School of Health and Behavioural Sciences, University of the Sunshine Coast, Queensland Australia.
School of Health and Behavioural Sciences, University of the Sunshine Coast, Queensland Australia.
Nutr Metab Cardiovasc Dis. 2021 Mar 10;31(3):827-833. doi: 10.1016/j.numecd.2020.11.018. Epub 2020 Nov 25.
Frailty has emerged as a third category of complication in patients with type 2 diabetes mellitus (T2DM). It has been suggested that adequate protein intake is an important dietary strategy for counteracting frailty. Therefore, we explored the association between protein intake and functional biomarkers of frailty in older adults with T2DM.
Frailty was operationalized as the presence of three of the following: exhaustion, low muscle strength, low physical activity, slow gait speed, and weight loss. Functional biomarkers included handgrip strength (HGS), chair stands, the short physical performance battery and gait speed. Eighty-seven older adults (71.2 ± 8.2 years; 66.7% males) were included. A total of n = 6 (7%) and n = 32 (37%) participants were identified as frail and pre-frail respectively. No significant difference was observed for protein intake across staging of frailty (pre-frail/frail: 1.3 ± 0.4 g/kg BW; non-frail: 1.4 ± 0.4 g/kg BW; P = 0.320). A significant association was observed for total protein intake and HGS (β = 0.44; 95% CI: 0.23-1.8; P = 0.01). However, this was no longer significant after adjusting for age, gender, physical activity, energy intake and total appendicular lean muscle (β = 0.03; 95% CI: -0.45-0.60; P = 0.78). Nil other associations were observed between total protein intake and functional biomarkers of frailty.
Adequate protein intake was not associated with functional biomarkers in older adults with T2DM. Future research should focus on the efficacy of protein on attenuating functional decline in vulnerable older adults with low protein intake.
衰弱已成为 2 型糖尿病(T2DM)患者的第三类并发症。有研究表明,充足的蛋白质摄入是对抗衰弱的重要饮食策略。因此,我们探讨了 T2DM 老年患者蛋白质摄入与衰弱功能生物标志物之间的关系。
衰弱定义为存在以下三种情况:疲惫、肌肉力量弱、身体活动少、步态缓慢和体重减轻。功能生物标志物包括握力(HGS)、椅站、简易体能测试和步态速度。共纳入 87 名老年人(71.2±8.2 岁;66.7%为男性)。共有 n=6(7%)和 n=32(37%)参与者分别被确定为衰弱和衰弱前期。衰弱分期之间的蛋白质摄入量无显著差异(衰弱前期/衰弱:1.3±0.4g/kg BW;非衰弱:1.4±0.4g/kg BW;P=0.320)。总蛋白质摄入量与 HGS 呈显著相关(β=0.44;95%CI:0.23-1.8;P=0.01)。然而,在调整年龄、性别、身体活动、能量摄入和四肢瘦体重后,这一相关性不再显著(β=0.03;95%CI:-0.45-0.60;P=0.78)。总蛋白质摄入量与衰弱的其他功能生物标志物之间无其他关联。
T2DM 老年患者的充足蛋白质摄入与功能生物标志物无关。未来的研究应集中在低蛋白质摄入的脆弱老年患者中,蛋白质对减缓功能下降的疗效上。