Evidence map›Paper›PMID 18607530›Full record

ArticleJournal of human genetics2008

Comparison of multivariate adaptive regression splines and logistic regression in detecting SNP-SNP interactions and their application in prostate cancer.

Hui-Yi Lin, Wenquan Wang, Yung-Hsin Liu, Seng-Jaw Soong, Timothy P York, Leann Myers, Jennifer J Hu

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In one paragraph

Article in Journal of human genetics, 2008. 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. Trial
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Robust genetic interaction analysis.Briefings in bioinformatics · 2019
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Mixture modelling as an exploratory framework for genotype-trait associations.Journal of the Royal Statistical Society. Series C, Applied statistics · 2011
    Article
  17. Article
  18. 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

7 authors.

Hui-Yi LinMedical Statistics Section, University of Alabama at Birmingham, Birmingham, AL, USA.
Wenquan WangMedical Statistics Section, University of Alabama at Birmingham, Birmingham, AL, USA.
Yung-Hsin LiuINC Research, Raleigh, NC, USA.
Seng-Jaw SoongMedical Statistics Section, University of Alabama at Birmingham, Birmingham, AL, USA.
Timothy P YorkDepartment of Human Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Leann MyersDepartment of Biostatistics, Tulane University, New Orleans, LA, USA.
Jennifer J HuSylvester Comprehensive Cancer Center and Department of Epidemiology and Public Health, University of Miami School of Medicine, Miami, FL, USA. jhu@med.miami.edu.

Funding

Molecular Epidemiology and Prevention of Breast CancerR01CA073629 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HU, JENNIFER J. · 2003 to 2007
$1.3M
Molecular Genetics of Colon Cancer in Blacks and WhitesR01CA090898 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HU, JENNIFER J · 2002 to 2005
$803k
MOLECULAR EPIDEMIOLOGY AND PREVENTION OF BREAST CANCERR29CA073629 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HU, JENNIFER J · 1997 to 2001
$253k
NCI NIH HHS CA090898NCI NIH HHS CA73629
6 · The paper itself

Abstract

Single nucleotide polymorphism (SNP) interaction plays a critical role for complex diseases. The primary limitation of logistic regressions (LR) in testing SNP-SNP interactions is that coefficient estimates may not be valid because of numerous terms in a model. Multivariate adaptive regression splines (MARS) have useful features to effectively reduce the number of terms in a model. To study how MARS can address these drawbacks possibly better than LR, the power of MARS and LR with SNPs using the reference-coding and additive-mode scheme was compared using simulated data of ten SNPs for 400 subjects based on 1,000 replications for five interaction models. In overall scenarios, MARS performed better than LR. In the model with a dominant two-way interaction, the power range was 76-96% for MARS and 1-8% for LR in both coding schemes. In the dominant three-way interaction model, the power was 57-85% for MARS and less than 4% for LR. In the prostate cancer example, we evaluated the association between ten SNPs and prostate cancer risk in 649 Caucasians. The best model with one two-way and one three-way interaction was selected using MARS. The findings supported that MARS may provide a useful tool for exploring SNP-SNP interactions.

Indexed as

Computer SimulationEpistasis, GeneticPolymorphism, Single NucleotideCase-Control StudiesGene FrequencyGenotypeHumansLogistic ModelsMaleModels, GeneticProstatic NeoplasmsRisk FactorsWhite PeopleXeroderma Pigmentosum Group D ProteinERCC2 protein, humanXeroderma Pigmentosum Group D Protein

Identifiers

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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.