老化
多发病率
自噬
免疫衰老
PI3K/AKT/mTOR通路
医学
肌萎缩
疾病
表观遗传学
衰老
炎症
纺神星
神经退行性变
慢性阻塞性肺病
生物信息学
生物
神经科学
信号转导
免疫学
内科学
细胞生物学
遗传学
免疫系统
细胞凋亡
基因
肾
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2015-01-22
卷期号:45 (3): 790-806
被引量:165
标识
DOI:10.1183/09031936.00229714
摘要
In ageing populations many patients have multiple diseases characterised by acceleration of the normal ageing process. Better understanding of the signalling pathways and cellular events involved in ageing shows that these are characteristic of many chronic degenerative diseases, such as chronic obstructive pulmonary disease (COPD), chronic cardiovascular and metabolic diseases, and neurodegeneration. Common mechanisms have now been identified in these diseases, which show evidence of cellular senescence with telomere shortening, activation of PI3K–AKT–mTOR signalling, impaired autophagy, mitochondrial dysfunction, stem cell exhaustion, epigenetic changes, abnormal microRNA profiles, immunosenescence and low grade chronic inflammation (“inflammaging”). Many of these pathways are driven by chronic oxidative stress. There is also a reduction in anti-ageing molecules, such as sirtuins and Klotho, which further accelerates the ageing process. Understanding these molecular mechanisms has identified several novel therapeutic targets and several drugs have already been developed that may slow the ageing process, as well as lifestyle interventions, such as diet and physical activity. This indicates that in the future new treatment approaches may target the common pathways involved in multimorbidity and this area of research should be given high priority. Thus, COPD should be considered as a component of multimorbidity and common disease pathways, particularly accelerated ageing, should be targeted.
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