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TREATMENT OF ALZHEIMER'S DISEASE

机译:阿尔茨海默病的治疗

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BACKGROUNDndash; Alzheimer's disease (AD) is a progressive dementia associated with distinct neuropathologic changes and characterized by memory loss and impairment in at least one other area of cognition. The underlying neuropathologic substrate for cognitive and noncognitive behavioral disturbances in AD is uncertain, but likely includes deficiencies of cholinergic and other transmitters in addition to plaques and tangles.REVIEWndash; Therapies based on cholinergic hypotheses have lead to two approved drugs, tacrine and donepezil; other cholinergic drugs, including cholinesterase inhibitors, muscarinic agonists, and nicotinic agonists, are under development. Other therapies have been devised based on presumed risk and protective factors, such as aging, APO E genotype, head trauma, menopause/estrogen deficiency, the effect of education on the brain, anti-inflammatory drugs, and anti-oxidants. Recently, numerous basic studies have demonstrated the significance of amyloid protein, tau; protein, and apolipoprotein E in the pathogenesis of plaques and tangles.SUMMARYndash; Treatment of the cognitive disturbances in AD will likely use multiple approaches to improve symptoms and to slow progression. Therapy for the noncognitive disturbances involves communication between the clinician and the caregiver, as well as pharmacologic and nonpharmacologic treatments.CONCLUSIONSndash; AD is a heterogeneous disorder. Treatment must be individualized and must address both cognitive and noncognitive disturbances. Future therapies may also take various genetic risk factors and gender into account.
机译:背景– 阿尔茨海默病 (AD) 是一种进行性痴呆,与不同的神经病理学变化相关,其特征是记忆丧失和至少一个其他认知领域的障碍。AD 中认知和非认知行为障碍的潜在神经病理学基质尚不确定,但除了斑块和缠结外,还可能包括胆碱能和其他递质的缺乏。评论– 基于胆碱能假说的疗法导致了两种获批的药物,他克林和多奈哌齐;其他胆碱能药物,包括胆碱酯酶抑制剂、毒蕈碱激动剂和烟碱激动剂,正在开发中。其他疗法是根据假定的风险和保护因素设计的,例如衰老、APO E 基因型、头部外伤、更年期/雌激素缺乏、教育对大脑的影响、抗炎药和抗氧化剂。近年来,大量基础研究证明了淀粉样蛋白、τ蛋白和载脂蛋白E在斑块和缠结发病机制中的重要性。摘要– AD认知障碍的治疗可能会使用多种方法来改善症状并减缓进展。非认知障碍的治疗包括临床医生和照料者之间的沟通,以及药物和非药物治疗。结论– AD 是一种异质性疾病。治疗必须个体化,必须同时解决认知和非认知障碍。未来的治疗也可能考虑各种遗传风险因素和性别。

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