Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA.
Cardiovascular & Pulmonary Branch, National Heart, Lung, and Blood Institute, The National Institutes of Health, Bethesda, Maryland, USA.
Birth Defects Res. 2021 Jan 1;113(1):63-76. doi: 10.1002/bdr2.1834. Epub 2020 Oct 28.
BACKGROUND: Holoprosencephaly is the most common malformation of the forebrain (1 in 250 embryos) with severe consequences for fetal and child development. This study evaluates nongenetic factors associated with holoprosencephaly risk, severity, and gene-environment interactions. METHODS: For this retrospective case control study, we developed an online questionnaire focusing on exposures to common and rare toxins/toxicants before and during pregnancy, nutritional factors, maternal health history, and demographic factors. Patients with holoprosencephaly were primarily ascertained from our ongoing genetic and clinical studies of holoprosencephaly. Controls included children with Williams-Beuren syndrome (WBS) ascertained through online advertisements in a WBD support group and fliers. RESULTS: Difference in odds of exposures between cases and controls as well as within cases with varying holoprosencephaly severity were studied. Cases included children born with holoprosencephaly (n = 92) and the control group consisted of children with WBS (n = 56). Pregnancy associated risk associated with holoprosencephaly included maternal pregestational diabetes (9.2% of cases and 0 controls, p = .02), higher alcohol consumption (adjusted odds ratio [aOR], 1.73; 95% CI, 0.88-15.71), and exposure to consumer products such as aerosols or sprays including hair sprays (aOR, 2.46; 95% CI, 0.89-7.19). Significant gene-environment interactions were identified including for consumption of cheese (p < .05) and espresso drinks (p = .03). CONCLUSION: The study identifies modifiable risk factors and gene-environment interactions that should be considered in future prevention of holoprosencephaly. Studies with larger HPE cohorts will be needed to confirm these findings.
背景:前脑无脑畸形(holoprosencephaly,HPE)是最常见的前脑畸形(1/250 胚胎),对胎儿和儿童发育有严重影响。本研究评估了与 HPE 风险、严重程度相关的非遗传因素以及基因-环境相互作用。
方法:本回顾性病例对照研究通过在线问卷调查的方式,重点调查了妊娠前和妊娠期间常见和罕见的毒素/毒物、营养因素、母体健康史和人口统计学因素。HPE 患者主要通过我们正在进行的 HPE 遗传和临床研究确定,对照组包括通过 WBS 支持组织的在线广告和传单确定的患有威廉姆斯-比伦综合征(Williams-Beuren syndrome,WBS)的儿童。
结果:研究了病例与对照组之间以及不同严重程度 HPE 病例之间暴露差异的比值比(odds ratio,OR)。病例组包括出生时患有 HPE 的儿童(n=92),对照组由患有 WBS 的儿童组成(n=56)。与 HPE 相关的妊娠风险包括母亲孕前糖尿病(病例中为 9.2%,对照组中为 0,p=0.02)、更高的酒精摄入量(校正 OR,1.73;95%置信区间,0.88-15.71),以及接触气溶胶或喷雾等消费品,包括发胶(aOR,2.46;95%CI,0.89-7.19)。确定了显著的基因-环境相互作用,包括奶酪(p<0.05)和浓咖啡(p=0.03)的摄入量。
结论:该研究确定了可改变的危险因素和基因-环境相互作用,应在未来预防 HPE 中考虑。需要有更大的 HPE 队列研究来证实这些发现。
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