Suwazono Yasushi, Sand Salomon, Vahter Marie, Filipsson Agneta Falk, Skerfving Staffan, Lidfeldt Jonas, Akesson Agneta
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Environ Health Perspect. 2006 Jul;114(7):1072-6. doi: 10.1289/ehp.9028.
Our goal in this study was to explore the use of a hybrid approach to calculate benchmark doses (BMDs) and their 95% lower confidence bounds (BMDLs) for renal effects of cadmium in a population with low environmental exposure.
Morning urine and blood samples were collected from 820 Swedish women 53-64 years of age. We measured urinary cadmium (U-Cd) and tubular effect markers [N-acetyl-beta-d-glucosaminidase (NAG) and human complex-forming protein (protein HC) ] in 790 women and estimated glomerular filtration rate (GFR; based on serum cystatin C) in 700 women. Age, body mass index, use of nonsteroidal anti-inflammatory drugs, and blood lead levels were used as covariates for estimated GFR. BMDs/BMDLs corresponding to an additional risk (benchmark response) of 5 or 10% were calculated (the background risk at zero exposure was set to 5%) . The results were compared with the estimated critical concentrations obtained by applying logistic models used in previous studies on the present data.
For both NAG and protein HC, the BMDs (BMDLs) of U-Cd were 0.5-1.1 (0.4-0.8) microg/L (adjusted for specific gravity of 1.015 g/mL) and 0.6-1.1 (0.5-0.8) microg/g creatinine. For estimated GFR, the BMDs (BMDLs) were 0.8-1.3 (0.5-0.9) microg/L adjusted for specific gravity and 1.1-1.8 (0.7-1.2) microg/g creatinine.
The obtained benchmark doses of U-Cd were lower than the critical concentrations previously reported. The critical dose level for glomerular effects was only slightly higher than that for tubular effects. We suggest that the hybrid approach is more appropriate for estimation of the critical U-Cd concentration, because the choice of cutoff values in logistic models largely influenced the obtained critical U-Cd.
本研究的目的是探索一种混合方法,用于计算低环境暴露人群中镉对肾脏影响的基准剂量(BMDs)及其95%下限置信区间(BMDLs)。
收集了820名年龄在53 - 64岁的瑞典女性的晨尿和血样。我们在790名女性中测量了尿镉(U - Cd)和肾小管效应标志物[N - 乙酰 - β - d - 氨基葡萄糖苷酶(NAG)和人复合形成蛋白(蛋白HC)],并在700名女性中估计了肾小球滤过率(GFR;基于血清胱抑素C)。年龄、体重指数、非甾体抗炎药的使用情况和血铅水平用作估计GFR的协变量。计算了对应于5%或10%额外风险(基准反应)的BMDs/BMDLs(零暴露时的背景风险设定为5%)。将结果与通过对本数据应用先前研究中使用的逻辑模型获得的估计临界浓度进行比较。
对于NAG和蛋白HC,U - Cd的BMDs(BMDLs)分别为0.5 - 1.1(0.4 - 0.8)μg/L(校正比重为1.015 g/mL)和0.6 - 1.1(0.5 - 0.8)μg/g肌酐。对于估计的GFR,BMDs(BMDLs)分别为校正比重后的0.8 - 1.3(0.5 - 0.9)μg/L和1.1 - 1.8(0.7 - 1.2)μg/g肌酐。
获得的U - Cd基准剂量低于先前报道的临界浓度。肾小球效应的临界剂量水平仅略高于肾小管效应的临界剂量水平。我们认为混合方法更适合估计临界U - Cd浓度,因为逻辑模型中截断值的选择在很大程度上影响了获得的临界U - Cd。