Related Experiment Video
Updated: Sep 6, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Complement Factor H and Related Proteins as Markers of Cardiovascular Risk in Pediatric Chronic Kidney Disease
Wei-Ting Liao1, Wei-Ling Chen1, You-Lin Tain1,2
1Division of Pediatric Nephrology, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 833, Taiwan.
Insights
Complement factor H (CFH) and related proteins like CFHR2 and CFHR3 are linked to cardiovascular disease (CVD) risk in children with chronic kidney disease (CKD). These biomarkers may help identify CVD risk in pediatric CKD patients.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Cardiovascular disease (CVD) is the leading cause of mortality in pediatric patients with chronic kidney disease (CKD).
- Hypertension is a significant risk factor for CVD in this population.
- Congenital anomalies of the kidney and urinary tract (CAKUT) are primary causes of pediatric CKD.
Purpose of the Study:
- To investigate the association between complement factor H (CFH) and related proteins (CFHR2, CFHR3) and CVD risk in children with CKD.
- To determine if these proteins can differentiate CVD risk based on CKD etiology (CAKUT vs. non-CAKUT).
Main Methods:
- Evaluated 102 children (aged 6-18 years) with CKD.
- Assessed CVD risk factors using 24-hour ambulatory blood pressure monitoring (ABPM), cardiosonography, and arterial stiffness.
- Measured plasma levels of CFH, CFHR2, and CFHR3.
Main Results:
- Higher plasma CFHR3 levels were observed in the non-CAKUT group compared to the CAKUT group (p=0.046).
- CFHR3 showed a negative correlation with left ventricular (LV) mass (p=0.009).
- Elevated CFHR2 levels were associated with 24-hour hypertension (p<0.05), while lower CFHR3 levels were linked to daytime hypertension and increased BP load in non-CAKUT CKD children.
Conclusions:
- CFH and related proteins (CFHR2, CFHR3) play a role in cardiovascular risk among children with CKD.
- These proteins may serve as potential biomarkers for early CVD risk assessment in pediatric CKD patients.
- Differential expression of CFHR3 may help distinguish CVD risk in children with different CKD etiologies.
Abstract:
Cardiovascular disease (CVD) is the main cause of mortality among chronic kidney disease (CKD) patients, both in adults and in children. Hypertension is one of the risk factors of CVD. For early detection of subclinical CVD in pediatric CKD, 24 h ambulatory blood pressure monitoring (ABPM), cardiosonography, and arterial stiffness assessment were evaluated. CAKUT (congenital anomalies of the kidney and urinary tract) are the main etiologies of pediatric CKD. Previously, by a proteomic approach, we identified complement factor H (CFH) and related proteins differentially expressed between children with CAKUT and non-CAKUT CKD. In this study, we aimed to evaluate whether CFH, CFH-related protein-2 (CFHR2), and CFH-related protein-3 (CFHR3) were related to CVD risk in children with CKD. This study included 102 subjects aged 6 to 18 years old. The non-CAKUT group had higher plasma CFHR3 levels than the CAKUT group (p = 0.046). CFHR3 was negatively correlated with LV mass (p = 0.009). CFHR2 was higher in children with CKD with 24 h hypertension in the ABPM profile (p < 0.05). In addition, children with non-CAKUT CKD with day-time hypertension (p = 0.036) and increased BP load (p = 0.018) displayed a lower plasma CFHR3 level. Our results highlight that CFH and related proteins play a role for CVD in children with CKD. Early assessment of CFH, CFHR2, and CFHR3 may have clinical utility in discriminating CV risk in children with CKD with different etiologies.
Related Concept Videos
Chronic Kidney Disease II: Clinical Manifestations
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
Chronic Kidney Disease I: Introduction
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Chronic Kidney Disease III: Interprofessional Care
Acute Kidney Injury II: Pathophysiology

