文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

未结合胆汁酸和次级胆汁酸谱对高脂肪、低碳水化合物饮食的反应及与相关肠道微生物群的关系:一项为期 6 个月的随机对照喂养试验。

Unconjugated and secondary bile acid profiles in response to higher-fat, lower-carbohydrate diet and associated with related gut microbiota: A 6-month randomized controlled-feeding trial.

机构信息

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.

出版信息

Clin Nutr. 2020 Feb;39(2):395-404. doi: 10.1016/j.clnu.2019.02.037. Epub 2019 Feb 27.


DOI:10.1016/j.clnu.2019.02.037
PMID:30876827
Abstract

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.

摘要

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。

相似文献

[1]
Unconjugated and secondary bile acid profiles in response to higher-fat, lower-carbohydrate diet and associated with related gut microbiota: A 6-month randomized controlled-feeding trial.

Clin Nutr. 2020-2

[2]
Exploring changes in the human gut microbiota and microbial-derived metabolites in response to diets enriched in simple, refined, or unrefined carbohydrate-containing foods: a post hoc analysis of a randomized clinical trial.

Am J Clin Nutr. 2020-12-10

[3]
Effects of dietary fat on gut microbiota and faecal metabolites, and their relationship with cardiometabolic risk factors: a 6-month randomised controlled-feeding trial.

Gut. 2019-2-19

[4]
Effects of Bile Acid Modulation by Dietary Fat, Cholecystectomy, and Bile Acid Sequestrant on Energy, Glucose, and Lipid Metabolism and Gut Microbiota in Mice.

Int J Mol Sci. 2022-5-25

[5]
Dietary fat and gut microbiota interactions determine diet-induced obesity in mice.

Mol Metab. 2016-10-13

[6]
Dietary cholesterol drives the development of nonalcoholic steatohepatitis by altering gut microbiota mediated bile acid metabolism in high-fat diet fed mice.

J Nutr Biochem. 2023-7

[7]
Bile acid is a significant host factor shaping the gut microbiome of diet-induced obese mice.

BMC Biol. 2017-12-14

[8]
Comprehensive Analysis of Serum and Fecal Bile Acid Profiles and Interaction with Gut Microbiota in Primary Biliary Cholangitis.

Clin Rev Allergy Immunol. 2020-2

[9]
Dietary bile acids supplementation improves the growth performance and alleviates fatty liver in broilers fed a high-fat diet via improving the gut microbiota.

Poult Sci. 2024-2

[10]
Bile acids associate with specific gut microbiota, low-level alcohol consumption and liver fibrosis in patients with non-alcoholic fatty liver disease.

Liver Int. 2020-6

引用本文的文献

[1]
Novel Approaches in Glucose and Lipid Metabolism Disorder Therapy: Targeting the Gut Microbiota-Bile Acid Axis.

Biology (Basel). 2025-7-2

[2]
High-fat diet driven post-operative colon cancer recurrence is dependent upon genetic susceptibility to deoxycholic acid.

Cancer Lett. 2025-7-22

[3]
Association between dietary index for gut microbiota and diarrhea among US adults: a cross-sectional analysis of NHANES 2005-2010.

Front Nutr. 2025-4-11

[4]
The gut microbiota-inflammation-HFpEF axis: deciphering the role of gut microbiota dysregulation in the pathogenesis and management of HFpEF.

Front Cell Infect Microbiol. 2025-3-13

[5]
Carcinogenic and anticancer activities of microbiota-derived secondary bile acids.

Front Oncol. 2025-1-29

[6]
Study of Microbiota Associated to Early Tumors Can Shed Light on Colon Carcinogenesis.

Int J Mol Sci. 2024-12-11

[7]
Bile acids as a key target: traditional Chinese medicine for precision management of insulin resistance in type 2 diabetes mellitus through the gut microbiota-bile acids axis.

Front Endocrinol (Lausanne). 2024-12-10

[8]
Microbiota-Focused Dietary Approaches to Support Health: A Systematic Review.

J Nutr. 2025-2

[9]
Colon or semicolon: gut sampling microdevices for omics insights.

NPJ Biofilms Microbiomes. 2024-10-2

[10]
Diet, Gut Microbes, and Cancer.

Cancer Treat Res. 2024

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索