Assessment of Antiphospholipid Antibodies, CD4 Count and Some Haematological Parameters in HIV Patients attending a Tertiary Health Institution in South-Western Nigeria

Olayanju, Ayodeji OluSola and Afolabi, Temitope and Ezigbo,, Eyiuche Doris and Enitan, Seyi Samson and Oluwatayo, Beatrice Olatundun (2018) Assessment of Antiphospholipid Antibodies, CD4 Count and Some Haematological Parameters in HIV Patients attending a Tertiary Health Institution in South-Western Nigeria. International Blood Research & Reviews, 8 (2). ISSN 2321–7219

Text document.pdf Download (264kB)

Abstract

Antiphospholipid antibodies (aPLs) are the serological markers used in the diagnosis of the antiphospholipid syndrome (APS). HIV infe ction has been as sociated with an elevated aPls level, but its link to the APS with clin ical thrombosis is still been investigated . This study is designed to determine and correlate serum level of antiphospholipid antibodies with CD4 count and some haematological parameters of HIV se ropositive subjects in comparison to those of healthy controls and also to compare these parameters between an tiretroviral therapy (ART) naïve and treated patients. Methodology: A cohort of 110 patients which consist of 90 HIV positive Patients (22 males and 68 females) and 20 HIV negative patients (10 males and 10 females) which serve as control attending Babcock University Teaching Hospital (BUTH) Ilisha n-Remo, Ogun State, Nigeria were recruited for the cross-sectional study. HIV anti bodies were detected using 3 rapid diagnostic kits (Determine, Unigold and Stat Pak). CD4+ cells were counted us ing Partec® Cyflow Counter (Germany). The Full Blood Count was analyzed using the Sysmex® Auto mated Haematology Analyzer (Kobe-Japan). Antiphospholipid antibodies (aPLs) were assayed using the Human Anti-Phospholipid Screen IgG/IgM ELISA kit (Alpha Diagnostic International, Texas, U SA). Results: The present study showed that the mean se rum antiphospholipid antibody level was significantly (P<0.001) higher in HIV positive Pa tients (11.83±7.36u/ml) compared to the control group (7.30±3.95u/ml). While on one hand, there was a strong positive correlation between serum aPLs level and PLT (r= 0.044), MCHC (r= 0.084) and LYM (r= 0.105) in HIV infection; on the other hand, there was a strong negative correl ation with CD4 count (r= -0.094), PCV (r= -0.099), Hb (r= - 0.072), RBC (r= -0.003), WBC (r= -0.063), MNO (r= -0 .213), GRA (r= -0.003), MCV (r= -0.023) and MCH (r= -0.005). Also, there was no significant diffe rences (P>0.05) between the aPLs level of HIV group on ART (11.44±7.74 u/ml) and those not on ART (12.00±7.24 u/ml). Some haematological parameters like PLT, PCV, Hb, RBC and red cell indices of the HIV group on ART did not differ significantly from those not on ART. However, the CD4 count (638.89±119.56 cell/ μ L), WBC (5.38±1.49X10 3 / μ L), LYM (51.43±7.99%) and GRA (46.30±10. 18%) of the HIV group on ART were significant higher than those not on ART (465.30±145.92 cell/ μ L, 4.55±1.57X10 3 / μ L, 42.23±10.96% and 39.10±7.81%, respectively). Conclusion: Significant elevated aPLs level is present in HIV infection; however, the information obtained is not sufficient to indicate the occurrence of anti-phospholipid sy ndrome in HIV infection. There was no strong relationship between aPLs level and indicators of immunohaematological abnormalities in HIV infection. This finding is plausible and would therefore require further investigation.

Actions (login required)

View Item