Geographic distributions of motor neuron disease mortality and well water use in U.S. counties

IF 2.5 4区 医学 Q2 CLINICAL NEUROLOGY Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Pub Date : 2017-04-03 DOI:10.1080/21678421.2016.1264975
G. Schwartz, B. Rundquist, Isaac J. Simon, S. Swartz
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引用次数: 14

Abstract

Abstract Objective: We recently reported that U.S. mortality rates for motor neuron disease (MND) at the level of the state are associated with well water use. However, data at the state level may not accurately reflect data at the individual level. We therefore examined the association between MND mortality and well water use utilizing data from smaller geographic units that may better reflect exposure and disease at the individual level. Methods: We used data on age-adjusted MND mortality rates at the level of the county, obtained from the CDC, and corresponding data on the prevalence of well water use, obtained from the U.S. Geological Survey. Data were analyzed by multivariate linear regression and by Getis-Ord Gi*, a measure of spatial clustering. Results: Age-adjusted mortality rates for MND in 923 U.S. counties were significantly correlated with the prevalence of well water (p < 0.0001). ‘Hot spots’ of MND mortality were significantly associated with ‘hot spots’ of well water use (p < 0.0005). Conclusions: These findings support the hypothesis that an agent present in well water plays an etiologic role in ALS. Further study of water use among individuals with ALS is warranted.
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美国各县运动神经元疾病死亡率和井水使用的地理分布
摘要目的:我们最近报道了美国运动神经元疾病(MND)的死亡率与井水的使用有关。然而,国家层面的数据可能无法准确反映个人层面的数据。因此,我们利用较小地理单元的数据研究了MND死亡率与井水使用之间的关系,这些数据可能更好地反映个体水平上的暴露和疾病。方法:我们使用了从美国疾病控制与预防中心获得的该县经年龄调整的MND死亡率数据,以及从美国地质调查局获得的井水使用率的相应数据。数据通过多元线性回归和Getis Ord Gi*(一种空间聚类的度量)进行分析。结果:923例MND的年龄调整死亡率 美国各县与井水的流行率显著相关(p < 0.0001)。MND死亡率的“热点”与井水使用的“热点点”显著相关(p < 0.0005)。结论:这些发现支持了存在于井水中的药剂在ALS中起病因作用的假设。有必要对ALS患者的用水情况进行进一步研究。
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来源期刊
CiteScore
5.40
自引率
10.70%
发文量
64
期刊介绍: Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration is an exciting new initiative. It represents a timely expansion of the journal Amyotrophic Lateral Sclerosis in response to the clinical, imaging pathological and genetic overlap between ALS and frontotemporal dementia. The expanded journal provides outstanding coverage of research in a wide range of issues related to motor neuron diseases, especially ALS (Lou Gehrig’s disease) and cognitive decline associated with frontotemporal degeneration. The journal also covers related disorders of the neuroaxis when relevant to these core conditions.
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