Evidence map›Paper›PMID 31193788›Full record

ArticleSchizophrenia research. Cognition2019

Association of genetic variants at 22q11.2 chromosomal region with cognitive performance in Japanese patients with schizophrenia.

Kazufumi Akiyama, Atsushi Saito, Satoshi Saito, Yuji Ozeki, Takashi Watanabe, Kumiko Fujii, Kazutaka Shimoda

Open access · goldAbstract read
In one paragraph

Article in Schizophrenia research. Cognition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 98% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

7 authors at 2 institutions in 2 countries.

Kazufumi AkiyamaDepartment of Biological Psychiatry and Neuroscience, Dokkyo Medical University, School of Medicine, Mibu, Tochigi, Japan.
Atsushi SaitoDepartment of Biological Psychiatry and Neuroscience, Dokkyo Medical University, School of Medicine, Mibu, Tochigi, Japan.
Satoshi SaitoDepartment of Biological Psychiatry and Neuroscience, Dokkyo Medical University, School of Medicine, Mibu, Tochigi, Japan.
Yuji OzekiDepartment of Psychiatry, Dokkyo Medical University School of Medicine, Mibu, Tochigi, Japan.
Takashi WatanabeDepartment of Psychiatry, Dokkyo Medical University School of Medicine, Mibu, Tochigi, Japan.
Kumiko FujiiDepartment of Psychiatry, Dokkyo Medical University School of Medicine, Mibu, Tochigi, Japan.
Kazutaka ShimodaDepartment of Psychiatry, Dokkyo Medical University School of Medicine, Mibu, Tochigi, Japan.
Dokkyo Medical University · JPJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

22q11.2 heterozygous multigene deletions confer an increased risk of schizophrenia with marked impairment of cognition. We explored whether genes on 22q11.2 are associated with cognitive performance in patients with idiopathic schizophrenia. A total of 240 schizophrenia patients and 240 healthy controls underwent the Japanese-language version of the Brief Assessment of Cognition in Schizophrenia (BACS) and were genotyped for 115 tag single-nucleotide polymorphisms (tag SNPs) at the 22q11.2 region using the golden gate assay (Illumina®). Associations between z-scores of the BACS cognitive domains and SNPs and haplotypes were analyzed using linear regression in PLINK 1.07. An additional set of 149 patients with bipolar disorder were included for cognitive assessment and selected SNPs were genotyped using real-time PCR. Patients with schizophrenia and bipolar disorder showed qualitatively comparable profiles of cognitive impairment across BACS subdomains, as revealed by significant correlation between the two groups in the resulting cognitive effect sizes relative to controls. rs4819522 (

Indexed as

22q11.2BACSSchizophreniaSymbol codingTBX1UFD1L

Identifiers

PMID31193788
PMCPMC6543121
OpenAlexW2922541278

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.