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Comparative Study
. 2015 Aug 30:15:71.
doi: 10.1186/s12874-015-0066-2.

Comparison of subset selection methods in linear regression in the context of health-related quality of life and substance abuse in Russia

Affiliations
Comparative Study

Comparison of subset selection methods in linear regression in the context of health-related quality of life and substance abuse in Russia

Olga Morozova et al. BMC Med Res Methodol. .

Abstract

Background: Automatic stepwise subset selection methods in linear regression often perform poorly, both in terms of variable selection and estimation of coefficients and standard errors, especially when number of independent variables is large and multicollinearity is present. Yet, stepwise algorithms remain the dominant method in medical and epidemiological research.

Methods: Performance of stepwise (backward elimination and forward selection algorithms using AIC, BIC, and Likelihood Ratio Test, p = 0.05 (LRT)) and alternative subset selection methods in linear regression, including Bayesian model averaging (BMA) and penalized regression (lasso, adaptive lasso, and adaptive elastic net) was investigated in a dataset from a cross-sectional study of drug users in St. Petersburg, Russia in 2012-2013. Dependent variable measured health-related quality of life, and independent correlates included 44 variables measuring demographics, behavioral, and structural factors.

Results: In our case study all methods returned models of different size and composition varying from 41 to 11 variables. The percentage of significant variables among those selected in final model varied from 100 % to 27 %. Model selection with stepwise methods was highly unstable, with most (and all in case of backward elimination: BIC, forward selection: BIC, and backward elimination: LRT) of the selected variables being significant (95 % confidence interval for coefficient did not include zero). Adaptive elastic net demonstrated improved stability and more conservative estimates of coefficients and standard errors compared to stepwise. By incorporating model uncertainty into subset selection and estimation of coefficients and their standard deviations, BMA returned a parsimonious model with the most conservative results in terms of covariates significance.

Conclusions: BMA and adaptive elastic net performed best in our analysis. Based on our results and previous theoretical studies the use of stepwise methods in medical and epidemiological research may be outperformed by alternative methods in cases such as ours. In situations of high uncertainty it is beneficial to apply different methodologically sound subset selection methods, and explore where their outputs do and do not agree. We recommend that researchers, at a minimum, should explore model uncertainty and stability as part of their analyses, and report these details in epidemiological papers.

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Figures

Fig. 1
Fig. 1
Bootstrap frequency of covariates selection in the final model using stepwise algorithms. Dependent variable is EuroQoL 5D visual analogue scale measure of the health-related quality of life. a shows results of backward elimination regression using AIC, b—using BIC, and c—using Likelihood Ratio Test (p = 0.05). d, e and f show results of forward selection regression with AIC, BIC and LRT (p = 0.05) correspondingly. Black bars represent variables selected in the final model, and light grey bars—variables excluded from the final model. Solid line and the number next to it correspond to the minimum frequency among variables included in the final model; dashed line and the number next to it correspond to the maximum frequency among variables excluded from final subset. Dotted line corresponds to the frequency = 0.9, and number next to it shows the percentage of variables in the final model with inclusion frequency over 0.9 (out of the number of variables selected in the final model). Description of variable names is provided in the Additional file 2
Fig. 2
Fig. 2
Bootstrap frequency of covariates selection in the final model using penalized regression. Dependent variable is EuroQoL 5D visual analogue scale measure of the health-related quality of life. a shows results of lasso corresponding to λmin, b—lasso corresponding to λ1se ; c and d—adaptive lasso with λmin (c) and λ1se (d); and e and f—adaptive elastic net with λmin (e) and λ1se (f). Black bars represent variables selected in the final model, and light grey bars—variables excluded from the final model. Solid line and the number next to it correspond to the minimum frequency among variables included in the final model; dashed line and the number next to it correspond to the maximum frequency among variables excluded from final subset. Dotted line corresponds to the frequency = 0.9, and number next to it shows the percentage of variables in the final model with inclusion frequency over 0.9 (out of the number of variables selected in the final model). Description of variable names is provided in the Additional file 2
Fig. 3
Fig. 3
Bayesian model averaging: posterior inclusion probabilities of independent variables in linear regression. Dependent variable is EuroQoL 5D visual analogue scale measure of the health-related quality of life. a shows covariates posterior inclusion probabilities (PIP) based on aggregate information from sampling chain with posterior model distribution based on MCMC frequencies. b shows covariates PIP based on 100 best models from sampling chain with posterior model distributions based on exact marginal likelihoods. Dashed line corresponds to the subset selection PIP threshold, which equals 0.5 (median inclusion probability model). Description of variable names is provided in the Additional file 2
Fig. 4
Fig. 4
Summary of the resulting linear regression models obtained with different subset selection methods. Dependent variable is EuroQoL 5D visual analogue scale measure of the health-related quality of life. 95 % CI, 95 % Confidence/Credible interval; Full MV, full multivariate regression; HRQoL, health-related quality of life. Description of variable names is provided in the Additional file 2

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