Department of Epidemiology, Columbia University, 722 West 168(th) Street, NY, New York 10032, USA.
Department of Epidemiology and Biostatistics, University at Albany, 1 University Place, Rensselaer, NY 12144, USA; Department of Environmental Health Sciences, University at Albany, 1 University Place, Rensselaer, NY, 12144, USA.
Sci Total Environ. 2022 Feb 20;808:152150. doi: 10.1016/j.scitotenv.2021.152150. Epub 2021 Dec 3.
BACKGROUND/OBJECTIVE: Research suggests gestational exposure to particulate matter ≤2.5 μm (PM) and extreme heat may independently increase risk of birth defects. We investigated whether duration of gestational extreme heat exposure modifies associations between PM exposure and specific congenital heart defects (CHDs). We also explored nonlinear exposure-outcome relationships.
We identified CHD case children (n = 2824) and non-malformed live-birth control children (n = 4033) from pregnancies ending between 1999 and 2007 in the National Birth Defects Prevention Study, a U.S. population-based multicenter case-control study. We assigned mothers 6-week averages of PM exposure during the cardiac critical period (postconceptional weeks 3-8) using the closest monitor within 50 km of maternal residence. We assigned a count of extreme heat days (EHDs, days above the 90th percentile of daily maximum temperature for year, season, and weather station) during this period using the closest weather station. Using generalized additive models, we explored logit-nonlinear exposure-outcome relationships, concluding logistic models were reasonable. We estimated joint effects of PM and EHDs on six CHDs using logistic regression models adjusted for mean dewpoint and maternal age, education, and race/ethnicity. We assessed multiplicative and additive effect modification.
Conditional on the highest observed EHD count (15) and at least one critical period day during spring/summer, each 5 μg/m increase in average PM exposure was significantly associated with perimembranous ventricular septal defects (VSDpm; OR: 1.54 [95% CI: 1.01, 2.41]). High EHD counts (8+) in the same population were positively, but non-significantly, associated with both overall septal defects and VSDpm. Null or inverse associations were observed for lower EHD counts. Multiplicative and additive effect modification estimates were consistently positive in all septal models.
Results provide limited evidence that duration of extreme heat exposure modifies the PM-septal defects relationship. Future research with enhanced exposure assessment and modeling techniques could clarify these relationships.
背景/目的:研究表明,孕妇在妊娠期接触粒径≤2.5μm(PM)和极端高温可能会独立增加出生缺陷的风险。我们调查了妊娠期极端高温暴露时间是否会改变 PM 暴露与特定先天性心脏病(CHD)之间的关联。我们还探索了非线性暴露-结果关系。
我们从 1999 年至 2007 年期间在美国国家出生缺陷预防研究(一项基于人群的多中心病例对照研究)中结束妊娠的 CHD 病例儿童(n=2824)和非畸形活产对照儿童(n=4033)中确定了病例儿童。我们使用距离母亲居住地 50 公里以内的最近监测器,为母亲在心脏关键期(受孕后第 3-8 周)分配了 6 周的 PM 暴露平均值。我们使用最近的气象站,为这段时间内的极端高温天数(EHD,每天的最高温度超过年、季节和气象站的第 90 个百分位数的天数)分配了一个计数。使用广义加性模型,我们探索了 logit 非线性暴露-结果关系,得出逻辑模型是合理的。我们使用逻辑回归模型,调整了平均露点、母亲年龄、教育程度和种族/民族,估计了 PM 和 EHD 对六种 CHD 的联合效应。我们评估了乘法和加法效应修饰。
在观察到的最高 EHD 计数(15)和春季/夏季至少有一天关键期的条件下,平均 PM 暴露每增加 5μg/m,与膜周室间隔缺损(VSDpm;OR:1.54 [95%CI:1.01,2.41])显著相关。同一人群中高 EHD 计数(8+)与总室间隔缺损和 VSDpm 均呈正相关,但无统计学意义。较低的 EHD 计数观察到的结果为零或负相关。所有室间隔模型的乘法和加法效应修饰估计值均为正值。
结果提供了有限的证据表明,极端高温暴露时间会改变 PM-室间隔缺损的关系。未来的研究可以使用增强的暴露评估和建模技术来澄清这些关系。