Evidence map›Paper›PMID 27065294›Full record

ArticleDementia and geriatric cognitive disorders extra

Genetic Association between Presenilin 2 Polymorphisms and Alzheimer's Disease and Dementia of Lewy Body Type in a Japanese Population.

Ayako Suzuki, Nobuto Shibata, Koji Kasanuki, Tomoyuki Nagata, Shunichiro Shinagawa, Nobuyuki Kobayashi, Tohru Ohnuma, Yoshihide Takeshita, Eri Kawai, Toshiki Takayama and 6 more

Open access · goldAbstract read
In one paragraph

Article in Dementia and geriatric cognitive disorders extra. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

16 authors at 2 institutions in 1 country.

Ayako SuzukiDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Nobuto ShibataDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Koji KasanukiDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Tomoyuki NagataDepartment of Psychiatry, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan; Division of Molecular Genetics, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan.
Shunichiro ShinagawaDepartment of Psychiatry, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan.
Nobuyuki KobayashiDepartment of Psychiatry, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan.
Tohru OhnumaDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Yoshihide TakeshitaDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Eri KawaiDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Toshiki TakayamaDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Kenya NishiokaDepartments of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
Yumiko MotoiDepartments of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
Nobutaka HattoriDepartments of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
Kazuhiko NakayamaDepartment of Psychiatry, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan.
Hisashi YamadaDivision of Molecular Genetics, Institute of DNA Medicine, Jikei University School of Medicine, Tokyo, Japan.
Heii AraiDepartments of Psychiatry, Juntendo University School of Medicine, Tokyo, Japan.
Juntendo University · JPJikei University School of Medicine · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimsMutations in the presenilin 2 (PSEN2) gene cause familial Alzheimer's disease (AD). Common polymorphisms affect gene activity and increase the risk of AD. Nonsynonymous polymorphisms in the PSEN2 gene showed Lewy body dementia (LBD) phenotypes clinically. Therefore, we aimed to investigate whether PSEN2 gene polymorphisms were associated with AD or LBD.

methodsSeven single nucleotide polymorphisms (SNPs) of the gene were analyzed using a case-control study design comprising 288 AD patients, 76 LBD patients, and 105 age-matched controls.

resultsLinkage disequilibrium (LD) examination showed strong LD from rs1295645 to rs8383 on the gene in our cases from Japan. There were no associations between the SNPs studied here and AD onset, and haplotypic analyses did not detect genetic associations between AD and the PSEN2 gene. Although the number of the cases was small, the SNPs studied did not modify the risk of developing LBD in a Japanese population.

conclusionThe common SNPs of the PSEN2 gene did not affect the risk of AD or LBD in a Japanese population. Because genetic variability of the PSEN2 gene is associated with behavioral and psychological symptoms of dementia (BPSD) in AD and LBD, further detailed analyses considering BPSD of both diseases would be required.

Indexed as

Alzheimer's diseaseApolipoprotein ELewy body dementiaPresenilin 2Single nucleotide polymorphism

Identifiers

PMID27065294
PMCPMC4821141
OpenAlexW2326381636

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.