The Effect of Inulin‐Type Fructans on Plasma Trimethylamine N‐Oxide Levels in Peritoneal Dialysis Patients: A Randomized Crossover Trial

Author:

Xiong Qianqian1,Li Li1,Xiao Yonghua2,He Shuiqing3,Zhao Jing1,Lin Xuechun1,He Yuqin1,Wang Jinxue1,Guo Xiaolei1,Liang Wangqun4,Zuo Xuezhi5,Ying Chenjiang1ORCID

Affiliation:

1. Department of Nutrition and Food Hygiene Hubei Key Laboratory of Food Nutrition and Safety School of Public Health Tongji Medical College Huazhong University of Science and Technology Wuhan Hubei 430030 China

2. Institute of Food and Environmental Health Wuhan Centers for Disease Control and Prevention Wuhan Hubei 430024 China

3. Hunan Institute for Tuberculosis Control Hunan Chest Hospital Department of Nutrition Changsha Hunan 410000 China

4. Division of Nephrology Tongji Hospital Tongji Medical College Huazhong University of Science and Technology Wuhan Hubei 430030 China

5. Department of Clinical Nutrition Tongji Hospital Tongji Medical College Huazhong University of Science and Technology Wuhan Hubei 430030 China

Abstract

ScopeTrimethylamine N‐oxide (TMAO), an important proatherogenic uremic toxin, is oxidized by hepatic‐flavin monooxygenases from gut microbiome‐generated trimethylamine (TMA). The present study aims to explore whether manipulating the gut microbiota by inulin‐type fructans (ITFs) can reduce circulating TMAO levels in peritoneal dialysis patients.Methods and resultsThis is a randomized, double‐blind, placebo‐controlled, crossover trial with 10 g day−1 ITFs intervention for 3 months in continuous ambulatory peritoneal dialysis patients. The gut microbiome is measured, and TMA‐producing gene clusters are annotated using shotgun metagenomic sequencing. Fecal and plasma TMA, plasma TMAO, and daily urine excretion and dialysis removal of TMAO are measured. Finally, 22 participants complete the trial. The daily intake of macronutrients and TMAO precursors is comparable during the prebiotics, washout, and placebo interventions. The ITFs intervention increases the Firmicutes/Bacteroidetes (F/B) ratio (p = 0.049) of gut microbiome. However, no significant influences are observed on fecal TMA content, circulating TMAO levels, or TMA‐producing gene clusters, including choline TMA‐lyase (CutC/D), carnitine monooxygenase (CntA/B), and betaine reductase (GrdH).ConclusionsIntervention with 10 g day−1 of ITFs for 3 months is not sufficient to reduce plasma TMAO levels in peritoneal dialysis patients, but it improves the gut microbiome composition.

Publisher

Wiley

Subject

Food Science,Biotechnology

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