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首页> 外文期刊>Journal of psychiatry & neuroscience: JPN >Diabetes mellitus during pregnancy and increased risk of schizophrenia in offspring: a review of the evidence and putative mechanisms.
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Diabetes mellitus during pregnancy and increased risk of schizophrenia in offspring: a review of the evidence and putative mechanisms.

机译:妊娠期糖尿病和后代精神分裂症风险增加:证据和推定机制的综述。

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OBJECTIVE: To identify converging themes from the neurodevelopmental hypothesis of schizophrenia and the pathophysiology of diabetic pregnancy and to examine mechanisms by which diabetes mellitus in a pregnant mother may increase the risk of schizophrenia in offspring. METHODS: We reviewed relevant publications on clinical, epidemiologic and animal studies of diabetic pregnancy and the neurodevelopmental aspects of schizophrenia. RESULTS: Epidemiologic studies have shown that the offspring of mothers who experienced diabetes mellitus during their pregnancies are 7 times more likely to develop schizophrenia, compared with those who were not exposed to diabetic pregnancy. Maternal hyperglycemia during pregnancy could predispose to schizophrenia in adult life through at least 3 prenatal mechanisms: hypoxia, oxidative stress and increased inflammation. Hyperglycemia increases oxidative stress, alters lipid metabolism, affects mitochondrial structure, causes derangements in neural cell processes and neuronal architecture and results in premature specialization before neural tube closure. The molecular mechanisms underlying these processes include the generation of excess oxyradicals and lipid peroxide intermediates as well as reductions in levels of polyunsaturated fatty acids that are known to cause increased dopaminergic and lowered gamma-aminobutyric acidergic activity. The combination of hyperglycemia and hypoxia in pregnancy also leads to altered immune function including increased tumour necrosis factor-alpha, C-reactive protein and upregulation of other proinflammatory cytokines. Finally, maternal hyperglycemia could have a lasting impact on fetal cellular physiology, resulting in increased vulnerability to stress and predisposition to schizophrenia via a mechanism known as programming. These prenatal events can also result in obstetric complications such as fetal growth abnormalities and increased susceptibility to prenatal infection, all of which are associated with a spectrum of neurodevelopmental anomalies and an enhanced risk of schizophrenia. CONCLUSION: On the basis of the evidence presented and taking into consideration the projected increases in the rates of diabetes mellitus among younger women of child-bearing potential, it is imperative that the neurodevelopmental sequelae of diabetic pregnancy in general, and the increased risk for schizophrenia in particular, receive further study.
机译:目的:从精神分裂症的神经发育假说和糖尿病妊娠的病理生理学中确定趋同的主题,并探讨怀孕母亲的糖尿病可能增加后代精神分裂症风险的机制。方法:我们回顾了有关糖尿病妊娠的临床,流行病学和动物研究以及精神分裂症的神经发育方面的相关出版物。结果:流行病学研究表明,与未接受糖尿病妊娠的母亲相比,怀孕期间患有糖尿病的母亲的后代患精神分裂症的可能性高7倍。怀孕期间的孕妇高血糖症可能通过至少三种产前机制在成人生活中易患精神分裂症:低氧,氧化应激和炎症增加。高血糖症会增加氧化应激,改变脂质代谢,影响线粒体结构,导致神经细胞过程和神经元结构紊乱,并导致神经管闭合前的早熟。这些过程的分子机制包括产生过量的氧自由基和脂质过氧化物中间体,以及降低已知会引起多巴胺能和γ-氨基丁酸能活性降低的多不饱和脂肪酸含量降低。妊娠期间高血糖和低氧的结合还导致免疫功能改变,包括肿瘤坏死因子-α,C反应蛋白增加以及其他促炎细胞因子的上调。最后,母亲的高血糖症可能会对胎儿的细胞生理产生持久的影响,从而通过一种被称为“编程”的机制导致对压力的易感性增加和易患精神分裂症。这些产前事件还可能导致产科并发症,例如胎儿生长异常和对产前感染的敏感性增加,所有这些都与一系列神经发育异常和精神分裂症的风险增加有关。结论:在提供的证据的基础上,并考虑到有生育能力的年轻妇女中糖尿病发病率的预计增加,必须使糖尿病妊娠的神经发育后遗症普遍增加,并且精神分裂症的风险增加尤其需要进一步研究。

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