The Gut–Kidney Axis in Uric Acid Nephropathy: Microbiota, Metabolic Crosstalk, and Translational Prospects

Jiahao Liang,1 Yanzhi Qiu,1 Tong Fu,2 Jianing Li,1 Jiamin Yang,1 Ying Tong1 1Graduate School, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, 150040, People’s Republic of China; 2Department of Psychology, Brandeis University, Waltham, MA, 02453, USACorrespondence: Ying Tong, Graduate School, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, 150040, People’s Republic of China, Email [email protected]: Uric acid nephropathy (UAN) represents a critical and multifactorial renal disorder closely linked to hyperuricemia, inflammation, and gut microbiota dysregulation. Recent advances have revealed the pivotal role of the gut–kidney axis in modulating urate metabolism, immune activation, and oxidative stress. This review synthesizes emerging preclinical and clinical evidence to construct an integrative framework for understanding UAN, highlighting both crystal-dependent and crystal-independent mechanisms that drive tubular injury and fibrosis. Accumulating data underscore the reciprocal crosstalk between renal dysfunction and gut dysbiosis, mediated by microbial metabolites such as short-chain fatty acids (SCFAs), indoxyl sulfate, and p-cresol sulfate. We further evaluate therapeutic interventions targeting the gut–kidney axis—including probiotics, synbiotics, postbiotics, fecal microbiota transplantation (FMT), and engineered microbial therapies—which have shown promise in restoring microbial balance and improving urate handling. By integrating multi-omics profiling with systems biology, this review proposes a precision-medicine roadmap that leverages microbiome signatures and metabolic phenotyping for risk stratification and personalized intervention. Moreover, we emphasize the need for supportive regulatory frameworks and interdisciplinary collaboration to enable the clinical translation of microbiota-based strategies. Collectively, this work provides a strengthened conceptual foundation for microbiome-informed prevention and treatment of uric acid–related kidney disease.Keywords: uric acid nephropathy, hyperuricemia, gut–kidney axis, microbiota, inflammation, oxidative stress, probiotics

Publication Details

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Dove Medical Press (Taylor and Francis Group)
Published
2025-12-18
Primary Topic
Gout, Hyperuricemia, Uric Acid
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article
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article

The Gut–Kidney Axis in Uric Acid Nephropathy: Microbiota, Metabolic Crosstalk, and Translational Prospects

Dove Medical Press (Taylor and Francis Group)
Gout, Hyperuricemia, Uric Acid
article

The Gut–Kidney Axis in Uric Acid Nephropathy: Microbiota, Metabolic Crosstalk, and Translational Prospects

article en

Abstract

Jiahao Liang,1 Yanzhi Qiu,1 Tong Fu,2 Jianing Li,1 Jiamin Yang,1 Ying Tong1 1Graduate School, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, 150040, People’s Republic of China; 2Department of Psychology, Brandeis University, Waltham, MA, 02453, USACorrespondence: Ying Tong, Graduate School, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, 150040, People’s Republic of China, Email [email protected]: Uric acid nephropathy (UAN) represents a critical and multifactorial renal disorder closely linked to hyperuricemia, inflammation, and gut microbiota dysregulation. Recent advances have revealed the pivotal role of the gut–kidney axis in modulating urate metabolism, immune activation, and oxidative stress. This review synthesizes emerging preclinical and clinical evidence to construct an integrative framework for understanding UAN, highlighting both crystal-dependent and crystal-independent mechanisms that drive tubular injury and fibrosis. Accumulating data underscore the reciprocal crosstalk between renal dysfunction and gut dysbiosis, mediated by microbial metabolites such as short-chain fatty acids (SCFAs), indoxyl sulfate, and p-cresol sulfate. We further evaluate therapeutic interventions targeting the gut–kidney axis—including probiotics, synbiotics, postbiotics, fecal microbiota transplantation (FMT), and engineered microbial therapies—which have shown promise in restoring microbial balance and improving urate handling. By integrating multi-omics profiling with systems biology, this review proposes a precision-medicine roadmap that leverages microbiome signatures and metabolic phenotyping for risk stratification and personalized intervention. Moreover, we emphasize the need for supportive regulatory frameworks and interdisciplinary collaboration to enable the clinical translation of microbiota-based strategies. Collectively, this work provides a strengthened conceptual foundation for microbiome-informed prevention and treatment of uric acid–related kidney disease.Keywords: uric acid nephropathy, hyperuricemia, gut–kidney axis, microbiota, inflammation, oxidative stress, probiotics

Dove Medical Press (Taylor and Francis Group)
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Gout, Hyperuricemia, Uric Acid
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