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Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency

BACKGROUND: Anaemia commonly complicates both human immunodeficiency virus (HIV) infection and tuberculosis (TB), contributing substantially to morbidity and mortality. The mechanisms underlying anaemia and corresponding treatments in co-infected patients are poorly defined. OBJECTIVE: To determine...

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Autores principales: Kerkhoff, A. D., Meintjes, G., Opie, J., Vogt, M., Jhilmeet, N., Wood, R., Lawn, S. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union Against Tuberculosis and Lung Disease 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371921/
https://www.ncbi.nlm.nih.gov/pubmed/26792471
http://dx.doi.org/10.5588/ijtld.15.0558
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author Kerkhoff, A. D.
Meintjes, G.
Opie, J.
Vogt, M.
Jhilmeet, N.
Wood, R.
Lawn, S. D.
author_facet Kerkhoff, A. D.
Meintjes, G.
Opie, J.
Vogt, M.
Jhilmeet, N.
Wood, R.
Lawn, S. D.
author_sort Kerkhoff, A. D.
collection PubMed
description BACKGROUND: Anaemia commonly complicates both human immunodeficiency virus (HIV) infection and tuberculosis (TB), contributing substantially to morbidity and mortality. The mechanisms underlying anaemia and corresponding treatments in co-infected patients are poorly defined. OBJECTIVE: To determine the relative contributions of anaemia of chronic disease (ACD) and iron deficiency to anaemia in patients with HIV-associated TB. DESIGN: Consecutively recruited hospitalised (n = 102) and matched ambulatory patients (n = 51) with microbiologically confirmed HIV-associated TB in Cape Town, South Africa, were included. Haemoglobin levels, iron status markers, hepcidin and pro-inflammatory cytokines in blood were measured. We determined the prevalence of ACD and iron-deficiency anaemia (IDA) using seven different published definitions of IDA. RESULTS: More than 80% of enrolled HIV-associated TB patients were anaemic, and anaemia was more severe among in-patients. Over 95% of anaemic HIV-associated TB patients had ACD, whereas the proportion with IDA using a range of seven different definitions was low overall (median < 3%, range 0–32.6) in both patient groups. The proportion with IDA and hepcidin concentration ⩽ 20.0 ng/ml (predictive of responsiveness to oral iron supplementation) was also very low (median < 3%, range 0–15.1). CONCLUSIONS: ACD was the predominant cause underlying anaemia in HIV-associated TB patients, and IDA was very uncommon in this setting. The majority of anaemic HIV-associated TB patients were unlikely to benefit from oral iron supplementation.
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spelling pubmed-63719212019-02-22 Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency Kerkhoff, A. D. Meintjes, G. Opie, J. Vogt, M. Jhilmeet, N. Wood, R. Lawn, S. D. Int J Tuberc Lung Dis Original Articles BACKGROUND: Anaemia commonly complicates both human immunodeficiency virus (HIV) infection and tuberculosis (TB), contributing substantially to morbidity and mortality. The mechanisms underlying anaemia and corresponding treatments in co-infected patients are poorly defined. OBJECTIVE: To determine the relative contributions of anaemia of chronic disease (ACD) and iron deficiency to anaemia in patients with HIV-associated TB. DESIGN: Consecutively recruited hospitalised (n = 102) and matched ambulatory patients (n = 51) with microbiologically confirmed HIV-associated TB in Cape Town, South Africa, were included. Haemoglobin levels, iron status markers, hepcidin and pro-inflammatory cytokines in blood were measured. We determined the prevalence of ACD and iron-deficiency anaemia (IDA) using seven different published definitions of IDA. RESULTS: More than 80% of enrolled HIV-associated TB patients were anaemic, and anaemia was more severe among in-patients. Over 95% of anaemic HIV-associated TB patients had ACD, whereas the proportion with IDA using a range of seven different definitions was low overall (median < 3%, range 0–32.6) in both patient groups. The proportion with IDA and hepcidin concentration ⩽ 20.0 ng/ml (predictive of responsiveness to oral iron supplementation) was also very low (median < 3%, range 0–15.1). CONCLUSIONS: ACD was the predominant cause underlying anaemia in HIV-associated TB patients, and IDA was very uncommon in this setting. The majority of anaemic HIV-associated TB patients were unlikely to benefit from oral iron supplementation. International Union Against Tuberculosis and Lung Disease 2016-02 2016-02-01 /pmc/articles/PMC6371921/ /pubmed/26792471 http://dx.doi.org/10.5588/ijtld.15.0558 Text en © 2016 Kerkhoff et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Articles
Kerkhoff, A. D.
Meintjes, G.
Opie, J.
Vogt, M.
Jhilmeet, N.
Wood, R.
Lawn, S. D.
Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency
title Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency
title_full Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency
title_fullStr Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency
title_full_unstemmed Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency
title_short Anaemia in patients with HIV-associated TB: relative contributions of anaemia of chronic disease and iron deficiency
title_sort anaemia in patients with hiv-associated tb: relative contributions of anaemia of chronic disease and iron deficiency
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6371921/
https://www.ncbi.nlm.nih.gov/pubmed/26792471
http://dx.doi.org/10.5588/ijtld.15.0558
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