Buch Assaf, Carmeli Eli, Boker Lital Keinan, Marcus Yonit, Shefer Gabi, Kis Ofer, Berner Yitshal, Stern Naftali
Institute of Endocrinology, Metabolism and Hypertension, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel; The Sackler Faculty of Medicine, Tel-Aviv University, Israel.
Institute of Endocrinology, Metabolism and Hypertension, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel; School of Public Health, Haifa University, Haifa, Israel.
Exp Gerontol. 2016 Apr;76:25-32. doi: 10.1016/j.exger.2016.01.008. Epub 2016 Jan 16.
In western countries, the proportion of people over age 60 is increasing faster than any other group. This is linked to higher rates of obesity. Older age, co-morbidities and obesity are all associated with frailty syndrome. In the core of both frailty and sarcopenia there are dysfunction and deterioration of the muscle and the fat tissues. This overview interlinks the phenotypes presented in older adults such as sarcopenia and frailty-alone and with relation to obesity, muscle function and fat tissue accumulation.
Observational studies have well described the loss of muscle mass and strength through the years of adult life, both components of frailty and sarcopenia. They have shown that these changes are associated with dysmetabolism and functional deterioration, independent of common explanatory variables. In the metabolic mechanism core of this link, insulin resistance and higher ectopic fat accumulation may play a role. Basic experiments have partially validated this hypothesis. Whether there is a synergistic effect of obesity and frailty phenotype on morbidity risk is still questionable and currently under investigation; however, few cohort studies have shown that the frail-obese or sarcopenic-obese group have higher probability for metabolic complications.
Muscle mass loss and fat accumulation in the muscle in the elderly, with or without the presence of obesity, may explain some of the functional and metabolic defects shown in the frail, sarcopenic population.
在西方国家,60岁以上人群的比例增长速度超过其他任何群体。这与肥胖率上升有关。老年、合并症和肥胖都与衰弱综合征相关。在衰弱和肌肉减少症的核心,存在肌肉和脂肪组织的功能障碍与退化。本综述将老年人出现的表型相互联系起来,如肌肉减少症和单纯衰弱,以及与肥胖、肌肉功能和脂肪组织堆积的关系。
观察性研究已经很好地描述了成年期多年来肌肉质量和力量的丧失,这两者都是衰弱和肌肉减少症的组成部分。研究表明,这些变化与代谢紊乱和功能退化有关,与常见的解释变量无关。在这一联系的代谢机制核心中,胰岛素抵抗和更高的异位脂肪堆积可能起作用。基础实验已部分验证了这一假设。肥胖和衰弱表型对发病风险是否存在协同作用仍存在疑问,目前正在研究中;然而,很少有队列研究表明衰弱肥胖或肌肉减少症肥胖组发生代谢并发症的可能性更高。
老年人肌肉质量丧失和肌肉内脂肪堆积,无论是否存在肥胖,都可能解释衰弱、肌肉减少症人群中出现的一些功能和代谢缺陷。