Evidence map›Paper›PMID 14989417›Full record

ArticleSchizophrenia bulletin2003

Proton magnetic resonance spectroscopy in first episode psychosis and ultra high-risk individuals.

Stephen J Wood, Gregor Berger, Dennis Velakoulis, Lisa J Phillips, Patrick D McGorry, Alison R Yung, Patricia Desmond, Christos Pantelis

Abstract read
PubMed Publisher
In one paragraph

Article in Schizophrenia bulletin, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 2 syntheses or guidelines pooled it, 123 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. A Review of Potential Neuroimaging Biomarkers of Schizophrenia-Risk.Journal of psychiatry and brain science · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Whither the attenuated psychosis syndrome?Schizophrenia bulletin · 2012
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cognitive control deficits in schizophrenia: mechanisms and meaning.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2011
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Stephen J WoodMelbourne Neuropsychiatry Centre, University of Melbourne and Sunshine Hospital, Melbourne, Australia. stephen.wood@wh.org.au
Gregor Berger
Dennis Velakoulis
Lisa J Phillips
Patrick D McGorry
Alison R Yung
Patricia Desmond
Christos Pantelis
Orygen Youth Health · AUUniversity of Melbourne · AUThe Royal Melbourne Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The underlying neurobiology of emerging psychotic disorders is not well understood. Recent neuroimaging findings have suggested that some brain areas are affected prior to the onset of psychosis, while changes occur in other brain regions during the transition to illness. Further, previous research using magnetic resonance spectroscopy (MRS) has generally demonstrated that there are changes to the brain chemistry of patients with schizophrenia. However, it is unclear whether these changes are present prior to or at the onset of the disorder, and to what extent they are specific to schizophrenia. In this study, we assessed the left medial temporal and left dorsolateral prefrontal regions of 56 patients in their first episode of a psychotic disorder, 30 young people at ultra high-risk (UHR) of developing psychosis, and 21 healthy controls, using proton MRS. Six of the UHR group developed a first episode psychosis over the study period. No differences were identified between the first episode and control groups for any metabolite ratio in either region of interest. This may reflect intact neuronal circuits in the early phase of psychotic disorders. There were also no differences between the UHR and control groups for the medial temporal region. However, there was a significant elevation of the NAA/Creatine and the Choline/Creatine ratios in the dorsolateral prefrontal region of the UHR group, which was interpreted as a decline in creatine indicative of hypometabolism. This finding did not discriminate between those UHR individuals who later became psychotic and those who did not.

Indexed as

Image Processing, Computer-AssistedMagnetic Resonance ImagingMagnetic Resonance SpectroscopyAdolescentAdultAspartic AcidBipolar DisorderBrain MappingCholineCreatineDominance, CerebralEnergy MetabolismFemaleHippocampusHumansMajor Depressive DisorderAspartic AcidCholineCreatineN-acetylaspartate

Identifiers

PMID14989417
OpenAlexW2088772672

What OpenQuestion holds

Textmetadata
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.