Evidence map›Paper›PMID 14745454›Full record

ArticleMolecular psychiatry2004

Association study of an SNP combination pattern in the dopaminergic pathway in paranoid schizophrenia: a novel strategy for complex disorders.

Q Xu, Y-B Jia, B-Y Zhang, K Zou, Y-B Tao, Y-P Wang, B-Q Qiang, G-Y Wu, Y Shen, H-K Ji and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2004. 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
3.1field-weighted citation impact, top 9% 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, 41 citations in OpenAlex.

  1. Trial
  2. Review
  3. Toward a phenomic analysis of chronic postsurgical pain following cardiac surgery.Canadian journal of pain = Revue canadienne de la douleur · 2019
    Article
  4. Review
  5. Review
  6. Article
  7. Non-P450 aldehyde oxidizing enzymes: the aldehyde dehydrogenase superfamily.Expert opinion on drug metabolism & toxicology · 2008
    Review
  8. Analysis of phenotype-genotype connection: the story of dissecting disease pathogenesis in genomic era in China, and beyond.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2007
    Review
  9. Expression and initial characterization of human ALDH3B1.Biochemical and biophysical research communications · 2007
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 6 institutions in 1 country.

Q XuNational Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
Y-B Jia
B-Y Zhang
K Zou
Y-B Tao
Y-P Wang
B-Q Qiang
G-Y Wu
Y Shen
H-K Ji
Y Huang
X-Q Sun
L Ji
Y-D Li
Y-B Yuan
L Shu
X Yu
Y-C Shen
Y-Q Yu
G-Z Ju
Chinese Schizophrenia Consortium
Chinese Academy of Medical Sciences & Peking Union Medical College · CNTsinghua University · CNChinese National Human Genome Center · CNJilin University · CNPeking University · CNPeking University Sixth Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schizophrenia is a common mental disorder with a complex pattern of inheritance. Despite a large number of studies in the past decades, its molecular etiology remains unknown. In this study, we proposed a 'system-thinking' strategy in seeking the combined effect of susceptibility genes for a complex disorder by using paranoid schizophrenia as an example. We genotyped 85 reported single-nucleotide polymorphisms (SNPs) present in 23 genes for the dopamine (DA) metabolism pathway among 83 paranoid schizophrenics and 108 normal controls with detailed clinical and genetic information. We developed two novel multilocus approaches-the potential effective SNP combination pattern and potential effective dynamic effects analysis, by which three susceptibility genotype combinations were found to be associated with schizophrenia. These results were also validated in a family-based cohort consisting of 95 family trios of paranoid schizophrenia. The present findings suggest that the COMT and ALDH3 combination may be the most common type involved in predisposing to schizophrenia. Since the combination blocks the whole pathways for the breakdown of DA and noradrenaline, it is very likely to play a central role in developing paranoid schizophrenia.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAldehyde DehydrogenaseAsian PeopleCatechol O-MethyltransferaseCluster AnalysisCohort StudiesComputational BiologyDopamineGenetic Predisposition to DiseaseHumansMultifactorial InheritancePhenotypeSchizophrenia, ParanoidAldehyde DehydrogenaseCatechol O-Methyltransferasecorneal protein 54, bovineDopamine

Identifiers

PMID14745454
OpenAlexW1979020314

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.