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IJE Advance Access originally published online on November 23, 2007
International Journal of Epidemiology 2008 37(1):136-146; doi:10.1093/ije/dym234
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Published by Oxford University Press on behalf of the International Epidemiological Association © The Author 2007; all rights reserved.

How should we use information about HWE in the meta-analyses of genetic association studies?

Cosetta Minelli1,*, John R Thompson2, Keith R Abrams2, Ammarin Thakkinstian3,4 and John Attia4

1Respiratory Epidemiology and Public Health Group, National Heart and Lung Institute, Imperial College London, SW3 6LR, London, UK.
2 Department of Health Sciences, Centre for Biostatistics and Genetic Epidemiology, University of Leicester, LE 1 7 RH Leicester, UK.
3 Clinical Epidemiology Unit, Mahidol University, 10400 Bangkok, Thailand.
4 Centre for Clinical Epidemiology and Biostatistics, University of Newcastle, NSW 2300 Newcastle, Australia.

* Corresponding author. Respiratory Epidemiology and Public Health Group, NHLI, Imperial College London, Emmanuel Kaye Building, Manresa Road, London, SW3 6LR, UK. E-mail: cosetta.minelli{at}imperial.ac.uk


   Abstract

Background: It is often recommended that control groups in meta-analyses of genetic association studies are checked for Hardy-Weinberg equilibrium (HWE) as a surrogate for assessing study quality. However, tests for HWE have low power and there is currently no consensus about how to handle studies that deviate significantly from HWE.

Methods: We identified 72 papers describing 114 meta-analyses of 1603 primary gene–disease comparisons. Based on these studies and on related simulations, we evaluated four different strategies for handling studies that appear not to be in HWE: (i) include them in the meta-analysis; (ii) exclude them if the test for HWE results in P < 0.05; (iii) exclude them if a measure of the size of departure from HWE is large and (iv) exclude them if (ii) and (iii).

Results: Of the 72 papers, 26 did not report information on HWE, with a trend toward increased reporting with time. HWE was evaluated through testing, with only three papers assessing the size of departure. On re-analysis, 9% of the 1603 primary comparisons showed significant deviation from HWE. The chance of an extreme departure from HWE was inversely related to the sample size of the study. Simulations suggest that there is no advantage in excluding studies that appear not to be in HWE.

Conclusions: Meta-analyses should report both the magnitude and the statistical significance of departures from HWE. Studies that appear to deviate from HWE should be investigated further for weaknesses in their design, but these studies should not be excluded unless there are other grounds for doubting the quality of the study.


Keywords Hardy-Weinberg equilibrium, genetic association studies, meta-analysis

Accepted 26 September 2007


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