Evidence map›Paper›PMID 19772658›Full record

ArticleBMC medical genomics2009

Exon expression in lymphoblastoid cell lines from subjects with schizophrenia before and after glucose deprivation.

Maureen V Martin, Brandi Rollins, P Adolfo Sequeira, Andrea Mesén, William Byerley, Richard Stein, Emily A Moon, Huda Akil, Edward G Jones, Stanley J Watson and 6 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 23 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

16 authors at 9 institutions in 2 countries.

Maureen V MartinDepartment of Psychiatry and Human Behavior, Univ. of California, Irvine, CA, USA. martinmv@uci.edu
Brandi Rollins
P Adolfo Sequeira
Andrea Mesén
William Byerley
Richard Stein
Emily A Moon
Huda Akil
Edward G Jones
Stanley J Watson
Jack Barchas
Lynn E DeLisi
Richard M Myers
Alan Schatzberg
William E Bunney
Marquis P Vawter
University of California, Irvine · USUniversity of Michigan–Ann Arbor · USCornell University · USHudsonAlpha Institute for Biotechnology · USNew York University · USPalo Alto University · USUniversidad Hispanoamerica · CRUniversity of California, Davis · USUniversity of California, San Francisco · US

Funding

Project 5: High-Throughput Analysis of Gene RegulationP50MH060398 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI BUNNEY, WILLIAM E · 1999 to 2008
$12.7M
NIMH NIH HHS MH40730NIMH NIH HHS P50 MH060398NIMH NIH HHS P50 MH60398
6 · The paper itself

Abstract

backgroundThe purpose of this study was to examine the effects of glucose reduction stress on lymphoblastic cell line (LCL) gene expression in subjects with schizophrenia compared to non-psychotic relatives.

methodsLCLs were grown under two glucose conditions to measure the effects of glucose reduction stress on exon expression in subjects with schizophrenia compared to unaffected family member controls. A second aim of this project was to identify cis-regulated transcripts associated with diagnosis.

resultsThere were a total of 122 transcripts with significant diagnosis by probeset interaction effects and 328 transcripts with glucose deprivation by probeset interaction probeset effects after corrections for multiple comparisons. There were 8 transcripts with expression significantly affected by the interaction between diagnosis and glucose deprivation and probeset after correction for multiple comparisons. The overall validation rate by qPCR of 13 diagnosis effect genes identified through microarray was 62%, and all genes tested by qPCR showed concordant up- or down-regulation by qPCR and microarray. We assessed brain gene expression of five genes found to be altered by diagnosis and glucose deprivation in LCLs and found a significant decrease in expression of one gene, glutaminase, in the dorsolateral prefrontal cortex (DLPFC). One SNP with previously identified regulation by a 3' UTR SNP was found to influence IRF5 expression in both brain and lymphocytes. The relationship between the 3' UTR rs10954213 genotype and IRF5 expression was significant in LCLs (p = 0.0001), DLPFC (p = 0.007), and anterior cingulate cortex (p = 0.002).

conclusionExperimental manipulation of cells lines from subjects with schizophrenia may be a useful approach to explore stress related gene expression alterations in schizophrenia and to identify SNP variants associated with gene expression.

Indexed as

Gene Expression ProfilingAdultBrainCell Line, TransformedExonsGene ExpressionGlucoseHumansLymphocytesMaleMiddle AgedOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideReproducibility of ResultsReverse Transcriptase Polymerase Chain ReactionSchizophreniaGlucose

Identifiers

PMID19772658
PMCPMC2760574
OpenAlexW2056634473

What OpenQuestion holds

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LicenceCC BY
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.