INRS-Institut Armand-Frappier, Université du Québec, Laval, Quebec, Canada.
Department of Environmental and Occupational Health, School of Public Health, Université de Montréal, Montreal, Quebec, Canada.
Occup Environ Med. 2018 Aug;75(8):562-572. doi: 10.1136/oemed-2018-105058. Epub 2018 Jul 6.
While several monocyclic aromatic hydrocarbons are classified as definite or possible carcinogens to humans, little data exist on their role in prostate cancer (PCa). We examined occupational exposure to benzene, toluene, xylene (BTX) and styrene and PCa risk in a population-based case-control study in Montreal, Canada.
Cases aged ≤75 years diagnosed with PCa in 2005-2009 (n=1920) and population controls frequency-matched on age (n=1989) provided detailed work histories. Experts evaluated the certainty, frequency and concentration of exposure to monocyclic aromatic hydrocarbons in each job lasting ≥2 years. Logistic regression estimated OR and 95% CIs for PCa risk, adjusting for potential confounders.
Exposures to BTX were highly intercorrelated, except for durations of exposure at substantial levels. Ever exposure to any BTX was associated with overall PCa (OR 1.27, 95% CI 1.05 to 1.53), while the OR for styrene was 1.19. However, increases in risk were largely confined to low-grade tumours, with ORs of 1.33 (95%CI 1.08 to 1.64) and 1.41 (95% CI 0.85 to 2.31) for ever exposure to any BTX and styrene, respectively, and a duration response pattern for any BTX. Risks for low-grade tumours were elevated among men exposed ≥25 years at substantial levels of benzene (OR 2.32) and styrene (OR 2.44). Some cumulative exposure categories showed increased risks but without clear trends.
Exposure to any BTX was associated with higher risks of overall PCa. Prolonged exposures at the substantial level to benzene and styrene increased risks of low-grade tumours. These novel findings were independent from PCa screening.
虽然有几种单环芳烃被归类为人类的明确或可能的致癌物,但关于它们在前列腺癌(PCa)中的作用的数据很少。我们在加拿大蒙特利尔进行了一项基于人群的病例对照研究,研究了苯、甲苯、二甲苯(BTX)和苯乙烯的职业暴露与 PCa 风险之间的关系。
2005-2009 年间诊断为 PCa 的年龄≤75 岁的病例(n=1920)和按年龄匹配的人群对照(n=1989)提供了详细的工作经历。专家评估了每种持续时间≥2 年的工作中,单环芳烃暴露的确定性、频率和浓度。使用逻辑回归估计了 PCa 风险的 OR 和 95%CI,调整了潜在混杂因素。
BTX 的暴露高度相关,除了暴露时间在较高水平时。BTX 的任何暴露都与整体 PCa 相关(OR 1.27,95%CI 1.05-1.53),而苯乙烯的 OR 为 1.19。然而,风险的增加主要局限于低级别肿瘤,BTX 和苯乙烯的任何暴露的 OR 分别为 1.33(95%CI 1.08-1.64)和 1.41(95%CI 0.85-2.31),BTX 的任何暴露都呈现出剂量-反应关系。暴露于高浓度 BTX 和苯乙烯≥25 年的男性,低级别肿瘤的风险增加(OR 2.32 和 2.44)。一些累积暴露类别显示出风险增加,但没有明显趋势。
BTX 的任何暴露都与整体 PCa 风险增加相关。苯和苯乙烯在高浓度水平的长期暴露增加了低级别肿瘤的风险。这些新发现独立于 PCa 筛查。