在子宫内砷暴露和早期儿童运动发育在新罕布什尔州出生队列研究

Frontiers in epidemiology Pub Date : 2023-05-09 eCollection Date: 2023-01-01 DOI:10.3389/fepid.2023.1139337
Erin E Butler, Margaret R Karagas, Eugene Demidenko, David C Bellinger, Susan A Korrick
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引用次数: 0

摘要

引言亚洲几个地区(如孟加拉国)的产前和儿童期高水平砷暴露特征可能会影响运动功能。然而,尽管儿童时期缺乏运动技能可能会产生不利的长期后果,但较低水平的砷暴露(其他地区的特征)与运动发育之间的关系在很大程度上尚未得到研究。因此,我们试图在新罕布什尔州出生队列研究中调查395名儿童的产前砷暴露与运动功能之间的关系,该研究是一项来自新英格兰北部的农村队列研究。方法通过使用高效液相色谱(HPLC)电感耦合等离子体质谱(ICP-MS)测量妊娠24-28周时母体尿液中特定的As,并将无机As、一甲基亚砷酸和二甲基亚胂酸相加,获得总尿As(tAs),来估计产前暴露量。在平均(SD)年龄5.5(0.4)岁时,用Bruininks-Oseretsky运动能力测试第二版(BOT-2)评估运动功能。结果完成这项考试的孩子主要是白人(97%),已婚母亲(86%)拥有大学或更高学历(67%)所生。中位(IQR)妊娠期尿液tAs浓度为4.0(5.0)µg/L。整体运动能力的平均(SD)BOT-2分为48.6(8.4),精细手动控制的平均(标准分)为48.2(9.6) = 50(10)],精细运动积分为16.3(5.1),精细运动精度为12.5(4.1)[标准分 = 15(5)]。我们发现了非线性剂量-反应关系的证据,并使用变化点模型来评估tAs与整体运动能力、精细运动整合指数、精细运动精度及其复合精细手动控制的关系,并根据年龄和性别进行调整。在针对潜在混杂因素进行调整的模型中,当tAs浓度大于9.5的变化点时,尿液tAs每增加一倍,整体运动能力就会降低-3.3分(95%置信区间:-6.1,-0.4) µg/L,并且当tAs浓度大于17.0的变化点时,精细运动积分降低了–4.3个点(95%置信区间:–8.0,–0.6) µg/L。讨论总之,我们发现,在美国人群中,产前As暴露水平高于经验推导的阈值(即变化点)与儿童运动发育下降有关。
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In utero arsenic exposure and early childhood motor development in the New Hampshire Birth Cohort Study.

Introduction: High-level prenatal and childhood arsenic (As) exposure characteristic of several regions in Asia (e.g., Bangladesh), may impact motor function. However, the relationship between lower-level arsenic exposure (characteristic of other regions) and motor development is largely unstudied, despite the potential for deficient motor skills in childhood to have adverse long-term consequences. Thus, we sought to investigate the association between prenatal As exposure and motor function among 395 children in the New Hampshire Birth Cohort Study, a rural cohort from northern New England.

Methods: Prenatal exposure was estimated by measuring maternal urine speciated As at 24-28 weeks of gestation using high-performance liquid chromatography (HPLC) inductively coupled plasma mass spectrometry (ICP-MS) and summing inorganic As, monomethylarsonic acid, and dimethylarsinic acid to obtain total urinary As (tAs). Motor function was assessed with the Bruininks-Oseretsky Test of Motor Proficiency, 2nd Edition (BOT-2) at a mean (SD) age of 5.5 (0.4) years.

Results: Children who completed this exam were largely reported as white race (97%), born to married mothers (86%) with a college degree or higher (67%). The median (IQR) gestational urine tAs concentration was 4.0 (5.0) µg/L. Mean (SD) BOT-2 scores were 48.6 (8.4) for overall motor proficiency and 48.2 (9.6) for fine manual control [standard score = 50 (10)], and were 16.3 (5.1) for fine motor integration and 12.5 (4.1) for fine motor precision [standard score = 15 (5)]. We found evidence of a non-linear dose response relationship and used a change-point model to assess the association of tAs with overall motor proficiency and indices of fine motor integration, fine motor precision, and their composite, fine manual control, adjusted for age and sex. In models adjusted for potential confounders, each doubling of urine tAs decreased overall motor proficiency by -3.3 points (95% CI: -6.1, -0.4) for tAs concentrations greater than the change point of 9.5 µg/L and decreased fine motor integration by -4.3 points (95% CI: -8.0, -0.6) for tAs concentrations greater than the change point of 17.0 µg/L.

Discussion: In summary, we found that levels of prenatal As exposure above an empirically-derived threshold (i.e., the change point) were associated with decrements in childhood motor development in a US population.

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