黄连解毒汤对代谢综合征的有益作用:前瞻性随机对照临床试验

X U Pingyuan, Zhu Heng, Zhou Ruonan, Wei Yaping, Zhu Ziwei, X U Fangyuan, Xiang Yingying, Cao Yue, Shen Lixuan, Wang Ziwei, Xue Yingying, Y U Xizhong, Fang Penghua, Shang Wenbin
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引用次数: 0

摘要

目的:评价黄连解毒汤(HLJDD)治疗代谢综合征(MS)的临床疗效,并探讨其作用机制。方法:共纳入132例受试者,随机分为HLJDD组和对照组。HLJDD组接受为期3个月的HLJDD治疗和生活方式指导,而对照组只接受生活方式指导。在基线和试验结束时测量人体测量指数、血脂谱、肝功能指数、葡萄糖稳态、胰岛素敏感性、炎症谱和棕色脂肪因子成纤维细胞生长因子21 (FGF-21)。结果:研究表明,与对照组相比,给予HLJDD 3个月可显著降低体重[8.91% (6.03% ~ 10.22%)vs5.58% (3.31% ~ 8.70%), pv5.37% (3.27% ~ 8.54%), pv7.43% (3.11% ~ 11.69%), Pvs -22.90%, P < 0.01], IL-17A (-23.34% vs -9.13%, P < 0.05), TNF-α (-33.78% vs-11.02%, P < 0.01)和FGF-21 (P < 0.05)]。结论:HLJDD对代谢综合征患者的代谢紊乱有改善作用。这些数据还表明,HLJDD对代谢的有益作用可能归因于其促进FGF-21分泌的作用,否则FGF-21会因代谢性炎症而受到损害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Beneficial effects of Huanglian Jiedu decoction ( ) on metabolic syndrome: a prospective randomized controlled clinical trial.

Objective: To evaluate the clinical efficacy of Huanglian Jiedu decoction (, HLJDD) in patients with metabolic syndrome (MS) and to elucidate its potential underlying mechanisms.

Methods: A total of 132 participants were enrolled and randomly divided into the HLJDD group and the control group. Participants in the HLJDD group received a 3-month HLJDD treatment in addition to lifestyle guidance, while the control group received only lifestyle guidance. Anthropometric indices, blood lipid profiles, liver function indices, glucose homeostasis, insulin sensitivity, inflammatory profiles, and the brown adipokine fibroblast growth factor 21 (FGF-21) were measured both at baseline and at the end of the trial.

Results: The study demonstrated that administering HLJDD for three months significantly reduces the body weight [8.91% (6.03%-10.22%) vs5.58% (3.31%-8.70%), P<0.01], body mass index [8.55% (6.08%-10.16%) vs5.37% (3.27%-8.54%), P<0.01], waist circumference [9.56% (6.63%-14.41%) vs 7.43% (3.11%-11.69%), P <0.01] as well as the metabolic profiles of patients with metabolic syndrome. Additionally, it was observed that the HLJDD regimen led to lower serum levels of inflammatory cytokines IL-6 (-45.03% vs-22.90%, P < 0.01), IL-17A (-23.34% vs -9.13%, P < 0.05), TNF-α (-33.78% vs-11.02%, P < 0.01) and FGF-21 (P < 0.05) when compared to the control group.

Conclusion: It can be concluded that HLJDD contributes to ameliorating metabolic disorders in individuals suffering from metabolic syndrome. The data also imply that the beneficial effects of HLJDD on metabolism might be attributed to its role in enhancing FGF-21 secretion, which is otherwise compromised due to metabolic inflammation.

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