Evidence map›Paper›PMID 36155836›Full record

ArticleCardiovascular pathology : the official journal of the Society for Cardiovascular Pathology

Apolipoprotein E genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study.

Regina Silva Paradela, Daniela Souza Farias-Itao, Renata E P Leite, Carlos A Pasqualucci, Lea T Grinberg, Michel Satya Naslavsky, Mayana Zatz, Ricardo Nitrini, Wilson Jacob-Filho, Claudia Kimie Suemoto

Open access · greenAbstract read
In one paragraph

Article in Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Current perspectives on the pathogenesis of cerebral atherosclerosis.Journal of inflammation (London, England) · 2025
    Review
  3. International journal of general medicine · 2024
    Article
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

10 authors at 2 institutions in 3 countries.

Regina Silva ParadelaDivision of Geriatrics, University of Sao Paulo Medical School, Brazil. Electronic address: reginarpds@gmail.com.
Daniela Souza Farias-ItaoDepartment of Pathology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
Renata E P LeiteDepartment of Pathology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
Carlos A PasqualucciDepartment of Pathology, University of Sao Paulo Medical School, Sao Paulo, Brazil.
Lea T GrinbergMemory and Aging Center, University of California San Francisco, USA.
Michel Satya NaslavskyHuman Genome and Stem Cell Center, Biosciences Institute, University of São Paulo, São Paulo, Brazil.
Mayana ZatzHuman Genome and Stem Cell Center, Biosciences Institute, University of São Paulo, São Paulo, Brazil.
Ricardo NitriniDepartment of Neurology, University of São Paulo Medical School, Brazil.
Wilson Jacob-FilhoDivision of Geriatrics, University of Sao Paulo Medical School, Brazil.
Claudia Kimie SuemotoDivision of Geriatrics, University of Sao Paulo Medical School, Brazil.
Universidade de São Paulo · BRUniversity of California, San Francisco · US

Funding

Clinical Features and Neuropathological Basis of Sleep Wake Behavior in Alzheimer's and PSPR01AG060477 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Lea Tenenholz Grinberg, Thomas C Neylan · 2019 to 2026
$8.2M
Neuropathological changes underlying clinical heterogeneity in Alzheimer diseaseK24AG053435 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRINBERG, LEA TENENHOLZ · 2016 to 2025
$1.8M
NIA NIH HHS K24 AG053435NIA NIH HHS R01 AG060477
6 · The paper itself

Abstract

backgroundApolipoprotein E gene (APOE) ε4 allele is associated with a higher risk of carotid atherosclerosis, but less is known about the association of APOE with intracranial atherosclerotic disease (IAD). We aimed to investigate the association of APOE alleles with IAD in a cross-sectional autopsy study.

methodsWe measured the stenosis in the 12 arteries of the Circle of Willis using postmortem morphometric measurements. The APOE polymorphism was determined by real-time polymerase chain reaction. We assessed the association between APOE polymorphism and IAD using regression models adjusted for sociodemographic and clinical variables. We also verified the modifier effect of age, sex, and race on this association. We stratified the analysis by age group to investigate the possibility of attrition bias.

resultsIn 400 participants (mean age=73.2±12.3 years old, 51% female, and 64% White), IAD was evaluated in 4,504 artery segments. APOE-ε4 was not associated with IAD nor with the number of artery stenosis compared to non-APOE-ε4 carriers. Sociodemographic variables did not modify this relationship. Among participants older than 70 years, there was a trend towards an association between APOE allele ε4 and a lower stenosis index in the middle cerebral artery, suggesting attrition bias related to the APOE-ε4 effect on mortality.

conclusionsAPOE alleles were not associated with IAD in this population-based autopsy study. Lower stenosis in older participants suggests the possibility of attrition bias.

Indexed as

Intracranial ArteriosclerosisAgedAged, 80 and overApolipoproteinsAutopsyConstriction, PathologicCross-Sectional StudiesFemaleHumansMaleMiddle AgedApolipoproteinsApolipoprotein EAtherosclerosisCerebral arteriesEpidemiologyRisk factors

Identifiers

PMID36155836
PMCPMC9990746
OpenAlexW4296700212

What OpenQuestion holds

Textmetadata
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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.