Effect of the relationship between anaemia and systemic inflammation on the risk of incident tuberculosis and death in people with advanced HIV: a sub-analysis of the REMEMBER trial.

Anaemia Death HIV Haemoglobin Incident TB Inflammation Systemic inflammation Tuberculosis

Journal

EClinicalMedicine
ISSN: 2589-5370
Titre abrégé: EClinicalMedicine
Pays: England
ID NLM: 101733727

Informations de publication

Date de publication:
Jun 2023
Historique:
received: 09 11 2022
revised: 12 05 2023
accepted: 16 05 2023
medline: 8 6 2023
pubmed: 8 6 2023
entrez: 8 6 2023
Statut: epublish

Résumé

Tuberculosis (TB) is an infectious morbidity that commonly occurs in people living with HIV (PWH) and increases the progression of HIV disease, as well as the risk of death. Simple markers of progression are much needed to identify those at highest risk for poor outcome. This study aimed to assess how baseline severity of anaemia and associated inflammatory profiles impact death and the incidence of TB in a cohort of PWH who received TB preventive therapy (TPT). This study is a secondary posthoc analysis of the AIDS Clinical Trials Group A5274 REMEMBER clinical trial (NCT0138008), an open-label randomised clinical trial of antiretroviral-naïve PWH with CD4 <50 cells/μL, performed from October 31, 2011 to June 9, 2014, from 18 outpatient research clinics in 10 low- and middle-income countries (Malawi, South Africa, Haiti, Kenya, Zambia, India, Brazil, Zimbabwe, Peru, and Uganda) who initiated antiretroviral therapy and either isoniazid TPT or 4-drug empiric TB therapy. Plasma concentrations of several soluble inflammatory biomarkers were measured prior to the commencement of antiretroviral and anti-TB therapies, and participants were followed up for at least 48 weeks. Incident TB or death during this period were primary outcomes. We performed multidimensional analyses, logistic regression analyses, survival curves, and Bayesian network analyses to delineate associations between anaemia, laboratory parameters, and clinical outcomes. Of all 269 participants, 76.2% (n = 205) were anaemic, and 31.2% (n = 84) had severe anaemia. PWH with moderate/severe anaemia exhibited a pronounced systemic pro-inflammatory profile compared to those with mild or without anaemia, hallmarked by a substantial increase in IL-6 plasma concentrations. Moderate/severe anaemia was also associated with incident TB incidence (aOR: 3.59, 95% CI: 1.32-9.76, p = 0.012) and death (aOR: 3.63, 95% CI: 1.07-12.33, p = 0.039). Our findings suggest that PWH with moderate/severe anaemia display a distinct pro-inflammatory profile. The presence of moderate/severe anaemia pre-ART was independently associated with the development of TB and death. PWH with anaemia should be monitored closely to minimise the occurrence of unfavourable outcomes. National Institutes of Health.

Sections du résumé

Background UNASSIGNED
Tuberculosis (TB) is an infectious morbidity that commonly occurs in people living with HIV (PWH) and increases the progression of HIV disease, as well as the risk of death. Simple markers of progression are much needed to identify those at highest risk for poor outcome. This study aimed to assess how baseline severity of anaemia and associated inflammatory profiles impact death and the incidence of TB in a cohort of PWH who received TB preventive therapy (TPT).
Methods UNASSIGNED
This study is a secondary posthoc analysis of the AIDS Clinical Trials Group A5274 REMEMBER clinical trial (NCT0138008), an open-label randomised clinical trial of antiretroviral-naïve PWH with CD4 <50 cells/μL, performed from October 31, 2011 to June 9, 2014, from 18 outpatient research clinics in 10 low- and middle-income countries (Malawi, South Africa, Haiti, Kenya, Zambia, India, Brazil, Zimbabwe, Peru, and Uganda) who initiated antiretroviral therapy and either isoniazid TPT or 4-drug empiric TB therapy. Plasma concentrations of several soluble inflammatory biomarkers were measured prior to the commencement of antiretroviral and anti-TB therapies, and participants were followed up for at least 48 weeks. Incident TB or death during this period were primary outcomes. We performed multidimensional analyses, logistic regression analyses, survival curves, and Bayesian network analyses to delineate associations between anaemia, laboratory parameters, and clinical outcomes.
Findings UNASSIGNED
Of all 269 participants, 76.2% (n = 205) were anaemic, and 31.2% (n = 84) had severe anaemia. PWH with moderate/severe anaemia exhibited a pronounced systemic pro-inflammatory profile compared to those with mild or without anaemia, hallmarked by a substantial increase in IL-6 plasma concentrations. Moderate/severe anaemia was also associated with incident TB incidence (aOR: 3.59, 95% CI: 1.32-9.76, p = 0.012) and death (aOR: 3.63, 95% CI: 1.07-12.33, p = 0.039).
Interpretation UNASSIGNED
Our findings suggest that PWH with moderate/severe anaemia display a distinct pro-inflammatory profile. The presence of moderate/severe anaemia pre-ART was independently associated with the development of TB and death. PWH with anaemia should be monitored closely to minimise the occurrence of unfavourable outcomes.
Funding UNASSIGNED
National Institutes of Health.

Identifiants

pubmed: 37287871
doi: 10.1016/j.eclinm.2023.102030
pii: S2589-5370(23)00207-9
pmc: PMC10242630
doi:

Types de publication

Journal Article

Langues

eng

Pagination

102030

Subventions

Organisme : NIAID NIH HHS
ID : UM1 AI069423
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI068634
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069469
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069518
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069453
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069463
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI108568
Pays : United States
Organisme : Medical Research Council
ID : MC_PC_16022
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : UM1 AI068636
Pays : United States

Informations de copyright

© 2023 The Author(s).

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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Auteurs

Mariana Araújo-Pereira (M)

Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Multinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Salvador, Brazil.
Programa de Pós-Graduação em Patologia Humana e Experimental, Universidade Federal da Bahia, Salvador, Bahia, Brazil.
Curso de Medicina, Faculdade de Tecnologia e Ciências (FTC), Salvador, Brazil.

Sonya Krishnan (S)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Padmini Salgame (P)

Department of Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.

Yukari C Manabe (YC)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Mina C Hosseinipour (MC)

Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

Gregory Bisson (G)

University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

Damocles Patrice Severe (DP)

Les Centres Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince HT6110, Haiti.

Vanessa Rouzier (V)

Les Centres Haitian Group for the Study of Kaposi's Sarcoma and Opportunistic Infections (GHESKIO), Port-au-Prince HT6110, Haiti.

Samantha Leong (S)

Department of Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.

Vidya Mave (V)

BJ Medical College Clinical Research Site, Pune, India.

Fredrick Kipyego Sawe (FK)

Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD, USA.

Abraham M Siika (AM)

Department of Medicine, School of Medicine, Moi University, Eldoret, Kenya.

Cecilia Kanyama (C)

University of North Carolina Project, Kamazu Central Hospital, Lilongwe, Malawi.

Sufia S Dadabhai (SS)

Johns Hopkins Bloomberg School of Public Health, Blantyre, Malawi.

Javier R Lama (JR)

Asociacion Civil Impacta Salud y Educacion, Lima, Peru.

Javier Valencia-Huamani (J)

Asociacion Civil Impacta Salud y Educacion, Lima, Peru.

Sharlaa Badal-Faesen (S)

Clinical HIV Research Unit, School of Clinical Medicine, University of Witwatersrand, Johannesburg, South Africa.

Umesh Gangaram Lalloo (UG)

Morningside Mediclinic, Sandton, Johannesburg, South Africa.

Kogieleum Naidoo (K)

Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal Nelson R Mandela School of Medicine, Durban, South Africa.
SA-Medical Research Council (MRC)-CAPRISA-HIV-TB Pathogenesis and Treatment Research Unit, University of KwaZulu-Natal Nelson R Mandela School of Medicine, Durban, South Africa.

Lerato Mohapi (L)

School of Clinical Medicine, University of Witwatersrand, Johannesburg, South Africa.

Cissy Kityo (C)

HIV Medicine, Joint Clinical Research Centre, Kampala, Uganda.

Bruno B Andrade (BB)

Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.
Multinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Salvador, Brazil.
Programa de Pós-Graduação em Patologia Humana e Experimental, Universidade Federal da Bahia, Salvador, Bahia, Brazil.
Curso de Medicina, Faculdade de Tecnologia e Ciências (FTC), Salvador, Brazil.

Amita Gupta (A)

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Classifications MeSH