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
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
102030Subventions
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.
Références
J Infect Dis. 2007 Aug 15;196 Suppl 1:S52-62
pubmed: 17624827
Environ Health Prev Med. 2021 Jan 23;26(1):13
pubmed: 33485299
Eur Respir J. 2011 May;37(5):1248-59
pubmed: 20817712
Front Immunol. 2022 Jun 23;13:916216
pubmed: 35812431
J Immunol. 1990 Jan 15;144(2):480-4
pubmed: 2295799
Semin Arthritis Rheum. 2009 Apr;38(5):382-8
pubmed: 18336871
PLoS One. 2016 May 12;11(5):e0155100
pubmed: 27171281
Tuberculosis (Edinb). 2019 Sep;118:101863
pubmed: 31561185
EBioMedicine. 2022 Nov;85:104309
pubmed: 36283285
N Engl J Med. 2005 Mar 10;352(10):1011-23
pubmed: 15758012
J Infect Dis. 2010 Jun 15;201(12):1788-95
pubmed: 20446848
Clin Microbiol Rev. 2011 Apr;24(2):351-76
pubmed: 21482729
PLoS One. 2017 Mar 30;12(3):e0173976
pubmed: 28358846
Blood. 1997 Jun 1;89(11):4100-3
pubmed: 9166851
Front Immunol. 2020 Sep 24;11:588405
pubmed: 33072136
Environ Health Prev Med. 2021 Sep 21;26(1):93
pubmed: 34548015
Int J STD AIDS. 2016 Oct;27(11):1019-22
pubmed: 26468273
BMC Med. 2015 Apr 02;13:70
pubmed: 25889688
AIDS. 2017 Oct 23;31(16):2217-2225
pubmed: 28742529
Int Rev Immunol. 2014 Nov-Dec;33(6):511-36
pubmed: 24654626
J Exp Med. 2011 Jun 6;208(6):1203-14
pubmed: 21624938
Lancet. 2016 Mar 19;387(10024):1198-209
pubmed: 27025337
Clin Infect Dis. 2020 Dec 17;71(10):2645-2654
pubmed: 31761933
Clin Infect Dis. 2015 Jul 1;61(1):102-10
pubmed: 25828994
Am J Med. 2004 Apr 5;116 Suppl 7A:27S-43S
pubmed: 15050884
J Res Med Sci. 2012 Feb;17(2):138-42
pubmed: 23264786
AIDS. 1999 May 28;13(8):943-50
pubmed: 10371175
Life (Basel). 2020 Oct 29;10(11):
pubmed: 33138069
Nat Rev Microbiol. 2018 Feb;16(2):80-90
pubmed: 29109555
AIDS. 2014 Jul 31;28(12):1791-6
pubmed: 25003720
J Infect Dis. 2015 Aug 15;212(4):585-95
pubmed: 25722296
J Acquir Immune Defic Syndr. 2011 Apr;56(4):349-55
pubmed: 20926954
PLoS One. 2013 May 17;8(5):e63541
pubmed: 23691062
Microorganisms. 2021 Nov 04;9(11):
pubmed: 34835417
Lancet Infect Dis. 2015 Apr;15(4):429-38
pubmed: 25672566
J Infect Dis. 2011 Jun 1;203(11):1637-46
pubmed: 21592994