Evidence map›Paper›PMID 32954402›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2021

Sex-Dependent Effects of the APOE ɛ4 Allele on Behavioral Traits and White Matter Structures in Young Adults.

Hikaru Takeuchi, Hiroaki Tomita, Ryan Browne, Yasuyuki Taki, Yoshie Kikuchi, Chiaki Ono, Zhiqian Yu, Rui Nouchi, Ryoichi Yokoyama, Yuka Kotozaki and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 44% 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

6 citing papers in PubMed, 8 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

23 authors at 6 institutions in 2 countries.

Hikaru TakeuchiDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Hiroaki TomitaDepartment of Psychiatry, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Japan.
Ryan BrowneDepartment of Advanced Brain Science, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Yasuyuki TakiDivision of Medical Neuroimaging Analysis, Department of Community Medical Supports, Tohoku Medical Megabank Organization, Tohoku University, Sendai 980-8575, Japan.
Yoshie KikuchiDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai 980-8575, Japan.
Chiaki OnoDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai 980-8575, Japan.
Zhiqian YuDepartment of Disaster Psychiatry, International Research Institute of Disaster Science, Tohoku University, Sendai 980-8575, Japan.
Rui NouchiDepartment of Advanced Brain Science, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Ryoichi YokoyamaSchool of Medicine, Kobe University, Kobe 650-0017, Japan.
Yuka KotozakiDivision of Clinical research, Medical-Industry Translational Research Center, Fukushima Medical University School of Medicine, Fukushima 960-1925, Japan.
Seishu NakagawaDepartment of Human Brain Science, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Atsushi SekiguchiDivision of Medical Neuroimaging Analysis, Department of Community Medical Supports, Tohoku Medical Megabank Organization, Tohoku University, Sendai 980-8575, Japan.
Kunio IizukaDepartment of Psychiatry, Graduate School of Medicine, Tohoku University, Sendai 980-8575, Japan.
Sugiko HanawaDepartment of Human Brain Science, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Tsuyoshi ArakiADVANTAGE Risk Management Co., Ltd. , Tokyo 153-0051, Japan.
Carlos Makoto MiyauchiDepartment of Advanced Brain Science, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Kohei SakakiDepartment of Advanced Brain Science, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Takayuki NozawaResearch Institute for the Earth Inclusive Sensing, Tokyo Institute of Technology, Tokyo 152-8550, Japan.
Shigeyuki IkedaDepartment of Ubiquitous Sensing, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Susumu YokotaDivision for Experimental Natural Science, Faculty of Arts and Science, Kyushu University, Fukuoka 819-0385, Japan.
Daniele MagistroDepartment of Sport Science, School of Science and Technology, Nottingham Trent University, Nottingham NG11 8NS, UK.
Yuko SassaDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Ryuta KawashimaDivision of Developmental Cognitive Neuroscience, Institute of Development, Aging and Cancer, Tohoku University, Sendai 980-8575, Japan.
Tohoku University · JPFukushima Medical University · JPKobe University · JPKyushu University · JPNottingham Trent University · GBTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The APOE ɛ4 allele is associated with a risk of Alzheimer's disease in the elderly, with the association being pronounced in females. Conversely, findings of the effects of the APOE ɛ4 allele in young adults are mixed. Here, we investigated the sex-genotype interaction effects of the APOE ɛ4 allele on cognitive functions as well as brain structures among 1258 young adults. After adjusting for multiple comparisons, there were significant effects of the interaction between sex and the number of APOE ɛ4 allele on some speed tasks (e.g., simple processing speed tasks and the reverse Stroop task) as well as on regional white matter volume (rWMV). The observed sex-genotype interaction conferred better cognitive performance and greater rWMV in the anterior frontal and precentral white matter areas in females having more APOE ɛ4 alleles and reduced rWMV in the same areas in male having more APOE ɛ4 alleles. These findings support the long-debated antagonistic pleiotropic effects of the APOE ɛ4 allele in females.

Indexed as

Sex FactorsAdolescentAdultAlzheimer DiseaseApolipoprotein E4Apolipoproteins EBehaviorCognitionFemaleGenotypeHumansMaleNeuropsychological TestsWhite MatterYoung AdultApoE protein, humanApolipoprotein E4Apolipoproteins EAPOE genotypeimaging geneticssex interaction effectswhite matter structuresyoung adults

Identifiers

PMID32954402
PMCPMC7727389
OpenAlexW3087282842

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.