Evidence map›Paper›PMID 21196378›Full record

ReviewFrontiers in bioscience (Scholar edition)2011

Cognition, dopamine and bioactive lipids in schizophrenia.

Ruth Condray, Jeffrey K Yao

Open access · bronzeAbstract readReview
In one paragraph

Review in Frontiers in bioscience (Scholar edition), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Association between theSchizophrenia research. Cognition · 2024
    Article
  3. Article
  4. Review
  5. Observational
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Benzotriazole: An overview on its versatile biological behavior.European journal of medicinal chemistry · 2015
    Review
  14. Article
  15. Article
  16. Inflammation and the two-hit hypothesis of schizophrenia.Neuroscience and biobehavioral reviews · 2014
    Review
  17. Article
  18. Article
  19. Article
  20. Article
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

2 authors at 1 institution in 1 country.

Ruth CondrayDepartment of Psychiatry and Western Psychiatric Institute and Clinic University of Pittsburgh School of Medicine, 3811 O'Hara Street, Pittsburgh, PA 15213, USA.
Jeffrey K Yao
University of Pittsburgh · US

Funding

MEMBRANE DEFICITS AND OUTCOME IN SCHIZOPHRENIAR01MH058141 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI YAO, JEFFREY K · 1999 to 2003
$979k
NEUROCOGNITIVE BOUNDARIES OF THE SCHIZOPHRENIA SPECTRUMR01MH050631 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CONDRAY, RUTH · 1998 to 2002
$749k
LANGUAGE PROCESSES IN SCHIZOPHRENIA AND SPDR29MH050631 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CONDRAY, RUTH · 1993 to 1996
–
NIMH NIH HHS MH50631NIMH NIH HHS MH58141NIMH NIH HHS R01 MH050631NIMH NIH HHS R01 MH058141
6 · The paper itself

Abstract

Schizophrenia is a remarkably complex disorder with a multitude of behavioral and biological perturbations. Cognitive deficits are a core feature of this disorder, and involve abnormalities across multiple domains, including memory, attention, and perception. The complexity of this debilitating illness has led to a view that the key to unraveling its pathophysiology lies in deconstructing the clinically-defined syndrome into pathophysiologically distinct intermediate phenotypes. Accumulating evidence suggests that one of these intermediate phenotypes may involve phospholipid signaling abnormalities, particularly in relation to arachidonic acid (AA). Our data show relationships between levels of AA and performance on tests of cognition for schizophrenia patients, with defects in AA signaling associated with deficits in cognition. Moreover, dopamine may moderate these relationships between AA and cognition. Taken together, cognitive deficits, dopaminergic neurotransmission, and bioactive lipids have emerged as related features of schizophrenia. Existing treatment options for cognitive deficits in schizophrenia do not specifically target lipid-derived signaling pathways; understanding these processes could inform efforts to identify novel targets for treatment innovation.

Indexed as

Models, NeurologicalAnimalsCognitionDopamineEicosanoidsFatty Acids, UnsaturatedHumansMemory DisordersPhospholipidsSchizophreniaSignal TransductionSynaptic TransmissionDopamineEicosanoidsFatty Acids, UnsaturatedPhospholipids

Identifiers

PMID21196378
PMCPMC3060944
OpenAlexW2087334855

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.