Evidence map›Paper›PMID 21130223›Full record

SynthesisBiological psychiatry2010

Meta-analysis of genetic variation in DTNBP1 and general cognitive ability.

Jian-Ping Zhang, Katherine E Burdick, Todd Lencz, Anil K Malhotra

Abstract readMeta-Analysis
In one paragraph

Synthesis in Biological psychiatry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Cognitive Deficit in Schizophrenia: From Etiology to Novel Treatments.International journal of molecular sciences · 2021
    Review
  2. Article
  3. Association ofFrontiers in psychiatry · 2020
    Article
  4. Article
  5. Review
  6. Cognitive Deficits in Schizophrenia: Understanding the Biological Correlates and Remediation Strategies.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2018
    Review
  7. Dysregulation of Specialized Delay/Interference-Dependent Working Memory Following Loss of Dysbindin-1A in Schizophrenia-Related Phenotypes.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Beyond the GWAS in schizophrenia.EMBO molecular medicine · 2011
    Article
  18. Review
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

4 authors.

Jian-Ping ZhangThe Zucker Hillside Hospital, Glen Oaks, New York, USA. jzhang1@nshs.edu
Katherine E Burdick
Todd Lencz
Anil K Malhotra

Funding

Striatal D2/D3 Dopamine receptor availability in first episode schizophreniaP50MH080173 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI GOLDBERG, TERRY · 2008 to 2012
$10.4M
Genetic Variation and Functional Disability in SchizophreniaR01MH079800 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI MALHOTRA, ANIL K · 2007 to 2011
$1.9M
Neurocognition as an endophenotype in bipolar disorderK23MH077807 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BURDICK, KATHERINE ELIZABETH · 2008 to 2012
$774k
NIMH NIH HHS K23 MH077807NIMH NIH HHS K23MH077807NIMH NIH HHS P50 MH080173NIMH NIH HHS P50MH080173NIMH NIH HHS R01 MH079800NIMH NIH HHS R01MH79800
6 · The paper itself

Abstract

backgroundThe human dystrobrevin binding protein 1 (DTNBP1) gene has been linked to risk for schizophrenia. Recent studies indicate that several single nucleotide polymorphisms (SNPs) in the DTNBP1 gene may also influence general cognitive ability in both schizophrenic patients and healthy control subjects. We examined the relationship between DTNBP1 SNPs and general cognitive ability in nonpsychiatric healthy samples via meta-analysis.

methodsMEDLINE search (12/31/09) yielded 11 articles examining DTNBP1 variation and general cognitive ability, of which 8 studies had data available encompassing 10 independent cohorts (total n = 7592). The phenotype was defined as either the first principal component score from multiple neuropsychological tests (Spearman's g) or full-scale IQ. Meta-analyses were conducted for nine SNPs for which cognitive data were available from at least three cohorts. For each SNP in each cohort, effect size was computed between major allele homozygotes and minor allele carriers; effect size was then pooled across studies using a random effect model.

resultsPooled effect sizes from two of the nine SNPs (rs1018381 and rs2619522) were -.123 and -.083, ps < .01, respectively, suggesting that the minor allele carriers of these SNPs had lower cognitive ability scores than the major allele homozygotes. Results remained significant after examining heterogeneity among samples and potential publication biases. Other SNPs did not show significant effects on general cognitive ability.

conclusionsGenetic variation in DTNBP1 modestly influences general cognitive ability. Further studies are needed to elucidate the biological mechanisms that may account for this relationship.

Indexed as

Polymorphism, Single NucleotideCarrier ProteinsCognitionDysbindinDystrophin-Associated ProteinsHumansMeta-Analysis as TopicCarrier ProteinsDTNBP1 protein, humanDysbindinDystrophin-Associated Proteins

Identifiers

PMID21130223
PMCPMC3026311

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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.