Evidence map›Paper›PMID 36849934›Full record

ArticleBMC psychiatry2023

Association of HTR3B gene polymorphisms with depression and its executive dysfunction: a case-control study.

Lina Wang, Miao Wang, Chaoben Zhao, Jia Jian, Dongdong Qiao

Open access · goldAbstract read
In one paragraph

Article in BMC psychiatry, 2023. 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
0.9field-weighted citation impact, top 28% 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, 4 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

5 authors at 3 institutions in 1 country.

Lina Wang *Department of Psychology, Shandong Normal University, Jinan, 250358, Shandong, China.
Miao Wang *School of Mental Health, Jining Medical University, Jining, 272000, Shandong, China.
Chaoben ZhaoSchool of Mental Health, Jining Medical University, Jining, 272000, Shandong, China.
Jia JianDepartment of Psychiatry, Shandong Mental Health Center, Shandong University, Jinan, 250014, Shandong, China.
Dongdong QiaoDepartment of Psychiatry, Shandong Mental Health Center, Shandong University, Jinan, 250014, Shandong, China. qiaovincent@163.com.
Jining Medical University · CNShandong University · CNShandong Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have shown that depression was associated with HTR3B gene. The aim of this study was to investigate the relationship between polymorphisms of the HTR3B gene and depression and its executive dysfunction in Chinese Han population.

methodsA total of 229 patients with depressive disorder and 202 healthy controls were enrolled. Six Single nucleotide polymorphism sites (SNPs) including rs10789970, rs4938056, rs12421126, rs1176744, rs2276305 and rs12795805 were genotyped by Snapshot. Clinical features were collected using a general demographic questionnaire. The 24-item Hamilton Depression Scale (HAMD) was used to assess the symptoms' severity of the patients. The patients' executive function was assessed using a series of cognitive tests including Maze Test, Symbolic Coding Test, Spatial Span Inverse Order Test, Linking Test, and Emotional Management Test.

resultsThe genotypic and allelic distributions of rs1176744 in HTR3B gene were significantly different (χ

conclusionsThe polymorphisms of HTR3B gene may be associated with depression in Chinese Han population. The A allele of rs1176744 may increase the risk of developing depression and executive dysfunction while C alleles of rs1176744 and rs12795805 may be the protective factors for executive dysfunction in patients with depression.

Indexed as

Cognitive DysfunctionDepressionCase-Control StudiesGenotypeHumansPolymorphism, Single NucleotideReceptors, Serotonin, 5-HT3HTR3B protein, humanReceptors, Serotonin, 5-HT3DepressionExecutive dysfunctionHTR3BPolymorphism

Identifiers

PMID36849934
PMCPMC9972617
OpenAlexW4322489420

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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.