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科萨科夫综合征的演变和治疗:视而不见,听而不闻?

The evolution and treatment of Korsakoff's syndrome: out of sight, out of mind?

机构信息

Molecular Psychiatry Laboratory, Rockefeller Building, University College London, 21 University Street, London, UK.

出版信息

Neuropsychol Rev. 2012 Jun;22(2):81-92. doi: 10.1007/s11065-012-9196-z. Epub 2012 May 9.

Abstract

Wernicke's Encephalopathy is an acute neuro-psychiatric condition caused by an insufficient supply of thiamine (Vitamin B1) to the brain. If undiagnosed or inadequately treated, it is likely to proceed to Korsakoff's Syndrome. Wernicke's Encephalopathy can result from dietary deficiency alone and this form is usually successfully treated, with little chance of Korsakoff's Syndrome supervening. On the other hand, thiamine deficiency associated with alcohol misuse/dependence may require up to 1 gram of thiamine IV in the first 24 hours to be treated successfully. The reasons for this difference in treatment will be discussed. Thiamine diphosphate acts as a co-factor for a number of thiamine-dependent enzymes. Thiamine deficiency leads to a reduction in the activity of these enzymes, and this leads to alterations in mitochondrial activity, impairment of oxidative metabolism, decreased energy status and eventually selective neuronal death. The damage caused by the combination of thiamine deficiency and alcohol metabolism probably interferes with adequate thiamine transport at a number of sites in the body, including the blood-brain barrier, as well as causing damage to the apoenzymes which then require higher concentrations of thiamine to work normally. The accumulated damage is likely to render the use of oral thiamine therapeutically inadequate since the body is unable to produce high enough concentrations of thiamine in the blood to traverse the blood-brain barrier. Some individuals are probably genetically predisposed to develop Wernicke's. Long before individuals with alcohol misuse or dependence develop Wernicke's Encephalopathy the neurons and other cells of the body are functioning sub-optimally because of the inadequate supply of thiamine and the neurotoxic effect of alcohol. This relative deficiency initiates a series of pathological changes which accumulate and further interfere with the supply of thiamine and its utilisation at a time when the requirements are increased. The best treatment for Korsakoff's Syndrome is timely recognition of Wernicke's Encephalopathy and appropriate intervention and prevention.

摘要

韦尼克脑病是一种由于大脑缺乏足够的硫胺素(维生素 B1)引起的急性神经精神疾病。如果未经诊断或治疗不当,很可能会发展为柯萨科夫综合征。韦尼克脑病仅因饮食中缺乏硫胺素即可引起,这种形式通常可以成功治疗,很少有柯萨科夫综合征发生的机会。另一方面,与酒精滥用/依赖相关的硫胺素缺乏可能需要在最初的 24 小时内静脉注射高达 1 克硫胺素才能成功治疗。这种治疗差异的原因将在讨论中说明。硫胺素二磷酸作为许多依赖硫胺素的酶的辅助因子。硫胺素缺乏会导致这些酶的活性降低,进而导致线粒体活性改变、氧化代谢受损、能量状态下降,最终导致选择性神经元死亡。硫胺素缺乏和酒精代谢相结合造成的损害可能会干扰体内许多部位(包括血脑屏障)的硫胺素转运,同时也会损害需要更高浓度硫胺素才能正常发挥作用的脱辅基酶。累积的损伤可能使口服硫胺素的治疗效果不足,因为身体无法在血液中产生足够高浓度的硫胺素来穿过血脑屏障。一些个体可能存在发生韦尼克脑病的遗传倾向。在有酒精滥用或依赖的个体出现韦尼克脑病之前很久,身体的神经元和其他细胞由于硫胺素供应不足和酒精的神经毒性作用,功能就已经处于次优状态。这种相对缺乏会引发一系列病理变化,这些变化会在需求增加时积累并进一步干扰硫胺素的供应及其利用。柯萨科夫综合征的最佳治疗方法是及时发现韦尼克脑病并进行适当的干预和预防。

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