Evidence map›Paper›PMID 30134963›Full record

ArticleAlzheimer's research & therapy2018

Synergistic interaction between APOE and family history of Alzheimer's disease on cerebral amyloid deposition and glucose metabolism.

Dahyun Yi, Younghwa Lee, Min Soo Byun, Jun Ho Lee, Kang Ko, Bo Kyung Sohn, Young Min Choe, Hyo Jung Choi, Hyewon Baek, Chul-Ho Sohn and 3 more

Abstract read
In one paragraph

Article in Alzheimer's research & therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

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

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  9. Connectomic analysis of Alzheimer's disease using percolation theory.Network neuroscience (Cambridge, Mass.) · 2022
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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

13 authors.

Dahyun YiInstitute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul, Republic of Korea.
Younghwa LeeDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
Min Soo ByunInstitute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul, Republic of Korea.
Jun Ho LeeDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
Kang KoDepartment of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea.
Bo Kyung SohnDepartment of Psychiatry, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Republic of Korea.
Young Min ChoeDepartment of Neuropsychiatry, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, Republic of Korea.
Hyo Jung ChoiDepartment of Neuropsychiatry, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea.
Hyewon BaekDepartment of Neuropsychiatry, Kyunggi Provincial Hospital for the Elderly, Yongin, Republic of Korea.
Chul-Ho SohnDepartment of Radiology, Seoul National University College of Medicine & Seoul National University Hospital, Seoul, Republic of Korea.
Yu Kyeong KimDepartment of Nuclear Medicine, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea.
Dong Young LeeInstitute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul, Republic of Korea. selfpsy@snu.ac.kr.
KBASE research group

Funding

Ministry of Science and ICT, Republic of Korea NRF-2014M3C7A1046042
6 · The paper itself

Abstract

backgroundRecently, the field of gene-gene or gene-environment interaction research appears to have gained growing interest, although it is seldom investigated in Alzheimer's disease (AD). Hence, the current study aims to investigate interaction effects of the key genetic and environmental risks-the apolipoprotein ε4 allele (APOE4) and family history of late-onset AD (FH)-on AD-related brain changes in cognitively normal (CN) middle-aged and older adults.

methods[

resultsA significant synergistic interaction effect was found between the APOE4 and FH on amyloid-beta (Aβ) deposition in the AD signature ROIs as well as other regions. Synergistic interaction effects on cerebral glucose metabolism were observed in the regions not captured by the AD signature ROIs, particularly in the medial temporal regions.

conclusionsStrong synergistic effects of APOE4 and FH on Aβ deposition and cerebral glucose metabolism in CN adults indicate possible gene-to-gene or gene-to-environment interactions that are crucial for pathogenesis of AD involving Aβ. Other unspecified risk factors-genes and/or environmental-that are captured by the positive FH status might either coexpress or interact with APOE4 to alter AD-related brain changes in CN. Healthy people with both FH and APOE4 need more attention for AD prevention.

Indexed as

AgedAlzheimer DiseaseAmyloid beta-PeptidesApolipoprotein E4Cerebral CortexFemaleGene-Environment InteractionGenetic Predisposition to DiseaseGlucoseHumansMagnetic Resonance ImagingMaleMiddle AgedPositron-Emission TomographyAmyloid beta-PeptidesApolipoprotein E4GlucoseAmyloid beta depositionAPOECerebral glucose metabolismCognitively normal adultsFamily history of Alzheimer’s disease

Identifiers

PMID30134963
PMCPMC6106945

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LicenceCC BY
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Registered trials

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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.