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The impact of saturable metabolism on exposure-response relations in 2 studies of benzene-induced leukemia.

机译:在2篇关于苯诱发的白血病的研究中,饱和代谢对暴露-反应关系的影响。

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摘要

Enzymatic saturation of metabolic pathways is one factor that potentially contributes to the nonlinear exposure-response relations that are frequently reported in occupational epidemiologic studies. The authors propose an approach to explore the contribution of saturable metabolism to previously reported exposure-response relations by integrating predictive models of relevant biomarkers of exposure into the epidemiologic analysis. The approach is demonstrated with 2 studies of leukemia in benzene-exposed workers, one conducted in the Australian petroleum industry (1981-1999) and one conducted in a US rubber hydrochloride production factory in Ohio (1940-1996). The studies differed greatly in their magnitudes and durations of exposure. Substitution of biomarker levels for external estimates of benzene exposure reduced the fold difference of the log relative risk of leukemia per unit of cumulative exposure between the 2 studies by 11%-44%. Nevertheless, a considerable difference in the log relative risk per unit of cumulative exposure remained between the 2 studies, suggesting that exposure misclassification, differences in study design, and potential confounding factors also contributed to the heterogeneity in risk estimates.
机译:代谢途径的酶饱和是可能导致职业流行病学研究中经常报道的非线性暴露-反应关系的因素之一。作者提出了一种方法,通过将相关的相关生物标志物的预测模型整合到流行病学分析中,探索饱和代谢对先前报道的暴露-反应关系的贡献。有2项针对苯接触工人的白血病研究证明了这种方法,其中一项是在澳大利亚石油工业中进行的(1981-1999年),另一项是在俄亥俄州的美国橡胶盐酸盐生产厂进行的(1940-1996年)。这些研究在暴露的程度和持续时间方面差异很大。用生物标志物水平代替外部估计的苯暴露可以使这两项研究之间每单位累积暴露的对数白血病相对危险度的对数差异减少11%-44%。然而,在这两项研究之间,每单位累积暴露的对数相对风险仍然存在相当大的差异,这表明暴露分类错误,研究设计的差异以及潜在的混杂因素也导致了风险估计的异质性。

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