A rare case of early onset lewy body dementia with parkinsonism associated with chronic exposure to copper contaminated drinking water.

IF 3.6 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2024-09-02 eCollection Date: 2024-01-01 DOI:10.3389/ftox.2024.1451235
Marcia H Ratner, Jonathan S Rutchik
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Abstract

There is a well-recognized relationship between a person's body burden of essential trace elements such as copper and their neurological function in which both deficiencies and exposures to excessive concentrations are associated with adverse clinical outcomes. Preclinical studies indicate chronic excess copper exposure is associated with altered motor function, dopaminergic neuronal loss, astrocytosis, and microgliosis. Copper also promotes oligomerization and fibrilization of α-synuclein suggesting it may hasten the course of an α-synucleinopathy. Here we report a rare case of early onset Lewy Body Dementia with Parkinsonism in a 53-year-old Caucasian woman exposed to copper contaminated drinking water for more than 10 years. Her hair and that of her daughter had streaks of blue-green discoloration as did the porcelain sinks in their home. Testing confirmed copper contamination of the drinking water. A neurologist diagnosed her with Lewy Body Dementia with Parkinsonism. Skin biopsy for phosphorylated α was consistent with a diagnosis of an α-synucleinopathy. These findings suggest chronic exposure to excessive copper may act as disease modifying factor in Lewy Body Dementia with Parkinsonism. It has previously been recommended that individuals at risk of Alzheimer's disease (AD) avoid excessive intake of copper. Genetic studies indicate that Lewy Body Dementia shares risk factors and pathways with AD. Based on the observations in this patient we recommend that individuals at risk for an α-synucleinopathy based on a positive family history, genetic testing, and/or positive results on a skin biopsy for phosphorylated α-synuclein avoid exposure to excess copper.

一例与长期接触受铜污染的饮用水有关的早发性白质痴呆伴帕金森病的罕见病例。
铜等人体必需微量元素的含量与其神经功能之间存在着公认的关系,缺乏铜或铜含量过高都会导致不良的临床结果。临床前研究表明,长期过量接触铜与运动功能改变、多巴胺能神经元丧失、星形胶质细胞增多症和小胶质细胞增多症有关。铜还能促进α-突触核蛋白的寡聚化和纤维化,这表明铜可能会加速α-突触核蛋白病的进程。在此,我们报告了一例罕见的早发卢瓦体痴呆伴帕金森病病例,患者是一名 53 岁的白种女性,接触铜污染的饮用水长达 10 多年。她和她女儿的头发以及家中的陶瓷水槽都出现了蓝绿色变色条纹。检测证实饮用水受到铜污染。神经科医生诊断她患有路易体痴呆症和帕金森症。皮肤活检的磷酸化 α 与 α-突触核蛋白病的诊断一致。这些研究结果表明,长期接触过量铜可能会成为路易体痴呆伴帕金森病的疾病改变因素。以前曾建议有阿尔茨海默病(AD)风险的人避免摄入过量的铜。遗传学研究表明,路易体痴呆症与阿兹海默症具有相同的风险因素和发病途径。根据对该患者的观察,我们建议有α-突触核蛋白病风险的人,如果家族史、基因检测和/或皮肤活检中磷酸化α-突触核蛋白检测结果呈阳性,则应避免接触过量铜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
0.00%
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0
审稿时长
13 weeks
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