Protein C and procollagen III peptide levels in patients with hepatic dysfunction after allogeneic hematopoietic stem cell transplantation

Bone Marrow Transplant. 2005 Oct;36(7):631-7. doi: 10.1038/sj.bmt.1705114.

Abstract

Veno-occlusive disease (VOD) is one of the most serious complications following hematopoietic stem cell transplantation (HSCT) and is associated with a high mortality. We conducted a large trial on the clinical significance of protein C (PC) and procollagen III peptide (PNPIII) levels, which have been described as possible diagnostic markers of VOD. In total, 350 patients undergoing allogeneic HSCT were included. PC and PNPIII levels were analyzed prior to conditioning and weekly until 8 weeks after the HSCT. Signs of VOD and other transplantation-related complications (graft-versus-host disease (GVHD), toxicity, microangiopathic hemolytic anemia, infection) were recorded weekly throughout the trial. Patients showed a significant drop of the PC levels in VOD (70.3 vs 96.3%, P<0.001) and with increasing severity of aGVHD. Steroids increased the PC levels (69.4% vs 109.4%, P<0.001). The highest PNPIII levels were registered in patients with VOD (mean 6.3 IU/ml). Patients with aGVHD showed an elevation of PNPIII, especially patients with hepatic aGVHD. PC levels during conditioning do not predict VOD (98.5 vs 76.5%, NS). Although PC and PNPIII may play a role in the pathogenesis of VOD they cannot discriminate between complications with jaundice and are only of limited help in the differential diagnosis of VOD.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anemia, Hemolytic / metabolism
  • Cell Transplantation
  • Clinical Trials as Topic
  • Collagen Type III / biosynthesis*
  • Collagen Type III / blood
  • Diagnosis, Differential
  • Female
  • Genetic Markers
  • Graft vs Host Disease
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Hepatic Veno-Occlusive Disease / genetics
  • Humans
  • Liver / pathology*
  • Liver Diseases / etiology*
  • Liver Diseases / metabolism
  • Male
  • Middle Aged
  • Peptides / chemistry
  • Procollagen / biosynthesis*
  • Procollagen / blood
  • Prospective Studies
  • Protein C / biosynthesis*
  • Stem Cells / cytology
  • Steroids / pharmacology
  • Time Factors
  • Transplantation, Homologous / adverse effects*

Substances

  • Collagen Type III
  • Genetic Markers
  • Peptides
  • Procollagen
  • Protein C
  • Steroids