Increased Metabolic Activity on 18F-Fluorodeoxyglucose Positron Emission Tomography-Computed Tomography in Human Immunodeficiency Virus-Associated Immune Reconstitution Inflammatory Syndrome.


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:
07 01 2019
Historique:
received: 03 03 2018
accepted: 23 05 2018
pubmed: 15 9 2018
medline: 31 1 2020
entrez: 15 9 2018
Statut: ppublish

Résumé

Immune reconstitution inflammatory syndrome (IRIS) represents an unexpected inflammatory response shortly after initiation of antiretroviral therapy (ART) in some human immunodeficiency virus (HIV)-infected patients with underlying neoplasia or opportunistic infections, including tuberculosis. We hypothesized that IRIS is associated with increased glycolysis and that 18F-fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET/CT) could help identify high-risk subjects. In this prospective cohort study, 30 HIV-infected patients (CD4+ count <100 cells/µL) underwent FDG-PET/CT scans at baseline and 4-8 weeks after ART initiation. Ten patients developed IRIS (6 mycobacterial). At baseline, total glycolytic activity, total lesion volume, and maximum standardized uptake values (SUVs) of pathologic FDG uptake (reflective of opportunistic disease burden) were significantly higher in IRIS vs non-IRIS (P = .010, .017, and .029, respectively) and significantly correlated with soluble inflammatory biomarkers (interferon-γ, myeloperoxidase, tumor necrosis factor, interleukin 6, soluble CD14). Baseline bone marrow (BM) and spleen FDG uptake was higher in mycobacterial IRIS specifically. After ART initiation, BM and spleen mean SUV decreased in non-IRIS (P = .004, .013) but not IRIS subjects. Our results were supported by significantly higher glucose transporter 1 (Glut-1) expression of CD4+ cells and monocytes after ART initiation in IRIS/mycobacterial IRIS compared with non-IRIS patients. We conclude that increased pathologic metabolic activity on FDG-PET/CT prior to ART initiation is associated with IRIS development and correlates with inflammatory biomarkers. Abnormally elevated BM and spleen metabolism is associated with mycobacterial IRIS, HIV viremia, and Glut-1 expression on CD4+ cells and monocytes. NCT02147405.

Sections du résumé

Background
Immune reconstitution inflammatory syndrome (IRIS) represents an unexpected inflammatory response shortly after initiation of antiretroviral therapy (ART) in some human immunodeficiency virus (HIV)-infected patients with underlying neoplasia or opportunistic infections, including tuberculosis. We hypothesized that IRIS is associated with increased glycolysis and that 18F-fluorodeoxyglucose (FDG) positron emission tomography-computed tomography (PET/CT) could help identify high-risk subjects.
Methods
In this prospective cohort study, 30 HIV-infected patients (CD4+ count <100 cells/µL) underwent FDG-PET/CT scans at baseline and 4-8 weeks after ART initiation. Ten patients developed IRIS (6 mycobacterial).
Results
At baseline, total glycolytic activity, total lesion volume, and maximum standardized uptake values (SUVs) of pathologic FDG uptake (reflective of opportunistic disease burden) were significantly higher in IRIS vs non-IRIS (P = .010, .017, and .029, respectively) and significantly correlated with soluble inflammatory biomarkers (interferon-γ, myeloperoxidase, tumor necrosis factor, interleukin 6, soluble CD14). Baseline bone marrow (BM) and spleen FDG uptake was higher in mycobacterial IRIS specifically. After ART initiation, BM and spleen mean SUV decreased in non-IRIS (P = .004, .013) but not IRIS subjects. Our results were supported by significantly higher glucose transporter 1 (Glut-1) expression of CD4+ cells and monocytes after ART initiation in IRIS/mycobacterial IRIS compared with non-IRIS patients.
Conclusions
We conclude that increased pathologic metabolic activity on FDG-PET/CT prior to ART initiation is associated with IRIS development and correlates with inflammatory biomarkers. Abnormally elevated BM and spleen metabolism is associated with mycobacterial IRIS, HIV viremia, and Glut-1 expression on CD4+ cells and monocytes.
Clinical Trials Registration
NCT02147405.

Identifiants

pubmed: 30215671
pii: 5095310
doi: 10.1093/cid/ciy454
pmc: PMC6321853
doi:

Substances chimiques

Anti-HIV Agents 0
Biomarkers 0
Glucose Transporter Type 1 0
Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Banques de données

ClinicalTrials.gov
['NCT02147405']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

229-238

Subventions

Organisme : CCR NIH HHS
ID : HHSN261200800001C
Pays : United States
Organisme : NCI NIH HHS
ID : HHSN261200800001E
Pays : United States

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Auteurs

Dima A Hammoud (DA)

Center for Infectious Diseases Imaging, Clinical Center, National Institutes of Health (NIH).

Afroditi Boulougoura (A)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Georgios Z Papadakis (GZ)

Center for Infectious Diseases Imaging, Clinical Center, National Institutes of Health (NIH).

Jing Wang (J)

Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc, National Cancer Institute, Frederick.

Lori E Dodd (LE)

Biostatistics Research Branch, NIAID, NIH, Bethesda.

Adam Rupert (A)

Leidos Biomedical Research Inc, Frederick National Laboratory for Cancer Research.

Jeanette Higgins (J)

Leidos Biomedical Research Inc, Frederick National Laboratory for Cancer Research.

Gregg Roby (G)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Dorinda Metzger (D)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Elizabeth Laidlaw (E)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

JoAnn M Mican (JM)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Alice Pau (A)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Silvia Lage (S)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Chun-Shu Wong (CS)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Andrea Lisco (A)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Maura Manion (M)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Virginia Sheikh (V)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

Corina Millo (C)

Positron Emission Tomography Department, Clinical Center, NIH, Bethesda, Maryland.

Irini Sereti (I)

Division of Intramural Research, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda.

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Classifications MeSH