Early Environmental Upheaval and the Risk for Schizophrenia.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2021-05-07 Epub Date: 2021-02-05 DOI:10.1146/annurev-clinpsy-081219-103805
Vincent Paquin, Mylène Lapierre, Franz Veru, Suzanne King
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引用次数: 21

Abstract

Why does prenatal exposure to wars, natural disasters, urbanicity, or winter increase the risk for schizophrenia? Research from the last two decades has provided rich insight about the underlying chains of causation at play during environmental upheaval, from conception to early infancy. In this review, we appraise the evidence linking schizophrenia spectrum disorder to prenatal maternal stress, obstetric complications, early infections, and maternal nutrition and other lifestyle factors. We discuss putative mechanisms, including the maternal stress system, perinatal hypoxia, and maternal-offspring immune activation. We propose that gene-environment interactions, timing during development, and sex differentiate the neuropsychiatric outcomes. Future research should pursue the translation of animal studies to humans and the longitudinal associations between early exposures, intermediate phenotypes, and psychiatric disorders. Finally, to paint a comprehensive model of risk and to harness targets for prevention, we argue that risk factors should be situated within the individual's personal ecosystem.

早期环境剧变与精神分裂症的风险。
为什么产前暴露于战争、自然灾害、城市化或冬季会增加患精神分裂症的风险?过去二十年的研究提供了丰富的见解,揭示了从怀孕到婴儿早期,在环境剧变中起作用的潜在因果链。在这篇综述中,我们评估了将精神分裂症谱系障碍与产前产妇压力、产科并发症、早期感染、产妇营养和其他生活方式因素联系起来的证据。我们讨论了可能的机制,包括母亲的应激系统,围产期缺氧,和母婴免疫激活。我们认为,基因-环境相互作用、发育时间和性别会区分神经精神病学结果。未来的研究应该将动物研究转化为人类研究,以及早期暴露、中间表型和精神疾病之间的纵向关联。最后,为了描绘一个全面的风险模型并利用预防目标,我们认为风险因素应该位于个人的个人生态系统中。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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