Rahman Mohammad L, Valeri Linda, Kile Molly L, Mazumdar Maitreyi, Mostofa Golam, Qamruzzaman Qazi, Rahman Mahmudur, Baccarelli Andrea, Liang Liming, Hauser Russ, Christiani David C
Harvard T.H. Chan School of Public Health, Department of Environmental Health, Boston, MA, USA.
McLean Hospital, Belmont, Massachusetts, USA, Harvard Medical School, Boston, MA, USA.
Environ Int. 2017 Nov;108:32-40. doi: 10.1016/j.envint.2017.07.026. Epub 2017 Aug 5.
Shortening of gestation and intrauterine growth restriction (IUGR) are the two main determinants of birthweight. Low birthweight has been linked with prenatal arsenic exposure, but the causal relation between arsenic and birthweight is not well understood.
We applied a quantile causal mediation analysis approach to determine the association between prenatal arsenic exposure and birthweight in relation to shortening of gestation and IUGR, and whether the susceptibility of arsenic exposure varies by infant birth sizes.
In a longitudinal birth cohort in Bangladesh, we measured arsenic in drinking water (n=1182) collected at enrollment and maternal toenails (n=1104) collected ≤1-month postpartum using inductively coupled plasma mass spectrometry. Gestational age was determined using ultrasound at ≤16weeks' gestation. Demographic information was collected using a structured questionnaire.
Of 1184 singleton livebirths, 16.4% (n=194) were low birthweight (<2500g), 21.9% (n=259) preterm (<37weeks' gestation), and 9.2% (n=109) both low birthweight and preterm. The median concentrations of arsenic in drinking water and maternal toenails were 2.2μg/L (range: below the level of detection [LOD]-1400) and 1.2μg/g (range: <LOD-46.6), respectively. Prenatal arsenic exposure was negatively associated with birthweight, where the magnitude of the association varied across birthweight percentiles. The effect of arsenic on birthweight mediated via shortening of gestation affected all infants irrespective of birth sizes (β range: 10th percentile=-19.7g [95% CI: -26.7, -13.3] to 90th percentile=-10.9g [95% CI: -18.5, -5.9] per natural log water arsenic increase), whereas the effect via pathways independent of gestational age affected only the smaller infants (β range: 10th percentile=-28.0g [95% CI: -43.8, -9.9] to 20th percentile=-14.9g [95% CI: -30.3, -1.7] per natural log water arsenic increase). Similar pattern was observed for maternal toenail arsenic.
The susceptibility of prenatal arsenic exposure varied by infant birth sizes, placing smaller infants at greater risk of lower birthweight by shortening of gestation and possibly growth restriction. It is important to mitigate prenatal arsenic exposure to improve perinatal outcomes in Bangladesh.
孕期缩短和宫内生长受限(IUGR)是出生体重的两个主要决定因素。低出生体重与产前砷暴露有关,但砷与出生体重之间的因果关系尚未完全明确。
我们采用分位数因果中介分析方法,以确定产前砷暴露与出生体重之间在孕期缩短和IUGR方面的关联,以及砷暴露的易感性是否因婴儿出生大小而异。
在孟加拉国的一个纵向出生队列中,我们使用电感耦合等离子体质谱法测量了入组时收集的饮用水中的砷(n = 1182)和产后≤1个月收集的产妇趾甲中的砷(n = 1104)。在妊娠≤16周时通过超声确定孕周。使用结构化问卷收集人口统计学信息。
在1184例单胎活产中,16.4%(n = 194)为低出生体重(<2500g),21.9%(n = 259)为早产(<37周妊娠),9.2%(n = 109)既为低出生体重又为早产。饮用水和产妇趾甲中砷的中位数浓度分别为2.2μg/L(范围:低于检测限[LOD] - 1400)和1.2μg/g(范围:<LOD - 46.6)。产前砷暴露与出生体重呈负相关,且这种关联的程度在不同出生体重百分位数之间有所不同。砷通过孕期缩短对出生体重的影响在所有婴儿中均有体现,无论出生大小如何(β范围:第10百分位数=-19.7g [95%置信区间:-26.7,-13.3]至第90百分位数=-10.9g [95%置信区间:-18.5,-5.9],每自然对数单位的饮用水砷增加),而通过独立于孕周的途径产生的影响仅在较小的婴儿中出现(β范围:第10百分位数=-28.0g [95%置信区间:-43.8,-9.9]至第20百分位数=-14.9g [95%置信区间:-30.3,-1.7],每自然对数单位的饮用水砷增加)。产妇趾甲砷也观察到类似模式。
产前砷暴露的易感性因婴儿出生大小而异,较小的婴儿因孕期缩短和可能的生长受限而面临更低出生体重的更大风险。在孟加拉国减轻产前砷暴露对于改善围产期结局很重要。