Evidence map›Paper›PMID 37644438›Full record

ArticleBMC psychiatry2023

Genetic contribution of synapse-associated protein 97 to cerebellar functional connectivity changes in first-episode schizophrenia.

Xusan Xu, Shucun Luo, Xiaoxia Wang, Xia Wen, Jingwen Yin, Xudong Luo, Bin He, Chunmei Liang, Susu Xiong, Dongjian Zhu and 9 more

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. 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 42% 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, 2 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

19 authors at 2 institutions in 1 country.

Xusan Xu *Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Shucun Luo *Department of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Xiaoxia Wang *Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Xia WenInstitute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Jingwen YinDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Xudong LuoDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Bin HeDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Chunmei LiangInstitute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Susu XiongDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Dongjian ZhuDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Dong LvDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Zhun DaiDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Juda LinDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
You LiInstitute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Zhixiong LinDepartment of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Wubiao ChenDepartment of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China.
Zebin LuoDepartment of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China. gdmcfsjd@163.com.
Yajun WangMaternal and Children's Health Research Institute, Shunde Women and Children's Hospital, Guangdong Medical University, Foshan, 528300, China. wangyajuny1977@aliyun.com.
Guoda MaInstitute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, China. sihan1107@126.com.
Guangdong Medical College · CNFoshan Maternity and Child Health Care Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous study data suggested that the synapse-associated protein 97 (SAP97) rs3915512 polymorphism is significantly related to clinical performance in schizophrenia. The cerebellum exhibits abundant expression of SAP97, which is involved with negative symptoms, cognition and emotion in schizophrenia. As functional dysconnectivity with the cortical-subcortical-cerebellar circuitry has been widely shown in patients with schizophrenia, cortical-subcortical-cerebellar dysconnectivity can therefore be considered a possible intermediate phenotype that connects risk genes with schizophrenia. In this study, resting-state functional magnetic resonance imaging (fMRI) was applied to evaluate whether the SAP97 rs3915512 polymorphism changes cortical/subcortical-cerebellar resting-state functional connectivity (RSFC) in 104 Han Chinese subjects (52 first-episode schizophrenia (FES) patients and 52 matched healthy controls (HCs)). To examine RSFC between cortical/subcortical regions and the cerebellum, a ROI (region of interest)-wise functional connectivity analysis was conducted. The association between abnormal cortical/subcortical-cerebellar connectivity and clinical manifestation was further assessed in FES patients with different genotypes. The interactive effect of disease and genotype on RSFC was found between the frontal gyrus (rectus) and cerebellum. A positive correlation was suggested between RSFC in the cerebellum and the hostility scores in FES patients with the A allele, and no correlation was found in FES patients with the TT genotype. The current findings identified that SAP97 may be involved in the process of mental symptoms in FES patients via cerebellar connectivity depending on the rs3915512 polymorphism genotype.

Indexed as

Discs Large Homolog 1 ProteinSchizophreniaAllelesAsian PeopleCerebellumHumansDiscs Large Homolog 1 ProteinDLG1 protein, humanCerebellumResting-state functional connectivityRs3915512SAP97Schizophrenia

Identifiers

PMID37644438
PMCPMC10464201
OpenAlexW4386252111

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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.