Evidence map›Paper›PMID 41408315›Full record

ArticleDiabetology & metabolic syndrome2025

Serum RAC1 as a potential biomarker in the early stages of diabetic kidney disease.

Yao Fang, Xianyang Mo, Nan Wang, Qunwei Ma, Ruirui Fu, Ying Sun, Tingting Yang, Jaishi Bishnu Raj, Xiaoyan Zhou, Changjiang Ying

Abstract read
In one paragraph

Article in Diabetology & metabolic syndrome, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Salt and chronic kidney disease.Nature reviews. Nephrology · 2026
    Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Yao FangAffiliated Hospital of Xuzhou Medical University, Xuzhou, China.
Xianyang MoThe Graduate School, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Nan WangThe Graduate School, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Qunwei MaThe Graduate School, Capital Medical University, Beijing, China.
Ruirui FuThe Graduate School, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Ying SunJiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Tingting YangJiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Jaishi Bishnu RajThe Graduate School, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xiaoyan ZhouLaboratory of Morphology, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Changjiang YingAffiliated Hospital of Xuzhou Medical University, Xuzhou, China. ycj321651@163.com.ORCID http://orcid.org/0000-0002-0224-0265

Funding

Medical and Health Science and Technology Project of the National Health Commission WKZX2022JG0111National Natural Science Foundation of China 82271205Research Foundation of Medical Key Project of Jiangsu Provincial Health Commission K2023063the Jiangsu Provincial Traditional Chinese Medicine Science and Technology Development Plan Project MS2022141
6 · The paper itself

Abstract

backgroundPreclinical studies have suggested that Ras-related C3 botulinum toxin substrate 1 (RAC1) accelerates diabetic kidney disease (DKD) progression by triggering renal inflammation/fibrosis. Nevertheless, the clinical relevance of RAC1 with DKD is undefined. In this study, we aimed to investigate the association between circulating RAC1 levels and early DKD to evaluate its potential as a novel biomarker for early disease detection.

methodsA total of 150 participants were recruited. They were divided into three groups: the type-2 diabetes mellitus (T2DM) group, the early DKD group, and the healthy volunteers (HVs). We measured the circulating level of RAC1 with ELISAs. In addition, we measured levels of two indicators of inflammation (NOD-like receptor pyrin domain-containing 3 (NLRP3) inflammasome, and interleukin (IL)-1β) and two serological indicators reflecting renal fibrosis (fibrillin 1 (FBN1) and matrix metalloproteinase-10 (MMP-10)).

resultsThe serum level of RAC1 was increased in individuals with early DKD. The serum level of RAC1 was positively correlated with urinary clinical biomarkers, including the urine albumin-to-creatinine ratio (UACR), urine microalbumin (UMA), and α1-microglobulin (α1-MG), but inversely associated with the estimated glomerular filtration rate (eGFR). Serum levels of RAC1, NLRP3, IL-1β, and MMP-10 were strongly inter-correlated in DKD patients. In addition, after correction for pertinent clinical features and the other four biomarkers, an increased risk of early DKD was linked to a higher serum RAC1 level. Analyses of receiver operating characteristic (ROC) curves revealed the area under the ROC curve of serum levels of RAC1, NLRP3, IL-1β, and MMP-10 for identifying early DKD to be 0.785, 0.728, 0.697, and 0.714, respectively.

conclusionsThe circulating RAC1 level was associated with early DKD and might be a biomarker for the early stages of DKD.

Indexed as

Diabetic kidney diseaseFibrosisInflammationNLRP3 inflammasomeRAC1

Identifiers

PMID41408315
PMCPMC12709860

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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.