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首页> 外文期刊>Annals of epidemiology >Use of penalized splines in extended Cox-type additive hazard regression to flexibly estimate the effect of time-varying serum uric acid on risk of cancer incidence: a prospective, population-based study in 78,850 men.
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Use of penalized splines in extended Cox-type additive hazard regression to flexibly estimate the effect of time-varying serum uric acid on risk of cancer incidence: a prospective, population-based study in 78,850 men.

机译:在扩展的Cox型加性危害回归分析中使用惩罚性样条曲线灵活地估计随时间变化的血清尿酸对癌症发病风险的影响:一项针对人群的前瞻性研究,研究对象为78,850名男性。

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摘要

PURPOSE: We sought to investigate the effect of serum uric acid (SUA) levels on risk of cancer incidence in men and to flexibly determine the shape of this association by using a novel analytical approach. METHODS: A population-based cohort of 78,850 Austrian men who received 264,347 serial SUA measurements was prospectively followed-up for a median of 12.4 years. Data were collected between 1985 and 2003. Penalized splines (P-splines) in extended Cox-type additive hazard regression were used to flexibly model the association between SUA, as a time-dependent covariate, and risk of overall and site-specific cancer incidence and to calculate adjusted hazard ratios with their 95% confidence intervals. RESULTS: During follow-up 5189 incident cancers were observed. Restricted maximum-likelihood optimizing P-spline models revealed a moderately J-shaped effect of SUA on risk of overall cancer incidence, with statistically significantly increased hazard ratios in the upper third of the SUA distribution. Increased SUA (>/=8.00 mg/dL) further significantly increased risk for several site-specific malignancies, with P-spline analyses providing detailed insight about the shape of the association with these outcomes. CONCLUSIONS: Our study is the first to demonstrate a dose-response association between SUA and cancer incidence in men, simultaneously reporting on the usefulness of a novel methodological framework in epidemiologic research.
机译:目的:我们试图研究血清尿酸(SUA)水平对男性癌症发病风险的影响,并通过一种新颖的分析方法灵活地确定这种关联的形状。方法:前瞻性随访了以人群为基础的78850名奥地利男性患者,他们接受了264,347次连续SUA测量,平均随访时间为12.4年。收集了1985年至2003年之间的数据。使用了扩展的Cox型加性危害回归分析中的惩罚样条线(P-splines)来灵活地建模SUA之间的关联(时间相关协变量)以及整体和特定部位癌症发生风险并以95%的置信区间计算调整后的危险比。结果:在随访中发现5189例癌症。受限制的最大似然优化P样条曲线模型显示,SUA对总体癌症发生风险具有中等J形影响,在SUA分布的上三分之一中,危险比在统计学上显着增加。 SUA升高(> / = 8.00 mg / dL)进一步显着增加了几种特定部位恶性肿瘤的风险,P样条分析提供了有关与这些结局相关性的详细信息。结论:我们的研究是第一个证明SUA和男性癌症发病率之间存在剂量反应关系的研究,同时报道了新型方法学框架在流行病学研究中的有用性。

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