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      Genetically Predicted Gut Microbiota Mediate the Association Between Fatty Acids and Intrahepatic Cholestasis of Pregnancy: A Mendelian Randomization Analysis

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          ABSTRACT

          Fatty acids (FAs) and gut bacteria likely play vital roles in intrahepatic cholestasis of pregnancy (ICP). However, the causal connection between FAs, gut microbiota, and ICP has not yet been confirmed. To investigate the associations of FAs, gut bacteria, and ICP, a Mendelian randomization (MR) analysis with two samples was performed to identify the potential causal relationships between FAs and ICP. The potential mediating role of gut bacteria in FAs and ICP was analyzed by a two‐step MR analysis. False discovery rate (FDR) correction was conducted to correct the bias of multiple tests. MR analysis revealed that higher omega‐6 FAs/total FAs (odds ratio [OR] = 2.563, 95% confidence interval [CI] = 1.362–4.824, FDR p = 0.016), linoleic acids/total FAs (OR = 3.812, 95%CI = 1.966–7.388, FDR p = 0.001), and average number of methylene groups (OR = 1.968, 95%CI = 1.390–2.785, FDR p = 0.001) are potential risk factors for ICP. However, omega‐3 FAs (OR = 0.587, 95%CI = 0.394–0.874, FDR p = 0.031) and the average number of double bonds in an FA chain (OR = 0.575, 95%CI = 0.435–0.759, FDR p = 0.001) could reduce the risk of ICP. The abundance of 25 gut bacteria showed significant causal effects on ICP, among which Dokdonella may play a crucial role in modulating the effects of FAs on ICP. Our research results suggest that the effects of FA on ICP likely vary according to their different types. Dokdonella abundance plays a significant role in mediating the causal interactions between FAs and ICP.

          Abstract

          The effects of fatty acids (FAs) on intrahepatic cholestasis of pregnancy (ICP) likely vary according to their different types. Dokdonella abundance plays a significant role in mediating the causal interactions between FAs and ICP.

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          Most cited references35

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          Omega‐3 fatty acid supplementation in pregnancy—baseline omega‐3 status and early preterm birth: exploratory analysis of a randomised controlled trial

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            Gut microbiota alters host bile acid metabolism to contribute to intrahepatic cholestasis of pregnancy

            Intrahepatic cholestasis of pregnancy (ICP) is a female pregnancy-specific disorder that is characterized by increased serum bile acid and adverse fetal outcomes. The aetiology and mechanism of ICP are poorly understood; thus, existing therapies have been largely empiric. Here we show that the gut microbiome differed significantly between individuals with ICP and healthy pregnant women, and that colonization with gut microbiome from ICP patients was sufficient to induce cholestasis in mice. The gut microbiomes of ICP patients were primarily characterized by Bacteroides fragilis ( B. fragilis ), and B. fragilis was able to promote ICP by inhibiting FXR signaling via its BSH activity to modulate bile acid metabolism. B. fragilis -mediated FXR signaling inhibition was responsible for excessive bile acid synthesis and interrupted hepatic bile excretion to ultimately promote the initiation of ICP. We propose that modulation of the gut microbiota-bile acid-FXR axis may be of value for ICP treatment. Intrahepatic cholestasis of pregnancy (ICP) is a liver disease that sometimes develops during pregnancy and is characterized by increased serum bile acid levels. Here the authors report that the gut microbiome species B. fragilis is enriched in patients with ICP and promotes ICP development in mice via inhibition of signalling though the bile acid receptor FXR.
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              Porphyromonas gingivalis aggravates colitis via a gut microbiota-linoleic acid metabolism-Th17/Treg cell balance axis

              Periodontitis is closely related to inflammatory bowel disease (IBD). An excessive and non-self-limiting immune response to the dysbiotic microbiome characterizes the two. However, the underlying mechanisms that overlap still need to be clarified. We demonstrate that the critical periodontal pathogen Porphyromonas gingivalis (Pg) aggravates intestinal inflammation and Th17/Treg cell imbalance in a gut microbiota-dependent manner. Specifically, metagenomic and metabolomic analyses shows that oral administration of Pg increases levels of the Bacteroides phylum but decreases levels of the Firmicutes, Verrucomicrobia, and Actinobacteria phyla. Nevertheless, it suppresses the linoleic acid (LA) pathway in the gut microbiota, which was the target metabolite that determines the degree of inflammation and functions as an aryl hydrocarbon receptor (AHR) ligand to suppress Th17 differentiation while promoting Treg cell differentiation via the phosphorylation of Stat1 at Ser727. Therapeutically restoring LA levels in colitis mice challenged with Pg exerts anti-colitis effects by decreasing the Th17/Treg cell ratio in an AHR-dependent manner. Our study suggests that Pg aggravates colitis via a gut microbiota-LA metabolism-Th17/Treg cell balance axis, providing a potential therapeutically modifiable target for IBD patients with periodontitis.

                Author and article information

                Contributors
                9862022078@jiangnan.edu.cn
                Journal
                Food Sci Nutr
                Food Sci Nutr
                10.1002/(ISSN)2048-7177
                FSN3
                Food Science & Nutrition
                John Wiley and Sons Inc. (Hoboken )
                2048-7177
                30 December 2024
                January 2025
                : 13
                : 1 ( doiID: 10.1002/fsn3.v13.1 )
                : e4683
                Affiliations
                [ 1 ] Affiliated Women's Hospital of Jiangnan University, Jiangnan University Wuxi China
                Author notes
                [*] [* ] Correspondence:

                Ting Zhang ( 9862022078@ 123456jiangnan.edu.cn )

                Author information
                https://orcid.org/0009-0009-6804-8143
                Article
                FSN34683 FSN3-2024-06-1660.R2
                10.1002/fsn3.4683
                11717022
                63f9f1bc-fdd0-45ce-86a2-9be2e74b0e47
                © 2024 The Author(s). Food Science & Nutrition published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 November 2024
                : 11 June 2024
                : 03 December 2024
                Page count
                Figures: 5, Tables: 0, Pages: 8, Words: 5300
                Funding
                Funded by: National Natural Science Foundation of China , doi 10.13039/501100001809;
                Award ID: 81671489
                Award ID: 82171674
                Funded by: Major Research Foundation of Jiangsu Science and Technology Department
                Award ID: BE2017628
                Funded by: Jiangsu Province Health Committee Scientific Research Project
                Award ID: M2021023
                Funded by: Wuxi City Key Medical Talent of the Project of Invigorating Health Care through Science, Technology and Education
                Award ID: Z201601
                Funded by: Top Talent Support Program for young and middle‐aged people of Wuxi Health Committee
                Award ID: BJ2020077
                Award ID: HB2023078
                Funded by: Jiangsu Province Health Committee Six One Project Top Talent Project
                Award ID: LGY2020023
                Funded by: Wuxi City Science and Technology Development Fund Project
                Award ID: Y20212035
                Funded by: Scientific Research Program of Wuxi Health Commission
                Award ID: Q202121
                Award ID: ZH202109
                Funded by: Key Project of Jiangsu Medical Association Laboratory Medicine Research Special Fund
                Award ID: SYH‐3201160‐0058 (2023005)
                Funded by: Wuxi Maternal and Child Health Research Project
                Award ID: FYKY202308
                Categories
                Original Article
                Original Article
                Custom metadata
                2.0
                January 2025
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.5.2 mode:remove_FC converted:09.01.2025

                fatty acids,gut bacteria,intrahepatic cholestasis of pregnancy,mendelian randomization

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