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ORIGINAL RESEARCH article

Front. Endocrinol.

Sec. Diabetes: Molecular Mechanisms

Volume 16 - 2025 | doi: 10.3389/fendo.2025.1682136

U-TXM: A Novel Biomarker for Early Detection of Diabetic Kidney Disease

Provisionally accepted
Yujie  JinYujie Jin1Jiahao  XuJiahao Xu1Yan  MaYan Ma1Chunchen  NiChunchen Ni1Yan  YaoYan Yao1Shujuan  ShangShujuan Shang1Mengru  WangMengru Wang1Chunyan  XingChunyan Xing1Song  DongSong Dong1Chaoqun  XiongChaoqun Xiong1Kang  XieKang Xie1Ruixi  ZhangRuixi Zhang2Wenjun  PeiWenjun Pei2Shiqiang  LiuShiqiang Liu1Jinhan  ChengJinhan Cheng1Fan  LiuFan Liu1Siwen  ZhangSiwen Zhang1Dong  LiDong Li1Lizhuo  WangLizhuo Wang2Liuming  YuLiuming Yu1Jialin  GaoJialin Gao1*
  • 1First Affiliated Hospital of Wannan Medical College, Wuhu, China
  • 2Wannan Medical College, Wuhu, China

The final, formatted version of the article will be published soon.

Background and Aims: Diabetic kidney disease (DKD) is the leading cause of end-stage renal disease. This study aimed to investigate the potential of urinary 11-dehydrothromboxane B2 (U-TXM) as a biomarker for the early detection of DKD. Materials and Methods: A total of 690 patients were enrolled, including 422 with diabetes mellitus (DM) and 268 with DKD. Patients with type 1, type 2, and other specific forms of diabetes were consecutively recruited from the Department of Endocrinology, Yijishan Hospital of Wannan Medical College (April–September 2024). U-TXM levels were measured and their clinical relevance to DKD was evaluated using correlation analysis, logistic regression, and receiver operating characteristic (ROC) curve analysis. Results: Urinary U-TXM levels were significantly higher in patients with DKD than in those with DM (median: 1158.05 vs. 960.44 pg/mg Cr; P<0.001). When stratified by renal function, U-TXM remained elevated in DKD regardless of serum creatinine (Cr) level (>70 or ≤70 μmol/L, both P<0.001). Multivariate analysis confirmed the existence of an independent association between DKD and U-TXM (OR=1.778, P=0.001), serum Cr (odds ratio [OR]=2.861, P<0.001), and systolic blood pressure (SBP, OR=1.032, P=0.001). U-TXM correlated positively with the urine albumin-to-Cr ratio (r=0.225, P<0.001), but only weakly with Cr and blood urea nitrogen. ROC analysis showed limited diagnostic value for U-TXM alone (area under the curve [AUC]=0.625), which improved substantially when combined with serum Cr and SBP (AUC=0.803). Conclusion: U-TXM shows potential as a biomarker for DKD, particularly in patients at early disease stages. Validation through longitudinal, multicenter, and comparative studies is required to confirm its clinical utility.

Keywords: Diabetic kidney disease, early diagnosis, Novel biomarkers, Urinary 11-Dehydrothromboxane B2, Urinary albumin-to-creatinine ratio

Received: 08 Aug 2025; Accepted: 14 Oct 2025.

Copyright: © 2025 Jin, Xu, Ma, Ni, Yao, Shang, Wang, Xing, Dong, Xiong, Xie, Zhang, Pei, Liu, Cheng, Liu, Zhang, Li, Wang, Yu and Gao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Jialin Gao, gaojialin-ktz@wnmc.edu.cn

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