Association of Plasma Soluble Vascular Cell Adhesion Molecule-1 and sCD14 With Mortality in HIV-1-Infected West African Adults With High CD4 Counts.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 01 2021
Historique:
pubmed: 20 10 2020
medline: 16 7 2021
entrez: 19 10 2020
Statut: ppublish

Résumé

Several biomarkers of inflammation and coagulation were reported to be associated with HIV disease progression in different settings. In this article, we report the association between 11 biomarkers and medium-term mortality in HIV-infected West African adults. In Temprano ANRS 12136, antiretroviral therapy (ART)-naive HIV-infected adults with high CD4 counts were randomly assigned either to start ART immediately or defer ART until the World Health Organization criteria were met. Participants who completed the 30-month trial follow-up were invited to participate in a posttrial phase. The posttrial phase end point was all-cause death. We used multivariate Cox proportional models to analyze the association between baseline plasma biomarkers [IL-1ra, IL-6, soluble vascular cell adhesion molecule 1 (sVCAM-1), sCD14, D-dimer, fibrinogen, IP-10, sCD163, albumin, high-sensitivity C-reactive protein, and 16S rDNA] and all-cause death in the Temprano participants randomized to defer ART. Four hundred seventy-seven patients (median age 35 years, 78% women, and median CD4 count: 379 cells/mm) were randomly assigned to defer starting ART until the World Health Organization criteria were met. The participants were followed for 2646 person-years (median 5.8 years). In the follow-up, 89% of participants started ART and 30 died. In the multivariate analysis adjusted for the study center, sex, baseline CD4 count, isoniazid preventive therapy, plasma HIV-1 RNA, peripheral blood mononuclear cell HIV-1 DNA, and ART, the risk of death was significantly associated with baseline sVCAM-1 (≥1458 vs. <1458: adjusted hazard ratio 2.57, 95% confidence interval: 1.13 to 5.82) and sCD14 (≥2187 vs. <2187: adjusted hazard ratio 2.79, interquartile range 1.29-6.02) levels. In these sub-Saharan African adults with high CD4 counts, pre-ART plasma sVCAM-1 and sCD14 levels were independently associated with mortality.

Sections du résumé

BACKGROUND
Several biomarkers of inflammation and coagulation were reported to be associated with HIV disease progression in different settings. In this article, we report the association between 11 biomarkers and medium-term mortality in HIV-infected West African adults.
METHODS
In Temprano ANRS 12136, antiretroviral therapy (ART)-naive HIV-infected adults with high CD4 counts were randomly assigned either to start ART immediately or defer ART until the World Health Organization criteria were met. Participants who completed the 30-month trial follow-up were invited to participate in a posttrial phase. The posttrial phase end point was all-cause death. We used multivariate Cox proportional models to analyze the association between baseline plasma biomarkers [IL-1ra, IL-6, soluble vascular cell adhesion molecule 1 (sVCAM-1), sCD14, D-dimer, fibrinogen, IP-10, sCD163, albumin, high-sensitivity C-reactive protein, and 16S rDNA] and all-cause death in the Temprano participants randomized to defer ART.
RESULTS
Four hundred seventy-seven patients (median age 35 years, 78% women, and median CD4 count: 379 cells/mm) were randomly assigned to defer starting ART until the World Health Organization criteria were met. The participants were followed for 2646 person-years (median 5.8 years). In the follow-up, 89% of participants started ART and 30 died. In the multivariate analysis adjusted for the study center, sex, baseline CD4 count, isoniazid preventive therapy, plasma HIV-1 RNA, peripheral blood mononuclear cell HIV-1 DNA, and ART, the risk of death was significantly associated with baseline sVCAM-1 (≥1458 vs. <1458: adjusted hazard ratio 2.57, 95% confidence interval: 1.13 to 5.82) and sCD14 (≥2187 vs. <2187: adjusted hazard ratio 2.79, interquartile range 1.29-6.02) levels.
CONCLUSIONS
In these sub-Saharan African adults with high CD4 counts, pre-ART plasma sVCAM-1 and sCD14 levels were independently associated with mortality.

Identifiants

pubmed: 33074857
doi: 10.1097/QAI.0000000000002533
pii: 00126334-202101010-00019
doi:

Substances chimiques

Anti-Retroviral Agents 0
Biomarkers 0
Fibrin Fibrinogen Degradation Products 0
Lipopolysaccharide Receptors 0
Vascular Cell Adhesion Molecule-1 0
fibrin fragment D 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

138-145

Références

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Auteurs

Roseline Affi (R)

CeDReS, CHU de Treichville, Abidjan, Côte d'Ivoire.
PACCI-ANRS Research Site, Côte d'Ivoire.
Université Felix Houphouët Boigny, Abidjan, Côte d'Ivoire.

Delphine Gabillard (D)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Catherine Dunyach-Remy (C)

VBMI, INSERM U1047, Université de Montpellier, Service de Microbiologie et Hygiène Hospitalière, CHU de Carémeau, Nîmes, France.

Jean-Baptiste Ntakpe (JB)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Raoul Moh (R)

PACCI-ANRS Research Site, Côte d'Ivoire.
Université Felix Houphouët Boigny, Abidjan, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Anani Badje (A)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Gérard M Kouame (GM)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Sophie Karcher (S)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Jérome Le Carrou (J)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Christine Danel (C)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Mathieu F Chevalier (MF)

INSERM U976, Laboratory of Human Immunology, Pathophysiology and Immunotherapy, Hôpital Saint-Louis, Paris, France.
Université de Paris, Institut de Recherche Saint Louis, Hôpital Saint-Louis, Paris, France.

Christine Rouzioux (C)

AP-HP, CHU Necker Enfants Malades, EA 7327 Université Paris Descartes, Paris, France.

Serge P Eholie (SP)

PACCI-ANRS Research Site, Côte d'Ivoire.
Université Felix Houphouët Boigny, Abidjan, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Jean-Philippe Lavigne (JP)

VBMI, INSERM U1047, Université de Montpellier, Service de Microbiologie et Hygiène Hospitalière, CHU de Carémeau, Nîmes, France.

Andre Inwoley (A)

CeDReS, CHU de Treichville, Abidjan, Côte d'Ivoire.
PACCI-ANRS Research Site, Côte d'Ivoire.
Université Felix Houphouët Boigny, Abidjan, Côte d'Ivoire.

Xavier Anglaret (X)

PACCI-ANRS Research Site, Côte d'Ivoire.
INSERM U1219, University of Bordeaux, IRD, France.

Laurence Weiss (L)

Université de Paris, Institut de Recherche Saint Louis, Hôpital Saint-Louis, Paris, France.
Service d'Immunologie Clinique, Hôpital Européen Georges Pompidou, AP-HP, Paris, France ; and.
Faculté de Médecine Paris Descartes, Université de Paris, France.

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