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Correlation of antiphospholipid antibodies and protein S deficiency with thrombosis in HIV-infected men

K L Hassell1, D C Kressin, A Neumann

  • 1Department of Medicine, Denver VA Medical Center, CO 80220.

Insights

Antiphospholipid antibodies (aPL) and free protein S (PSF) deficiency are common in HIV-infected men. While these coagulation abnormalities were prevalent, they did not significantly correlate with thrombosis in this study group.

Area of Science:

  • Hematology
  • Immunology
  • Infectious Diseases

Background:

  • Antiphospholipid antibodies (aPL) and free protein S (PSF) deficiency are linked to thrombosis.
  • Previous studies indicated a high prevalence of these abnormalities in HIV-infected individuals, with limited associated thrombosis.
  • This study investigates the relationship between aPL, PSF deficiency, and thrombosis in HIV-infected men.

Purpose of the Study:

  • To determine the prevalence of aPL and PSF deficiency in HIV-infected men.
  • To assess the association between aPL, PSF deficiency, and the development of clinical thrombosis.
  • To explore correlations between these coagulation abnormalities and clinical features of HIV infection.

Main Methods:

  • A cohort of 74 HIV-infected men were analyzed for aPL and PSF deficiency.
  • Clinical data, including medication use, opportunistic infections, and CD4 cell counts, were collected.
  • Prospective follow-up was conducted to monitor the incidence of thrombosis over a median of 12 months.

Main Results:

  • aPL were detected in 86% and PSF deficiency in 33% of participants.
  • A strong correlation was found between a specific subset of aPL (reacting to phosphatidylethanolamine) and low PSF levels.
  • No significant correlation was observed between aPL, PSF deficiency, and clinical HIV features or the development of thrombosis.

Conclusions:

  • High prevalence of aPL and PSF deficiency exists in HIV-infected men, but their direct correlation with thrombosis requires further investigation.
  • Specific aPL subsets, particularly those associated with low PSF levels, may warrant closer examination in larger cohorts.
  • Larger studies with extended follow-up are needed to clarify the thrombotic risk associated with these coagulation abnormalities in HIV-infected individuals.

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