Pataky Zoltan, Genton Laurence, Spahr Laurent, Lazarevic Vladimir, Terraz Sylvain, Gaïa Nadia, Rubbia-Brandt Laura, Golay Alain, Schrenzel Jacques, Pichard Claude
Service of Therapeutic Education for Chronic Diseases, WHO Collaborating Centre, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.
Clinical Nutrition, Geneva University Hospitals, University of Geneva, Geneva, Switzerland.
Dig Dis Sci. 2016 Sep;61(9):2721-31. doi: 10.1007/s10620-016-4179-1. Epub 2016 May 3.
NAFLD is likely to become the most common cause of chronic liver disease. The first-line treatment includes weight loss.
To analyze the impact of a hypocaloric hyperproteic diet (HHD) on gut microbiota in NAFLD patients.
Fifteen overweight/obese patients with NAFLD were included. At baseline and after a 3-week HHD (Eurodiets(®), ~1000 kcal/day, ~125 g protein/day), we measured gut microbiota composition and function by shotgun metagenomics; body weight; body composition by bioelectrical impedance analysis; liver and visceral fat by magnetic resonance imaging; plasma C-reactive protein (CRP); and liver tests. Results between both time points, expressed as median (first and third quartile), were compared by Wilcoxon signed-rank tests.
At baseline, age was 50 (47-55) years and body mass index 34.6 (32.4, 36.7) kg/m(2). HDD decreased body weight by 3.6 % (p < 0.001), percent liver fat by 65 % (p < 0.001), and CRP by 19 % (p = 0.014). HDD was associated with a decrease in Lachnospira (p = 0.019), an increase in Blautia (p = 0.026), Butyricicoccus (p = 0.024), and changes in several operational taxonomic units (OTUs) of Bacteroidales and Clostridiales. The reduced liver fat was negatively correlated with bacteria belonging to the Firmicutes and Bacteroidetes phyla (a Ruminococcaceae OTU, r = -0.83; Bacteroides, r = -0.73). The associated metabolic changes concerned mostly enzymes involved in amino acid and carbohydrate metabolism.
In this pilot study, HHD changes gut microbiota composition and function in overweight/obese NAFLD patients, in parallel with decreased body weight, liver fat, and systemic inflammation. Future studies should aim to confirm these bacterial changes and understand their mode of action.
Under clinicaltrials.gov: NCT01477307.
非酒精性脂肪性肝病(NAFLD)可能会成为慢性肝病最常见的病因。一线治疗方法包括减重。
分析低热量高蛋白饮食(HHD)对NAFLD患者肠道微生物群的影响。
纳入15例超重/肥胖的NAFLD患者。在基线期以及为期3周的HHD饮食(欧洲饮食法(®),约1000千卡/天,约125克蛋白质/天)后,我们通过鸟枪法宏基因组学检测肠道微生物群的组成和功能;测量体重;通过生物电阻抗分析测定身体成分;通过磁共振成像测量肝脏和内脏脂肪;检测血浆C反应蛋白(CRP)以及肝功能。两个时间点的结果以中位数(第一和第三四分位数)表示,通过Wilcoxon符号秩检验进行比较。
在基线期,年龄为50(47 - 55)岁,体重指数为34.6(32.4,36.7)kg/m²。HHD使体重下降了3.6%(p < 0.001),肝脏脂肪百分比下降了65%(p < 0.001),CRP下降了19%(p = 0.014)。HHD与毛螺菌属减少(p = 0.019)、布劳特氏菌属增加(p = 0.026)、丁酸球菌属增加(p = 0.024)以及拟杆菌目和梭菌目的几个操作分类单元(OTU)的变化有关。肝脏脂肪减少与厚壁菌门和拟杆菌门的细菌呈负相关(一个瘤胃球菌科OTU,r = -0.83;拟杆菌属,r = -0.73)。相关的代谢变化主要涉及参与氨基酸和碳水化合物代谢的酶。
在这项初步研究中,HHD改变了超重/肥胖NAFLD患者肠道微生物群的组成和功能,同时体重、肝脏脂肪和全身炎症也有所减轻。未来的研究应旨在证实这些细菌变化并了解其作用方式。
在clinicaltrials.gov下:NCT01477307。