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Blood CXCR2 levels and artery calcium buildup in advanced chronic kidney disease

Studies whether CXCR2 on white blood cells predicts heart artery calcification in advanced kidney disease.

Plain-language title generated from the registry record
Registry title: CXCR2 Leucocyte Expression Level as a Predictive Factor of Coronary Artery Calcification Progression in Advanced Chronic Kidney Disease Patients

Key facts

Where
Amiens, FranceSee the site

Where in France

  • CHRU AmiensAmiens, FranceNo longer taking part

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Trial details

Who runs it
Centre Hospitalier Universitaire, Amiens
Trial code
NCT07811505
Record updated
10 September 2026
Original description
Chronic kidney disease (CKD) is associated with the development of coronary arteries calcifications (CAC) and increased cardiovascular mortality. Previously, the investigators demonstrated that interleukin 8 (IL-8) plays a role in the calcification process, and that blockade of its receptor, CXCR2 reduces cardiovascular calcifications. The investigators hypothesize that leucocytes expressing CXCR2 may contribute to the development and progression of CAC in CKD patients. Identifying CKD patients with a high calcification phenotype and therapeutic targets to prevent cardiovascular calcifications is essential. Advanced CKD patients (stages IV and V) will undergo analysis of CXCR2 expression from neutrophils and monocytes at inclusion by flow cytometry, followed by non-contrast thoracic CT scans at inclusion, 1 year and 3 years to assess calcification scores and progression. Patients will have a pre-inclusion visit for research information and consent. If consent is given, three protocol visits (inclusion, 1 year, 3 years) including clinical exam, laboratory tests and CT evaluations will be performed.Read full original descriptionShow less

CXCR2 Leucocyte Expression Level as a Predictive Factor of Coronary Artery Calcification Progression in Advanced Chronic Kidney Disease Patients

Chronic kidney disease (CKD) is associated with the development of coronary arteries calcifications (CAC) and increased cardiovascular mortality. Previously, the investigators demonstrated that interleukin 8 (IL-8) plays a role in the calcification process, and that blockade of its receptor, CXCR2 reduces cardiovascular calcifications. The investigators hypothesize that leucocytes expressing CXCR2 may contribute to the development and progression of CAC in CKD patients. Identifying CKD patients with a high calcification phenotype and therapeutic targets to prevent cardiovascular calcifications is essential. Advanced CKD patients (stages IV and V) will undergo analysis of CXCR2 expression from neutrophils and monocytes at inclusion by flow cytometry, followed by non-contrast thoracic CT scans at inclusion, 1 year and 3 years to assess calcification scores and progression. Patients will have a pre-inclusion visit for research information and consent. If consent is given, three protocol visits (inclusion, 1 year, 3 years) including clinical exam, laboratory tests and CT evaluations will be performed.

Inclusion: age > 18 years; CKD defined by eGFR < 30 mL/min/1,73m²; signed inform consent.

Exclusion: kidney transplant recipients,; current or recent (within 30 days) infection,; inflammatory diseases,; active cancer treatment,; patients on dialysis,; use of immunosuppressive agents,; presence of coronary stents or aortic valve protheses,; inability to provide informed consent.

ClinicalTrials.gov NCT07811505