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首页> 外文期刊>Evidence-based Preclinical Medicine >The relationship between risk of bias criteria, research outcomes, and study sponsorship in a cohort of preclinical thiazolidinedione animal studies: a meta‐analysis
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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

机译:临床前噻唑烷二酮动物研究队列中偏倚标准风险,研究结果和研究赞助之间的关系:荟萃分析

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ABSTRACTIntroductionThere 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.MethodsWe 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.ResultsSeven 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.ConclusionsIndustry-sponsored TZD animal studies have exaggerated efficacy and harms outcomes compared with studies funded by non-industry sources. There was poor reporting of COIs.
机译:摘要简介关于利益冲突对临床前研究的影响的证据很少。这项研究调查了行业赞助是否与已发表的临床前噻唑烷二酮(TZD)研究中偏倚风险和/或结果的效应大小增加有关。方法我们确定了1965年1月1日至2012年11月14日之间发表的临床前TZD研究。旨在减少偏见的研究设计标准的信息,所有相关结果的结果,赞助来源以及符合纳入标准的112项研究的研究者财务关系。计算各研究的平均标准化平均差异(SMD),以测定血浆葡萄糖(功效结果)和体重增加(伤害结果)。在亚组分析中,TZD结果通过赞助来源和偏见标准风险进行评估。结果七项研究仅由行业资助,17项研究由行业和非行业资助,49项研究由非行业资助,39项研究未披露。没有一项研究使用样本量计算,意向性分析,研究者不知情或隐瞒分配。大多数研究报告了支持TZD使用的有利结果(112的88)和结论(112的95)。仅由行业赞助的六项研究(−3.41; 95%CI −5.21,−1.53; I 2 = 93%)的功效估计值明显高于非行业来源的42项研究(−0.97) ; 95%CI -1.37,-0.56; I 2 = 81%; p值= 0.01)。仅由行业发起的四项研究的危害估计显着更大(5.00; 95%CI 1.22,8.77; I 2 = 93%),而由非行业来源发起的38项研究(0.30; 95%CI -0.08,0.68; I 2 = 79%; p值= 0.02)。结论TZD动物研究与非行业来源资助的研究相比,TZD动物研究夸大了功效和危害结果,因此TZD的功效和危害在财务COI披露或偏见风险方面没有差异。关于COI的报告很差。

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