ArticleGenetic epidemiology2011
Bias due to two-stage residual-outcome regression analysis in genetic association studies.
Article in Genetic epidemiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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.
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.
Who cites it
16 citing papers in PubMed.
- Impact of RAASIs on Potassium and Mortality in a Large Cohort of Hemodialysis Patients: Practical Excursus and Comparison Between Traditional Statistics and Machine Learning.Journal of clinical medicine · 2026Article
- Beyond the single-outcome approach: A comparison of outcome-wide analysis methods for exposome research.Environment international · 2023Article
- Use of Correct and Incorrect Methods of Accounting for Age in Studies of Epigenetic Accelerated Aging: Implications and Recommendations for Best Practices.American journal of epidemiology · 2023Review
- Power loss due to testing association between covariate-adjusted traits and genetic variants.Genetic epidemiology · 2020Article
- The role of physical activity in metabolic homeostasis before and after the onset of type 2 diabetes: an IMI DIRECT study.Diabetologia · 2020Article
- Genome-wide identification of loci associated with growth in rainbow trout.BMC genomics · 2020Article
- A rank-based normalization method with the fully adjusted full-stage procedure in genetic association studies.PloS one · 2020Article
- Analysis of Epigenetic Age Predictors in Pain-Related Conditions.Frontiers in public health · 2020Article
- Scalable Nonparametric Prescreening Method for Searching Higher-Order Genetic Interactions Underlying Quantitative Traits.Genetics · 2019Article
- A fully adjusted two-stage procedure for rank-normalization in genetic association studies.Genetic epidemiology · 2019Article
- The effect of phenotypic outliers and non-normality on rare-variant association testing.European journal of human genetics : EJHG · 2016Article
- Limits on the reproducibility of marker associations with southern leaf blight resistance in the maize nested association mapping population.BMC genomics · 2014Article
- A versatile omnibus test for detecting mean and variance heterogeneity.Genetic epidemiology · 2014Article
- A nonparametric test to detect quantitative trait loci where the phenotypic distribution differs by genotypes.Genetic epidemiology · 2013Article
- Loss of power in two-stage residual-outcome regression analysis in genetic association studies.Genetic epidemiology · 2012Article
- Challenges and opportunities in genome-wide environmental interaction (GWEI) studies.Human genetics · 2012Review
Corrections and comments
- Commented on by
Authors and funding
2 authors.
Funding
Abstract
Association studies of risk factors and complex diseases require careful assessment of potential confounding factors. Two-stage regression analysis, sometimes referred to as residual- or adjusted-outcome analysis, has been increasingly used in association studies of single nucleotide polymorphisms (SNPs) and quantitative traits. In this analysis, first, a residual-outcome is calculated from a regression of the outcome variable on covariates and then the relationship between the adjusted-outcome and the SNP is evaluated by a simple linear regression of the adjusted-outcome on the SNP. In this article, we examine the performance of this two-stage analysis as compared with multiple linear regression (MLR) analysis. Our findings show that when a SNP and a covariate are correlated, the two-stage approach results in biased genotypic effect and loss of power. Bias is always toward the null and increases with the squared-correlation between the SNP and the covariate (). For example, for , 0.1, and 0.5, two-stage analysis results in, respectively, 0, 10, and 50% attenuation in the SNP effect. As expected, MLR was always unbiased. Since individual SNPs often show little or no correlation with covariates, a two-stage analysis is expected to perform as well as MLR in many genetic studies; however, it produces considerably different results from MLR and may lead to incorrect conclusions when independent variables are highly correlated. While a useful alternative to MLR under , the two -stage approach has serious limitations. Its use as a simple substitute for MLR should be avoided.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.