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本文引用的文献

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Oxidative stress during acetaminophen hepatotoxicity: Sources, pathophysiological role and therapeutic potential.对乙酰氨基酚肝毒性中的氧化应激:来源、病理生理作用及治疗潜力。
Redox Biol. 2016 Dec;10:148-156. doi: 10.1016/j.redox.2016.10.001. Epub 2016 Oct 4.
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Acetaminophen from liver to brain: New insights into drug pharmacological action and toxicity.对乙酰氨基酚从肝脏到大脑:药物药理作用及毒性的新见解
Pharmacol Res. 2016 Jul;109:119-31. doi: 10.1016/j.phrs.2016.02.020. Epub 2016 Feb 26.
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The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.小鼠母体白细胞介素-17a通路促进后代出现自闭症样表型。
Science. 2016 Feb 26;351(6276):933-9. doi: 10.1126/science.aad0314. Epub 2016 Jan 28.
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Maternal use of acetaminophen during pregnancy and risk of autism spectrum disorders in childhood: A Danish national birth cohort study.孕期母亲使用对乙酰氨基酚与儿童自闭症谱系障碍风险:一项丹麦全国出生队列研究
Autism Res. 2016 Sep;9(9):951-8. doi: 10.1002/aur.1591. Epub 2015 Dec 21.
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Infections and Brain Development.感染与大脑发育
Obstet Gynecol Surv. 2015 Oct;70(10):644-55. doi: 10.1097/OGX.0000000000000236.
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Regulation of neuronal migration, an emerging topic in autism spectrum disorders.神经元迁移的调控,这是自闭症谱系障碍中一个新兴的研究课题。
J Neurochem. 2016 Feb;136(3):440-56. doi: 10.1111/jnc.13403. Epub 2015 Nov 13.
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Aniline Is Rapidly Converted Into Paracetamol Impairing Male Reproductive Development.苯胺可迅速转化为对乙酰氨基酚,损害雄性生殖发育。
Toxicol Sci. 2015 Nov;148(1):288-98. doi: 10.1093/toxsci/kfv179. Epub 2015 Aug 10.
8
Prenatal Infection and Autism Spectrum Disorders in Childhood: A Population-Based Case-Control Study in Taiwan.产前感染与儿童自闭症谱系障碍:台湾一项基于人群的病例对照研究
Paediatr Perinat Epidemiol. 2015 Jul;29(4):307-16. doi: 10.1111/ppe.12194. Epub 2015 May 19.
9
Association of maternal report of infant and toddler gastrointestinal symptoms with autism: evidence from a prospective birth cohort.婴幼儿胃肠道症状的母亲报告与自闭症的关联:来自一项前瞻性出生队列研究的证据
JAMA Psychiatry. 2015 May;72(5):466-74. doi: 10.1001/jamapsychiatry.2014.3034.
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The emerging picture of autism spectrum disorder: genetics and pathology.自闭症谱系障碍的新图景:遗传学和病理学。
Annu Rev Pathol. 2015;10:111-44. doi: 10.1146/annurev-pathol-012414-040405.

产前发热与自闭症风险。

Prenatal fever and autism risk.

机构信息

Center for Infection and Immunity, Mailman School of Public Health, Columbia University, New York, NY, USA.

Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.

出版信息

Mol Psychiatry. 2018 Mar;23(3):759-766. doi: 10.1038/mp.2017.119. Epub 2017 Jun 13.

DOI:10.1038/mp.2017.119
PMID:28607458
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5822459/
Abstract

Some studies suggest that prenatal infection increases risk of autism spectrum disorders (ASDs). This study was undertaken in a prospective cohort in Norway to examine whether we could find evidence to support an association of the prenatal occurrence of fever, a common manifestation of infection, with ASD risk. Prospective questionnaires provided maternal exposure data; case status was established from clinical assessments and registry linkages. In a large, prospectively ascertained cohort of pregnant mothers and their offspring, we examined infants born ⩾32 weeks for associations between fever exposure in each trimester and ASD risk using logistic regression. Maternal exposure to second-trimester fever was associated with increased ASD risk, adjusting for presence of fever in other trimesters and confounders (adjusted odds ratio (aOR), 1.40; 95% confidence interval, 1.09-1.79), with a similar, but nonsignificant, point estimate in the first trimester. Risk increased markedly with exposure to three or more fever episodes after 12 weeks' gestation (aOR, 3.12; 1.28-7.63). ASD risk appears to increase with maternal fever, particularly in the second trimester. Risk magnified dose dependently with exposure to multiple fevers after 12 weeks' gestation. Our findings support a role for gestational maternal infection and innate immune responses to infection in the pathogenesis of at least some cases of ASD.

摘要

一些研究表明,产前感染会增加自闭症谱系障碍(ASD)的风险。本研究在挪威的一项前瞻性队列中进行,旨在检验我们是否能够找到支持产前发热(感染的常见表现)与 ASD 风险之间存在关联的证据。前瞻性问卷调查提供了母亲暴露数据;病例状态是通过临床评估和登记处链接确定的。在一项大规模的、前瞻性确定的孕妇及其后代队列中,我们使用逻辑回归检验了每个孕期发热暴露与 ASD 风险之间的关系,研究对象为 ⩾32 周出生的婴儿。调整其他孕期发热情况和混杂因素后,母亲在孕中期发热与 ASD 风险增加相关(调整后的优势比(aOR),1.40;95%置信区间,1.09-1.79),在孕早期的点估计值相似但无统计学意义。在妊娠 12 周后暴露于三次或更多发热发作时,风险显著增加(aOR,3.12;1.28-7.63)。母亲发热似乎会增加 ASD 风险,尤其是在孕中期。风险随着孕 12 周后多次发热暴露呈剂量依赖性增加。我们的研究结果支持妊娠期间母体感染和对感染的固有免疫反应在至少某些 ASD 病例发病机制中的作用。