Exploring the Relationship between Gut Microbiome Composition and Blood Indole-3-acetic Acid in Hemodialysis Patients

Author:

Wu Ping-Hsun1234ORCID,Tseng Yu-Fang5,Liu Wangta6ORCID,Chuang Yun-Shiuan347ORCID,Tai Chi-Jung7ORCID,Tung Chun-Wei89ORCID,Lai Kean-Yee10,Kuo Mei-Chuan12ORCID,Chiu Yi-Wen12,Hwang Shang-Jyh12ORCID,Hung Wei-Chun11,Lin Yi-Ting2347ORCID

Affiliation:

1. Division of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan

2. Faculty of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan

3. Center for Big Data Research, Kaohsiung Medical University, Kaohsiung 807, Taiwan

4. Research Center for Precision Environmental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan

5. Department of Family Medicine, Kaohsiung Municipal Hsiao-Kang Hospital, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan

6. Department of Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan

7. Department of Family Medicine, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan

8. Institute of Biotechnology and Pharmaceutical Research, National Health Research Institutes, Miaoli 350, Taiwan

9. Graduate Institute of Data Science, College of Management, Taipei Medical University, Taipei 110, Taiwan

10. Post Baccalaureate Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan

11. Department of Microbiology and Immunology, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan

Abstract

Indole-3-acetic acid (IAA), a protein-bound uremic toxin resulting from gut microbiota-driven tryptophan metabolism, increases in hemodialysis (HD) patients. IAA may induce endothelial dysfunction, inflammation, and oxidative stress, elevating cardiovascular and cognitive risk in HD patients. However, research on the microbiome–IAA association is limited. This study aimed to explore the gut microbiome’s relationship with plasma IAA levels in 72 chronic HD patients aged over 18 (August 2016–January 2017). IAA levels were measured using tandem mass spectrometry, and gut microbiome analysis utilized 16s rRNA next-generation sequencing. Linear discriminative analysis effect size and random forest analysis distinguished microbial species linked to IAA levels. Patients with higher IAA levels had reduced microbial diversity. Six microbial species significantly associated with IAA levels were identified; Bacteroides clarus, Bacteroides coprocola, Bacteroides massiliensi, and Alisteps shahii were enriched in low-IAA individuals, while Bacteroides thetaiotaomicron and Fusobacterium varium were enriched in high-IAA individuals. This study sheds light on specific gut microbiota species influencing IAA levels, enhancing our understanding of the intricate interactions between the gut microbiota and IAA metabolism.

Funder

Ministry of Science and Technology

Kaohsiung Medical University Hospital

Kaohsiung Medical University

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

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