临床前噻唑烷二酮动物研究队列中偏倚风险标准、研究结果和研究赞助之间的关系:一项荟萃分析

M. Abdel-Sattar, D. Krauth, A. Anglemyer, L. Bero
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引用次数: 14

摘要

很少有证据表明利益冲突对临床前研究的影响。本研究探讨了在已发表的临床前噻唑烷二酮(TZD)研究中,行业赞助是否与偏倚风险增加和/或结果效应大小有关。方法选取1965年1月1日至2012年11月14日期间发表的临床前TZD研究。编码器独立地从符合纳入标准的112项研究中提取有关旨在减少偏倚的研究设计标准、所有相关结果的结果、赞助来源和研究者经济关系的信息。计算各研究的平均标准化平均差(SMD)对血糖(疗效结果)和体重增加(危害结果)的影响。在亚组分析中,通过赞助来源和偏倚风险标准评估TZD结果。结果7项研究由工业界单独资助,17项研究由工业界和非工业界共同资助,49项研究由非工业界单独资助,39项研究没有披露。没有一项研究使用了样本量计算、意向治疗分析、调查人员的盲法或隐瞒分配。大多数研究报告了有利的结果(112项中的88项)和支持使用TZD的结论(112项中的95项)。在由工业界单独赞助的6项研究中,疗效估计明显更大(- 3.41;95% ci为−5.21,−1.53;I2 = 93%),而非工业来源赞助的研究为42项(- 0.97;95% ci为−1.37,−0.56;I2 = 81%;p值= 0.01)。在仅由工业界赞助的四项研究中,危害估计要大得多(5.00;95% ci 1.22, 8.77;I2 = 93%),而非工业来源赞助的研究有38项(0.30;95% ci−0.08,0.68;I2 = 79%;p值= 0.02)。TZD的疗效和危害没有因财务coi或偏倚风险的披露而不同。与非工业资助的研究相比,工业资助的TZD动物研究夸大了疗效和危害结果。coi报告不完善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta-analysis

Introduction

There is little evidence regarding the influence of conflicts of interest on preclinical research. This study examines whether industry sponsorship is associated with increased risks of bias and/or effect sizes of outcomes in published preclinical thiazolidinedione (TZD) studies.

Methods

We identified preclinical TZD studies published between January 1, 1965, and November 14, 2012. Coders independently extracted information on study design criteria aimed at reducing bias, results for all relevant outcomes, sponsorship source and investigator financial ties from the 112 studies meeting the inclusion criteria. The average standardized mean difference (SMD) across studies was calculated for plasma glucose (efficacy outcome) and weight gain (harm outcome). In subgroup analyses, TZD outcomes were assessed by sponsorship source and risk of bias criteria.

Results

Seven studies were funded by industry alone, 17 studies funded by both industry and non-industry, 49 studies funded by non-industry alone and 39 studies had no disclosures. None of the studies used sample size calculations, intention-to-treat analyses, blinding of investigators or concealment of allocation. Most studies reported favourable results (88 of 112) and conclusions (95 of 112) supporting TZD use. Efficacy estimates were significantly larger in six studies sponsored by industry alone (−3.41; 95% CI −5.21, −1.53; I2 = 93%) versus 42 studies sponsored by non-industry sources (−0.97; 95% CI −1.37, −0.56; I2 = 81%; p-value = 0.01). Harms estimates were significantly larger in four studies sponsored by industry alone (5.00; 95% CI 1.22, 8.77; I2 = 93%) versus 38 studies sponsored by non-industry sources (0.30; 95% CI −0.08, 0.68; I2 = 79%; p-value = 0.02). TZD efficacy and harms did not differ by disclosure of financial COIs or risks of bias.

Conclusions

Industry-sponsored TZD animal studies have exaggerated efficacy and harms outcomes compared with studies funded by non-industry sources. There was poor reporting of COIs.

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