Evidence map›Paper›PMID 23529008›Full record

ArticleThe pharmacogenomics journal2014

Synapsin II gene expression in the dorsolateral prefrontal cortex of brain specimens from patients with schizophrenia and bipolar disorder: effect of lifetime intake of antipsychotic drugs.

M L Tan, B A Dyck, J Gabriele, R P Daya, N Thomas, C Sookram, D Basu, M A Ferro, V Z Chong, R K Mishra

Open access · greenAbstract read
In one paragraph

Article in The pharmacogenomics journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 27 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

M L TanDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
B A DyckDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
J GabrieleDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
R P DayaDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
N ThomasDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
C SookramDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
D BasuDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
M A FerroDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
V Z ChongDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
R K MishraDepartment of Psychiatry and Behavioural Neurosciences, McMaster UniversityHamilton, Ontario, Canada.
McMaster University · CA

Funding

CIHR 126004-1
6 · The paper itself

Abstract

Synapsins are neuronal phosphoproteins crucial to regulating the processes required for normal neurotransmitter release. Synapsin II, in particular, has been implied as a candidate gene for schizophrenia. This study investigated synapsin II mRNA expression, using real-time reverse transcriptase-PCR, in coded dorsolateral prefrontal cortical samples provided by the Stanley Foundation Neuropathology Consortium. Synapsin IIa was decreased in patients with schizophrenia when compared with both healthy subjects and patients with bipolar disorder, whereas synapsin IIb was only significantly reduced in patients with schizophrenia when compared with healthy subjects but not in patients with bipolar disorder. Furthermore, lifetime antipsychotic drug use was positively associated with synapsin IIa expression in patients with schizophrenia. Results suggest that impairment of synaptic transmission by synapsin II reduction may contribute to dysregulated convergent molecular mechanisms, which result in aberrant neural circuits that characterize schizophrenia, while implicating involvement of synapsin II in therapeutic mechanisms of currently prescribed antipsychotic drugs.

Indexed as

Antipsychotic AgentsBipolar DisorderCase-Control StudiesDose-Response Relationship, DrugFemaleGene ExpressionHumansMaleMiddle AgedPrefrontal CortexReal-Time Polymerase Chain ReactionSchizophreniaSynapsinsSynaptic TransmissionTime FactorsAntipsychotic AgentsSynapsins

Identifiers

PMID23529008
PMCPMC3970980
OpenAlexW2031423947

What OpenQuestion holds

Textmetadata
LicenceTDM
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.