Le SIDA en Afrique subsaharienne (serveur d'exploration)

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HIV viral load as an independent risk factor for tuberculosis in South Africa: collaborative analysis of cohort studies.

Identifieur interne : 004367 ( Ncbi/Merge ); précédent : 004366; suivant : 004368

HIV viral load as an independent risk factor for tuberculosis in South Africa: collaborative analysis of cohort studies.

Auteurs : Lukas Fenner [Suisse] ; Andrew Atkinson [Suisse] ; Andrew Boulle [Afrique du Sud] ; Matthew P. Fox [Afrique du Sud] ; Hans Prozesky [Afrique du Sud] ; Kathrin Zürcher [Suisse] ; Marie Ballif [Suisse] ; Hansjakob Furrer [Suisse] ; Marcel Zwahlen [Suisse] ; Mary-Ann Davies [Afrique du Sud] ; Matthias Egger [Suisse]

Source :

RBID : pubmed:28691438

Abstract

Chronic immune activation due to ongoing HIV replication may lead to impaired immune responses against opportunistic infections such as tuberculosis (TB). We studied the role of HIV replication as a risk factor for incident TB after starting antiretroviral therapy (ART).

DOI: 10.7448/IAS.20.1.21327
PubMed: 28691438

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Le document en format XML

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<name sortKey="Davies, Mary Ann" sort="Davies, Mary Ann" uniqKey="Davies M" first="Mary-Ann" last="Davies">Mary-Ann Davies</name>
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<name sortKey="Egger, Matthias" sort="Egger, Matthias" uniqKey="Egger M" first="Matthias" last="Egger">Matthias Egger</name>
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<div type="abstract" xml:lang="en">Chronic immune activation due to ongoing HIV replication may lead to impaired immune responses against opportunistic infections such as tuberculosis (TB). We studied the role of HIV replication as a risk factor for incident TB after starting antiretroviral therapy (ART).</div>
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<DateCreated>
<Year>2017</Year>
<Month>07</Month>
<Day>10</Day>
</DateCreated>
<DateRevised>
<Year>2017</Year>
<Month>09</Month>
<Day>27</Day>
</DateRevised>
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<Volume>20</Volume>
<Issue>1</Issue>
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<Year>2017</Year>
<Month>06</Month>
<Day>23</Day>
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<Title>Journal of the International AIDS Society</Title>
<ISOAbbreviation>J Int AIDS Soc</ISOAbbreviation>
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<ArticleTitle>HIV viral load as an independent risk factor for tuberculosis in South Africa: collaborative analysis of cohort studies.</ArticleTitle>
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<Abstract>
<AbstractText Label="INTRODUCTION">Chronic immune activation due to ongoing HIV replication may lead to impaired immune responses against opportunistic infections such as tuberculosis (TB). We studied the role of HIV replication as a risk factor for incident TB after starting antiretroviral therapy (ART).</AbstractText>
<AbstractText Label="METHODS">We included all HIV-positive adult patients (≥16 years) in care between 2000 and 2014 at three ART programmes in South Africa. Patients with previous TB were excluded. Missing CD4 cell counts and HIV-RNA viral loads at ART start (baseline) and during follow-up were imputed. We used parametric survival models to assess TB incidence (pulmonary and extrapulmonary) by CD4 cell and HIV-RNA levels, and estimated the rate ratios for TB by including age, sex, baseline viral loads, CD4 cell counts, and WHO clinical stage in the model. We also used Poisson general additive regression models with time-updated CD4 and HIV-RNA values, adjusting for age and sex.</AbstractText>
<AbstractText Label="RESULTS">We included 44,260 patients with a median follow-up time of 2.7 years (interquartile range [IQR] 1.0-5.0); 3,819 incident TB cases were recorded (8.6%). At baseline, the median age was 34 years (IQR 28-41); 30,675 patients (69.3%) were female. The median CD4 cell count was 156 cells/µL (IQR 79-229) and the median HIV-RNA viral load 58,000 copies/mL (IQR 6,000-240,000). Overall TB incidence was 26.2/1,000 person-years (95% confidence interval [CI] 25.3-27.0). Compared to the lowest viral load category (0-999 copies/mL), the adjusted rate ratio for TB was 1.41 (95% CI 1.15-1.75, p < 0.001) in the highest group (>10,000 copies/mL). Time-updated analyses for CD4/HIV-RNA confirmed the association of viral load with the risk for TB.</AbstractText>
<AbstractText Label="CONCLUSIONS">Our results indicate that ongoing HIV replication is an important risk factor for TB, regardless of CD4 cell counts, and underline the importance of early ART start and retention on ART.</AbstractText>
</Abstract>
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<LastName>Fenner</LastName>
<ForeName>Lukas</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, Basel, Switzerland.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>University of Basel, Basel, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Atkinson</LastName>
<ForeName>Andrew</ForeName>
<Initials>A</Initials>
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<Affiliation>Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
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<LastName>Boulle</LastName>
<ForeName>Andrew</ForeName>
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<Affiliation>Khayelitsha ART Programme, Médecins Sans Frontières, Cape Town, South Africa.</Affiliation>
</AffiliationInfo>
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<Affiliation>Health Economics and Epidemiology Research Office, Department of Internal Medicine, School of Clinical Medicine, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Departments of Epidemiology and Global Health, Boston University, Boston, MA, USA.</Affiliation>
</AffiliationInfo>
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<LastName>Prozesky</LastName>
<ForeName>Hans</ForeName>
<Initials>H</Initials>
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<Affiliation>Division of Infectious Diseases, Department of Medicine, University of Stellenbosch and Tygerberg Hospital, Cape Town, South Africa.</Affiliation>
</AffiliationInfo>
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</AffiliationInfo>
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<Initials>M</Initials>
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<Affiliation>Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Furrer</LastName>
<ForeName>Hansjakob</ForeName>
<Initials>H</Initials>
<AffiliationInfo>
<Affiliation>Department of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zwahlen</LastName>
<ForeName>Marcel</ForeName>
<Initials>M</Initials>
<AffiliationInfo>
<Affiliation>Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Davies</LastName>
<ForeName>Mary-Ann</ForeName>
<Initials>MA</Initials>
<AffiliationInfo>
<Affiliation>Centre for Infectious Disease Epidemiology and Research (CIDER), School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.</Affiliation>
</AffiliationInfo>
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<LastName>Egger</LastName>
<ForeName>Matthias</ForeName>
<Initials>M</Initials>
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<Affiliation>Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Centre for Infectious Disease Epidemiology and Research (CIDER), School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.</Affiliation>
</AffiliationInfo>
</Author>
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<CollectiveName>International Epidemiology Database to Evaluate AIDS in Southern Africa (IeDEA-SA)</CollectiveName>
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<Language>eng</Language>
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<Grant>
<GrantID>U01AI069924</GrantID>
<Agency>US National Institutes of Health (NIAID, NICHD, NCI, NIMH, and NIDA)</Agency>
<Country>International</Country>
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