Nøst Therese Haugdahl, Sandanger Torkjel Manning, Nieboer Evert, Odland Jon Øyvind, Breivik Knut
NILU - Norwegian Institute for Air Research, The FRAM Centre, P.O. Box 6606 Langnes, NO-9296 Tromsø, Norway; Department of Community Medicine, Faculty of Health Sciences, UiT - The Arctic University of Norway, P.O. Box 6050 Langnes, NO-9037 Tromsø, Norway.
NILU - Norwegian Institute for Air Research, The FRAM Centre, P.O. Box 6606 Langnes, NO-9296 Tromsø, Norway; Department of Community Medicine, Faculty of Health Sciences, UiT - The Arctic University of Norway, P.O. Box 6050 Langnes, NO-9037 Tromsø, Norway.
Int J Hyg Environ Health. 2017 Jun;220(4):776-781. doi: 10.1016/j.ijheh.2017.01.015. Epub 2017 Feb 20.
In this short communication, our focus is on the relationship between human concentrations of select persistent organic pollutants (POPs) and environmental emissions. It is based on a longitudinal study (1979-2007) conducted in Norway.
Our aim was to extract general insights from observed and predicted temporal trends in human concentrations of 49 POPs to assist in the design and interpretation of future monitoring studies.
Despite considerable decline for polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) since 1986, the sum of the targeted POPs increased from 1979 until 2001, with per- and polyfluorinated alkyl substances (PFASs) dominating recent blood burden measurements. Specifically, the time trends in serum concentrations of POPs, exemplified by PCB-153, 1,1'-(2,2,2-Trichloroethane-1,1-diyl)bis(4-chlorobenzene) (DDT) and perfluorooctane sulfonic acid (PFOS), resembled the trends in available data on their emissions, production or use. These observations suggest that interpretations of human biomonitoring data on persistent compounds must consider historic emissions, which likely vary spatially across the globe. Based on the different temporal trends observed across POP groups, it is evident that generalizations regarding temporal aspects have limitations.
The discussion herein underscores the importance of understanding temporal variations in environmental emissions when designing and interpreting human biomonitoring studies.
在本简短通讯中,我们关注的是人类体内特定持久性有机污染物(POPs)浓度与环境排放之间的关系。它基于在挪威进行的一项纵向研究(1979 - 2007年)。
我们的目标是从观察到的和预测的49种POPs在人体内浓度的时间趋势中提取一般性见解,以协助设计和解释未来的监测研究。
尽管自1986年以来多氯联苯(PCBs)和有机氯农药(OCPs)的含量大幅下降,但目标POPs的总量从1979年到2001年有所增加,全氟和多氟烷基物质(PFASs)在近期血液负荷测量中占主导地位。具体而言,以PCB - 153、1,1' -(2,2,2 - 三氯乙烷 - 1,1 - 二基)双(4 - 氯苯)(滴滴涕)和全氟辛烷磺酸(PFOS)为例,POPs血清浓度的时间趋势与它们的排放、生产或使用的现有数据趋势相似。这些观察结果表明,对持久性化合物的人体生物监测数据的解释必须考虑历史排放,而历史排放在全球范围内可能存在空间差异。基于不同POPs组观察到的不同时间趋势,很明显关于时间方面的概括存在局限性。
本文的讨论强调了在设计和解释人体生物监测研究时理解环境排放时间变化的重要性。