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精神分裂症理论:一种遗传-炎症-血管综合理论。

Theories of schizophrenia: a genetic-inflammatory-vascular synthesis.

作者信息

Hanson Daniel R, Gottesman Irving I

机构信息

Department of Psychiatry, VA Medical Center (116A), One Veterans Drive, Minneapolis, MN 55417, USA.

出版信息

BMC Med Genet. 2005 Feb 11;6:7. doi: 10.1186/1471-2350-6-7.

Abstract

BACKGROUND

Schizophrenia, a relatively common psychiatric syndrome, affects virtually all brain functions yet has eluded explanation for more than 100 years. Whether by developmental and/or degenerative processes, abnormalities of neurons and their synaptic connections have been the recent focus of attention. However, our inability to fathom the pathophysiology of schizophrenia forces us to challenge our theoretical models and beliefs. A search for a more satisfying model to explain aspects of schizophrenia uncovers clues pointing to genetically mediated CNS microvascular inflammatory disease.

DISCUSSION

A vascular component to a theory of schizophrenia posits that the physiologic abnormalities leading to illness involve disruption of the exquisitely precise regulation of the delivery of energy and oxygen required for normal brain function. The theory further proposes that abnormalities of CNS metabolism arise because genetically modulated inflammatory reactions damage the microvascular system of the brain in reaction to environmental agents, including infections, hypoxia, and physical trauma. Damage may accumulate with repeated exposure to triggering agents resulting in exacerbation and deterioration, or healing with their removal. There are clear examples of genetic polymorphisms in inflammatory regulators leading to exaggerated inflammatory responses. There is also ample evidence that inflammatory vascular disease of the brain can lead to psychosis, often waxing and waning, and exhibiting a fluctuating course, as seen in schizophrenia. Disturbances of CNS blood flow have repeatedly been observed in people with schizophrenia using old and new technologies. To account for the myriad of behavioral and other curious findings in schizophrenia such as minor physical anomalies, or reported decreased rates of rheumatoid arthritis and highly visible nail fold capillaries, we would have to evoke a process that is systemic such as the vascular and immune/inflammatory systems.

SUMMARY

A vascular-inflammatory theory of schizophrenia brings together environmental and genetic factors in a way that can explain the diversity of symptoms and outcomes observed. If these ideas are confirmed, they would lead in new directions for treatments or preventions by avoiding inducers of inflammation or by way of inflammatory modulating agents, thus preventing exaggerated inflammation and consequent triggering of a psychotic episode in genetically predisposed persons.

摘要

背景

精神分裂症是一种相对常见的精神综合征,几乎影响所有脑功能,但100多年来一直无法得到解释。无论是通过发育和/或退行性过程,神经元及其突触连接的异常一直是最近关注的焦点。然而,我们无法深入了解精神分裂症的病理生理学,这迫使我们挑战我们的理论模型和信念。寻找一个更令人满意的模型来解释精神分裂症的各个方面,发现了指向基因介导的中枢神经系统微血管炎症性疾病的线索。

讨论

精神分裂症理论中的血管成分假定,导致疾病的生理异常涉及正常脑功能所需的能量和氧气供应的精确调节的破坏。该理论进一步提出,中枢神经系统代谢异常是因为基因调节的炎症反应在对包括感染、缺氧和身体创伤在内的环境因素作出反应时损害了脑微血管系统。随着反复接触触发因素,损害可能会累积,导致病情加重和恶化,或者随着触发因素的消除而愈合。有明确的例子表明,炎症调节因子中的基因多态性会导致过度的炎症反应。也有充分的证据表明,脑部炎症性血管疾病可导致精神病,通常病情有波动,病程呈起伏变化,如在精神分裂症中所见。使用新旧技术,在精神分裂症患者中反复观察到中枢神经系统血流紊乱。为了解释精神分裂症中无数的行为和其他奇怪发现,如轻微身体异常,或报告的类风湿性关节炎发病率降低以及明显可见的甲襞毛细血管,我们必须唤起一个全身性的过程,如血管和免疫/炎症系统。

总结

精神分裂症的血管炎症理论以一种能够解释所观察到的症状和结果多样性的方式,将环境和遗传因素结合在一起。如果这些观点得到证实,它们将为治疗或预防带来新的方向,即通过避免炎症诱导剂或通过炎症调节剂,从而防止在基因易感人群中发生过度炎症以及随之引发的精神病发作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce9b/554096/5651f4f8b4ab/1471-2350-6-7-1.jpg

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