Soluble Adhesion Molecules in Patients Coinfected with HIV and HCV: A Predictor of Outcome

PLoS One. 2016 Feb 5;11(2):e0148537. doi: 10.1371/journal.pone.0148537. eCollection 2016.

Abstract

Background: Higher serum levels of adhesion molecules (sICAM-1 and sVCAM-1) are associated with advanced liver fibrosis in patients coinfected with human immunodeficiency virus and hepatitis C virus. We assessed the relationship between serum levels of adhesion molecules and liver-related events (LRE) or death, in coinfected patients.

Methods: We studied clinical characteristics and outcomes of 182 coinfected patients with a baseline liver biopsy (58 with advanced fibrosis) and simultaneous plasma samples who were followed for median of 9 years. We used receiver-operating characteristic (ROC) curves to calculate optimized cutoff values (OCV) of sICAM-1 and sVCAM-1, defined as the values with the highest combination of sensitivity and specificity for LRE. We used multivariate regression analysis to test the association between OCVs of sICAM-1 and sVCAM-1 and outcomes. The variables for adjustment were age, HIV transmission category, liver fibrosis, baseline CD4+ T-cell counts, antiretroviral therapy, and sustained virologic response (SVR).

Results: During the study period 51 patients had SVR, 19 had LRE, and 16 died. The OCVs for LRE were 5.68 Log pg/mL for sICAM-1 and 6.25 Log pg/mL for sVCAM-1, respectively. The adjusted subhazard ratio (aSHR) (95% confidence interval [CI]) of death or LRE, whichever occurred first, for sICAM-1 and sVCAM-1 > OCV were 3.98 ([1.14; 13.89], P = 0.030) and 2.81 ([1.10; 7.19], respectively (P = 0.030).

Conclusions: Serum levels of sICAM-1 and sVCAM-1 can serve as markers of outcome in HIV/HCV-coinfected patients. Therapies targeting necroinflammatory damage and fibrogenesis may have a role in the management chronic hepatitis C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / blood
  • CD4-Positive T-Lymphocytes
  • Coinfection
  • Female
  • Follow-Up Studies
  • HIV Infections / blood
  • HIV Infections / drug therapy
  • HIV Infections / mortality
  • HIV Infections / pathology*
  • Hepatitis C / blood
  • Hepatitis C / drug therapy
  • Hepatitis C / mortality
  • Hepatitis C / pathology*
  • Humans
  • Intercellular Adhesion Molecule-1 / blood*
  • Kaplan-Meier Estimate
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / virology
  • Male
  • Retrospective Studies
  • Vascular Cell Adhesion Molecule-1 / blood*

Substances

  • Biomarkers
  • Vascular Cell Adhesion Molecule-1
  • Intercellular Adhesion Molecule-1

Grants and funding

This work was supported by grants PI11/01556, PI14/01094, PI11/00245 and PI14CIII/00011 given by Fondo de Investigación de Sanidad en España (FIS) (Spanish Health Funds for Research) and by grants RD12/0017/0004 and RD12/0017/0024 from Plan Nacional R+D+I and cofinanced by ISCIII Subdirección General de Evaluación y el Fondo Europeo de Desarrollo Regional (FEDER). JB is an investigator from the Programa de Intensificación de la Actividad Investigadora en el Sistema Nacional de Salud (I3SNS; Refs INT10/009 and INT12/154). DPT and MAJS are supported by ISCIII grants CM12/00043 and CD13/00013, respectively.