Szekely Christine A, Town Terrence, Zandi Peter P
Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.
Subcell Biochem. 2007;42:229-48. doi: 10.1007/1-4020-5688-5_11.
Epidemiologic and laboratory studies suggest that non-steroidal anti-inflammatory drug (NSAID) use reduces the risk of Alzheimer's disease (AD). Initial reports in the early 1990's indicated that a history of arthritis, a presumed surrogate of NSAID use, was associated with a lower risk of AD. [1] These reports were followed by epidemiologic studies in which NSAID use was assessed directly and the majority of these reports confirmed the inverse association with risk for AD. [2, 3] Postmortem studies in humans [4], studies in animal models of AD [5, 6], and in vitro studies [7, 8] generally support the notion that NSAIDs can reduce the deleterious inflammation which surrounds amyloid beta (Abeta) plaques in the AD brain. In addition, some studies conducted in vitro and in rodents point to a subgroup of NSAIDs that may work by inhibiting amyloidogenic APP metabolism rather than through traditional anti-inflammatory mechanisms. [9-11] This novel property of NSAIDs is currently being explored in epidemiologic studies. Results from randomized clinical trials of NSAIDs and established AD and one trial on secondary prevention have not been promising and there have been no prevention trials completed. The feasibility of using NSAIDs as a chemopreventive agent in AD is discussed.
流行病学和实验室研究表明,使用非甾体抗炎药(NSAID)可降低患阿尔茨海默病(AD)的风险。20世纪90年代初的初步报告指出,关节炎病史(一种推测的NSAID使用替代指标)与较低的AD风险相关。[1] 随后进行了流行病学研究,其中直接评估了NSAID的使用情况,这些报告中的大多数证实了其与AD风险呈负相关。[2, 3] 人体尸检研究[4]、AD动物模型研究[5, 6]以及体外研究[7, 8]总体上支持NSAIDs可减轻AD大脑中围绕淀粉样β(Aβ)斑块的有害炎症这一观点。此外,一些体外和啮齿动物研究指出,一部分NSAIDs可能通过抑制淀粉样前体蛋白(APP)的淀粉样生成代谢起作用,而非通过传统的抗炎机制。[9 - 11] NSAIDs的这一新颖特性目前正在流行病学研究中进行探索。NSAIDs用于已确诊AD的随机临床试验结果以及一项二级预防试验均未取得理想结果,且尚无预防试验完成。本文讨论了将NSAIDs用作AD化学预防剂的可行性。