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Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates
BACKGROUND: HIV infection is associated with a high prevalence of antiphospholipid antibodies (aPL) and increased thrombotic events but the aetiopathogenic link between the two is unclear. FINDINGS: Prospective single centre study from Soweto, South Africa, comparing the prevalence of aPL in highly...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199261/ https://www.ncbi.nlm.nih.gov/pubmed/21970576 http://dx.doi.org/10.1186/1756-0500-4-379 |
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author | Becker, Anthony C Libhaber, Elena Sliwa, Karen Singh, Sham Stewart, Simon Tikly, Mohammed Essop, Mohammed R |
author_facet | Becker, Anthony C Libhaber, Elena Sliwa, Karen Singh, Sham Stewart, Simon Tikly, Mohammed Essop, Mohammed R |
author_sort | Becker, Anthony C |
collection | PubMed |
description | BACKGROUND: HIV infection is associated with a high prevalence of antiphospholipid antibodies (aPL) and increased thrombotic events but the aetiopathogenic link between the two is unclear. FINDINGS: Prospective single centre study from Soweto, South Africa, comparing the prevalence of aPL in highly active anti-retroviral therapy (HAART) naïve HIV positive and negative patients presenting with Acute Coronary Syndromes (ACS). Between March 2004 and February 2008, 30 consecutive black South African HIV patients with ACS were compared to 30 black HIV negative patients with ACS. The HIV patients were younger (43 ± 7 vs. 54 ± 13, p = 0.004) and besides smoking (73% vs. 33%, p = 0.002) and lower HDL levels (0.8 ± 0.3 vs. 1.1 ± 0.4, p = 0.001) had fewer risk factors than the control group. HIV patients had a higher prevalence of anticardiolipin (aCL) IgG (47% vs. 10%, p = 0.003) and anti-prothrombin (aPT) IgG antibodies (87% vs. 21%, p < 0.001) but there was no difference in the prevalence of the antiphospholipid syndrome (44% vs. 24%, p = N/S) and aPL were not predictive of clinical or angiographic outcomes. CONCLUSIONS: Treatment naïve black South African HIV patients with ACS are younger with fewer traditional coronary risk factors than HIV negative patients but have a higher prevalence and different expression of aPL which is likely to be an epiphenomenon of the HIV infection rather than causally linked to thrombosis and the pathogenesis of ACS. |
format | Online Article Text |
id | pubmed-3199261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31992612011-10-24 Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates Becker, Anthony C Libhaber, Elena Sliwa, Karen Singh, Sham Stewart, Simon Tikly, Mohammed Essop, Mohammed R BMC Res Notes Short Report BACKGROUND: HIV infection is associated with a high prevalence of antiphospholipid antibodies (aPL) and increased thrombotic events but the aetiopathogenic link between the two is unclear. FINDINGS: Prospective single centre study from Soweto, South Africa, comparing the prevalence of aPL in highly active anti-retroviral therapy (HAART) naïve HIV positive and negative patients presenting with Acute Coronary Syndromes (ACS). Between March 2004 and February 2008, 30 consecutive black South African HIV patients with ACS were compared to 30 black HIV negative patients with ACS. The HIV patients were younger (43 ± 7 vs. 54 ± 13, p = 0.004) and besides smoking (73% vs. 33%, p = 0.002) and lower HDL levels (0.8 ± 0.3 vs. 1.1 ± 0.4, p = 0.001) had fewer risk factors than the control group. HIV patients had a higher prevalence of anticardiolipin (aCL) IgG (47% vs. 10%, p = 0.003) and anti-prothrombin (aPT) IgG antibodies (87% vs. 21%, p < 0.001) but there was no difference in the prevalence of the antiphospholipid syndrome (44% vs. 24%, p = N/S) and aPL were not predictive of clinical or angiographic outcomes. CONCLUSIONS: Treatment naïve black South African HIV patients with ACS are younger with fewer traditional coronary risk factors than HIV negative patients but have a higher prevalence and different expression of aPL which is likely to be an epiphenomenon of the HIV infection rather than causally linked to thrombosis and the pathogenesis of ACS. BioMed Central 2011-10-04 /pmc/articles/PMC3199261/ /pubmed/21970576 http://dx.doi.org/10.1186/1756-0500-4-379 Text en Copyright ©2010 Becker et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Becker, Anthony C Libhaber, Elena Sliwa, Karen Singh, Sham Stewart, Simon Tikly, Mohammed Essop, Mohammed R Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
title | Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
title_full | Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
title_fullStr | Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
title_full_unstemmed | Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
title_short | Antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
title_sort | antiphospholipid antibodies in black south africans with hiv and acute coronary syndromes: prevalence and clinical correlates |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199261/ https://www.ncbi.nlm.nih.gov/pubmed/21970576 http://dx.doi.org/10.1186/1756-0500-4-379 |
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