Suppr超能文献

联合生活方式干预(含或不含蛋白质饮料)对肥胖 2 型糖尿病老年患者炎症的影响。

The effect of a combined lifestyle intervention with and without protein drink on inflammation in older adults with obesity and type 2 diabetes.

机构信息

Faculty of Sports and Nutrition, Center of Expertise Urban Vitality, Amsterdam University of Applied Sciences (AUAS), 1067 SM Amsterdam, the Netherlands; Amsterdam Movement Sciences research institute, Amsterdam UMC location Vrije Universiteit Amsterdam, 1081 HV Amsterdam, the Netherlands; Gerontology Department, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

Frailty & Resilience in Ageing (FRIA) research department, Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel, 1090 Brussels, Belgium.

出版信息

Exp Gerontol. 2024 Jun 1;190:112410. doi: 10.1016/j.exger.2024.112410. Epub 2024 Apr 1.

Abstract

BACKGROUND

Chronic low-grade inflammatory profile (CLIP) is one of the pathways involved in type 2 diabetes (T2D). Currently, there is limited evidence for ameliorating effects of combined lifestyle interventions on CLIP in type 2 diabetes. We investigated whether a 13-week combined lifestyle intervention, using hypocaloric diet and resistance exercise plus high-intensity interval training with or without consumption of a protein drink, affected CLIP in older adults with T2D.

METHODS

In this post-hoc analysis of the PROBE study 114 adults (≥55 years) with obesity and type 2 (pre-)diabetes had measurements of C-reactive protein (CRP), pro-inflammatory cytokines interleukin (IL)-6, tumor-necrosis-factor (TNF)-α, and monocyte chemoattractant protein (MCP)-1, anti-inflammatory cytokines IL-10, IL-1 receptor antagonist (RA), and soluble tumor-necrosis-factor receptor (sTNFR)1, adipokines leptin and adiponectin, and glycation biomarkers carboxymethyl-lysine (CML) and soluble receptor for advanced glycation end products (sRAGE) from fasting blood samples. A linear mixed model was used to evaluate change in inflammatory biomarkers after lifestyle intervention and effect of the protein drink. Linear regression analysis was performed with parameters of body composition (by dual-energy X-ray absorptiometry) and parameters of insulin resistance (by oral glucose tolerance test).

RESULTS

There were no significant differences in CLIP responses between the protein and the control groups. For all participants combined, IL-1RA, leptin and adiponectin decreased after 13 weeks (p = 0.002, p < 0.001 and p < 0.001), while ratios TNF-α/IL-10 and TNF-α/IL-1RA increased (p = 0.003 and p = 0.035). CRP increased by 12 % in participants with low to average CLIP (pre 1.91 ± 0.39 mg/L, post 2.13 ± 1.16 mg/L, p = 0.006) and decreased by 36 % in those with high CLIP (pre 5.14 mg/L ± 1.20, post 3.30 ± 2.29 mg/L, p < 0.001). Change in leptin and IL-1RA was positively associated with change in fat mass (β = 0.133, p < 0.001; β = 0.017, p < 0.001) and insulin resistance (β = 0.095, p = 0.024; β = 0.020, p = 0.001). Change in lean mass was not associated with any of the biomarkers.

CONCLUSION

13 weeks of combined lifestyle intervention, either with or without protein drink, reduced circulating adipokines and anti-inflammatory cytokine IL-1RA, and increased inflammatory ratios TNF-α/IL-10 and TNF-α/IL-1RA in older adults with obesity and T2D. Effect on CLIP was inversely related to baseline inflammatory status.

摘要

背景

慢性低度炎症特征(CLIP)是 2 型糖尿病(T2D)的相关途径之一。目前,对于联合生活方式干预对 T2D 患者 CLIP 的改善效果的证据有限。我们研究了 13 周的联合生活方式干预(使用低热量饮食和抗阻运动加高强度间歇训练,加或不加蛋白质饮料)是否会影响老年 T2D 患者的 CLIP。

方法

在 PROBE 研究的事后分析中,114 名肥胖和 2 型(前)糖尿病成年人(≥55 岁)进行了 C 反应蛋白(CRP)、促炎细胞因子白细胞介素(IL)-6、肿瘤坏死因子(TNF)-α、单核细胞趋化蛋白(MCP)-1、抗炎细胞因子白细胞介素(IL)-10、IL-1 受体拮抗剂(IL-1RA)和可溶性肿瘤坏死因子受体(sTNFR)1、脂肪因子瘦素和脂联素、糖基化生物标志物羧甲基赖氨酸(CML)和可溶性晚期糖基化终产物受体(sRAGE)的检测,检测来自空腹血样。使用线性混合模型评估生活方式干预后炎症生物标志物的变化,并评估蛋白质饮料的作用。采用线性回归分析方法对身体成分(双能 X 射线吸收法)和胰岛素抵抗参数(口服葡萄糖耐量试验)进行参数分析。

结果

蛋白质组和对照组之间的 CLIP 反应无显著差异。对于所有参与者,13 周后 IL-1RA、瘦素和脂联素下降(p=0.002、p<0.001 和 p<0.001),而 TNF-α/IL-10 和 TNF-α/IL-1RA 比值增加(p=0.003 和 p=0.035)。CLIP 较低或平均的参与者的 CRP 增加了 12%(前 1.91±0.39mg/L,后 2.13±1.16mg/L,p=0.006),而 CLIP 较高的参与者降低了 36%(前 5.14mg/L±1.20,后 3.30±2.29mg/L,p<0.001)。瘦素和 IL-1RA 的变化与脂肪量的变化呈正相关(β=0.133,p<0.001;β=0.017,p<0.001)和胰岛素抵抗(β=0.095,p=0.024;β=0.020,p=0.001)。瘦体重的变化与任何生物标志物均无相关性。

结论

13 周的联合生活方式干预,无论是否添加蛋白质饮料,均可降低肥胖和 T2D 老年患者的循环脂肪因子和抗炎细胞因子 IL-1RA,并增加 TNF-α/IL-10 和 TNF-α/IL-1RA 的炎症比值。对 CLIP 的影响与基线炎症状态呈反比。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验