# Urinary stress hormones and their metabolites as predictive biomarkers for CKD with diabetes

**Authors:** Yujie Jin, Song Dong, Yan Ma, Chunchen Ni, Yan Yao, Shujuan Shang, Mengru Wang, Jiahao Xu, Fan Liu, MengMeng Qian, Shiqiang Liu, Dong Li, Lizhuo Wang, Liuming Yu, Jialin Gao

PMC · DOI: 10.1186/s12882-025-04717-9 · BMC Nephrology · 2025-12-24

## TL;DR

This study found that urinary stress hormones and their metabolites could serve as noninvasive biomarkers for chronic kidney disease in people with diabetes.

## Contribution

The study identifies urinary stress hormones as potential biomarkers for CKD with diabetes and explores their diagnostic value.

## Key findings

- Norepinephrine, cortisol, and 17-ketosteroids levels were significantly lower in CKD with diabetes compared to diabetes alone.
- Norepinephrine was inversely correlated with markers of kidney dysfunction and positively with estimated glomerular filtration rate.
- A composite model using norepinephrine and other metabolites achieved high diagnostic accuracy (AUC of 0.831).

## Abstract

This study aimed to characterize urinary stress hormones and their metabolites in patients with chronic kidney disease associated with diabetes (CKD with diabetes) and to evaluate their associations with renal function, providing insights into stress-related mechanisms and potential biomarker utility.

We enrolled 735 participants, including 449 with type 2 diabetes mellitus(T2D)and 286 with CKD with diabetes. Urinary concentrations of norepinephrine, cortisol, aldosterone, and 17-ketosteroids were analyzed. Statistical methods included correlation and regression analyses, receiver operating characteristic (ROC) curves, and orthogonal partial least squares discriminant analysis (OPLS-DA) to evaluate diagnostic value.

Urinary norepinephrine, cortisol, and 17-ketosteroids levels were significantly lower in CKD patients with diabetes than in those with diabetes alone. Norepinephrine was inversely correlated with albumin-to-creatinine ratio, urinary microalbumin, blood urea nitrogen, and serum creatinine, and positively with estimated glomerular filtration rate. Similar trends were observed for cortisol and 17-ketosteroids. Aldosterone was also negatively correlated with urinary microalbumin and creatinine. OPLS-DA showed distinct metabolic profiles between CKD with diabetes and diabetes, suggesting metabolic heterogeneity. Multivariate logistic regression identified norepinephrine as an independent protective factor, while diastolic blood pressure, urinary glucose, and homovanillic acid were risk factors. A composite model integrating norepinephrine, 17-ketosteroids, and homovanillic acid demonstrated high diagnostic performance, with the norepinephrine-based model achieving an AUC of 0.831 in validation.

Urinary adrenal hormones and their metabolites provide valuable insights into stress-related mechanisms in CKD with diabetes and may hold potential as complementary noninvasive biomarkers for disease assessment.

Not applicable.

The online version contains supplementary material available at 10.1186/s12882-025-04717-9.

## Linked entities

- **Chemicals:** norepinephrine (PubChem CID 951), cortisol (PubChem CID 5754), aldosterone (PubChem CID 5839), 17-ketosteroids (PubChem CID 4226429), homovanillic acid (PubChem CID 1738)
- **Diseases:** chronic kidney disease (MONDO:0005300), diabetes (MONDO:0005015), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Diseases:** CKD (MESH:D012080), diabetes (MESH:D003920)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12849337/full.md

## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849337/full.md

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Source: https://tomesphere.com/paper/PMC12849337