36年以上慢性多氯联苯中毒(玉树事故)患者的神经症状和体征

Hirokazu Furuya , Takeshi Yamada , Yasumasa Ohyagi , Koji Ikezoe , Tasuku Miyoshi , Naoki Fujii , Jun-ichi Kira , on behalf of the Study Group for Yusho
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引用次数: 3

摘要

背景:由于关于多氯联苯对周围神经系统影响的研究很少,因此慢性接触多氯联苯后周围神经病变的存在仍然存在争议。目的:本研究的目的是确定神经体征和症状与血清多氯联苯浓度的相关性。材料和方法:从36年前接触的450名男性和557名女性玉树受害者(慢性多氯联苯中毒)的全国健康检查结果中收集的神经学数据与最近的血清多氯联苯浓度和模式测量结果进行了比较。结果:经神经学检查发现感觉障碍的频率在正式承认的受害者组中明显高于男性(P = 0.014;女性,P = 0.001)比年龄匹配的对照组。血清多氯联苯模式与神经学检查结果无显著差异,但在官方和非官方承认的女性鱼松受害者中,腱鞘反射下降组的血清多氯联苯浓度显著高于官方承认的女性鱼松受害者(男性,P = 0.994;女性,P = 0.014)。结论:多氯联苯的长半衰期及其在脂肪组织中的蓄积可导致暴露后长时间持续的周围神经系统轻度损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurological signs and symptoms in patients with chronic PCB poisoning (Yusho accident) for more than 36 years

Background:

The existence of peripheral neuropathy after chronic exposure to polychlorinated biphenyls (PCBs) is still controversial because studies concerning the effects of PCBs on the peripheral nervous system are rare.

Objective:

The purpose of this study was to determine the correlation between neurological signs and symptoms and the concentration of serum PCBs.

Materials and methods:

Neurological data collected from the results of a nationwide health examination of 450 male and 557 female Yusho victims (chronic PCB poisoning) exposed more than 36 years ago were compared with recent measurements of the serum PCB concentration and patterns.

Results:

The frequency of sensory disturbance detected by neurological examination was significantly higher in the group of officially acknowledged victims (male, P = 0.014; female, P = 0.001) than in age-matched controls. Significant differences were not observed between the serum PCB patterns and the neurological findings, but the serum PCB concentration was significantly higher in the group with decreased tendon reflex in officially and non-officially acknowledged female Yusho victims (male, P = 0.994; female, P = 0.014).

Conclusion:

These results suggest that the long half-life of PCBs and their accumulation in fatty tissue can lead to persistent mild impairment of the peripheral nervous system even long after exposure.

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