Related Experiment Video
Updated: May 24, 2026

Strategic Endothelial Cell Tube Formation Assay: Comparing Extracellular Matrix and Growth Factor Reduced Extracellular Matrix
Published on: August 14, 2016
Effect of GFR on plasma N-terminal connective tissue growth factor (CTGF) concentrations
Karin G Gerritsen1, Alferso C Abrahams, Hilde P Peters
1Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands. k.g.f.gerritsen@umcutrecht.nl
Background:
Connective tissue growth factor (CTGF) has a key role in the pathogenesis of renal and cardiac fibrosis. Its amino-terminal fragment (N-CTGF), the predominant form of CTGF detected in plasma, has a molecular weight in the middle molecular range (18 kDa). However, it is unknown whether N-CTGF is a uremic retention solute that accumulates in chronic kidney disease (CKD) due to decreased renal clearance and whether it can be removed by hemodiafiltration.
Study Design:
4 observational studies in patients and 2 pharmacokinetic studies in rodents.
Setting & Participants:
4 single-center studies. First study (cross-sectional): 88 patients with CKD not receiving kidney replacement therapy. Second study (cross-sectional): 23 patients with end-stage kidney disease undergoing low-flux hemodialysis. Third study: 9 kidney transplant recipients before and 6 months after transplant. Fourth study: 11 low-flux hemodialysis patients and 12 hemodiafiltration patients before and after one dialysis session.
Predictor:
First, second, and third study: (residual) glomerular filtration rate (GFR). Fourth study: dialysis modality.
Outcomes & Measurements:
Plasma (N-)CTGF concentrations, measured by enzyme-linked immunosorbent assay.
Results:
In patients with CKD, we observed an independent association between plasma CTGF level and estimated GFR (β = -0.72; P < 0.001). In patients with end-stage kidney disease, plasma CTGF level correlated independently with residual kidney function (β = -0.55; P = 0.046). Successful kidney transplant resulted in a decrease in plasma CTGF level (P = 0.008) proportional to the increase in estimated GFR. Plasma CTGF was not removed by low-flux hemodialysis, whereas it was decreased by 68% by a single hemodiafiltration session (P < 0.001). Pharmacokinetic studies in nonuremic rodents confirmed that renal clearance is the major elimination route of N-CTGF.
Limitations:
Observational studies with limited number of patients. Fourth study: nonrandomized, evaluation of the effect of one session; randomized longitudinal study is warranted.
Conclusion:
Plasma (N-)CTGF is eliminated predominantly by the kidney, accumulates in CKD, and is decreased substantially by a single hemodiafiltration session.
Related Concept Videos
Glomerular Filtration Rate and its Regulation
GFR regulation involves two primary intrinsic controls: the myogenic and tubuloglomerular feedback mechanisms.
The myogenic...
TGF - β Signaling Pathway
Drug Dosing in Renal Diseases: Measurement of Glomerular Filtration Rate
Intracellular Signaling Affects Focal Adhesions
Some...
Mitogens and the Cell Cycle
Drug Dosing in Renal Diseases: Estimation of Glomerular Filtration Rate Based on Serum Creatinine Concentration
