Kawamoto T, Murata K, Koga M, Hattori Y, Kodama Y
Department of Environmental Health, University of Occupational and Environmental Health, Kitakyushu, Japan.
Occup Environ Med. 1994 Dec;51(12):817-21. doi: 10.1136/oem.51.12.817.
To clarify the relation between the genetic polymorphism of ALDH2 (low Km aldehyde dehydrogenase) and toluene metabolism.
The study subjects were 253 toluene workers (192 men and 61 women with an age range of 18-66). The genotypes of ALDH2 were classified by artificial restriction fragment length polymorphism into the homozygous genotype of normal ALDH2 (NN), the homozygous genotype of an inactive ALDH2 (DD), and the heterozygous genotype of normal and inactive ALDH2 (ND). The concentrations of hippuric acid (HA), the main metabolite of toluene, was determined in urine specimens of 253 toluene workers. The HA measurements in previous occupational health examinations were also referenced. The HA concentrations corrected for creatinine (HA/C) were compared with the biological exposure index (BEI) for toluene, which is 2.5 g/g creatinine. To estimate the toluene exposures, urinary o-cresol concentrations were also determined and compared with another BEI for toluene--that is, 1.0 mg urinary o-cresol/g creatinine.
Incidence of each genotype in the toluene workers was almost the same as that in non-exposed controls who lived in the same area as the toluene workers. The incidence of each of the three genotypes also did not differ by smoking habit. Mean urinary HA concentrations were not significantly different in the groups with the different genotypes of ALDH2. The HA concentrations of > 70% of the 890 total samples were < 1.0 g/l. The number of urine samples > 3.0 g/l was 28 (5.4%) in the NN group and 19 (6.4%) in the ND group. No urine samples in the DD group were > 3.0 g/l HA. The distribution of urinary HA in the DD group was significantly different from those in both the NN and ND groups (P < 0.05). Seven (4.9%) of the 136 total specimens in the NN group and four (4.7%) of the 82 total specimens in the ND group exceeded the BEI. There were, however, no urine specimens that exceeded the BEI in the DD group. The maximum HA concentration after correction for creatinine in the DD group was 1.86 g/g creatinine. The percentages of urine specimens in which o-cresol concentrations exceeded this BEI were 14.3% in the NN group, 9.1% in the ND group, and 15.4% in the DD group. Therefore, the exposure rate for all three genotypic groups of workers was almost the same.
The HA concentrations of toluene workers with ALDH2 DD genotype were lower than those of the NN and ND genotypes when they were exposed to relatively high concentrations of toluene. The exposures of the DD group were suspected to be underestimates because they were based on the BEI for the NN genotype.
阐明乙醛脱氢酶2(低Km醛脱氢酶)基因多态性与甲苯代谢之间的关系。
研究对象为253名甲苯作业工人(192名男性和61名女性,年龄范围为18 - 66岁)。通过人工限制性片段长度多态性将乙醛脱氢酶2的基因型分为正常乙醛脱氢酶2的纯合基因型(NN)、无活性乙醛脱氢酶2的纯合基因型(DD)以及正常和无活性乙醛脱氢酶2的杂合基因型(ND)。测定了253名甲苯作业工人尿液样本中甲苯的主要代谢产物马尿酸(HA)的浓度。还参考了以往职业健康检查中的HA测量值。将校正肌酐后的HA浓度(HA/C)与甲苯的生物接触指数(BEI)进行比较,甲苯的BEI为2.5 g/g肌酐。为评估甲苯暴露情况,还测定了尿邻甲酚浓度,并与甲苯的另一个BEI(即1.0 mg尿邻甲酚/g肌酐)进行比较。
甲苯作业工人中各基因型的发生率与居住在甲苯作业工人同一地区的非暴露对照人群几乎相同。三种基因型各自的发生率在吸烟习惯方面也无差异。不同乙醛脱氢酶2基因型组的尿HA平均浓度无显著差异。890个总样本中超过70%的HA浓度<1.0 g/l。NN组中HA浓度>3.0 g/l的尿样有28个(5.4%),ND组有19个(6.4%)。DD组中没有尿样的HA浓度>3.0 g/l。DD组尿HA的分布与NN组和ND组均有显著差异(P<0.05)。NN组136个总样本中有7个(4.9%)、ND组82个总样本中有4个(4.7%)超过了BEI。然而,DD组没有尿样超过BEI。DD组校正肌酐后的HA最大浓度为1.86 g/g肌酐。邻甲酚浓度超过该BEI的尿样百分比在NN组为14.3%,ND组为9.1%,DD组为15.4%。因此,所有三个基因型组工人的暴露率几乎相同。
当暴露于相对高浓度甲苯时,乙醛脱氢酶2基因DD型的甲苯作业工人的HA浓度低于NN型和ND型。DD组的暴露情况被怀疑被低估了,因为它们是基于NN基因型的BEI。