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首页> 外文期刊>Movement disorders >Interaction between blood lead concentration and delta-amino-levulinic acid dehydratase gene polymorphisms increases the odds of essential tremor.
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Interaction between blood lead concentration and delta-amino-levulinic acid dehydratase gene polymorphisms increases the odds of essential tremor.

机译:血铅浓度和δ-氨基乙酰丙酸脱水酶基因多态性之间的相互作用增加了原发性震颤的几率。

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摘要

Blood lead (BPb) concentrations are elevated in essential tremor (ET) cases. The delta-amino-levulinic acid dehydratase (ALAD) gene codes for ALAD, the principal enzyme involved in lead kinetics. Carriers of the ALAD-2 allele may be more susceptible to lead toxicity. The objective of this study was to test, using a case-control design, whether an interaction between BPb concentration and ALAD allele status increases the odds of ET. Mean log BPb concentration was significantly higher in 63 cases than 101 controls (0.47+/-0.26 vs. 0.35+/-0.25 microg/dl). Eighteen (28.6%) cases vs. 17 (16.8%) controls had an ALAD-2 allele (OR=1.98; 95% CI=0.93--4.21). In an adjusted logistic regression analysis, the interaction term (ALAD allele status x log BPb concentration) was associated with increased odds for ET. In stratified analyses, log BPb concentration was not associated with odds of ET in individuals with two ALAD-1 alleles (OR=2.69; 95% CI=0.61--11.82), but in individuals with an ALAD-2 allele, BPb concentration was significantly associated with odds of ET (OR=80.29; 95% CI=3.08--2,096.36). There was an interaction between BPb concentration and ALAD allele status; the odds of ET were greatly elevated in individuals with both an ALAD-2 allele and an elevated BPb concentration. The presence of increased circulating BPb concentrations along with a greater potential for lead toxicity (ALAD-2 allele) could result in greater cerebellar damage, thereby increasing the risk of developing tremor.
机译:在原发性震颤(ET)病例中血铅(BPb)浓度升高。 δ-氨基乙酰丙酸脱水酶(ALAD)基因编码ALAD,ALAD是参与铅动力学的主要酶。 ALAD-2等位基因的携带者可能更容易受到铅毒性的影响。这项研究的目的是使用病例对照设计来测试BPb浓度和ALAD等位基因状态之间的相互作用是否增加ET的几率。 63例患者的平均log BPb浓度显着高于101例对照(0.47 +/- 0.26 vs.0.35 +/- 0.25 microg / dl)。 18例(28.6%)的病例与17例(16.8%)的对照组具有ALAD-2等位基因(OR = 1.98; 95%CI = 0.93--4.21)。在调整后的逻辑回归分析中,相互作用项(ALAD等位基因状态x log BPb浓度)与ET的优势增加相关。在分层分析中,log BPb浓度与两个ALAD-1等位基因(OR = 2.69; 95%CI = 0.61--11.82)的个体的ET几率无关,但在ALAD-2等位基因的个体中,BPb的浓度与ET的几率显着相关(OR = 80.29; 95%CI = 3.08--2,096.36)。 BPb浓度与ALAD等位基因状态之间存在相互作用。既有ALAD-2等位基因又有BPb浓度升高的个体,ET的几率大大提高。循环中BPb浓度增加以及潜在的铅毒性(ALAD-2等位基因)可能会导致小脑损伤,从而增加发生震颤的风险。

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