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The effect of assessing genetic risk of prostate cancer on the use of PSA tests in primary care: A cluster randomized controlled trial

机译:评估前列腺癌的遗传风险对初级保健中PSA试验的遗传风险:簇随机对照试验

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Background Assessing genetic lifetime risk for prostate cancer has been proposed as a means of risk stratification to identify those for whom prostate-specific antigen (PSA) testing is likely to be most valuable. This project aimed to test the effect of introducing a genetic test for lifetime risk of prostate cancer in general practice on future PSA testing. Methods and findings We performed a cluster randomized controlled trial with randomization at the level of general practices (73 in each of two arms) in the Central Region (Region Midtjylland) of Denmark. In intervention practices, men were offered a genetic test (based on genotyping of 33 risk-associated single nucleotide polymorphisms) in addition to the standard PSA test that informed them about lifetime genetic risk of prostate cancer and distinguished between “normal” and “high” risk. The primary outcome was the proportion of men having a repeated PSA test within 2 years. A multilevel logistic regression model was used to test the association. After applying the exclusion criteria, 3,558 men were recruited in intervention practices, with 1,235 (34.7%) receiving the genetic test, and 4,242 men were recruited in control practices. Men with high genetic risk had a higher propensity for repeated PSA testing within 2 years than men with normal genetic risk (odds ratio [OR] = 8.94, p 0.01). The study was conducted in routine practice and had some selection bias, which is evidenced by the relatively large proportion of younger and higher income participants taking the genetic test. Conclusions Providing general practitioners (GPs) with access to a genetic test to assess lifetime risk of prostate cancer did not reduce the overall number of future PSA tests. However, among men who had a genetic test, knowledge of genetic risk significantly influenced future PSA testing. Trial registration This study is registered with ClinicalTrials.gov, number NCT01739062.
机译:背景技术已经提出评估前列腺癌的遗传寿命风险作为风险分层的手段,以确定前列腺特异性抗原(PSA)测试可能是最有价值的那些。该项目旨在测试在未来PSA检测中介绍前列腺癌的终身风险的遗传测试的效果。方法和调查结果我们在丹麦中央区域(区域Midtjylland)的一般实践(每个武器中的73个)的随机化随机化控制试验中进行了随机随机对照试验。在干预实践中,除了标准的PSA试验之外,男性还提供了遗传测试(基于33个风险相关的单核苷酸多态性的基因分型),这些PSA试验告诉他们前列腺癌的终生遗传风险并区分“正常”和“高”风险。主要结果是2年内重复PSA测试的男性的比例。使用多级逻辑回归模型来测试关联。在申请排除标准后,招募3,558名男性在干预实践中招募,1,235名(34.7%)接受遗传检验,并在控制实践中招募了4,242名男性。具有高遗传风险的男性比具有正常遗传风险的男性在2年内对重复的PSA检测有更高的倾向(差异率[或] = 8.94,P <0.01)。该研究在常规实践中进行,并进行了一些选择偏见,这是通过相对较大的年轻和更高的收入参与者进行遗传测试的比例所证明。结论提供通用从业者(GPS)随着遗传检测获得遗传检测,以评估前列腺癌的寿命风险并没有减少未来PSA测试的整体数量。然而,在具有遗传测试的男性中,遗传风险的知识显着影响未来的PSA测试。试用注册本研究在ClinicalTrials.gov中注册,NCT01739062号码。

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