Nogawa K, Tsuritani I, Kido T, Honda R, Yamada Y, Ishizaki M
Int Arch Occup Environ Health. 1987;59(1):21-30. doi: 10.1007/BF00377675.
To investigate the mechanism for bone disease caused by exposure to cadmium serum samples were collected from 5 itai-itai disease patients, 36 Cd-exposed residents with renal tubular damage and 17 non-exposed individuals and analyzed for 1 alpha,25-dihydroxyvitamin D[1 alpha,25(OH)2D], parathyroid hormone, beta 2-microglobulin, calcium and inorganic phosphorus. Measurement of percentage tubular reabsorption of phosphate (%TRP) were performed only on the Cd-exposed subjects. Serum 1 alpha,25(OH)2D levels were lower in itai-itai disease patients and cadmium-exposed subjects with renal damage than in non-exposed subjects. Parathyroid hormone and beta 2-microglobulin concentrations in serum were higher in the Cd-exposed subjects. Decrease in serum 1 alpha,25(OH)2D levels were closely related to serum concentrations of parathyroid hormone, beta 2-microglobulin and %TRP. This study suggests that cadmium-induced bone effects were mainly due to a disturbance in vitamin D and parathyroid hormone metabolism, which was caused by the cadmium-induced kidney damage.
为研究镉暴露所致骨病的机制,采集了5例痛痛病患者、36例有肾小管损伤的镉暴露居民及17例未暴露个体的血清样本,分析其中1α,25 - 二羟基维生素D[1α,25(OH)₂D]、甲状旁腺激素、β₂ - 微球蛋白、钙及无机磷水平。仅对镉暴露受试者进行了磷酸盐肾小管重吸收百分比(%TRP)测定。痛痛病患者及有肾损伤的镉暴露受试者血清1α,25(OH)₂D水平低于未暴露受试者。镉暴露受试者血清中甲状旁腺激素和β₂ - 微球蛋白浓度较高。血清1α,25(OH)₂D水平降低与甲状旁腺激素、β₂ - 微球蛋白血清浓度及%TRP密切相关。本研究提示,镉诱导的骨骼效应主要归因于维生素D和甲状旁腺激素代谢紊乱,而这是由镉诱导的肾损伤所致。