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The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia

BACKGROUND: Anemia is frequent during HIV infection and is predictive of mortality. Although cART has demonstrated to reduce its prevalence, several patients still experience unresolved anemia. We aimed to characterize iron homeostasis and inflammation in HIV-infected individuals with mild anemia in...

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Autores principales: Quiros-Roldan, Eugenia, Castelli, Francesco, Lanza, Paola, Pezzoli, Chiara, Vezzoli, Marika, Biasiotto, Giorgio, Zanella, Isabella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735890/
https://www.ncbi.nlm.nih.gov/pubmed/29258550
http://dx.doi.org/10.1186/s12967-017-1358-6
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author Quiros-Roldan, Eugenia
Castelli, Francesco
Lanza, Paola
Pezzoli, Chiara
Vezzoli, Marika
Biasiotto, Giorgio
Zanella, Isabella
author_facet Quiros-Roldan, Eugenia
Castelli, Francesco
Lanza, Paola
Pezzoli, Chiara
Vezzoli, Marika
Biasiotto, Giorgio
Zanella, Isabella
author_sort Quiros-Roldan, Eugenia
collection PubMed
description BACKGROUND: Anemia is frequent during HIV infection and is predictive of mortality. Although cART has demonstrated to reduce its prevalence, several patients still experience unresolved anemia. We aimed to characterize iron homeostasis and inflammation in HIV-infected individuals with mild anemia in relation to cART. METHODS: In this retrospective cohort study, HIV-infected patients with mild anemia, CD4(+) cells > 200/mm(3) at baseline, maintaining virological response for 12 months after cART starting were selected within the Standardized Management of Antiretroviral Therapy Cohort (MASTER) cohort. Several inflammation and immune activation markers and iron homeostasis indexes were measured in stored samples, obtained at cART initiation (T0) and 12 months later (T1). Patients were grouped on the basis of hemoglobin values at T1: group A (> 13 g/dl) and B (< 13 g/dl). Wilcoxon rank sum test was used to compare biomarker values. Pearson correlation coefficients were calculated for all variables. RESULTS: cART improved CD4(+) and CD8(+) cell counts and their ratio, but this effect was significant only in group A. Only these patients had mild iron deficiency at T0 and showed higher transferrin and lower percentage of transferrin saturation than patients of group B, but differences disappeared with cART. cART decreased inflammation in all patients, but group B had higher levels of all markers than group A, reaching statistical significance only for IL-8 values at T1 (16 vs 2.9 pg/ml; p = 0.017). Hepcidin and IL-6 levels did not show significant differences between groups. Hemoglobin levels both at T0 and T1 did not correlate with any marker. CONCLUSIONS: Baseline mild anemia in HIV-infected patients cannot always be resolved with durable efficient cART, possibly due to residual inflammation or immune activation rather than unbalanced iron homeostasis. Further research is needed on cytokine profiling to understand the mechanisms that induce anemia in HIV with suppressive cART. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-017-1358-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-57358902017-12-21 The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia Quiros-Roldan, Eugenia Castelli, Francesco Lanza, Paola Pezzoli, Chiara Vezzoli, Marika Biasiotto, Giorgio Zanella, Isabella J Transl Med Research BACKGROUND: Anemia is frequent during HIV infection and is predictive of mortality. Although cART has demonstrated to reduce its prevalence, several patients still experience unresolved anemia. We aimed to characterize iron homeostasis and inflammation in HIV-infected individuals with mild anemia in relation to cART. METHODS: In this retrospective cohort study, HIV-infected patients with mild anemia, CD4(+) cells > 200/mm(3) at baseline, maintaining virological response for 12 months after cART starting were selected within the Standardized Management of Antiretroviral Therapy Cohort (MASTER) cohort. Several inflammation and immune activation markers and iron homeostasis indexes were measured in stored samples, obtained at cART initiation (T0) and 12 months later (T1). Patients were grouped on the basis of hemoglobin values at T1: group A (> 13 g/dl) and B (< 13 g/dl). Wilcoxon rank sum test was used to compare biomarker values. Pearson correlation coefficients were calculated for all variables. RESULTS: cART improved CD4(+) and CD8(+) cell counts and their ratio, but this effect was significant only in group A. Only these patients had mild iron deficiency at T0 and showed higher transferrin and lower percentage of transferrin saturation than patients of group B, but differences disappeared with cART. cART decreased inflammation in all patients, but group B had higher levels of all markers than group A, reaching statistical significance only for IL-8 values at T1 (16 vs 2.9 pg/ml; p = 0.017). Hepcidin and IL-6 levels did not show significant differences between groups. Hemoglobin levels both at T0 and T1 did not correlate with any marker. CONCLUSIONS: Baseline mild anemia in HIV-infected patients cannot always be resolved with durable efficient cART, possibly due to residual inflammation or immune activation rather than unbalanced iron homeostasis. Further research is needed on cytokine profiling to understand the mechanisms that induce anemia in HIV with suppressive cART. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12967-017-1358-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-19 /pmc/articles/PMC5735890/ /pubmed/29258550 http://dx.doi.org/10.1186/s12967-017-1358-6 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Quiros-Roldan, Eugenia
Castelli, Francesco
Lanza, Paola
Pezzoli, Chiara
Vezzoli, Marika
Biasiotto, Giorgio
Zanella, Isabella
The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia
title The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia
title_full The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia
title_fullStr The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia
title_full_unstemmed The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia
title_short The impact of antiretroviral therapy on iron homeostasis and inflammation markers in HIV-infected patients with mild anemia
title_sort impact of antiretroviral therapy on iron homeostasis and inflammation markers in hiv-infected patients with mild anemia
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5735890/
https://www.ncbi.nlm.nih.gov/pubmed/29258550
http://dx.doi.org/10.1186/s12967-017-1358-6
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