United States of America.ORCID 0000-0002-6973-418X
Lisa SchneperDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
Sarinnapha M VasunilashornDivision of General Medicine and Primary Care, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts, United States of America.
Daniel NottermanDepartment of Molecular Biology, Princeton University, Princeton, New Jersey, United States of America.
Michael T UllmanDepartment of Neuroscience, Georgetown University, Washington, D.C., United States of America.
Noreen GoldmanOffice of Population Research and Woodrow Wilson School of Public and International Affairs, Princeton University, Princeton, New Jersey, United States of America.
Princeton University · USBeth Israel Deaconess Medical Center · USColumbia University · USGeorgetown University · USWoodrow Wilson International Center for Scholars · US

Funding

BIODEMOGRAPHY OF HEALTH, SOCIAL FACTORS &LIFE CHALLENGER01AG016661 · NIA · RAND CORPORATION · PI WEINSTEIN, MAXINE A · 1999 to 2013
$9.5M
Reciprocal Genetic-Environmental Interactions During Childhood and AdolescenceR01HD076592 · NICHD · PRINCETON UNIVERSITY · PI NOTTERMAN, DANIEL A. · 2013 to 2023
$6.8M
BIODEMOGRAPHY OF HEALTH, SOCIAL FACTORS AND LIFE CHANGER01AG016790 · NIA · PRINCETON UNIVERSITY · PI GOLDMAN, NOREEN · 1999 to 2014
$5.6M
Development CoreP2CHD058486 · NICHD · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Jane Waldfogel · 2014 to 2026
$4.3M
Scientific and Technical Computing CoreP2CHD047879 · NICHD · PRINCETON UNIVERSITY · PI SALGANIK, MATTHEW J. · 2014 to 2018
$2.0M
Genomics for Social Scientists: 2022-2027R25AG053227 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Jessica Faul, COLTER M.S. MITCHELL · 2016 to 2026
$1.6M
Shared Pathophysiology of Postoperative Delirium and Alzheimer’s Disease and Related DementiasK01AG057836 · NIA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI VASUNILASHORN, SARINNAPHA · 2018 to 2022
$565k
NIA NIH HHS K01 AG057836NIA NIH HHS R01 AG016661NIA NIH HHS R01 AG016790NIA NIH HHS R25 AG053227NICHD NIH HHS P2C HD047879NICHD NIH HHS P2C HD058486NICHD NIH HHS R01 HD076592
6 · The paper itself

Abstract

Apolipoprotein E (APOE) genotype is believed to play a role in the onset of dementia, though less is known about its relationship with non-pathogenic age-related cognitive decline. We assessed whether APOE was a risk factor for cognitive decline among older Taiwanese adults using nationally representative data. General cognition was measured longitudinally over eleven years; domain-specific cognitive assessments of working memory, declarative learning and three aspects of attention (executive function, alerting, and orientation) were performed once. Having at least one risky APOE allele was associated with more rapid longitudinal cognitive decline compared to those with no risky alleles. Some evidence from the cross-sectional analysis of domain-specific cognitive assessments suggested that APOE genotype may be more closely associated with working memory and declarative learning than with attention. Most genetic studies of cognition include only populations of European descent; extension is crucial. This study confirmed the association between APOE genotype and the rate of cognitive decline in a predominantly Han Chinese population. Additional studies on diverse populations are warranted.

Indexed as

CognitionAgedAged, 80 and overAllelesApolipoproteins ECognitive DysfunctionCross-Sectional StudiesExecutive FunctionFemaleGenetic Association StudiesGenotypeGenotyping TechniquesHumansLongitudinal StudiesMaleMemory, Short-TermApoE protein, humanApolipoproteins E

Identifiers

PMID30339707
PMCPMC6195295
OpenAlexW2896011315

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.