Literature DB >> 29387290

The MAX Statistic is Less Powerful for Genome Wide Association Studies Under Most Alternative Hypotheses.

Benjamin Shifflett1,2, Rong Huang3, Steven D Edland2,4.   

Abstract

Genotypic association studies are prone to inflated type I error rates if multiple hypothesis testing is performed, e.g., sequentially testing for recessive, multiplicative, and dominant risk. Alternatives to multiple hypothesis testing include the model independent genotypic χ2 test, the efficiency robust MAX statistic, which corrects for multiple comparisons but with some loss of power, or a single Armitage test for multiplicative trend, which has optimal power when the multiplicative model holds but with some loss of power when dominant or recessive models underlie the genetic association. We used Monte Carlo simulations to describe the relative performance of these three approaches under a range of scenarios. All three approaches maintained their nominal type I error rates. The genotypic χ2 and MAX statistics were more powerful when testing a strictly recessive genetic effect or when testing a dominant effect when the allele frequency was high. The Armitage test for multiplicative trend was most powerful for the broad range of scenarios where heterozygote risk is intermediate between recessive and dominant risk. Moreover, all tests had limited power to detect recessive genetic risk unless the sample size was large, and conversely all tests were relatively well powered to detect dominant risk. Taken together, these results suggest the general utility of the multiplicative trend test when the underlying genetic model is unknown.

Entities:  

Keywords:  Armitage test; MAX statistic; Type I error; case-control study; efficiency robust statistics; multiple comparisons

Year:  2017        PMID: 29387290      PMCID: PMC5788028          DOI: 10.6000/1929-6029.2017.06.04.2

Source DB:  PubMed          Journal:  Int J Stat Med Res        ISSN: 1929-6029


  9 in total

1.  On power and efficiency robust linkage tests for affected sibs.

Authors:  J L Gastwirth; B Freidlin
Journal:  Ann Hum Genet       Date:  2000-09       Impact factor: 1.670

2.  Biased tests of association: comparisons of allele frequencies when departing from Hardy-Weinberg proportions.

Authors:  D J Schaid; S J Jacobsen
Journal:  Am J Epidemiol       Date:  1999-04-15       Impact factor: 4.897

3.  Re: "Biased tests of association: comparisons of allele frequencies when departing from Hardy-Weinberg proportions".

Authors:  M Knapp
Journal:  Am J Epidemiol       Date:  2001-08-01       Impact factor: 4.897

Review 4.  Candidate-gene approaches for studying complex genetic traits: practical considerations.

Authors:  Holly K Tabor; Neil J Risch; Richard M Myers
Journal:  Nat Rev Genet       Date:  2002-05       Impact factor: 53.242

5.  Case-control studies of genetic markers: power and sample size approximations for Armitage's test for trend.

Authors:  S L Slager; D J Schaid
Journal:  Hum Hered       Date:  2001       Impact factor: 0.444

6.  Exact tests for the analysis of case-control studies of genetic markers.

Authors:  Markus Neuhäuser
Journal:  Hum Hered       Date:  2002       Impact factor: 0.444

7.  Genetic association studies in Alzheimer's disease research: challenges and opportunities.

Authors:  Steven D Edland; Susan Slager; Matthew Farrer
Journal:  Stat Med       Date:  2004-01-30       Impact factor: 2.373

8.  Trend tests for case-control studies of genetic markers: power, sample size and robustness.

Authors:  B Freidlin; G Zheng; Z Li; J L Gastwirth
Journal:  Hum Hered       Date:  2002       Impact factor: 0.444

9.  From genotypes to genes: doubling the sample size.

Authors:  P D Sasieni
Journal:  Biometrics       Date:  1997-12       Impact factor: 2.571

  9 in total

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