Year in Review: Advances in Research in Gout Pathophysiology in 2024

This review provides an overview of the most significant developments in gout pathophysiology research published in 2024. Thirteen studies were selected based on originality, scientific rigor, and potential clinical impact and grouped into four major categories: inflammation and pain mechanisms (LRRC8 anion channels, CXCL5-CXCR2 axis, CD38 and NAD+ metabolism, PLK1 and NLRP3 inflammasome localization, and IFN1 suppression), biomarkers and proteomics (scRNA-seq reveals monocyte and T-cell flare signatures, and Olink serum profiling reveals a proinflammatory signature in hyperuricemia and also identifies TNFSF14 as a novel flare biomarker, while a multi-omics integrative study implicates TRIM46 as a key causal gene), gut virome, and novel therapies (vagus nerve stimulation, biomimetic nanosystem, and restoration of Urate Oxidase (Uox) function). The studies selected focused primarily on work on subjects other than on hyperuricemia. The findings collectively expand our understanding of gout’s complex pathophysiology and highlight potential strategies for diagnosis, management, and innovative treatments.

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Institutions

Publication Details

Journal
Gout Urate and Crystal Deposition Disease
Published
2025-08-18
DOI
https://doi.org/10.3390/gucdd3030015
Citations
1
Primary Topic
Gout, Hyperuricemia, Uric Acid
Type
article
Field-Weighted Citation Impact
1.43
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article

Year in Review: Advances in Research in Gout Pathophysiology in 2024

Mónica Gumá, Rocío Paz-González
1 citations
Gout Urate and Crystal Deposition Disease
Gout, Hyperuricemia, Uric Acid
1.43
article

Year in Review: Advances in Research in Gout Pathophysiology in 2024

Mónica Gumá, Rocío Paz-González
article en
1 citations

Abstract

This review provides an overview of the most significant developments in gout pathophysiology research published in 2024. Thirteen studies were selected based on originality, scientific rigor, and potential clinical impact and grouped into four major categories: inflammation and pain mechanisms (LRRC8 anion channels, CXCL5-CXCR2 axis, CD38 and NAD+ metabolism, PLK1 and NLRP3 inflammasome localization, and IFN1 suppression), biomarkers and proteomics (scRNA-seq reveals monocyte and T-cell flare signatures, and Olink serum profiling reveals a proinflammatory signature in hyperuricemia and also identifies TNFSF14 as a novel flare biomarker, while a multi-omics integrative study implicates TRIM46 as a key causal gene), gut virome, and novel therapies (vagus nerve stimulation, biomimetic nanosystem, and restoration of Urate Oxidase (Uox) function). The studies selected focused primarily on work on subjects other than on hyperuricemia. The findings collectively expand our understanding of gout’s complex pathophysiology and highlight potential strategies for diagnosis, management, and innovative treatments.

Gout Urate and Crystal Deposition DiseaseVol. 3(3)
University of California San Diego (US), VA San Diego Healthcare System (US), Instituto de Investigación Biomédica de A Coruña (ES)
Openalex Percentile: Top 17%
Gout, Hyperuricemia, Uric Acid
1.43
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Year in Review: Advances in Research in Gout Pathophysiology in 2024 — Mónica Gumá, Rocío Paz-González · Gout Urate and Crystal Deposition Disease (2025) | TGRS Research Map | TGRS