Galloway Tamara S, Fletcher Tony, Thomas Oliver J, Lee Ben P, Pilling Luke C, Harries Lorna W
Biosciences, College of Life and Environmental Sciences, University of Exeter, Exeter, UK.
Department of Social and Environmental Research, London School of Hygiene and Tropical Medicine, London, UK.
Chemosphere. 2015 Feb;120:555-62. doi: 10.1016/j.chemosphere.2014.09.066. Epub 2014 Oct 17.
Little is known about interactions between environmental and genetic risk factors for osteoarthritis (OA). Genetic factors include variation or mutation in genes involved in parathyroid hormone signalling. Exposure to the endocrine disrupting chemicals perfluoro-octanoic acid (PFOA) or perfluorooctane sulfonate (PFOS) have been suggested as potential environmental contributors, although evidence to support this association is conflicting. Here we test the hypothesis that PFOA and PFOS may alter the mRNA expression of genes in the parathyroid signalling cascade to provide evidence on possible pathways between these chemicals and OA. We measured the relationship between PFOA or PFOS serum levels and the in vivo expression of the Parathyroid hormone 1 and 2 genes (PTH, PTH2), Parathyroid hormone 1 and 2 receptor genes (PTH1R, PTH2R) and the parathyroid hormone-like (PTHLH) gene in peripheral blood from a cross-sectional population study designed to assess the potential health effects of these chemicals. We used multivariate linear regression models and found that PFOA or PFOS was inversely correlated with parathyroid hormone 2 receptor (PTH2R) expression (coefficients=-0.43 and -0.32, p=p=0.017 and 0.006 for PFOA and PFOS respectively) in 189 female subjects. The levels of PTH2 transcripts encoding the ligand of PTH2r, were also found to be lower in women with OA (median 2.08) compared with controls (median 3.41, p=0.046). As the parathyroid signalling cascade is a known candidate for osteoarthritis risk and our findings raise the possibility that exposure to these chemicals may contribute to the pathogenesis of OA in some individuals.
关于骨关节炎(OA)环境风险因素与遗传风险因素之间的相互作用,目前所知甚少。遗传因素包括参与甲状旁腺激素信号传导的基因变异或突变。尽管支持这种关联的证据相互矛盾,但接触内分泌干扰化学物质全氟辛酸(PFOA)或全氟辛烷磺酸(PFOS)被认为是潜在的环境因素。在此,我们检验这样一个假设,即PFOA和PFOS可能会改变甲状旁腺信号级联反应中基因的mRNA表达,以提供这些化学物质与OA之间可能途径的证据。在一项旨在评估这些化学物质潜在健康影响的横断面人群研究中,我们测量了PFOA或PFOS血清水平与外周血中甲状旁腺激素1和2基因(PTH、PTH2)、甲状旁腺激素1和2受体基因(PTH1R、PTH2R)以及甲状旁腺激素样(PTHLH)基因的体内表达之间的关系。我们使用多元线性回归模型,发现在189名女性受试者中,PFOA或PFOS与甲状旁腺激素2受体(PTH2R)表达呈负相关(PFOA和PFOS的系数分别为-0.43和-0.32,p值分别为0.017和0.006)。与对照组(中位数3.41,p=0.046)相比,OA女性中编码PTH2r配体的PTH2转录本水平也较低(中位数2.08)。由于甲状旁腺信号级联反应是骨关节炎风险的已知候选因素,我们的研究结果增加了这样一种可能性,即接触这些化学物质可能在某些个体中导致OA的发病机制。