Evidence map›Paper›PMID 40115374›Full record

ArticleJournal of clinical & translational endocrinology2025

Urinary DcR2/Cr level predicts renal outcomes in patients with diabetic kidney disease.

Jia Chen, Weidong Wang, Fang Yu, Xiaoyue Wang, Yani He, Kehong Chen

Abstract read
In one paragraph

Article in Journal of clinical & translational endocrinology, 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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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

6 authors.

Jia ChenDepartment of Nephrology, Daping Hospital, Army Medical University, Chongqing, China.
Weidong WangDepartment of Nephrology, Daping Hospital, Army Medical University, Chongqing, China.
Fang YuDepartment of Nephrology, Daping Hospital, Army Medical University, Chongqing, China.
Xiaoyue WangDepartment of Nephrology, Daping Hospital, Army Medical University, Chongqing, China.
Yani HeDepartment of Nephrology, Daping Hospital, Army Medical University, Chongqing, China.
Kehong ChenDepartment of Nephrology, Daping Hospital, Army Medical University, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In diabetic kidney disease (DKD), urinary decoy receptor 2 (uDcR2) levels are associated with tubulointerstitial fibrosis; however, whether uDcR2 can predict renal outcomes remains unclear. Herein, we analyzed the association between uDcR2 and renal outcomes (defined as a composite of a serum creatinine (SCr) increase of 50 % from baseline, or initiation of dialysis for end-stage renal disease) in 153 patients with biopsy-proven DKD. Patients were divided into the composite (n = 67) and no composite (n = 86) outcome groups. uDcR2 levels were measured using ELISA. The area under the receiver operating characteristic curve (AUC) for uDcR2 in discriminating DKD renal outcomes was calculated. Kaplan-Meier survival analysis and multifactorial Cox regression models evaluated the association between uDcR2 levels and renal outcomes. Renal DcR2 mRNA and protein expression were detected using in situ hybridization and immunohistochemical staining. Immunofluorescence revealed DcR2 and α-SMA colocalization. uDcR2/Cr levels were higher in patients in the composite than the no composite outcome group. uDcR2/Cr levels positively correlated with ACR, SCr, interstitial fibrosis and tubular atrophy (IFTA), and negatively correlated with eGFR. uDcR2/Cr had an AUC of 0.825 at the optimal cut-off value of 389 ng/gCr. Addition of uDcR2/Cr to ACR, eGFR, or IFTA improved renal outcome predictions. Renal survival was significantly lower at uDcR2/Cr ≥ 389 ng/gCr. Patients in the composite group had higher tubular DcR2 mRNA and protein level percentages. α-SMA was significantly increased in DcR2-positive renal tubules and their surroundings. Overall, uDcR2/Cr is an independent predictor of renal outcomes, with potential for improving the prevention and treatment of DKD.

Indexed as

Diabetic kidney diseaseRenal outcomeurinary DcR2/Cr

Identifiers

PMID40115374
PMCPMC11925566

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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.