Taglialatela Giulio, Rastellini Cristiana, Cicalese Luca
Mitchell Center for Neurodegenerative Disease, Department of Neurology, University of Texas Medical Branch, Galveston, Texas, USA.
Department of Surgery, University of Texas Medical Branch, Galveston, Texas, USA.
J Alzheimers Dis. 2015;47(2):329-33. doi: 10.3233/JAD-150065.
Experimental evidence suggests that the protein phosphatase calcineurin mediates the action of amyloid-β (Aβ) oligomers, the most toxic amyloid species thought to drive initial cognitive decline in Alzheimer's disease (AD). However, there is currently no evidence that inhibition of calcineurin could prevent the onset of AD in humans. Here, we report for the first time that individuals chronically treated with calcineurin inhibitors to prevent solid organ transplant rejection have a significantly lower incidence of AD/dementia as compared to the general population. This result prompts further clinical development of calcineurin inhibition as a viable treatment for AD.
实验证据表明,蛋白磷酸酶钙调神经磷酸酶介导淀粉样β(Aβ)寡聚体的作用,Aβ寡聚体是被认为在阿尔茨海默病(AD)中驱动初始认知衰退的毒性最强的淀粉样蛋白。然而,目前尚无证据表明抑制钙调神经磷酸酶可预防人类AD的发病。在此,我们首次报告,与普通人群相比,长期接受钙调神经磷酸酶抑制剂治疗以预防实体器官移植排斥反应的个体患AD/痴呆症的发生率显著更低。这一结果促使将钙调神经磷酸酶抑制作为AD的一种可行治疗方法进行进一步的临床开发。