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新型冠状病毒感染对阿尔茨海默病影响的研究进展

Research progress in the effect of SARS-CoV-2 infection on Alzheimer’s disease
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摘要 严重急性呼吸综合征冠状病毒2(SARS-CoV-2,新型冠状病毒)感染的全球发病率和病死率正逐渐降低,但老年人的死亡风险仍高于一般人群,特别是阿尔茨海默病(Alzheimer’s disease,AD)患者将面临更大风险。AD是一种缓慢进展的神经系统退行性疾病,是痴呆最常见的类型,其神经病理学特征包括β淀粉样蛋白的过度生成与清除失衡,以及过度磷酸化的tau蛋白导致神经原纤维缠结等。AD患者更容易感染新型冠状病毒,同样,该病毒也可能导致其感染者出现AD。新型冠状病毒感染机体后,通过引起免疫反应、炎症反应、细胞衰老、DNA损伤反应、自噬失调、脉络丛稳态紊乱、肾素-血管紧张素系统过度激活及氧化应激等对AD产生影响。本文主要就新型冠状病毒感染对AD影响的研究进展进行综述。 The global morbidity and mortality of severe acute respiratory syndrome coronavirus 2(SARS-CoV-2)infection are gradually decreasing,but the elderly people are still at higher risk of death than the general population,especially for those with Alzheimer’s disease(AD).AD is a slowly progressing degenerative disease of the nervous system,and is the most common type of dementia.Its neuropathological features include overproduction and clea-rance imbalance of amyloidβ-protein and overphosphorylated tau protein leading to neurofibrillary tangle.People with AD are more susceptible to be infected with SARS-CoV-2,likewise,the virus can also cause AD in those who are infected.After SARS-CoV-2 infection,it affects AD through immune response,inflammatory response,cell aging,DNA damage reaction,autophagy disorder,choroidal homeostasis disorder,over-activation of renin-angiotensin system,and oxidative stress.This article mainly reviews the research progress in the effect of SARS-CoV-2 infection on AD.
作者 王康 张琰 赵慧 邵龙 冯玲玲 赵同 WANG Kang;ZHANG Yan;ZHAO Hui;SHAO Long;FENG Ling-ling;ZHAO Tong(Department of Neurology,The Second Affiliated Hospital of Shandong First Medical University,Tai’an 271000,China;Department of Endocrinology,The First People’s Hospital of Tai’an,Tai’an 271000,China;Department of Imaging,The Second Affiliated Hospital of Shandong First Medical University,Tai’an 271000,China)
出处 《中国感染控制杂志》 CAS CSCD 北大核心 2024年第11期1450-1455,共6页 Chinese Journal of Infection Control
关键词 新型冠状病毒 阿尔茨海默病 免疫反应 炎症 细胞衰老 自噬 氧化应激 severe acute respiratory syndrome coronavirus 2 Alzheimer’s disease immune response inflammation cell aging autophagy oxidative stress
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