Evidence map›Paper›PMID 28283021›Full record

ArticleBMC genetics2017

Gain of power of the general regression model compared to Cochran-Armitage Trend tests: simulation study and application to bipolar disorder.

Marie-Hélène Dizier, Florence Demenais, Flavie Mathieu

Abstract readComparative Study
In one paragraph

Article in BMC genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Genome-wide association study of early-onset and late-onset postpartum depression: the IGEDEPP prospective study.European psychiatry : the journal of the Association of European Psychiatrists · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Decomposing Pearson's χAnnals of human genetics · 2018
    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

3 authors.

Marie-Hélène DizierGenetic Variation and Human Diseases Unit, UMR-946, Inserm, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France.
Florence DemenaisGenetic Variation and Human Diseases Unit, UMR-946, Inserm, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France.
Flavie MathieuInserm Siège, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France. Flavie.Mathieu@inserm.fr.ORCID 0000-0002-3386-0299

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundMost genome-wide association studies assumed an additive model of inheritance which may result in significant loss of power when there is a strong departure from additivity. The General Regression Model (GRM), which allows performing an assumption-free test for association by testing for both additive effect and deviation from additive effect, may be more appropriate for association tests. Additionally, GRM allows testing the underlying genetic model. We compared the power of GRM association test to additive and other Cochran-Armitage Trend (CAT) tests through simulations and by applying GRM to a large case/control sample, the bipolar Welcome Trust Case Control Cohort data. Simulations were performed on two sets of case/control samples (1000/1000 and 2000/2000), using a large panel of genetic models. Four association tests (GRM and additive, recessive and dominant CAT tests) were applied to all replicates.

resultsWe showed that GRM power to detect association was similar or greater than the additive CAT test, in particular in case of recessive inheritance, with up to 67% gain in power. GRM analysis of genome-wide bipolar disorder Welcome Trust Consortium data (1998 cases/3004 controls) showed significant association in the 16p12 region (rs420259; P = 3.4E-7) which has not been identified using the additive CAT test. As expected, rs42025 fitted a non-additive (recessive) model.

conclusionsGRM provides increased power compared to the additive CAT test for association studies and is easily applicable.

Indexed as

Genome-Wide Association StudyBipolar DisorderCase-Control StudiesDatabases, FactualGenomicsHumansModels, GeneticRegression AnalysisBipolarGenetic Association StudiesGRMSimulations

Identifiers

PMID28283021
PMCPMC5345257

What Socratic holds

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LicenceCC BY
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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 Socratic graph.