Effect of GFR on plasma N-terminal Connective Tissue Growth Factor (CTGF) concentrations

  • Karin G. Gerritsen
  • , Alferso C. Abrahams
  • , Hilde P. Peters
  • , Tri Q. Nguyen
  • , Maarten P. Koeners
  • , Claire H. Den Hoedt
  • , Amelie Dendooven
  • , Marinus A. Van Den Dorpel
  • , Peter J. Blankestijn
  • , Jack F. Wetzels
  • , Jaap A. Joles
  • , Roel Goldschmeding
  • , Robbert J. Kok

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

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. © 2012 National Kidney Foundation, Inc.
Original languageEnglish
Pages (from-to)619-627
Number of pages9
JournalAmerican Journal of Kidney Diseases
Volume59
Issue number5
DOIs
Publication statusPublished - 1 May 2012

Keywords

  • CCN2
  • Connective tissue growth factor
  • glomerular filtration rate
  • middle molecule
  • uremic toxin
  • connective tissue growth factor
  • adult
  • aged
  • animal experiment
  • animal model
  • animal tissue
  • article
  • chronic kidney disease
  • controlled study
  • correlation analysis
  • cross-sectional study
  • enzyme linked immunosorbent assay
  • female
  • glomerulus filtration rate
  • graft recipient
  • hemodiafiltration
  • hemodialysis
  • hemodialysis patient
  • human
  • kidney clearance
  • kidney disease
  • kidney failure
  • kidney graft
  • longitudinal study
  • male
  • nonhuman
  • observational study
  • plasma
  • protein blood level
  • rat
  • renal replacement therapy
  • rodent

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