Lack of utility of intestinal fatty acid binding protein levels in predicting intestinal allograft rejection

Transplantation. 2001 Apr 27;71(8):1058-60. doi: 10.1097/00007890-200104270-00008.

Abstract

Introduction: The enterocyte-specific protein, intestinal fatty acid binding protein (I-FABP), is detectable in serum only after intestinal injury. Previous studies in animals suggest that I-FABP might be a useful marker of intestinal allograft rejection.

Materials and methods: I-FABP was repetitively measured in nine intestinal transplant recipients and correlated with findings of surveillance endoscopy.

Results: Average interval between I-FABP determination and biopsy was 3.4 days (SD=4.2 days). Average number of rejection episodes per patient totalled 1.6+/-1.2. General linear modeling demonstrated no tendency for increases in serum FABP to precede histologic graft rejection (P=0.263). Restriction of the analysis to I-FABP determinations 1 day before or on the day of biopsy failed to affect these results. Minor increases in I-FABP were often associated with histologically normal grafts, whereas rejection often occurred when I-FABP was not detectable.

Discussion: Serum I-FABP levels do not predict clinical intestinal allograft rejection.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Biomarkers / urine
  • Carrier Proteins / blood*
  • Carrier Proteins / urine
  • Child
  • Child, Preschool
  • Fatty Acid-Binding Protein 7
  • Fatty Acid-Binding Proteins
  • Fatty Acids / metabolism
  • Graft Rejection / blood
  • Graft Rejection / diagnosis*
  • Graft Rejection / pathology
  • Humans
  • Intestines / pathology
  • Intestines / transplantation*
  • Monitoring, Physiologic / methods
  • Neoplasm Proteins*
  • Reproducibility of Results
  • Transplantation, Homologous / pathology
  • Transplantation, Homologous / physiology*
  • Tumor Suppressor Proteins*

Substances

  • Biomarkers
  • Carrier Proteins
  • FABP7 protein, human
  • Fatty Acid-Binding Protein 7
  • Fatty Acid-Binding Proteins
  • Fatty Acids
  • Neoplasm Proteins
  • Tumor Suppressor Proteins