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肠道微生物群和 PNPLA3 rs738409 变异对肥胖青少年非酒精性脂肪性肝病(NAFLD)的影响。

Effect of Gut Microbiota and PNPLA3 rs738409 Variant on Nonalcoholic Fatty Liver Disease (NAFLD) in Obese Youth.

机构信息

Frank H. Netter MD School of Medicine, North Haven, Connecticut.

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut.

出版信息

J Clin Endocrinol Metab. 2020 Oct 1;105(10):e3575-85. doi: 10.1210/clinem/dgaa382.


DOI:10.1210/clinem/dgaa382
PMID:32561908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7458486/
Abstract

CONTEXT: Nonalcoholic fatty liver disease (NAFLD) is the most common cause of liver disease, affecting approximately 3 in 10 obese children worldwide. OBJECTIVE: We aimed to investigate the potential relationship between gut microbiota and NAFLD in obese youth, while considering the role of PNPLA3 rs738409, a strong genetic contributor to NAFLD. DESIGN: In this cross-sectional study, participants completed an abdominal magnetic resonance imaging to measure hepatic fat fraction (HFF), oral glucose tolerance test, and PNPLA3 rs738409 genotyping. Fecal samples were collected to analyze the V4 region of the 16S rRNA gene for intestinal bacteria characterization. SETTING: Yale Pediatric Obesity Clinic. PARTICIPANTS: Obese youth (body mass index >95th percentile) with NAFLD (HFF ≥5.5%; n = 44) and without NAFLD (HFF <5.5%; n = 29). MAIN OUTCOME MEASURE: Shannon-Wiener diversity index values and proportional bacterial abundance by NAFLD status and PNPLA3 genotype. RESULTS: Subjects with NAFLD had decreased bacterial alpha-diversity compared with those without NAFLD (P = 0.013). Subjects with NAFLD showed a higher Firmicutes to Bacteroidetes (F/B) ratio (P = 0.019) and lower abundance of Bacteroidetes (P = 0.010), Prevotella (P = 0.019), Gemmiger (P = 0.003), and Oscillospira (P = 0.036). F/B ratio, Bacteroidetes, Gemmiger, and Oscillospira were associated with HFF when controlling for group variations. We also observed an additive effect on HFF by PNPLA3 rs738409 and Gemmiger, and PNPLA3 rs738409 and Oscillospira. CONCLUSIONS: Obese youth with NAFLD have a different gut microbiota composition than those without NAFLD. These differences were still statistically significant when controlling for factors associated with NAFLD, including PNPLA3 rs738409.

摘要

背景:非酒精性脂肪性肝病(NAFLD)是最常见的肝病病因,影响着全球约 3/10 的肥胖儿童。

目的:我们旨在研究肥胖青少年中肠道微生物群与 NAFLD 之间的潜在关系,同时考虑到 PNPLA3 rs738409 的作用,后者是 NAFLD 的一个强烈遗传因素。

设计:在这项横断面研究中,参与者完成了腹部磁共振成像以测量肝脂肪分数(HFF)、口服葡萄糖耐量试验和 PNPLA3 rs738409 基因分型。采集粪便样本以分析肠道细菌特征的 16S rRNA 基因 V4 区。

地点:耶鲁儿科肥胖诊所。

参与者:患有 NAFLD(HFF≥5.5%;n=44)和不患有 NAFLD(HFF<5.5%;n=29)的肥胖青少年(体重指数>第 95 百分位数)。

主要观察指标:根据 NAFLD 状态和 PNPLA3 基因型的 Shannon-Wiener 多样性指数值和细菌相对丰度。

结果:与无 NAFLD 者相比,有 NAFLD 者的细菌α多样性降低(P=0.013)。有 NAFLD 者的厚壁菌门与拟杆菌门比值(F/B 比值)更高(P=0.019),拟杆菌门(P=0.010)、普雷沃氏菌属(P=0.019)、动弯杆菌属(P=0.003)和真杆菌属(P=0.036)的丰度更低。在控制组间变异时,F/B 比值、拟杆菌门、动弯杆菌属和真杆菌属与 HFF 相关。我们还观察到 PNPLA3 rs738409 和动弯杆菌属以及 PNPLA3 rs738409 和真杆菌属对 HFF 的附加效应。

结论:患有 NAFLD 的肥胖青少年的肠道微生物群组成与无 NAFLD 者不同。当控制与 NAFLD 相关的因素,包括 PNPLA3 rs738409 时,这些差异仍然具有统计学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/b0fd1c641631/dgaa382_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/80d8b0a045bb/dgaa382_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/4ec3876282c0/dgaa382_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/b0fd1c641631/dgaa382_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/80d8b0a045bb/dgaa382_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/4ec3876282c0/dgaa382_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b46/7458486/b0fd1c641631/dgaa382_fig3.jpg

相似文献

[1]
Effect of Gut Microbiota and PNPLA3 rs738409 Variant on Nonalcoholic Fatty Liver Disease (NAFLD) in Obese Youth.

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[2]
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[3]
Association of PNPLA3 rs738409 G/C gene polymorphism with nonalcoholic fatty liver disease in children: a meta-analysis.

BMC Med Genet. 2020-8-18

[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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World J Hepatol. 2025-6-27

[2]
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[3]
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Front Microbiol. 2025-4-3

[4]
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[5]
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Environ Health Prev Med. 2025

[6]
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Nat Rev Gastroenterol Hepatol. 2025-5

[7]
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Front Microbiol. 2024-12-20

[8]
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World J Gastrointest Pharmacol Ther. 2024-11-5

[9]
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[10]
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