Division of Geriatric Medicine, Department of Medicine, National University Hospital, Singapore.
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
J Diabetes Res. 2023 Apr 28;2023:2519128. doi: 10.1155/2023/2519128. eCollection 2023.
Growth differentiation factor 15 (GDF-15) has been shown to be a metabolic and appetite regulator in diabetes mellitus (DM) and obesity. We aimed to investigate (i) the association between GDF-15 and DM with and without poor physical function independent of inflammation and (ii) the prediction model for poor physical function in prefrail older adults.
A cross-sectional study of 108-prefrail participants ≥60 years recruited for multidomain interventions. Data was collected for demographics, cognition, function, frailty, nutrition, handgrip strength (HGS), short physical performance battery (SPPB), and gait speed. Serum concentrations of GDF-15, IL-6, and TNF- were measured. GDF-15 was classified into tertiles (T1, T2, and T3), and its association was studied with DM and physical function (DM poor physical function, DM no poor physical function, no DM poor physical function, and no DM no poor physical function).
Compared with T1, participants in T3 were significantly older, had a lower education level, had almost three times higher prevalence of DM, slower gait speed, longer chair-stand time, and lower SPPB scores. On multivariate analysis, the odds of having both DM and poor physical performance compared to having no DM and no poor physical performance were significantly higher in GDF-15 T3 vs. GDF-15 T1 (aOR 9.7, 95% CI 1.4-67.7; = 0.021), and the odds of having DM no poor physical function compared to having no DM and no poor physical performance were significantly higher in GDF-15 T2 (aOR 12.7, 95% CI 1.1-143.7; = 0.040) independent of BMI, IL-6, TNF-, nutrition, physical function, education, age, and gender.
The association of GDF-15 with DM-associated poor physical function is independent of inflammation in prefrail older adults. Its causal-association link needs to be determined in longitudinal studies.
生长分化因子 15(GDF-15)已被证明是糖尿病(DM)和肥胖症的代谢和食欲调节剂。我们旨在研究(i)GDF-15 与 DM 以及与炎症无关的身体功能不良之间的关联,以及(ii)体弱老年人身体功能不良的预测模型。
对 108 名≥60 岁的体弱参与者进行横断面研究,这些参与者参与了多领域干预。收集了人口统计学、认知、功能、虚弱、营养、握力(HGS)、简短身体表现电池(SPPB)和步态速度的数据。测量了血清 GDF-15、IL-6 和 TNF-的浓度。将 GDF-15 分为三分位数(T1、T2 和 T3),并研究其与 DM 和身体功能(DM 身体功能不良、DM 无身体功能不良、无 DM 身体功能不良和无 DM 无身体功能不良)的关系。
与 T1 相比,T3 组参与者年龄较大,教育程度较低,DM 患病率高近三倍,步态速度较慢,坐立时间更长,SPPB 评分较低。多变量分析显示,与无 DM 且无身体功能不良相比,GDF-15 T3 组同时患有 DM 和身体功能不良的几率明显更高(OR9.7,95%CI1.4-67.7; = 0.021),与无 DM 且无身体功能不良相比,GDF-15 T2 组同时患有 DM 且无身体功能不良的几率明显更高(OR12.7,95%CI1.1-143.7; = 0.040),这独立于 BMI、IL-6、TNF-、营养、身体功能、教育、年龄和性别。
在体弱老年人中,GDF-15 与 DM 相关的身体功能不良之间的关联与炎症无关。需要在纵向研究中确定其因果关联。