Literature DB >> 16534212

The use of random controls in genetic association studies.

Chad Garner1.   

Abstract

BACKGROUND: The optimal control sample would be ethnically-matched and at minimal risk of developing the disease. Alternatively, one could collect random individuals from the population or select individuals to reduce the number of at-risk individuals in the sample. The effect of randomly selected individuals in a control sample on the statistical power and the odds ratio estimate was investigated.
METHODS: Case and control genotype distributions were simulated using standard genetic models with an additional term representing the proportion of unidentified cases in the control sample. Power and odds ratio were calculated from the genotype distributions generated under different sampling scenarios using established methods.
RESULTS: Random sampling of controls resulted in a loss in power and a reduction in the odds ratio estimate to a degree that is determined by the proportion of random sampling and the prevalence of the disease. Random sampling resulted in a 19% loss in power for a disease having prevalence of 0.20, compared to a control sample that contained no at-risk individuals. Having random controls results in a decrease in the odds ratio estimate.
CONCLUSIONS: Investigators planning case-control genetic association studies should be aware of the statistical costs of different ascertainment approaches.

Mesh:

Substances:

Year:  2006        PMID: 16534212     DOI: 10.1159/000091833

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  5 in total

1.  Replication of celiac disease UK genome-wide association study results in a US population.

Authors:  C P Garner; J A Murray; Y C Ding; Z Tien; D A van Heel; S L Neuhausen
Journal:  Hum Mol Genet       Date:  2009-07-31       Impact factor: 6.150

2.  Confounded by sequencing depth in association studies of rare alleles.

Authors:  Chad Garner
Journal:  Genet Epidemiol       Date:  2011-05       Impact factor: 2.135

3.  Genome-wide association studies--a summary for the clinical gastroenterologist.

Authors:  Espen Melum; Andre Franke; Tom H Karlsen
Journal:  World J Gastroenterol       Date:  2009-11-21       Impact factor: 5.742

4.  Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.

Authors:  Fumihiko Takeuchi; Masakuni Serizawa; Ken Yamamoto; Tomomi Fujisawa; Eitaro Nakashima; Keizo Ohnaka; Hiroshi Ikegami; Takao Sugiyama; Tomohiro Katsuya; Makoto Miyagishi; Naoki Nakashima; Hajime Nawata; Jiro Nakamura; Suminori Kono; Ryoichi Takayanagi; Norihiro Kato
Journal:  Diabetes       Date:  2009-04-28       Impact factor: 9.461

5.  Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.

Authors:  Chad Garner; Richard Ahn; Yuan Chun Ding; Linda Steele; Samantha Stoven; Peter H Green; Alessio Fasano; Joseph A Murray; Susan L Neuhausen
Journal:  PLoS One       Date:  2014-07-07       Impact factor: 3.240

  5 in total

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