Evidence map›Paper›PMID 42295602›Full record

ArticleIrish journal of medical science2026

Evaluation of CXCL12 levels in diabetic and non-diabetic chronic kidney disease.

Eda Şahin, Havva Yasemin Çinpolat, İlhan Kılıç, Serkan Bakırdöğen

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Article in Irish journal of medical science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Eda ŞahinDepartment of Medical Biochemistry, School of Graduate Studies, Çanakkale Onsekiz Mart University, Çanakkale, Türkiye.ORCID http://orcid.org/0009-0003-3274-5605
Havva Yasemin ÇinpolatDepartment of Medical Biochemistry, Faculty of Medicine, Çanakkale Onsekiz Mart University, Çanakkale, Türkiye. yaseminarattan@gmail.com.ORCID http://orcid.org/0000-0002-7161-2907
İlhan KılıçDepartment of Nephrology, Faculty of Medicine, Trakya University, Edirne, Türkiye.ORCID http://orcid.org/0000-0002-5990-8190
Serkan BakırdöğenDepartment of Nephrology, Faculty of Medicine, Çanakkale Onsekiz Mart University, Çanakkale, Türkiye.ORCID http://orcid.org/0000-0002-3448-0490

Funding

Çanakkale Onsekiz Mart University Scientific Research Projects Unit TYL-2025-5026
6 · The paper itself

Abstract

backgroundChronic kidney disease (CKD) constitutes a significant global health challenge due to its association with elevated morbidity and mortality rates. Diabetic nephropathy is a primary contributor to CKD progression, predominantly resulting from persistent inflammatory and fibrotic processes. CXCL12 is a multifunctional chemokine that has been implicated in renal pathology through context-dependent protective and deleterious effects.

aimThis study aimed to investigate circulating CXCL12 and CXCR4 levels in patients with diabetic nephropathy, and non-diabetic nephropathy, and to evaluate their association with disease severity.

methodsThis study included 177 participants comprising 60 patients with diabetic nephropathy, 57 patients with non-diabetic nephropathy, and 60 healthy controls. Plasma CXCL12 and CXCR4 concentrations were measured using ELISA method. The Kruskal-Wallis test and subsequent post hoc analyses were used to compare groups. ROC curve analysis evaluated the diagnostic value of the biomarkers. Also, binary logistic regression identified independent predictors of CKD.

resultsCXCL12 concentrations differed significantly between study groups and were highest in patients with diabetic nephropathy. CXCL12 levels increased with advancing CKD stage in the overall cohort. While no significant stage-related variation was observed in diabetic nephropathy, a pronounced stage-dependent increase was evident in non-diabetic nephropathy. CXCR4 levels showed minimal variation and weaker associations with disease stage. CXCL12 demonstrated good discriminatory performance and independently predicted CKD presence.

conclusionElevated CXCL12 levels are strongly associated with CKD irrespective of underlying etiology and may represent a valuable biomarker for disease detection and progression, particularly in non-diabetic CKD.

Indexed as

ChemokineChronic kidney diseaseCXCL12CXCR4Diabetic nephropathy

Identifiers

PMID42295602

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