SOP's for CKD-MBD-Biomarkers

RWTH Aachen University

Status: Completed

Conditions: Chronic Kidney Diseases

Treatments: Other: blood withdrawal

Study type: Observational

Funder types: Other

Identifiers

NCT02708368

15-109

Details and patient eligibility

About

CKD-MBD (Chronic Kidney Disease - Mineral and Bone Disorder) is an extensive disease and includes dysfunction of the mineral metabolism, the bone metabolism and cardiovascular diseases in the context of renal insufficiency. Clinical pictures of peripheral artery occlusive disease (PAOD), Coronary artery disease (CAD) and arterial hypertension favours among other main risk factors (smoking, obesity, etc.) additional cardiovascular complications. For this reason it makes sense to monitor these patients regularly. For this purpose the determination of different biomarkers would be appropriate for control of the course of disease.

During various studies the biomarkers FGF23, s-klotho, sclerostin, DKK1, BMP2, YKL-40 und MGP were established as indicators for the disease activity, as diagnostic criteria for the existence of CKD-MBD or as risk markers for the incidence of adverse events (incl. death) within the scope of CKD-MBD. For the clinical routine care application of these parameters standard operating procedures (SOP) are missing for the determination method relating to optimal pre-analytic and analytic procedures. These analyses are necessary to ensure the reproducibility of study results and to transfer these parameters in the clinical daily routine for risk stratification.

Enrollment: 32 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients who are regularly (3 times a week) on dialysis in the Maria-Hilf-Clinic or healthy subjects
• Male or Female at the age of at least 18 years
• Patients who will be admitted to the clinics of the University Hospital RWTH Aachen or of the Maria-Hilf-Clinic Mönchengladbach or healthy subjects
• written informed consent form
• Subjects who are contractually capable and mentally able to understand and follow the instructions of the study personnel

Exclusion criteria

• age < 18 years
• subjects who are unwilling or not able to consent
• pregnant or lactating women
• subject has been committed to an institution by legal or regulatory order
• dependency or working relationship with the investigator
• participation in a parallel interventional clinical study
• Hb-value < 10 g/dl

Trial design

32 participants in 2 patient groups

Patients on dialysis

Description:

16 patients on dialysis with a sex ratio 1:1; 8 patients on hemodialysis and 8 patients on hemodiafiltration

Treatment:

Other: blood withdrawal

Healthy Subjects

Description:

16 healthy subjects with a sex ratio 1:1

Treatment:

Other: blood withdrawal