Mansour Asieh, Mohajeri-Tehrani Mohammad Reza, Karimi Sara, Sanginabadi Milad, Poustchi Hossein, Enayati Samaneh, Asgarbeik Saeedeh, Nasrollahzadeh Javad, Hekmatdoost Azita
Department of Clinical Nutrition and Dietetics, Faculty of Nutrition and Food Technology, National Nutrition and Food Technology, Research Institute Shahid Beheshti University of Medical Science, Tehran, Iran.
Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.
EXCLI J. 2020 Mar 2;19:241-250. doi: 10.17179/excli2019-2021. eCollection 2020.
The aim of this study was to determine the effects of caffeine and chlorogenic acid supplementation on gut microbiota, and metabolic disturbances in patients with NAFLD and diabetes. In this randomized, placebo-controlled, clinical trial, 26 patients with diabetes and NAFLD were randomly assigned to four groups to receive either 200 mg caffeine plus 200 mg chlorogenic acid (CFCA), or 200 mg caffeine plus 200 mg placebo (starch) (CFPL), or 200 mg chlorogenic acid plus 200 mg placebo (CAPL), or 200 mg placebo plus 200 mg placebo (PLPL) for 12 weeks. After 3 months of supplementation, patients in the intervention groups showed a significant decrease in body weight (CFCA group =-3.69 kg; CFPL group=-0.7kg; CAPL group=-0.43kg; PLPL group=0.26 kg) (p=0.004). Weight reduced significantly more in CFCA group compared to all other three groups (p=0.005 for PLPL; p=0.023 for CAPL; and p=0.031 for CFPL). Although the number of gut Bifidobacteria increased in CFCA group, there were no statistically significant differences within and between the groups in any of bacteria numbers. In conclusion, our study showed that 12 weeks consumption of 200 mg/day caffeine plus 200 mg/day chlorogenic acid is effective in reduction of weight in patients with NAFLD and diabetes which might be at least partially through the rise in gut Bifidobacteria. This pilot study shed a light on the pathway of future clinical trials assessing the effects of coffee consumption in these patients. This trial has been registered at clinicaltrial.gov with registration number of NCT02929901.
本研究旨在确定补充咖啡因和绿原酸对非酒精性脂肪性肝病(NAFLD)合并糖尿病患者肠道微生物群及代谢紊乱的影响。在这项随机、安慰剂对照临床试验中,26例患有糖尿病和NAFLD的患者被随机分为四组,分别接受200毫克咖啡因加200毫克绿原酸(CFCA),或200毫克咖啡因加200毫克安慰剂(淀粉)(CFPL),或200毫克绿原酸加200毫克安慰剂(CAPL),或200毫克安慰剂加200毫克安慰剂(PLPL),为期12周。补充3个月后,干预组患者体重显著下降(CFCA组=-3.69千克;CFPL组=-0.7千克;CAPL组=-0.43千克;PLPL组=0.26千克)(p=0.004)。与其他三组相比,CFCA组体重下降更为显著(与PLPL组相比p=0.005;与CAPL组相比p=0.023;与CFPL组相比p=0.031)。虽然CFCA组肠道双歧杆菌数量增加,但各组内及组间的任何细菌数量均无统计学显著差异。总之,我们的研究表明,每天摄入200毫克咖啡因加200毫克绿原酸,持续12周,对降低NAFLD合并糖尿病患者的体重有效,这可能至少部分是通过肠道双歧杆菌数量的增加实现的。这项初步研究为未来评估这些患者饮用咖啡效果的临床试验途径提供了线索。该试验已在clinicaltrial.gov上注册,注册号为NCT02929901。