# U-TXM: a novel biomarker for early detection of diabetic kidney disease

## TL;DR

This study explores U-TXM as a potential early detection biomarker for diabetic kidney disease in patients with diabetes.

## Contribution

The study identifies U-TXM as a novel urinary biomarker for early detection of diabetic kidney disease.

## Key findings

- U-TXM levels were significantly higher in patients with diabetic kidney disease compared to those with diabetes alone.
- U-TXM remained elevated in diabetic kidney disease patients regardless of renal function.
- Combining U-TXM with serum creatinine and systolic blood pressure improved diagnostic accuracy.

## Abstract

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.

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.

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).

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.