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饱和代谢对苯致白血病的 2 项研究中暴露-反应关系的影响。

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

机构信息

Environmental Epidemiology Division, Institute for Risk Assessment Sciences, P.O. Box 80.178, NL-3508 TD Utrecht, the Netherlands.

出版信息

Am J Epidemiol. 2011 Sep 1;174(5):621-9. doi: 10.1093/aje/kwr118. Epub 2011 Jul 10.

Abstract

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.

摘要

代谢途径的酶饱和是导致职业流行病学研究中经常报告的非线性暴露-反应关系的因素之一。作者提出了一种方法,通过将相关暴露生物标志物的预测模型整合到流行病学分析中,来探讨饱和代谢对先前报告的暴露-反应关系的贡献。该方法通过对在澳大利亚石油工业(1981-1999 年)和美国俄亥俄州一家生产盐酸橡胶的工厂(1940-1996 年)进行的两项苯暴露工人白血病研究进行了演示。这两项研究在暴露程度和持续时间上有很大差异。用生物标志物水平替代苯暴露的外部估计值,使两项研究中每单位累积暴露的白血病对数相对风险的倍数差异降低了 11%-44%。然而,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、研究设计差异和潜在混杂因素也导致了风险估计的异质性。

相似文献

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Benzene and leukemia. An epidemiologic risk assessment.苯与白血病。一项流行病学风险评估。
N Engl J Med. 1987 Apr 23;316(17):1044-50. doi: 10.1056/NEJM198704233161702.

本文引用的文献

3
Evidence that humans metabolize benzene via two pathways.有证据表明人类通过两种途径代谢苯。
Environ Health Perspect. 2009 Jun;117(6):946-52. doi: 10.1289/ehp.0800510. Epub 2009 Feb 19.
9
Exposure and dose modelling in occupational epidemiology.职业流行病学中的暴露与剂量建模。
Occup Environ Med. 2007 Jul;64(7):492-8. doi: 10.1136/oem.2006.030031.

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