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探讨前脑无裂畸形的环境风险因素和基因-环境相互作用。

Identifying environmental risk factors and gene-environment interactions in holoprosencephaly.

机构信息

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.

出版信息

Birth Defects Res. 2021 Jan 1;113(1):63-76. doi: 10.1002/bdr2.1834. Epub 2020 Oct 28.


DOI:10.1002/bdr2.1834
PMID:33111505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9288838/
Abstract

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.

摘要

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。

相似文献

[1]
Identifying environmental risk factors and gene-environment interactions in holoprosencephaly.

Birth Defects Res. 2021-1-1

[2]
Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study.

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[3]
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[4]
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[5]
mutation and fetal alcohol converge on Nodal signaling in a mouse model of holoprosencephaly.

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[6]
Risk factors for nonsyndromic holoprosencephaly: a Manitoba case-control study.

Am J Med Genet A. 2012-3-14

[7]
Nongenetic risk factors for holoprosencephaly: An updated review of the epidemiologic literature.

Am J Med Genet C Semin Med Genet. 2018-5-15

[8]
Rescue of holoprosencephaly in fetal alcohol-exposed Cdon mutant mice by reduced gene dosage of Ptch1.

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[9]
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[10]
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引用本文的文献

[1]
Holoprosencephaly and cyclopia in and Crispant zebrafish.

Anim Cells Syst (Seoul). 2025-7-1

[2]
Examining the Neurodevelopmental Impact of Sonic Hedgehog Pathway Inhibition in Mice.

Birth Defects Res. 2025-4

[3]
Use of an Orthodontic and Otolaryngological Approach in an Infant with Holoprosencephaly.

Children (Basel). 2024-5-5

[4]
Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome.

J Am Heart Assoc. 2024-2-6

[5]
Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management.

Children (Basel). 2023-3-30

[6]
Birth defects data from hospital-based birth defect surveillance in Guilin, China, 2018-2020.

Front Public Health. 2022

[7]
Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man.

Hum Mol Genet. 2023-1-13

[8]
The Survey of the Health of Wisconsin (SHOW) Program: An Infrastructure for Advancing Population Health.

Front Public Health. 2022-3-31

[9]
Concepts in Multifactorial Etiology of Developmental Disorders: Gene-Gene and Gene-Environment Interactions in Holoprosencephaly.

Front Cell Dev Biol. 2021-12-22

[10]
The Role of Sonic Hedgehog in Human Holoprosencephaly and Short-Rib Polydactyly Syndromes.

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本文引用的文献

[1]
mutation and fetal alcohol converge on Nodal signaling in a mouse model of holoprosencephaly.

Elife. 2020-9-2

[2]
Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study.

Environ Health. 2020-6-8

[3]
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations.

Am J Hum Genet. 2019-12-26

[4]
Developmental Toxicity Assessment of Piperonyl Butoxide Exposure Targeting Sonic Hedgehog Signaling and Forebrain and Face Morphogenesis in the Mouse: An and Study.

Environ Health Perspect. 2019-10-23

[5]
Cohesin complex-associated holoprosencephaly.

Brain. 2019-9-1

[6]
Epidemiological characteristics of holoprosencephaly in China, 2007-2014: A retrospective study based on the national birth defects surveillance system.

PLoS One. 2019-6-6

[7]
A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly.

Am J Hum Genet. 2019-4-18

[8]
A forebrain undivided: Unleashing model organisms to solve the mysteries of holoprosencephaly.

Dev Dyn. 2019-5-1

[9]
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.

Brain. 2019-1-1

[10]
Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.

Hum Mutat. 2018-7-26

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