Department of Psychology, University of Georgia, Athens, GA 30602, USA.
Psychopharmacology (Berl). 2011 Aug;216(3):305-21. doi: 10.1007/s00213-011-2229-0. Epub 2011 Mar 4.
Delayed reward discounting (DRD) is a behavioral economic index of impulsivity and numerous studies have examined DRD in relation to addictive behavior. To synthesize the findings across the literature, the current review is a meta-analysis of studies comparing DRD between criterion groups exhibiting addictive behavior and control groups.
The meta-analysis sought to characterize the overall patterns of findings, systematic variability by sample and study type, and possible small study (publication) bias.
Literature reviews identified 310 candidate articles from which 46 studies reporting 64 comparisons were identified (total N=56,013).
From the total comparisons identified, a small magnitude effect was evident (d= .15; p< .00001) with very high heterogeneity of effect size. Based on systematic observed differences, large studies assessing DRD with a small number of self-report items were removed and an analysis of 57 comparisons (n=3,329) using equivalent methods and exhibiting acceptable heterogeneity revealed a medium magnitude effect (d= .58; p< .00001). Further analyses revealed significantly larger effect sizes for studies using clinical samples (d= .61) compared with studies using nonclinical samples (d=.45). Indices of small study bias among the various comparisons suggested varying levels of influence by unpublished findings, ranging from minimal to moderate.
These results provide strong evidence of greater DRD in individuals exhibiting addictive behavior in general and particularly in individuals who meet criteria for an addictive disorder. Implications for the assessment of DRD and research priorities are discussed.
延迟奖励折扣(DRD)是冲动性的行为经济学指标,许多研究已经研究了 DRD 与成瘾行为的关系。为了综合文献中的发现,本综述是对比较表现出成瘾行为的标准组和对照组之间 DRD 的研究进行的荟萃分析。
荟萃分析旨在描述总体发现模式、按样本和研究类型的系统可变性,以及可能存在的小样本(出版)偏差。
文献综述从 310 篇候选文章中确定了 46 项研究,共确定了 64 项比较(总 N=56013)。
从确定的总比较中,明显存在较小的效应量(d=.15;p<.00001),效应量的异质性非常高。基于系统观察到的差异,去除了评估 DRD 的大型研究,这些研究使用了少量的自我报告项目,并且对使用等效方法且表现出可接受异质性的 57 项比较(n=3329)进行了分析,结果显示中等效应量(d=.58;p<.00001)。进一步的分析表明,使用临床样本的研究(d=.61)的效应量明显大于使用非临床样本的研究(d=.45)。各比较中小样本偏差的指标表明,未发表的发现对结果的影响程度不同,从最小到中等。
这些结果为一般表现出成瘾行为的个体,特别是符合成瘾障碍标准的个体的 DRD 较大提供了强有力的证据。讨论了对 DRD 评估和研究重点的影响。