Evidence map›Paper›PMID 41905965›Full record

SynthesisNeuropsychopharmacology reports2026

Japanese Cohort Study and Meta-Analysis Demonstrate Significant Association Between Serotonin Transporter-Linked Polymorphic Region and Schizophrenia.

Masao Miyachi, Toshiyuki Shirai, Shohei Okada, Kiriko Minami, Ryo Tsukamoto, Kentaro Mouri, Satoshi Okazaki, Ikuo Otsuka, Akitoyo Hishimoto

Abstract readMeta-Analysis
In one paragraph

Synthesis in Neuropsychopharmacology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Masao MiyachiDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
Toshiyuki ShiraiDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID https://orcid.org/0009-0009-2058-1678
Shohei OkadaDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
Kiriko MinamiDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
Ryo TsukamotoDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
Kentaro MouriDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.
Satoshi OkazakiDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID https://orcid.org/0000-0001-5953-5526
Ikuo OtsukaDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.ORCID https://orcid.org/0000-0002-2831-9158
Akitoyo HishimotoDepartment of Psychiatry, Kobe University Graduate School of Medicine, Kobe, Japan.

Funding

Japan Agency for Medical Research and Development 22dk0307111Japan Society for the Promotion of Science JP21H02852Japan Society for the Promotion of Science JP21K07520Japan Society for the Promotion of Science JP24K02383Japan Society for the Promotion of Science JP24K10710Japan Society for the Promotion of Science JP24K10732Japan Society for the Promotion of Science JP25K19058Moonshot Research and Development Program JPMJMS239FSENSHIN Medical Research FoundationSmoking Research Foundation
6 · The paper itself

Abstract

Schizophrenia is a prevalent psychiatric disease that substantially affects health and increases mortality risk. The 5-hydroxytryptamine system has been implicated in its pathogenesis. The SLC6A4 gene encodes the serotonin transporter, which regulates synaptic 5-hydroxytryptamine through reuptake into presynaptic neurons. Within its promoter region, there is a 44-base pair insertion/deletion polymorphism, known as serotonin-transporter-linked polymorphic region (5-HTTLPR). We investigated the association between 5-HTTLPR polymorphism and schizophrenia in the cohorts, including the largest sample size of Asian schizophrenia patients to date. We included 467 patients with schizophrenia and 361 controls, all of Japanese ancestry. We extracted DNA from peripheral blood samples. After amplification with PCR, we analyzed the association between 5-HTTLPR genotypes and alleles and schizophrenia. Furthermore, we conducted a meta-analysis with previous literatures. 5-HTTLPR genotype distribution differed significantly between patients and controls (p = 0.007). The short allele was significantly more frequent in schizophrenia patients (odds ratio = 1.39 [95% Cl = 1.08-1.77], p = 0.007). The meta-analysis demonstrated a significant association between the short allele and schizophrenia (odds ratio = 1.06 [95% Cl = 1.01-1.11], p = 0.024). This study demonstrates a significant association between 5-HTTLPR polymorphism and schizophrenia. While further research is needed, the findings suggest 5-HTTLPR may represent a promising target for future therapeutic strategies.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticSchizophreniaSerotonin Plasma Membrane Transport ProteinsAdultCohort StudiesEast Asian PeopleFemaleGenetic Association StudiesGenotypeHumansJapanMaleMiddle AgedSerotonin Plasma Membrane Transport ProteinsSLC6A4 protein, humangeneticJapanmeta‐analysis as topicpolymorphismschizophreniaserotonin plasma membrane transport proteins

Identifiers

PMID41905965
PMCPMC13581099

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