Prospective International Study of Incidence and Predictors of Immune Reconstitution Inflammatory Syndrome and Death in People Living With Human Immunodeficiency Virus and Severe Lymphopenia.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
27 07 2020
Historique:
received: 03 05 2019
accepted: 03 09 2019
pubmed: 11 9 2019
medline: 28 4 2021
entrez: 11 9 2019
Statut: ppublish

Résumé

Patients living with human immunodeficiency virus (PLWH) with low CD4 counts are at high risk for immune reconstitution inflammatory syndrome (IRIS) and death at antiretroviral therapy (ART) initiation. We investigated the clinical impact of IRIS in PLWH and CD4 counts <100 cells/μL starting ART in an international, prospective study in the United States, Thailand, and Kenya. An independent review committee adjudicated IRIS events. We assessed associations between baseline biomarkers, IRIS, immune recovery at week 48, and death by week 48 with Cox models. We enrolled 506 participants (39.3% were women). Median age was 37 years, and CD4 count was 29 cells/μL. Within 6 months of ART, 97 (19.2%) participants developed IRIS and 31 (6.5%) died. Participants with lower hemoglobin at baseline were at higher IRIS risk (hazard ratio [HR], 1.2; P = .004). IRIS was independently associated with increased risk of death after adjustment for known risk factors (HR, 3.2; P = .031). Being female (P = .004) and having a lower body mass index (BMI; P = .003), higher white blood cell count (P = .005), and higher D-dimer levels (P = .044) were also significantly associated with increased risk of death. Decision-tree analysis identified hemoglobin <8.5 g/dL as predictive of IRIS and C-reactive protein (CRP) >106 μg/mL and BMI <15.6 kg/m2 as predictive of death. For PLWH with severe immunosuppression initiating ART, baseline low BMI and hemoglobin and high CRP and D-dimer levels may be clinically useful predictors of IRIS and death risk.

Sections du résumé

BACKGROUND
Patients living with human immunodeficiency virus (PLWH) with low CD4 counts are at high risk for immune reconstitution inflammatory syndrome (IRIS) and death at antiretroviral therapy (ART) initiation.
METHODS
We investigated the clinical impact of IRIS in PLWH and CD4 counts <100 cells/μL starting ART in an international, prospective study in the United States, Thailand, and Kenya. An independent review committee adjudicated IRIS events. We assessed associations between baseline biomarkers, IRIS, immune recovery at week 48, and death by week 48 with Cox models.
RESULTS
We enrolled 506 participants (39.3% were women). Median age was 37 years, and CD4 count was 29 cells/μL. Within 6 months of ART, 97 (19.2%) participants developed IRIS and 31 (6.5%) died. Participants with lower hemoglobin at baseline were at higher IRIS risk (hazard ratio [HR], 1.2; P = .004). IRIS was independently associated with increased risk of death after adjustment for known risk factors (HR, 3.2; P = .031). Being female (P = .004) and having a lower body mass index (BMI; P = .003), higher white blood cell count (P = .005), and higher D-dimer levels (P = .044) were also significantly associated with increased risk of death. Decision-tree analysis identified hemoglobin <8.5 g/dL as predictive of IRIS and C-reactive protein (CRP) >106 μg/mL and BMI <15.6 kg/m2 as predictive of death.
CONCLUSIONS
For PLWH with severe immunosuppression initiating ART, baseline low BMI and hemoglobin and high CRP and D-dimer levels may be clinically useful predictors of IRIS and death risk.

Identifiants

pubmed: 31504347
pii: 5560189
doi: 10.1093/cid/ciz877
pmc: PMC7384325
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

652-660

Subventions

Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States

Informations de copyright

Published by Oxford University Press for the Infectious Diseases Society of America 2019.

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Auteurs

Irini Sereti (I)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Virginia Sheikh (V)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Douglas Shaffer (D)

Walter Reed Army Institute of Research/US Army Medical Research Directorate-Africa, Nairobi, Kenya.
Walter Reed Army Institute of Research, US Military Human Immunodeficiency Virus Research Program, Silver Spring, Maryland, USA.

Nittaya Phanuphak (N)

South East Asia Research Collaboration with Hawaii, Thai Red Cross AIDS Research Centre, Bangkok, Thailand.

Erin Gabriel (E)

Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, Sweden.

Jing Wang (J)

Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc, National Cancer Institute Campus at Frederick, Maryland, USA.

Martha C Nason (MC)

Division of Clinical Research, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland, USA.

Gregg Roby (G)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Hellen Ngeno (H)

Walter Reed Army Institute of Research/US Army Medical Research Directorate-Africa, Nairobi, Kenya.

Fredrick Kirui (F)

Kenya Medical Research Institute/US Army Medical Research Directorate-Africa-Kenya/ Henry Jackson Foundation Medical Research International, Kericho Clinical Research Center, Kenya.

Alice Pau (A)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Joann M Mican (JM)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

Adam Rupert (A)

Applied and Developmental Research Directorate, AIDS Monitoring Laboratory, Leidos Biomedical Research, Inc, Frederick, Maryland, USA.

Rachel Bishop (R)

National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.

Brian Agan (B)

Infectious Disease Clinical Research Program, Department of Preventive Medicine and Biostatistics, Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.

Nitiya Chomchey (N)

South East Asia Research Collaboration with Hawaii, Thai Red Cross AIDS Research Centre, Bangkok, Thailand.

Nipat Teeratakulpisarn (N)

South East Asia Research Collaboration with Hawaii, Thai Red Cross AIDS Research Centre, Bangkok, Thailand.

Somsit Tansuphaswadikul (S)

Bamrasnaradura Infectious Diseases Institute, Department of Medicine, Nonthaburi, Thailand.

Deborah Langat (D)

Kenya Medical Research Institute/US Army Medical Research Directorate-Africa-Kenya/ Henry Jackson Foundation Medical Research International, Kericho Clinical Research Center, Kenya.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.

Josphat Kosgei (J)

Kenya Medical Research Institute/US Army Medical Research Directorate-Africa-Kenya/ Henry Jackson Foundation Medical Research International, Kericho Clinical Research Center, Kenya.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.

Martyn French (M)

University of Western Australia, Medical School and School of Biomedical Sciences, Nedlands, Australia.

Jintanat Ananworanich (J)

South East Asia Research Collaboration with Hawaii, Thai Red Cross AIDS Research Centre, Bangkok, Thailand.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
US Military Human Immunodeficiency Virus Research Program, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.
Department of Global Health, Amsterdam Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

Fredrick Sawe (F)

Kenya Medical Research Institute/US Army Medical Research Directorate-Africa-Kenya/ Henry Jackson Foundation Medical Research International, Kericho Clinical Research Center, Kenya.
Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.

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