Urinary connective tissue growth factor increases far earlier than histopathological damage and functional deterioration in early chronic renal allograft injury

Scand J Urol Nephrol. 2009;43(5):390-9. doi: 10.3109/00365520903142244.

Abstract

Objective: To date, serum biochemistry examination and routine biopsy are the most commonly used methods to assess renal function after allogenic kidney transplantation. Connective tissue growth factor (CTGF) has been considered as a biomarker of chronic renal allograft injury characterized by tubular atrophy and interstitial fibrosis (TA/IF). This study explored the potential value of urinary CTGF as an early predictor of TA/IF using a rat model.

Material and methods: A Fisher to Lewis allogenic rat kidney transplant model was established and the recipients were killed at weeks 4, 8 and 12 post-transplantation. TA/IF was graded based on Banff Schema 1997. The location and expression of CTGF mRNA were detected by oligonucleotide-primed in situ DNA synthesis and quantitative polymerase chain reaction. CTGF protein expression was examined with immunohistochemistry and immunoblotting. Urinary CTGF concentration was measured by enzyme-linked immunosorbent assay. The correlation between urinary CTGF concentration and serum creatinine (SCr) and Banff score was analysed statistically.

Results: Typical morphological changes including TA/IF in allograft appeared at week 8 and became very severe at week 12 post-transplantation. CTGF expression in epithelium was up-regulated early and urinary CTGF was markedly elevated from week 4. SCr in recipients was stable before week 8 but increased tremendously at week 12. Urinary CTGF concentration was positively correlated with SCr and degree of interstitial fibrosis.

Conclusion: Urinary CTGF increases earlier than the appearance of biochemical abnormalities and pathological changes. Measurement of urinary CTGF may offer a potential non-invasive strategy to predict the early onset of chronic renal allograft injury.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / urine
  • Blotting, Western
  • Connective Tissue Growth Factor / genetics
  • Connective Tissue Growth Factor / urine*
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Follow-Up Studies
  • Gene Expression
  • Graft Rejection / genetics
  • Graft Rejection / pathology
  • Graft Rejection / urine*
  • Immunohistochemistry
  • Kidney / pathology*
  • Kidney Failure, Chronic / genetics
  • Kidney Failure, Chronic / pathology
  • Kidney Failure, Chronic / urine*
  • Kidney Transplantation / pathology*
  • Male
  • Polymerase Chain Reaction
  • Prognosis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Inbred F344
  • Rats, Inbred Lew
  • Time Factors
  • Transplantation, Homologous

Substances

  • Biomarkers
  • RNA, Messenger
  • Connective Tissue Growth Factor