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Updated: Jan 19, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
A subset of low density granulocytes is associated with vascular calcification in chronic kidney disease patients
Javier Rodríguez-Carrio1,2, Natalia Carrillo-López2,3, Catalina Ulloa4
1Area of Immunology, Department of Functional Biology, University of Oviedo, Oviedo, Spain.
Insights
Low density granulocytes (LDGs) are increased in chronic kidney disease (CKD) patients, particularly a CD14-CD16-CD15+ subset linked to vascular calcification. This LDG expansion may serve as a biomarker for CKD progression and vascular complications.
Area of Science:
- Nephrology
- Immunology
- Vascular Biology
Background:
- Inflammation is a key driver in chronic kidney disease (CKD) and its associated vascular complications.
- The specific cellular players mediating this inflammation in CKD remain incompletely understood.
- Low density granulocytes (LDGs) are recognized as emerging inflammatory mediators.
Purpose of the Study:
- To investigate alterations in LDGs within the chronic kidney disease (CKD) population.
- To determine if LDGs correlate with clinical outcomes, specifically vascular calcification.
- To explore the potential of LDGs as diagnostic biomarkers in CKD.
Main Methods:
- Peripheral blood samples from 33 CKD patients on peritoneal dialysis and 15 healthy controls were analyzed using flow cytometry and confocal microscopy.
- LDG subsets, including CD14lowCD16+ and CD14-CD16- populations, were quantified.
- Gene expression of DEF3, a marker of early granulopoiesis, was measured in peripheral blood mononuclear cells (PBMCs) via qPCR.
Main Results:
- CKD patients exhibited an expansion of total CD15+ LDGs, with a notable increase in the CD14-CD16-CD15+ subset.
- The frequency of the CD14-CD16-CD15+ LDG subpopulation was significantly higher in CKD patients and remained stable over time.
- Increased CD14-CD16-CD15+ LDGs correlated with vascular calcification scores (Kauppila scores) and elevated DEF3 expression in PBMCs.
Conclusions:
- Low density granulocytes (LDGs) are expanded in chronic kidney disease (CKD) patients, characterized by a distinct CD14-CD16-CD15+ subset.
- This specific LDG subset is associated with the presence and severity of vascular calcification in CKD.
- DEF3 gene expression in PBMCs may serve as a valuable indicator of LDG expansion and potential disease progression in CKD.
Abstract:
Inflammation is central to chronic kidney disease (CKD) pathogenesis and vascular outcomes, but the exact players remain unidentified. Since low density granulocytes (LDGs) are emerging mediators in inflammatory conditions, we aimed to evaluate whether LDGs may be altered in CKD and related to clinical outcomes as biomarkers. To his end, LDGs subsets were measured in peripheral blood by flow cytometry and confocal microscopy in 33 CKD patients undergoing peritoneal dialysis and 15 healthy controls (HC). Analyses were replicated in an additional cohort. DEF3 (marker of early granulopoiesis) gene expression on PBMCs was quantified by qPCR. Total CD15+ LDGs and both CD14lowCD16+ and CD14-CD16- subsets were expanded in CKD. The relative frequency of the CD14-CD16- subpopulation was higher among the CD15+ pool in CKD. This alteration was stable over-time. The increased CD14-CD16-CD15+ paralleled Kauppila scores and DEF3 expression, whereas no association was found with CD14lowCD16+ CD15+. Both subsets differed in their CD11b, CD10, CD35, CD31, CD62L, IFNAR1 and CD68 expression, FSC/SSC features and nuclear morphology, pointing to different origins and maturation status. In conclusion, LDGs were expanded in CKD showing a skewed distribution towards a CD14-CD16-CD15+ enrichment, in association with vascular calcification. DEF3 expression in PBMC can be a marker of LDG expansion.
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