Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK; British Heart Foundation Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
British Heart Foundation Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK.
Clin Nutr. 2021 Apr;40(4):2427-2434. doi: 10.1016/j.clnu.2020.10.044. Epub 2020 Nov 1.
Sarcopenia and frailty are strongly associated with disease incidence and mortality. However, there is limited evidence regarding their joint association with health outcomes. This study aimed to investigate the joint association of sarcopenia and frailty with cardiovascular disease (CVD), respiratory disease and cancer incidence and mortality as well as all-cause mortality in middle-aged and older adults in the UK Biobank study.
316,980 UK Biobank participants were included in this prospective study (53.1% women). Sarcopenia was defined according to the EWGSOP2 2019. Frailty was defined using a modified version of the Fried criteria. Combined classifications of sarcopenia and frailty were generated with the following seven subgroups derived: i) normal, ii) non-sarcopenic/pre-frail, iii) non-sarcopenic/frail, iv) pre-sarcopenic/pre-frail, v) pre-sarcopenic/frail, vi) sarcopenic/pre-frail, and vii) sarcopenic/frail. No participants had (pre)sarcopenia but not frailty. Associations between these exposures and health outcomes (incidence and mortality from cardiovascular and respiratory diseases, cancer, as well as, all-cause mortality) were investigated using Cox-proportional hazard models.
51.7% of the participants were not sarcopenic nor frail (normal), 41.3% were pre-frail or frail, 6.5% pre-sarcopenia and frail (including pre-frail) and 0.5% as having both sarcopenia and frailty (including pre-frailty). The combination sarcopenic/frail showed the strongest association with CVD (HR: 1.68 [95% CI: 1.22 to 2.30]) and respiratory disease incidence (HR: 1.77 [95% CI: 1.40 to 2.24]) and for mortality from all-cause (HR: 2.27 [95% CI: 1.64 to 3.13]), respiratory disease (HR: 3.50 [95% CI: 1.97 to 6.23]), and cancer (HR: 1.92 [95% CI: 1.08 to 3.38]). Finally, when we investigated the associations between the outcomes and exposures by age groups (≥and <60 years), we identified that, for many outcomes and categories, the associations were higher in younger individuals compared with older adults.
Our findings indicate that different combinations of sarcopenia and frailty were associated with adverse health outcomes, highlighting the joint association between both conditions. However, those individuals with sarcopenia and frailty showed the strongest associations with CVD and respiratory disease incidence and mortality for all-cause and respiratory disease and cancer.
肌少症和衰弱与疾病发病率和死亡率密切相关。然而,关于它们与健康结果的联合关联的证据有限。本研究旨在调查肌少症和衰弱与心血管疾病(CVD)、呼吸疾病和癌症发病率和死亡率以及中年和老年人全因死亡率的联合关联在英国生物银行研究中。
316980 名英国生物银行参与者被纳入本前瞻性研究(53.1%为女性)。根据 EWGSOP2 2019 标准定义肌少症。使用 Fried 标准的改良版本定义衰弱。通过生成以下七个亚组来生成肌少症和衰弱的联合分类:i)正常,ii)非肌少症/前衰弱,iii)非肌少症/衰弱,iv)前肌少症/前衰弱,v)前肌少症/衰弱,vi)肌少症/前衰弱,和 vii)肌少症/衰弱。没有参与者存在(前)肌少症但不衰弱。使用 Cox 比例风险模型研究这些暴露与健康结果(心血管和呼吸疾病、癌症以及全因死亡率的发病率和死亡率)之间的关联。
51.7%的参与者既非肌少症也不衰弱(正常),41.3%为前衰弱或衰弱,6.5%为前肌少症和衰弱(包括前衰弱),0.5%为同时存在肌少症和衰弱(包括前衰弱)。肌少症/衰弱的组合与 CVD(HR:1.68 [95%CI:1.22 至 2.30])和呼吸疾病发病率(HR:1.77 [95%CI:1.40 至 2.24])以及全因死亡率(HR:2.27 [95%CI:1.64 至 3.13])、呼吸疾病(HR:3.50 [95%CI:1.97 至 6.23])和癌症(HR:1.92 [95%CI:1.08 至 3.38])的相关性最强。最后,当我们按年龄组(≥60 岁和<60 岁)调查结局和暴露之间的关联时,我们发现对于许多结局和类别,与老年人相比,年轻人的关联更高。
我们的研究结果表明,肌少症和衰弱的不同组合与不良健康结局相关,突出了这两种情况之间的联合关联。然而,那些同时存在肌少症和衰弱的人,与 CVD 和呼吸疾病发病率和死亡率以及全因和呼吸疾病以及癌症的相关性最强。