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益生菌治疗非酒精性脂肪性肝病(NAFLD)患者的随机试验。

Prebiotic Treatment in Patients with Nonalcoholic Fatty Liver Disease (NAFLD)-A Randomized Pilot Trial.

机构信息

Institute of Diabetes and Metabolism-Kaplan Medical Center, Rehovot 7661041, Israel.

School of Nutritional Sciences, Faculty of Agriculture, Food and Environment, The Hebrew University, Jerusalem 9112102, Israel.

出版信息

Nutrients. 2024 May 22;16(11):1571. doi: 10.3390/nu16111571.


DOI:10.3390/nu16111571
PMID:38892505
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11174003/
Abstract

Several studies show that gut microbiotas in patients with nonalcoholic fatty liver disease (NAFLD) differ from those in a healthy population, suggesting that this alteration plays a role in NAFLD pathogenesis. We investigated whether prebiotic administration affects liver fat content and/or liver-related and metabolic parameters. Patients with NAFLD and metabolic syndrome (age: 50 ± 11; 79% men) were randomized to receive either 16 g/day of prebiotic (ITFs-inulin-type fructans) ( = 8) or placebo (maltodextrin) ( = 11) for 12 weeks. Patients were instructed to maintain a stable weight throughout the study. Liver fat content (measured by HMRS), fecal microbiota, and metabolic, inflammatory, and liver parameters were determined before and after intervention. Fecal samples from patients who received the prebiotic had an increased content of ( = 0.025), which was not observed with the placebo. However, the baseline and end-of-study liver fat contents did not change significantly in the prebiotic and placebo groups, neither did the liver function tests' metabolic and inflammatory mediators, including fibroblast growth factor-19 and lipopolysaccharide-binding protein. Body weight remained stable in both groups. These findings suggest that prebiotic treatment without weight reduction is insufficient to improve NAFLD.

摘要

几项研究表明,非酒精性脂肪性肝病(NAFLD)患者的肠道微生物群与健康人群不同,这表明这种改变在 NAFLD 的发病机制中起作用。我们研究了益生菌的管理是否会影响肝脂肪含量和/或与肝脏相关的代谢参数。将非酒精性脂肪性肝病和代谢综合征患者(年龄:50 ± 11;79%男性)随机分为接受 16 克/天益生菌(ITFs-菊粉型果聚糖)(n = 8)或安慰剂(麦芽糊精)(n = 11)治疗 12 周。患者在整个研究期间被要求保持稳定的体重。在干预前后测定了肝脂肪含量(通过 HMRS 测量)、粪便微生物群和代谢、炎症和肝脏参数。接受益生菌的患者粪便样本中的含量增加(p = 0.025),而安慰剂组则没有观察到这种情况。然而,益生菌和安慰剂组的基线和研究结束时的肝脂肪含量没有显著变化,包括成纤维细胞生长因子 19 和脂多糖结合蛋白在内的肝功能试验的代谢和炎症介质也没有变化。两组的体重均保持稳定。这些发现表明,不减轻体重的益生菌治疗不足以改善非酒精性脂肪性肝病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/1c74d865805f/nutrients-16-01571-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/a768171e6110/nutrients-16-01571-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/6a0daf1f9432/nutrients-16-01571-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/45b7842b9223/nutrients-16-01571-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/86b7ced16894/nutrients-16-01571-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/1c74d865805f/nutrients-16-01571-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/a768171e6110/nutrients-16-01571-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/6a0daf1f9432/nutrients-16-01571-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/45b7842b9223/nutrients-16-01571-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/86b7ced16894/nutrients-16-01571-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca7b/11174003/1c74d865805f/nutrients-16-01571-g005.jpg

相似文献

[1]
Prebiotic Treatment in Patients with Nonalcoholic Fatty Liver Disease (NAFLD)-A Randomized Pilot Trial.

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[7]
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引用本文的文献

[1]
Type 2 Diabetes and the Multifaceted Gut-X Axes.

Nutrients. 2025-8-21

[2]
Gut microbiota in non-alcoholic fatty liver disease: Pathophysiology, diagnosis, and therapeutics.

World J Hepatol. 2025-6-27

[3]
Differential effects of inulin and fructooligosaccharides on gut microbiota composition and glycemic metabolism in overweight/obese and healthy individuals: a randomized, double-blind clinical trial.

BMC Med. 2025-7-1

[4]
Dietary Strategies to Modulate Gut Microbiota in Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD).

Nutrients. 2025-6-1

[5]
Advances in the acting mechanism and treatment of gut microbiota in metabolic dysfunction-associated steatotic liver disease.

Gut Microbes. 2025-12

[6]
Metabolic dysfunction-associated steatotic liver disease and the gut microbiome: pathogenic insights and therapeutic innovations.

J Clin Invest. 2025-4-1

[7]
Natural Bioactive Compounds in the Management of Type 2 Diabetes and Metabolic (Dysfunction)-Associated Steatotic Liver Disease.

Pharmaceuticals (Basel). 2025-2-19

[8]
The effect of gut microbiome-targeted therapies in nonalcoholic fatty liver disease: a systematic review and network meta-analysis.

Front Nutr. 2025-1-6

[9]
Insights of gut-liver axis in hepatic diseases: Mechanisms, clinical implications, and therapeutic potentials.

World J Gastrointest Pharmacol Ther. 2024-11-5

本文引用的文献

[1]
Non-alcoholic fatty liver disease and gut microbial dysbiosis- underlying mechanisms and gut microbiota mediated treatment strategies.

Rev Endocr Metab Disord. 2023-12

[2]
Prebiotics and Probiotics: Therapeutic Tools for Nonalcoholic Fatty Liver Disease.

Int J Mol Sci. 2023-10-5

[3]
Thioredoxin/Glutaredoxin Systems and Gut Microbiota in NAFLD: Interplay, Mechanism, and Therapeutical Potential.

Antioxidants (Basel). 2023-8-28

[4]
Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD): A State-of-the-Art Review.

J Obes Metab Syndr. 2023-9-30

[5]
Metabolic dysfunction: The silenced connection with fatty liver disease.

Ann Hepatol. 2023

[6]
Randomized, Controlled Trial of the FGF21 Analogue Pegozafermin in NASH.

N Engl J Med. 2023-9-14

[7]
Probiotic Supplementation, Hepatic Fibrosis, and the Microbiota Profile in Patients with Nonalcoholic Steatohepatitis: A Randomized Controlled Trial.

J Nutr. 2023-7

[8]
Pectin in Metabolic Liver Disease.

Nutrients. 2022-12-29

[9]
Inulin intervention attenuates hepatic steatosis in rats via modulating gut microbiota and maintaining intestinal barrier function.

Food Res Int. 2023-1

[10]
Safety, pharmacokinetics, and pharmacodynamics of pegozafermin in patients with non-alcoholic steatohepatitis: a randomised, double-blind, placebo-controlled, phase 1b/2a multiple-ascending-dose study.

Lancet Gastroenterol Hepatol. 2023-2

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