Department of Environmental and Occupational Health, College of Medicine, National Cheng Kung University, 138 Sheng-Li Road, Tainan 704, Taiwan.
Chemosphere. 2010 Sep;81(4):469-77. doi: 10.1016/j.chemosphere.2010.07.044. Epub 2010 Aug 24.
A congener profile of polychlorinated dibenzo-p-dioxin and dibenzofurans (PCDD/Fs) could provide valuable information for identifying possible sources of exposure to these compounds. The purpose of this study is to identify factors associated with PCDD/F congener profiles in the general population of Taiwan. Serum samples from 251 subjects of the general population in Taiwan were collected, and the levels of 17 2,3,7,8-chlorinated substituted PCDD/Fs were measured. The relationships between PCDD/F congener profiles and demographic parameters were evaluated using a multivariate analysis of variance method (MANOVA). Of the five demographic factors investigated, age was found to have the greatest impact on PCDD/F congener profiles. The PCDD/F congener pattern for the group I subjects (aged 18-29) was significantly different from those for the other three older age groups (p<0.001), and 12 congeners contributed to the effects (difference index: 71%). In addition, the group I subjects did not exhibit trends parallel to those of the other groups in the relationship between age and PCDD/F levels. Age was associated with PCDD/F levels and congener profiles in the general population of Taiwan and the young subjects (aged 18-29) was quite different from the other older subjects that could be influenced by the individual differences in pharmacokinetics and/or background exposure from dietary sources. We conclude that investigators must consider subjects' age and other underlying factors that could influence PCDD/F congener profiles in humans when identifying exposure sources.
多氯二苯并对二恶英和多氯二苯并呋喃(PCDD/Fs)同系物图谱可提供有价值的信息,有助于确定接触这些化合物的可能来源。本研究旨在确定与台湾普通人群中 PCDD/F 同系物图谱相关的因素。收集了台湾普通人群 251 名受试者的血清样本,并测量了 17 种 2,3,7,8-氯取代的 PCDD/Fs 水平。使用多变量方差分析方法(MANOVA)评估 PCDD/F 同系物图谱与人口统计学参数之间的关系。在所研究的五个人口统计学因素中,年龄对 PCDD/F 同系物图谱的影响最大。I 组(18-29 岁)的 PCDD/F 同系物模式与其他三个年龄较大的组明显不同(p<0.001),12 种同系物对这种差异有贡献(差异指数:71%)。此外,I 组受试者的年龄与 PCDD/F 水平之间的关系与其他组的趋势并不平行。年龄与台湾普通人群的 PCDD/F 水平和同系物图谱有关,18-29 岁的年轻受试者与其他年龄较大的受试者明显不同,这可能与个体差异的药代动力学和/或饮食来源的背景暴露有关。我们的结论是,在确定暴露源时,研究人员必须考虑到受试者的年龄和其他可能影响人类 PCDD/F 同系物图谱的潜在因素。