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补充主要咖啡成分(包括咖啡因和/或绿原酸)对非酒精性脂肪性肝病和 2 型糖尿病患者肝、代谢和炎症指标的影响:一项随机、双盲、安慰剂对照的临床试验。

Effects of supplementation with main coffee components including caffeine and/or chlorogenic acid on hepatic, metabolic, and inflammatory indices in patients with non-alcoholic fatty liver disease and type 2 diabetes: a randomized, double-blind, placebo-controlled, clinical trial.

机构信息

Department of Clinical Nutrition & Dietetics, Faculty of Nutrition Sciences and Food Technology, National Nutrition and Food Technology Research Institute, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Nutr J. 2021 Apr 10;20(1):35. doi: 10.1186/s12937-021-00694-5.

Abstract

BACKGROUND

Non-alcoholic fatty liver disease (NAFLD) is much more frequent and more severe, including cirrhosis, hepatocellular carcinoma in patients with type 2 diabetes. Coffee is a complex beverage with hundreds of compounds whereas caffeine and chlorogenic acid are the most abundant bioactive compounds. The published epidemiological data demonstrating beneficial associations between all categories of coffee exposure and ranges of liver outcomes are rapidly growing; however, the main contributors and cause-effect relationships have not yet been elucidated. To address existing knowledge gaps, we sought to determine the efficacy and safety of 6 months chlorogenic acid and/or caffeine supplementation in patients with type 2 diabetes affected by NAFLD.

METHODS

This trial was carried out at two Diabetes Centers to assess the effects of supplementation with daily doses of 200 mg chlorogenic acid, 200 mg caffeine, 200 mg chlorogenic acid plus 200 mg caffeine or placebo (starch) in patients with type 2 diabetes and NAFLD. The primary endpoint was reduction of hepatic fat and stiffness measured by FibroScan, and changes in serum hepatic enzymes and cytokeratin - 18 (CK-18) levels. Secondary endpoints were improvements in metabolic (including fasting glucose, homeostasis model assessment-estimated insulin resistance (HOMA-IR), hemoglobin A1c (HBA1C), C-peptide, insulin and lipid profiles) and inflammatory (including nuclear factor k-B (NF-KB), tumor necrosis factor (TNF-α), high sensitive- C reactive protein(hs-CRP)) parameters from baseline to the end of treatment.

RESULTS

Neither chlorogenic acid nor caffeine was superior to placebo in attenuation of the hepatic fat and stiffness and other hepatic outcomes in patients with diabetes and NAFLD. Except for the lower level of total cholesterol in caffeine group (p = 0.04), and higher level of insulin in chlorogenic acid plus caffeine group (p = 0.01) compared with placebo, there were no significant differences among the treatment groups.

CONCLUSION

These findings do not recommend caffeine and/or chlorogenic acid to treat NAFLD in type 2 diabetes patients.

TRIAL REGISTRATION

IRCT201707024010N21 . Registered 14 September 2017.

摘要

背景

非酒精性脂肪性肝病(NAFLD)在 2 型糖尿病患者中更为常见且更为严重,包括肝硬化和肝细胞癌。咖啡是一种含有数百种化合物的复杂饮料,而咖啡因和绿原酸是最丰富的生物活性化合物。表明咖啡暴露的所有类别与肝脏结果之间存在有益关联的已发表的流行病学数据正在迅速增加;然而,主要的贡献者和因果关系尚未阐明。为了解决现有知识差距,我们试图确定 6 个月绿原酸和/或咖啡因补充剂在患有非酒精性脂肪性肝病的 2 型糖尿病患者中的疗效和安全性。

方法

本试验在两个糖尿病中心进行,以评估每天补充 200mg 绿原酸、200mg 咖啡因、200mg 绿原酸加 200mg 咖啡因或安慰剂(淀粉)对 2 型糖尿病和非酒精性脂肪性肝病患者的影响。主要终点是通过 FibroScan 测量肝脂肪和硬度的减少,以及血清肝酶和细胞角蛋白-18(CK-18)水平的变化。次要终点是改善代谢(包括空腹血糖、稳态模型评估估计的胰岛素抵抗(HOMA-IR)、糖化血红蛋白(HBA1C)、C 肽、胰岛素和脂质谱)和炎症(包括核因子 k-B(NF-KB)、肿瘤坏死因子(TNF-α)、高敏-C 反应蛋白(hs-CRP))参数从基线到治疗结束时。

结果

绿原酸和咖啡因在降低糖尿病和非酒精性脂肪性肝病患者的肝脂肪和硬度及其他肝脏结局方面均不如安慰剂。与安慰剂相比,除了咖啡因组总胆固醇水平较低(p=0.04)和绿原酸加咖啡因组胰岛素水平较高(p=0.01)外,各组之间没有显著差异。

结论

这些发现不建议在 2 型糖尿病患者中使用咖啡因和/或绿原酸治疗非酒精性脂肪性肝病。

试验注册

IRCT201707024010N21。2017 年 9 月 14 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2865/8037901/74c357bf2ee6/12937_2021_694_Fig1_HTML.jpg

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