Evidence map›Paper›PMID 18001149›Full record

ArticlePLoS biology2007

Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype.

Akiko Watanabe, Tomoko Toyota, Yuji Owada, Takeshi Hayashi, Yoshimi Iwayama, Miho Matsumata, Yuichi Ishitsuka, Akihiro Nakaya, Motoko Maekawa, Tetsuo Ohnishi and 7 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

97 citing papers in PubMed, 218 citations in OpenAlex.

  1. Review
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  6. Hydrogen sulfide/polysulfides signaling and neuronal diseases.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
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  8. Review
  9. Article
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  12. Astrocytic FABP7 Alleviates Depression-Like Behaviors of Chronic Unpredictable Mild Stress Mice by Regulating Neuroinflammation and Hippocampal Spinogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  13. Cell-type-specificeLife · 2024
    Article
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  15. Review
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37 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 2 countries.

Akiko WatanabeLaboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Saitama, Japan.
Tomoko Toyota
Yuji Owada
Takeshi Hayashi
Yoshimi Iwayama
Miho Matsumata
Yuichi Ishitsuka
Akihiro Nakaya
Motoko Maekawa
Tetsuo Ohnishi
Ryoichi Arai
Katsuyasu Sakurai
Kazuo Yamada
Hisatake Kondo
Kenji Hashimoto
Noriko Osumi
Takeo Yoshikawa
RIKEN Center for Brain Science · JPTohoku University · JPCenter for Forensic Mental Health, Chiba University · JPInstitute of Agrobiological Sciences · JPPrinceton University · USThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Deficits in prepulse inhibition (PPI) are a biological marker for schizophrenia. To unravel the mechanisms that control PPI, we performed quantitative trait loci (QTL) analysis on 1,010 F2 mice derived by crossing C57BL/6 (B6) animals that show high PPI with C3H/He (C3) animals that show low PPI. We detected six major loci for PPI, six for the acoustic startle response, and four for latency to response peak, some of which were sex-dependent. A promising candidate on the Chromosome 10-QTL was Fabp7 (fatty acid binding protein 7, brain), a gene with functional links to the N-methyl-D-aspartic acid (NMDA) receptor and expression in astrocytes. Fabp7-deficient mice showed decreased PPI and a shortened startle response latency, typical of the QTL's proposed effects. A quantitative complementation test supported Fabp7 as a potential PPI-QTL gene, particularly in male mice. Disruption of Fabp7 attenuated neurogenesis in vivo. Human FABP7 showed altered expression in schizophrenic brains and genetic association with schizophrenia, which were both evident in males when samples were divided by sex. These results suggest that FABP7 plays a novel and crucial role, linking the NMDA, neurodevelopmental, and glial theories of schizophrenia pathology and the PPI endophenotype, with larger or overt effects in males. We also discuss the results from the perspective of fetal programming.

Indexed as

Genetic Predisposition to DiseaseAnimalsAstrocytesChromosome MappingChromosomes, MammalianCrosses, GeneticFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsGene ExpressionGene Expression Regulation, DevelopmentalGenetic MarkersHumansInhibition, PsychologicalMiceMice, Inbred StrainsNerve Tissue ProteinsFabp7 protein, mouseFatty Acid-Binding Protein 7Fatty Acid-Binding ProteinsGenetic MarkersNerve Tissue ProteinsReceptors, N-Methyl-D-AspartateRNA, Messenger

Identifiers

PMID18001149
PMCPMC2071943
OpenAlexW2007999164

What OpenQuestion holds

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Read underepoch 390

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.