Department of Food Science and Nutrition, Zhejiang University, Hangzhou, 310058, China.
No. 1 Department of Nutrition, Chinese People's Liberation Army General Hospital, Beijing, China.
Clin Nutr. 2020 Feb;39(2):395-404. doi: 10.1016/j.clnu.2019.02.037. Epub 2019 Feb 27.
BACKGROUND & AIMS: Observational studies have shown that diets high in fat and low in dietary fiber, might have an unfavorable impact on bile acid (BA) profiles, which might further affect host cardiometabolic health. In the current study, we aimed to evaluate the effects of dietary fat content on BA profiles and associated gut microbiota, and their correlates with cardiometabolic risk factors. METHODS: In a randomized controlled-feeding trial, healthy young adults were assigned to one of the three diets: a lower-fat diet (fat 20%, carbohydrate 66% and protein 14%), a moderate-fat diet (fat 30%, carbohydrate 56% and protein 14%) and a higher-fat diet (fat 40%, carbohydrate 46% and protein 14%) for 6 months. All the foods were provided during the entire intervention period. The BA profiles, associated gut microbiota and markers of cardiometabolic risk factors were determined before and after intervention. RESULTS: The higher-fat diet resulted in an elevated concentration of total BAs (p < 0.001), and unconjugated BAs (p = 0.03) compared with lower-fat diet. Secondary BAs, such as deoxycholic acid (DCA), taurodeoxycholic acid (TDCA), 12ketolithocholic acid (12keto-LCA), 3β-DCA and taurolithocholic acid (TLCA) (p < 0.05 after FDR correction) were significantly increased in the higher-fat diet group after the 6-month intervention. Consistently, the abundances of gut bacteria (Bacteroides, Clostridium, Bifidobacterium and Lactobacillus) which affect bile salt hydrolase gene expression were significantly increased after higher-fat consumption. The change of DCA was positively associated with the relative abundance of Bacteroides (r = 0.31, p = 0.08 after FDR correction). In addition, the changes of fecal concentrations of DCA and 12keto-LCA were positively associated with serum total cholesterol (r > 0.3, p = 0.02 and p = 0.008 after FDR correction, respectively). In line with these findings, serum fibroblast growth factor 19 (FGF19) was marginally significantly elevated in the higher-fat group after intervention (p = 0.05). CONCLUSIONS: The higher-fat diet resulted in an alteration of BAs, especially unconjugated BAs and secondary BAs, most likely through actions of gut microbiota. These alterations might confer potentially unfavorable impacts on colonic and host cardiometabolic health in healthy young adults. Clinical trial registry number: NCT02355795 listed on NIH website: ClinicalTrials.gov.
背景与目的:观察性研究表明,高脂肪、低膳食纤维的饮食可能对胆汁酸(BA)谱产生不利影响,进而可能影响宿主的心脏代谢健康。在本研究中,我们旨在评估饮食脂肪含量对 BA 谱和相关肠道微生物群的影响,以及它们与心脏代谢危险因素的相关性。
方法:在一项随机对照喂养试验中,健康的年轻成年人被分配到以下三种饮食之一:低脂肪饮食(脂肪 20%,碳水化合物 66%,蛋白质 14%)、中脂肪饮食(脂肪 30%,碳水化合物 56%,蛋白质 14%)和高脂肪饮食(脂肪 40%,碳水化合物 46%,蛋白质 14%),持续 6 个月。在整个干预期间都提供所有食物。在干预前后测定 BA 谱、相关肠道微生物群和心脏代谢危险因素标志物。
结果:与低脂肪饮食相比,高脂肪饮食导致总胆汁酸(BA)浓度升高(p<0.001),非结合胆汁酸(p=0.03)升高。次级 BA,如脱氧胆酸(DCA)、牛磺脱氧胆酸(TDCA)、12-酮石胆酸(12keto-LCA)、3β-DCA 和牛磺胆酸(TLCA)(FDR 校正后 p<0.05)在高脂肪饮食组中显著增加。一致地,影响胆汁盐水解酶基因表达的肠道细菌(拟杆菌、梭菌、双歧杆菌和乳酸杆菌)的丰度在高脂肪摄入后显著增加。DCA 的变化与拟杆菌的相对丰度呈正相关(r=0.31,FDR 校正后 p=0.08)。此外,粪便 DCA 和 12keto-LCA 浓度的变化与血清总胆固醇呈正相关(r>0.3,FDR 校正后分别为 p=0.02 和 p=0.008)。与此发现一致的是,干预后高脂肪组血清成纤维细胞生长因子 19(FGF19)水平略有升高(p=0.05)。
结论:高脂肪饮食导致 BA 谱发生改变,特别是非结合 BA 和次级 BA,很可能通过肠道微生物群的作用。这些变化可能对健康年轻成年人的结肠和宿主心脏代谢健康产生潜在不利影响。临床试验注册号:NCT02355795,在美国国立卫生研究院网站上登记:ClinicalTrials.gov。
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