EXPOSURE, DOSE, BODY BURDEN AND HEALTH EFFECTS OF LEAD
铅的暴露、剂量、身体负担和健康影响
基本信息
- 批准号:2882833
- 负责人:
- 金额:$ 55万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1997
- 资助国家:美国
- 起止时间:1997-03-01 至 2001-02-28
- 项目状态:已结题
- 来源:
- 关键词:binding proteins blood toxicology bone chemical binding chemical kinetics clearance rate clinical research cytotoxicity environmental toxicology epidemiology hemotoxin human subject lead lead poisoning longitudinal human study neurotoxicology neurotoxins outcomes research porphobilinogen synthase protein isoforms renal toxin succinates
项目摘要
Lead is a ubiquitous toxin and several biologic measures are available
to assess its absorption, deposition, and health consequences. Blood
lead (BLLs) and zinc protoporphyrin, commonly used measures, are
poor predictors of health effects and are influenced by external
exposure, internal lead stores, and interindividual differences in the
toxicokinetics of lead. Other measures of lead absorption and burden
have been developed (e.g., DMSA-chelatable lead, bone lead), but
these have not been evaluated in prospective studies of health effects.
Furthermore, there is little understanding of how individual factors may
influence relations between these biologic measures and health effects.
Increasingly, research has been directed at discovering interactions
between individual factors and hazardous exposures. Interindividual
differences in lead toxico-kinetics and toxicity are likely to be
mediated, in part, by genetic factors, including polymorph-isms in
proteins that differentially bind lead and affect its metabolism.
Accumulating evidence suggests that delta-aminolevulinic acid
dehydratase (ALAD), a polymorphic erythrocyte cytoplasmic enzyme,
modifies lead~s toxicokinetics. We propose a prospective study of the
relations among BLLs, DMSA-chelatable lead, bone lead, and health
effects (heme synthesis, renal early biologic effects and function, blood
pressure, and CNS and PNS function) in lead workers in South Korea.
Effect modification of these relations by ALAD genotype will also be
investigated. This population is uniquely suited to investigation of
gene-environment interaction because of its broad range of lead
exposures, covering the entire range observed in the U.S., and large
numbers of new hires. All current workers will be enrolled in the first
year (N=640) and new hires will be enrolled for 2 years (N=230);
these two groups will be compared with 120 nonexposed controls.
Study measures will be obtained longitudinally, 3 times during the 4
year study. This proposal offers an understanding of the composite
roles of BLLs, bone lead, and DMSA-chelatable lead, and effect
modification by ALAD genotype, in the prediction of important health
outcomes.
铅是一种普遍存在的毒素,有多种生物措施可供选择
评估其吸收、沉积和健康后果。 血
常用的测量方法是铅 (BLL) 和锌原卟啉
健康影响的预测能力较差,并受到外部因素的影响
暴露、内部铅储存以及个体间差异
铅的毒代动力学。 铅吸收和负担的其他措施
已经开发出来(例如,DMSA-螯合铅、骨铅),但是
这些尚未在健康影响的前瞻性研究中进行评估。
此外,人们对于个体因素如何影响我们知之甚少。
影响这些生物措施与健康效应之间的关系。
研究越来越多地致力于发现相互作用
个体因素和危险暴露之间的关系。 个体间
铅毒代动力学和毒性的差异可能是
部分由遗传因素介导,包括基因多态性
不同程度地结合铅并影响其代谢的蛋白质。
越来越多的证据表明 δ-氨基乙酰丙酸
脱水酶(ALAD),一种多态性红细胞胞质酶,
改变铅的毒代动力学。 我们提出一项前瞻性研究
BLL、DMSA 螯合铅、骨铅与健康之间的关系
影响(血红素合成、肾脏早期生物效应和功能、血液
韩国铅工人的压力、中枢神经系统和三七总皂甙功能)。
ALAD 基因型对这些关系的影响修改也将是
调查了。 这个人群特别适合调查
基因-环境相互作用,因为其广泛的铅
暴露范围,涵盖在美国观察到的整个范围,并且大
新员工数量。 所有现有工人将首先注册
年(N=640),新员工入职2年(N=230);
这两组将与 120 个未暴露的对照进行比较。
研究测量将纵向获得,在 4 年内进行 3 次
年学习。 该提案提供了对复合材料的理解
BLL、骨铅和 DMSA 螯合铅的作用和效果
通过 ALAD 基因型进行修饰,预测重要的健康状况
结果。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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BRIAN Seth SCHWARTZ其他文献
BRIAN Seth SCHWARTZ的其他文献
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{{ truncateString('BRIAN Seth SCHWARTZ', 18)}}的其他基金
Marcellus shale development, respiratory & reproductive outcomes in Pennsylvania
马塞勒斯页岩开发,呼吸
- 批准号:
8787106 - 财政年份:2013
- 资助金额:
$ 55万 - 项目类别:
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马塞勒斯页岩开发,呼吸
- 批准号:
8622523 - 财政年份:2013
- 资助金额:
$ 55万 - 项目类别:
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- 批准号:
6311316 - 财政年份:2000
- 资助金额:
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- 批准号:
6771794 - 财政年份:2000
- 资助金额:
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Explaining Disparities in Cognitive Function in Seniors
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- 批准号:
8062046 - 财政年份:2000
- 资助金额:
$ 55万 - 项目类别:
EXPLAINING DISPARITIES IN COGNITIVE FUNCTION IN SENIORS
解释老年人认知功能的差异
- 批准号:
6372563 - 财政年份:2000
- 资助金额:
$ 55万 - 项目类别:
EXPLAINING DISPARITIES IN COGNITIVE FUNCTION IN SENIORS
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- 批准号:
6649833 - 财政年份:2000
- 资助金额:
$ 55万 - 项目类别:
Explaining Disparities in Cognitive Function in Seniors
解释老年人认知功能的差异
- 批准号:
7459324 - 财政年份:2000
- 资助金额:
$ 55万 - 项目类别:
Explaining Disparities in Cognitive Function in Seniors
解释老年人认知功能的差异
- 批准号:
7617592 - 财政年份:2000
- 资助金额:
$ 55万 - 项目类别:














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