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对大鼠终生吸入柴油机尾气所致肺部肿瘤的荟萃分析。

Meta-analysis of rat lung tumors from lifetime inhalation of diesel exhaust.

作者信息

Valberg P A, Crouch E A

机构信息

Cambridge Environmental Inc., Cambridge, Massachusetts 02141, USA.

出版信息

Environ Health Perspect. 1999 Sep;107(9):693-9. doi: 10.1289/ehp.99107693.

Abstract

Estimating the carcinogenic potential of exposure to diesel-engine exhaust particulates (DEPs) is problematic. In rats, high concentrations of DEPs (> 1,000 microg/m(3)) inhaled over a lifetime result in excess lung tumors. However, data for rats exposed to DEP at concentrations not associated with lung overload are consistent with no tumorigenic effect. Individual rat studies have only a limited number of exposure groups; therefore, we combined the tumor data from eight chronic inhalation studies in a meta-analysis. Statistical analysis identified a threshold of response between 200 and 600 microg/m(3) average continuous lifetime exposure, consistent with biological-effect thresholds reported by other investigators. Our exposure-response analysis of all rats with < 600 microg/m(3) average continuous lifetime exposure found no tumorigenic effect of DEP in these rats. When we evaluated all rat studies, accounted for a threshold and for inhomogeneity between experiments, and expressed the results in terms of human unit risk (UR), we found a negative maximum-likelihood human UR of -32 (times) 10(-6) per microgram per cubic meter (microg/m(3)), but this was not statistically significantly different from zero. Extrapolating the rat upper 95th percentile confidence limit to humans gave an upper-bound human UR of 9.3 (times) 10(-6) per microg/m(3)]. This upper-bound human UR, derived from all of the data points (including 1,087 animals below the estimated threshold and 1,433 in the control groups), falls entirely below the range of estimates derived from lung-overloaded rats or from epidemiology of railroad workers. Our meta-analysis of the low-exposure data in rats does not support a lung cancer risk for DEP exposure at nonoverload conditions. Average ambient concentrations of DEP (0-3 microg/m(3)) are < 1% of the concentration associated here with a threshold of tumor response in the rat bioassay.

摘要

评估接触柴油发动机尾气颗粒物(DEP)的致癌潜力存在问题。在大鼠中,终生吸入高浓度的DEP(>1000微克/立方米)会导致肺部肿瘤增多。然而,接触DEP浓度未达到引起肺部负荷过重水平的大鼠的数据显示没有致瘤作用。单个大鼠研究的暴露组数量有限;因此,我们在一项荟萃分析中合并了八项慢性吸入研究的肿瘤数据。统计分析确定,终生平均连续暴露量在200至600微克/立方米之间存在反应阈值,这与其他研究人员报告的生物学效应阈值一致。我们对所有终生平均连续暴露量<600微克/立方米的大鼠进行的暴露-反应分析发现,DEP对这些大鼠没有致瘤作用。当我们评估所有大鼠研究,考虑到阈值和实验之间的不均匀性,并以人类单位风险(UR)表示结果时,我们发现最大似然人类UR为-32×10⁻⁶/(微克/立方米),但这与零没有统计学上的显著差异。将大鼠的第95百分位数置信上限外推至人类,得出人类UR上限为9.3×10⁻⁶/(微克/立方米)。这个上限人类UR来自所有数据点(包括1087只低于估计阈值的动物和1433只对照组动物),完全低于从肺部负荷过重的大鼠或铁路工人流行病学研究得出的估计范围。我们对大鼠低暴露数据的荟萃分析不支持在非过载条件下接触DEP会导致肺癌风险。DEP的平均环境浓度(0 - 3微克/立方米)<大鼠生物测定中与肿瘤反应阈值相关浓度的1%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3170/1566471/a4f552482ba8/envhper00514-0043-a.jpg

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