Translational Psychiatry Research Group and Department of Clinical Medicine, Faculty of Medicine, Federal University of Cearx00E1;, Fortaleza, Brazil.
Psychother Psychosom. 2016;85(2):81-90. doi: 10.1159/000441457. Epub 2016 Jan 26.
To aid in the differentiation of individuals with major depressive disorder (MDD) from healthy controls, numerous peripheral biomarkers have been proposed. To date, no comprehensive evaluation of the existence of bias favoring the publication of significant results or inflating effect sizes has been conducted.
Here, we performed a comprehensive review of meta-analyses of peripheral nongenetic biomarkers that could discriminate individuals with MDD from nondepressed controls. PubMed/MEDLINE, EMBASE, and PsycINFO databases were searched through April 10, 2015.
From 15 references, we obtained 31 eligible meta-analyses evaluating biomarkers in MDD (21,201 cases and 78,363 controls). Twenty meta-analyses reported statistically significant effect size estimates. Heterogeneity was high (I2 ≥ 50%) in 29 meta-analyses. We plausibly assumed that the true effect size for a meta-analysis would equal the one of its largest study. A significant summary effect size estimate was observed for 20 biomarkers. We observed an excess of statistically significant studies in 21 meta-analyses. The summary effect size of the meta-analysis was higher than the effect of its largest study in 25 meta-analyses, while 11 meta-analyses had evidence of small-study effects.
Our findings suggest that there is an excess of studies with statistically significant results in the literature of peripheral biomarkers for MDD. The selective publication of 'positive studies' and the selective reporting of outcomes are possible mechanisms. Effect size estimates of meta-analyses may be inflated in this literature.
为了帮助区分患有重度抑郁症(MDD)的个体和健康对照者,提出了许多外周生物标志物。迄今为止,尚未对有利于发表显著结果或夸大效应大小的偏倚的存在进行全面评估。
在这里,我们对能够区分 MDD 个体和非抑郁对照者的外周非遗传生物标志物的荟萃分析进行了全面综述。通过 2015 年 4 月 10 日检索了 PubMed/MEDLINE、EMBASE 和 PsycINFO 数据库。
从 15 篇参考文献中,我们获得了 31 项评估 MDD 生物标志物的合格荟萃分析(21201 例和 78363 例对照)。20 项荟萃分析报告了统计学上显著的效应大小估计值。29 项荟萃分析的异质性很高(I2≥50%)。我们合理地假设荟萃分析的真实效应大小与其最大研究的效应大小相等。20 个生物标志物观察到显著的汇总效应大小估计值。在 21 项荟萃分析中,我们观察到存在统计学上显著的研究数量过多。25 项荟萃分析的汇总效应大小高于其最大研究的效应大小,而 11 项荟萃分析有小样本研究效应的证据。
我们的研究结果表明,在 MDD 外周生物标志物的文献中,存在统计学上显著结果的研究数量过多。“阳性研究”的选择性发表和结果的选择性报告可能是其机制。荟萃分析的效应大小估计值可能在这一文献中被夸大。