Antiretroviral therapy for tuberculosis control in nine African countries
dc.contributor.author | Williams B.G. | |
dc.contributor.author | Granich R. | |
dc.contributor.author | De Cock K.M. | |
dc.contributor.author | Glaziou P. | |
dc.contributor.author | Sharma A. | |
dc.contributor.author | Dyeb C. | |
dc.date.accessioned | 2011-05-15T16:02:18Z | |
dc.date.available | 2011-05-15T16:02:18Z | |
dc.date.issued | 2010 | |
dc.description.abstract | HIV has increased the incidence of tuberculosis (TB) by up to sevenfold in African countries, but antiretroviral therapy (ART) reduces the incidence of AIDS-related TB. We use a mathematical model to investigate the short-term and long-term impacts of ART on the incidence of TB, assuming that people are tested for HIV once a year, on average, and start ART at a fixed time after HIV seroconversion or at a fixed CD4+ cell count. We fit the model to trend data on HIV prevalence and TB incidence in nine countries in sub-Saharan Africa. If HIV-positive people start ART within 5 y of seroconversion, the incidence of AIDS-related TB in 2015 will be reduced by 48% (range: 37-55%). Long-term reductions depend sensitively on the delay to starting ART. If treatment is started 5, 2, or 1 y after HIV seroconversion, or as soon as people test positive, the incidence in 2050 will be reduced by 66% (range: 57-80%), 95% (range: 93-96%), 97.7% (range: 96.9-98.2%) and 98.4% (range: 97.8-98.9%), respectively. In the countries considered here, early ART could avert 0.71 ± 0.36 [95% confidence interval (CI)] million of 3.4 million cases of TB between 2010 and 2015 and 5.8 ± 2.9 (95% CI) million of 15 million cases between 2015 and 2050. As more countries provide ART at higher CD4+ cell counts, the impact on TB should be investigated to test the predictions of this model. | |
dc.description.version | Conference Paper | |
dc.identifier.citation | Proceedings of the National Academy of Sciences of the United States of America | |
dc.identifier.citation | 107 | |
dc.identifier.citation | 45 | |
dc.identifier.issn | 278424 | |
dc.identifier.other | 10.1073/pnas.1005660107 | |
dc.identifier.uri | http://hdl.handle.net/10019.1/12410 | |
dc.subject | cytokine | |
dc.subject | glucosylceramidase | |
dc.subject | animal experiment | |
dc.subject | animal model | |
dc.subject | cell damage | |
dc.subject | cell lineage | |
dc.subject | conference paper | |
dc.subject | controlled study | |
dc.subject | dendritic cell | |
dc.subject | Gaucher disease | |
dc.subject | gene deletion | |
dc.subject | hematopoietic cell | |
dc.subject | immunophenotyping | |
dc.subject | macrophage | |
dc.subject | mesenchyme cell | |
dc.subject | microarray analysis | |
dc.subject | mouse | |
dc.subject | nonhuman | |
dc.subject | ossification | |
dc.subject | osteoblast | |
dc.subject | osteopenia | |
dc.subject | osteoporosis | |
dc.subject | priority journal | |
dc.subject | protein deficiency | |
dc.subject | T lymphocyte | |
dc.subject | Acquired Immunodeficiency Syndrome | |
dc.subject | Africa | |
dc.subject | Anti-Retroviral Agents | |
dc.subject | HIV Seropositivity | |
dc.subject | Humans | |
dc.subject | Incidence | |
dc.subject | Models, Statistical | |
dc.subject | Time Factors | |
dc.subject | Tuberculosis | |
dc.title | Antiretroviral therapy for tuberculosis control in nine African countries | |
dc.type | Conference Paper |