Unidad de Investigación Cardiovascular (IRYCIS/UFV), Hospital Universitario Ramón y Cajal, Madrid, Spain.
Instituto de Investigación Sanitaria de Getafe, Getafe, Madrid, Spain.
Mol Aspects Med. 2016 Aug;50:1-32. doi: 10.1016/j.mam.2016.06.001. Epub 2016 Jun 28.
Frailty is a functional status that precedes disability and is characterized by decreased functional reserve and increased vulnerability. In addition to disability, the frailty phenotype predicts falls, institutionalization, hospitalization and mortality. Frailty is the consequence of the interaction between the aging process and some chronic diseases and conditions that compromise functional systems and finally produce sarcopenia. Many of the clinical manifestations of frailty are explained by sarcopenia which is closely related to poor physical performance. Reduced regenerative capacity, malperfusion, oxidative stress, mitochondrial dysfunction and inflammation compose the sarcopenic skeletal muscle alterations associated to the frailty phenotype. Inflammation appears as a common determinant for chronic diseases, sarcopenia and frailty. The strategies to prevent the frailty phenotype include an adequate amount of physical activity and exercise as well as pharmacological interventions such as myostatin inhibitors and specific androgen receptor modulators. Cell response to stress pathways such as Nrf2, sirtuins and klotho could be considered as future therapeutic interventions for the management of frailty phenotype and aging-related chronic diseases.
衰弱是一种功能状态,先于残疾出现,其特征是功能储备减少和脆弱性增加。除了残疾外,衰弱表型还可预测跌倒、住院、住院和死亡。衰弱是衰老过程和一些影响功能系统的慢性疾病和状况相互作用的结果,最终导致肌肉减少症。衰弱的许多临床表现可以用肌肉减少症来解释,肌肉减少症与身体机能较差密切相关。再生能力下降、灌注不良、氧化应激、线粒体功能障碍和炎症构成了与衰弱表型相关的肌肉减少症骨骼肌肉改变。炎症似乎是慢性疾病、肌肉减少症和衰弱的共同决定因素。预防衰弱表型的策略包括适量的身体活动和锻炼,以及肌肉生长抑制素抑制剂和特定雄激素受体调节剂等药物干预。细胞对 Nrf2、sirtuins 和 klotho 等应激途径的反应可被视为管理衰弱表型和与衰老相关的慢性疾病的未来治疗干预措施。