Abstract

IntroductionAlthough factors initiating the inflammatory response to monosodium urate crystals have been identified, the role of the gut microbiota and their metabolites on gout remains unknown. This study aimed to investigate the changes in both gut microbiota and short-chain fatty acids (SCFAs) according to inflammatory states of gout in the same patients.MethodsThis study enrolled 20 patients with gout in the acute state who had active joints and were followed up until the recovery state with no active joints. Blood and fecal samples were simultaneously collected within 3 days for each disease state. The stool microbiome was analyzed using 16S rRNA sequencing, and serum SCFAs were measured by gas chromatography-mass spectrometry. Differences in the gut microbiome and serum SCFAs were compared between the acute and recovery states.ResultsBeta diversity of the microbiome was significantly different between the acute and recovery states in terms of weighted UniFrac distance. In the recovery state, Prevotellaceae (p = 0.006) and the genus Prevotella (p = 0.009) were significantly enriched, whereas Enterobacteriaceae (p = 0.019) and its derivative genus Shigella (p = 0.023) were significantly decreased compared to the acute state. Similarly, the levels of acetate were dramatically increased in the recovery state compared to the acute state (p < 0.010). The levels of propionate and butyrate tended to increase but without statistical significance.ConclusionSubstantial alterations of bacterial composition with the promotion of SCFA formation (especially acetate) were found after treatment in patients with gouty arthritis.

Highlights

  • Factors initiating the inflammatory response to monosodium urate crystals have been iden‐ tified, the role of the gut microbiota and their metabolites on gout remains unknown

  • A drug with an anti-inflammatory response on gouty arthritis could possibly exert its therapeutic effect by affecting the gut microbiota and enhancing short-chain fatty acids (SCFAs) production in mice induced by monosodium urate (MSU) crystals [6]

  • These studies suggest that the gut microbiota and SCFAs are involved in modulating the inflammatory response to MSU crystal-induced arthritis; these warrant further research for the possible therapeutic effects in patients with gouty arthritis

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Summary

Introduction

Factors initiating the inflammatory response to monosodium urate crystals have been iden‐ tified, the role of the gut microbiota and their metabolites on gout remains unknown. This study aimed to investigate the changes in both gut microbiota and short-chain fatty acids (SCFAs) according to inflammatory states of gout in the same patients. Park and Lee Arthritis Research & Therapy (2022) 24:51 polysaccharides, have an important role in regulating immune cell function and the inflammatory response [4]. Acetate, one such SCFA, promotes the resolution of the inflammatory response to MSU crystals by inducing neutrophil apoptosis [5]. A drug with an anti-inflammatory response on gouty arthritis could possibly exert its therapeutic effect by affecting the gut microbiota and enhancing SCFA production in mice induced by MSU crystals [6]. To understand the role of bacterial dysbiosis and SCFAs in its pathogenic mechanism, we analyzed the changes in the gut microbiota and SCFAs across the inflammatory states of gout in the same patients

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