Evidence map›Paper›PMID 40329424›Full record

ArticleMicrobiome2025

Gut microbiota dysbiosis orchestrates vitiligo-related oxidative stress through the metabolite hippuric acid.

Qingrong Ni, Lin Xia, Ye Huang, Xiaoying Yuan, Weijie Gu, Yueqi Chen, Yijin Wang, Meng Nian, Shengxi Wu, Hong Cai and 1 more

Abstract read
In one paragraph

Article in Microbiome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Qingrong Ni *Department of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China. niqingrong@fmmu.edu.cn.
Lin Xia *Department of Cardiovascular Surgery, General Hospital of Northern Theater Command, Shenyang, 110016, China.
Ye HuangDepartment of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China.
Xiaoying YuanDepartment of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China.
Weijie GuDepartment of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China.
Yueqi ChenDepartment of Orthopedics, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, 400038, China.
Yijin WangDepartment of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China.
Meng NianDepartment of Neurobiology, Basic Medical Science Academy, Fourth Military Medical University, Xi'an, 710032, China.
Shengxi WuDepartment of Neurobiology, Basic Medical Science Academy, Fourth Military Medical University, Xi'an, 710032, China.
Hong CaiDepartment of Dermatology, Air Force Medical Center, Fourth Military Medical University, Beijing, 100142, China. ch1031@163.com.
Jing HuangDepartment of Neurobiology, Basic Medical Science Academy, Fourth Military Medical University, Xi'an, 710032, China. jinghuang@fmmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVitiligo, a depigmenting autoimmune skin disease characterized by melanocyte dysfunction or death, is known to be associated with an imbalance in gut microbiota. Oxidative stress plays a critical role in the pathogenesis of vitiligo. However, the complex promising interaction between abnormal accumulation of reactive oxygen species (ROS) in the skin and gut microbiota has remained unclear.

resultsHere, we compared transcriptome data of vitiligo lesions and normal skin and identified a high expression of oxidative stress-related genes in vitiligo lesions. We also established a vitiligo mouse model and found that the presence of gut microbiota influenced the expression of ROS-related genes. Depletion of gut microbiota reduced abnormal ROS accumulation and mitochondrial abnormalities in melanocytes, significantly improving depigmentation. Our findings from manipulating gut microbiota through cohousing, fecal microbiota transplantation (FMT), and probiotic supplementation showed that transferring gut microbiota from mice with severe vitiligo-like phenotypes exacerbated skin depigmentation while probiotics inhibited its progression. Targeted metabolomics of fecal, serum, and skin tissues revealed gut microbiota-dependent accumulation of hippuric acid, mediating excessive ROS in the skin. Elevated serum hippuric acid levels were also confirmed in vitiligo patients. Additionally, a microbiota-dependent increase in intestinal permeability in vitiligo mice mediated elevated hippuric acid levels, and we found that hippuric acid could directly bind to ROS-related proteins (NOS2 and MAPK14).

conclusionsOur results suggested the important role of gut microbiota in regulating vitiligo phenotypes and oxidative stress. We identified hippuric acid, a gut microbiota-host co-metabolite, as a critical mediator of oxidative stress in vitiligo skin and its binding targets (NOS2 and MAPK14), resulting in oxidative stress. Validation in a small human cohort suggested that hippuric acid could serve as a novel diagnostic biomarker and therapeutic target for vitiligo. These findings provided new insights into how gut microbiota regulates skin oxidative stress in vitiligo and suggested potential treatment strategies for the disease. Video Abstract.

Indexed as

DysbiosisGastrointestinal MicrobiomeHippuratesOxidative StressVitiligoAnimalsDisease Models, AnimalFecal Microbiota TransplantationFemaleHumansMaleMelanocytesMiceMice, Inbred C57BLProbioticsReactive Oxygen SpeciesHippurateshippuric acidReactive Oxygen SpeciesGut microbiotaHippuric acidOxidative stressVitiligo

Identifiers

PMID40329424
PMCPMC12054231

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.