Effect Size Estimation From t-Statistics in the Presence of Publication Bias

2018 ◽  
Vol 226 (1) ◽  
pp. 56-80 ◽  
Author(s):  
Rolf Ulrich ◽  
Jeff Miller ◽  
Edgar Erdfelder

Abstract. Publication bias hampers the estimation of true effect sizes. Specifically, effect sizes are systematically overestimated when studies report only significant results. In this paper we show how this overestimation depends on the true effect size and on the sample size. Furthermore, we review and follow up methods originally suggested by Hedges (1984) , Iyengar and Greenhouse (1988) , and Rust, Lehmann, and Farley (1990) allowing the estimation of the true effect size from published test statistics (e.g., from the t-values of reported significant results). Moreover, we adapted these methods allowing meta-analysts to estimate the percentage of researchers who consign undesired results in a research domain to the file drawer. We also apply the same logic to the case when significant results tend to be underreported. We demonstrate the application of these procedures for conventional one-sample and two-sample t-tests. Finally, we provide R and MATLAB versions of a computer program to estimate the true unbiased effect size and the prevalence of publication bias in the literature.

2018 ◽  
Author(s):  
Robbie Cornelis Maria van Aert

More and more scientific research gets published nowadays, asking for statistical methods that enable researchers to get an overview of the literature in a particular research field. For that purpose, meta-analysis methods were developed that can be used for statistically combining the effect sizes from independent primary studies on the same topic. My dissertation focuses on two issues that are crucial when conducting a meta-analysis: publication bias and heterogeneity in primary studies’ true effect sizes. Accurate estimation of both the meta-analytic effect size as well as the between-study variance in true effect size is crucial since the results of meta-analyses are often used for policy making. Publication bias distorts the results of a meta-analysis since it refers to situations where publication of a primary study depends on its results. We developed new meta-analysis methods, p-uniform and p-uniform*, which estimate effect sizes corrected for publication bias and also test for publication bias. Although the methods perform well in many conditions, these and the other existing methods are shown not to perform well when researchers use questionable research practices. Additionally, when publication bias is absent or limited, traditional methods that do not correct for publication bias outperform p¬-uniform and p-uniform*. Surprisingly, we found no strong evidence for the presence of publication bias in our pre-registered study on the presence of publication bias in a large-scale data set consisting of 83 meta-analyses and 499 systematic reviews published in the fields of psychology and medicine. We also developed two methods for meta-analyzing a statistically significant published original study and a replication of that study, which reflects a situation often encountered by researchers. One method is a frequentist whereas the other method is a Bayesian statistical method. Both methods are shown to perform better than traditional meta-analytic methods that do not take the statistical significance of the original study into account. Analytical studies of both methods also show that sometimes the original study is better discarded for optimal estimation of the true effect size. Finally, we developed a program for determining the required sample size in a replication analogous to power analysis in null hypothesis testing. Computing the required sample size with the method revealed that large sample sizes (approximately 650 participants) are required to be able to distinguish a zero from a small true effect.Finally, in the last two chapters we derived a new multi-step estimator for the between-study variance in primary studies’ true effect sizes, and examined the statistical properties of two methods (Q-profile and generalized Q-statistic method) to compute the confidence interval of the between-study variance in true effect size. We proved that the multi-step estimator converges to the Paule-Mandel estimator which is nowadays one of the recommended methods to estimate the between-study variance in true effect sizes. Two Monte-Carlo simulation studies showed that the coverage probabilities of Q-profile and generalized Q-statistic method can be substantially below the nominal coverage rate if the assumptions underlying the random-effects meta-analysis model were violated.


2019 ◽  
Vol 227 (4) ◽  
pp. 261-279 ◽  
Author(s):  
Frank Renkewitz ◽  
Melanie Keiner

Abstract. Publication biases and questionable research practices are assumed to be two of the main causes of low replication rates. Both of these problems lead to severely inflated effect size estimates in meta-analyses. Methodologists have proposed a number of statistical tools to detect such bias in meta-analytic results. We present an evaluation of the performance of six of these tools. To assess the Type I error rate and the statistical power of these methods, we simulated a large variety of literatures that differed with regard to true effect size, heterogeneity, number of available primary studies, and sample sizes of these primary studies; furthermore, simulated studies were subjected to different degrees of publication bias. Our results show that across all simulated conditions, no method consistently outperformed the others. Additionally, all methods performed poorly when true effect sizes were heterogeneous or primary studies had a small chance of being published, irrespective of their results. This suggests that in many actual meta-analyses in psychology, bias will remain undiscovered no matter which detection method is used.


2018 ◽  
Author(s):  
V. S. Sundar ◽  
Chun-Chieh Fan ◽  
Dominic Holland ◽  
Anders M. Dale

AbstractDetermining the genetic causal variants and estimating their effect sizes are considered to be correlated but independent problems. Fine-mapping studies often rely on the ability to integrate useful functional annotation information into genome wide association univariate/multivariate analysis. In the present study, by modeling the probability of a SNP being causal and its effect size as a set of correlated Gaussian/non-Gaussian random variables, we design an optimization routine for simultaneous fine-mapping and effect size estimation. The algorithm is released as an open source C package MODE.Availability and Implementation:http://sites.google.com/site/sundarvelkur/modeContact:[email protected], [email protected]


2017 ◽  
Author(s):  
Hilde Augusteijn ◽  
Robbie Cornelis Maria van Aert ◽  
Marcel A. L. M. van Assen

One of the main goals of meta-analysis is to test and estimate the heterogeneity of effect size. We examined the effect of publication bias on the Q-test and assessments of heterogeneity, as a function of true heterogeneity, publication bias, true effect size, number of studies, and variation of sample sizes. The expected values of heterogeneity measures H2 and I2 were analytically derived, and the power and the type I error rate of the Q-test were examined in a Monte-Carlo simulation study. Our results show that the effect of publication bias on the Q-test and assessment of heterogeneity is large, complex, and non-linear. Publication bias can both dramatically decrease and increase heterogeneity. Extreme homogeneity can occur even when the population heterogeneity is large. Particularly if the number of studies is large and population effect size is small, publication bias can cause both extreme type I error rates and power of the Q-test close to 0 or 1. We therefore conclude that the Q-test of homogeneity and heterogeneity measures H2 and I2 are generally not valid in assessing and testing heterogeneity when publication bias is present, especially when the true effect size is small and the number of studies is large. We introduce a web application, Q-sense, which can be used to assess the sensitivity of the Q-test to publication bias, and we apply it to two published meta-analysis. Meta-analytic methods should be enhanced in order to be able to deal with publication bias in their assessment and tests of heterogeneity.


2018 ◽  
Author(s):  
Frank Renkewitz ◽  
Melanie Keiner

Publication biases and questionable research practices are assumed to be two of the main causes of low replication rates observed in the social sciences. Both of these problems do not only increase the proportion of false positives in the literature but can also lead to severely inflated effect size estimates in meta-analyses. Methodologists have proposed a number of statistical tools to detect and correct such bias in meta-analytic results. We present an evaluation of the performance of six of these tools in detecting bias. To assess the Type I error rate and the statistical power of these tools we simulated a large variety of literatures that differed with regard to underlying true effect size, heterogeneity, number of available primary studies and variation of sample sizes in these primary studies. Furthermore, simulated primary studies were subjected to different degrees of publication bias. Our results show that the power of the detection methods follows a complex pattern. Across all simulated conditions, no method consistently outperformed all others. Hence, choosing an optimal method would require knowledge about parameters (e.g., true effect size, heterogeneity) that meta-analysts cannot have. Additionally, all methods performed badly when true effect sizes were heterogeneous or primary studies had a small chance of being published irrespective of their results. This suggests, that in many actual meta-analyses in psychology bias will remain undiscovered no matter which detection method is used.


1997 ◽  
Vol 85 (2) ◽  
pp. 719-722 ◽  
Author(s):  
M. T. Bradley ◽  
R. D. Gupta

Although meta-analysis appears to be a useful technique to verify the existence of an effect and to summarize large bodies of literature, there are problems associated with its use and interpretation. Amongst difficulties is the “file drawer problem.” With this problem it is assumed that a certain percentage of studies are not published or are not available to be included in any given meta-analysis. We present a cautionary table to quantify the magnitude of this problem. The table shows that distortions exaggerating the effect size are substantial and that the exaggerations of effects are strongest when the true effect size approaches zero. A meta-analysis could be very misleading were the true effect size close to zero.


2020 ◽  
Author(s):  
Anton Olsson-Collentine ◽  
Marcel A. L. M. van Assen ◽  
Jelte M. Wicherts

We examined the evidence for heterogeneity (of effect sizes) when only minor changes to sample population and settings were made between studies and explored the association between heterogeneity and average effect size in a sample of 68 meta-analyses from thirteen pre-registered multi-lab direct replication projects in social and cognitive psychology. Amongst the many examined effects, examples include the Stroop effect, the “verbal overshadowing” effect, and various priming effects such as “anchoring” effects. We found limited heterogeneity; 48/68 (71%) meta-analyses had non-significant heterogeneity, and most (49/68; 72%) were most likely to have zero to small heterogeneity. Power to detect small heterogeneity (as defined by Higgins, 2003) was low for all projects (mean 43%), but good to excellent for medium and large heterogeneity. Our findings thus show little evidence of widespread heterogeneity in direct replication studies in social and cognitive psychology, suggesting that minor changes in sample population and settings are unlikely to affect research outcomes in these fields of psychology. We also found strong correlations between observed average effect sizes (standardized mean differences and log odds ratios) and heterogeneity in our sample. Our results suggest that heterogeneity and moderation of effects is unlikely for a zero average true effect size, but increasingly likely for larger average true effect size.


2021 ◽  
Author(s):  
Hilde Elisabeth Maria Augusteijn ◽  
Robbie Cornelis Maria van Aert ◽  
Marcel A. L. M. van Assen

Publication bias remains to be a great challenge when conducting a meta-analysis. It may result in overestimated effect sizes, increased frequency of false positives, and over- or underestimation of the effect size heterogeneity parameter. A new method is introduced, Bayesian Meta-Analytic Snapshot (BMAS), which evaluates both effect size and its heterogeneity and corrects for potential publication bias. It evaluates the probability of the true effect size being zero, small, medium or large, and the probability of true heterogeneity being zero, small, medium or large. This approach, which provides an intuitive evaluation of uncertainty in the evaluation of effect size and heterogeneity, is illustrated with a real-data example, a simulation study, and a Shiny web application of BMAS.


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