Department of Environmental and Occupational Health, Milken Institute of Public Health, George Washington University, 950 New Hampshire Ave NW #2, Washington, DC, 20052, USA.
Neonatal-Perinatal Medicine, Riley Children's Hospital, Indiana University School of Medicine, 699 Riley Hospital Dr RR 208, Indianapolis, IN, 46202, USA.
BMC Public Health. 2023 Nov 22;23(1):2308. doi: 10.1186/s12889-023-17171-9.
The objective of the Heartland Study is to address major knowledge gaps concerning the health effects of herbicides on maternal and infant health. To achieve this goal, a two-phased, prospective longitudinal cohort study is being conducted. Phase 1 is designed to evaluate associations between biomarkers of herbicide concentration and pregnancy/childbirth outcomes. Phase 2 is designed to evaluate potential associations between herbicide biomarkers and early childhood neurological development.
People (target enrollment of 2,000) who are seeking prenatal care, are ages 18 or older, and are ≤ 20 + 6 weeks gestation will be eligible for recruitment. The Heartland Study will utilize a combination of questionnaire data and biospecimen collections to meet the study objectives. One prenatal urine and buccal sample will be collected per trimester to assess the impact of herbicide concentration levels on pregnancy outcomes. Infant buccal specimens will be collected post-delivery. All questionnaires will be collected by trained study staff and clinic staff will remain blinded to all individual level research data. All data will be stored in a secure REDCap database. Hospitals in the agriculturally intensive states in the Midwestern region will be recruited as study sites. Currently participating clinical sites include Indiana University School of Medicine- affiliated Hospitals in Indianapolis, Indiana; Franciscan Health Center in Indianapolis, Indiana; Gundersen Lutheran Medical Center in La Crosse, Wisconsin, and University of Iowa in Iowa City, Iowa. An anticipated 30% of the total enrollment will be recruited from rural areas to evaluate herbicide concentrations among those pregnant people residing in the rural Midwest. Perinatal outcomes (e.g. birth outcomes, preterm birth, preeclampsia, etc.) will be extracted by trained study teams and analyzed for their relationship to herbicide concentration levels using appropriate multivariable models.
Though decades of study have shown that environmental chemicals may have important impacts on the health of parents and infants, there is a paucity of prospective longitudinal data on reproductive impacts of herbicides. The recent, rapid increases in herbicide use across agricultural regions of the United States necessitate further research into the human health effects of these chemicals, particularly in pregnant people. The Heartland Study provides an invaluable opportunity to evaluate health impacts of herbicides during pregnancy and beyond.
The study is registered at clinicaltrials.gov, NCT05492708 with initial registration and release 05 August, 2022.
“中心地带研究”旨在解决有关除草剂对母婴健康影响的主要知识空白。为了实现这一目标,正在进行一项两阶段、前瞻性纵向队列研究。第一阶段旨在评估除草剂浓度生物标志物与妊娠/分娩结局之间的关联。第二阶段旨在评估除草剂生物标志物与儿童早期神经发育之间的潜在关联。
正在寻求产前护理的人群(目标入组人数为 2000 人)年龄在 18 岁或以上,且妊娠 20+6 周以内,将有资格参加招募。“中心地带研究”将结合问卷调查数据和生物样本采集来实现研究目标。每个孕期将采集一次产前尿液和口腔样本,以评估除草剂浓度水平对妊娠结局的影响。分娩后将采集婴儿口腔样本。所有问卷将由经过培训的研究人员收集,临床工作人员将对所有个人研究数据保持盲态。所有数据将存储在一个安全的 REDCap 数据库中。将招募农业密集型中西部地区的医院作为研究点。目前参与的临床地点包括印第安纳大学医学院附属印第安纳波利斯医院、印第安纳州的弗朗西斯克健康中心、威斯康星州拉克罗斯的冈德森路德医学中心和爱荷华州的爱荷华大学。预计总入组人数的 30%将来自农村地区,以评估居住在中西部农村地区的孕妇的除草剂浓度。经过培训的研究团队将提取围产期结局(例如出生结局、早产、子痫前期等)数据,并使用适当的多变量模型分析其与除草剂浓度水平的关系。
尽管数十年来的研究表明环境化学物质可能对父母和婴儿的健康产生重要影响,但关于除草剂对生殖的影响,前瞻性纵向数据仍然很少。最近,美国农业地区除草剂使用的迅速增加需要进一步研究这些化学物质对人类健康的影响,特别是在孕妇中。“中心地带研究”为评估怀孕期间及以后除草剂的健康影响提供了宝贵的机会。
该研究在 clinicaltrials.gov 注册,注册号为 NCT05492708,初始注册和发布日期为 2022 年 8 月 5 日。