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[抗痴呆药物]

[Antidementia drugs].

作者信息

Müller-Spahn Franz, Sollberger Daniel, Wollmer M Axel

机构信息

Universitäre Psychiatrische Kliniken Basel, Basel.

出版信息

Ther Umsch. 2009 Jun;66(6):432-40. doi: 10.1024/0040-5930.66.6.432.

Abstract

The pharmacological treatment of dementias aims to improve cognitive deficits, activities of daily living and behavioural and psychiatric symptoms. The weighting of theses therapeutic aims varies with disease progression. Behavioural symptoms may dominate especially in the more severe stages of the disease and may further deteriorate global functional level of the patient. Today there is no causal therapy for Alzheimer's disease (AD). Based on preclinical disease models novel therapeutic approaches are under development that target the beta-amyloid and tau protein metabolism. Some of them aim to inhibit the formation, aggregation and toxicity of beta-amyloid peptides or promote their clearance from the brain. Others inhibit the formation of neurofibrillary tangles or have neuroprotective effects. Active or passive immunisation against beta-amyloid may be a very specific and effective approach. The efficacy of acetylcholine esterase inhibitors (AchEI) in the treatment of mild to moderate AD is well documented. They are first line therapeutics in the treatment of the disease and lead to a delay of symptomatic progression. Memantine is effective in the treatment of moderate to severe stages of AD. The evidence for the treatment of vascular dementia is comparatively weak. However, positive effects have been shown for all available AchEI and memantine. Non pharmacological therapy is an indispensable part of the treatment of dementia patients and should be adapted to the individual needs of the patient in the respective stage of the disease. The efficacy of antipsychotics in the treatment of behavioural and psychiatric symptoms of dementia is limited. These drugs are associated with increased morbidity and mortality in dementia patients. Therefore, their application should be based on a critical and individual evaluation of risks and benefits.

摘要

痴呆症的药物治疗旨在改善认知缺陷、日常生活活动以及行为和精神症状。这些治疗目标的权重会随着疾病进展而变化。行为症状可能在疾病的更严重阶段尤为突出,并可能进一步恶化患者的整体功能水平。目前尚无针对阿尔茨海默病(AD)的病因疗法。基于临床前疾病模型,正在开发针对β-淀粉样蛋白和tau蛋白代谢的新型治疗方法。其中一些旨在抑制β-淀粉样肽的形成、聚集和毒性,或促进其从大脑中清除。其他方法则抑制神经原纤维缠结的形成或具有神经保护作用。针对β-淀粉样蛋白的主动或被动免疫可能是一种非常特异且有效的方法。乙酰胆碱酯酶抑制剂(AchEI)在治疗轻度至中度AD方面的疗效已得到充分证实。它们是该疾病治疗的一线药物,可延缓症状进展。美金刚对中度至重度AD阶段有效。治疗血管性痴呆的证据相对较少。然而,所有可用的AchEI和美金刚均已显示出积极效果。非药物治疗是痴呆症患者治疗中不可或缺的一部分,应根据患者在疾病各个阶段的个体需求进行调整。抗精神病药物在治疗痴呆症行为和精神症状方面的疗效有限。这些药物与痴呆症患者的发病率和死亡率增加有关。因此,其应用应基于对风险和益处的严格个体化评估。

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