4.7 Article

Higher Levels of CRP, D-dimer, IL-6, and Hyaluronic Acid Before Initiation of Antiretroviral Therapy (ART) Are Associated With Increased Risk of AIDS or Death

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 203, Issue 11, Pages 1637-1646

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jir134

Keywords

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Funding

  1. National Institute of Allergy and Infectious Diseases (NIAID) of the National Institutes of Health [U01AI042170, U01AI046362, U01AI068641, CPCRA 058]
  2. INSIGHT
  3. NIAID [K23AI073192-02]
  4. National Cancer Institute, National Institutes of Health [HHSN261200800001E]
  5. [K12RR023247-05]
  6. MRC [MC_U122886352] Funding Source: UKRI
  7. Medical Research Council [MC_U122886352] Funding Source: researchfish

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Background. Substantial morbidity occurs during the first year of antiretroviral therapy (ART) in persons with advanced human immunodeficiency virus (HIV) disease despite HIV suppression. Biomarkers may identify high-risk groups. Methods. Pre-ART and 1-month samples from an initial ART trial were evaluated for biomarkers associated with AIDS events or death within 1-12 months. Case patients (n = 63) and control patients (n = 126) were 1: 2 matched on baseline CD4 cell count, hepatitis status, and randomization date. All had >= 1 log(10) HIV RNA level decrease at 1 month. Results. Case patients had more frequent prior AIDS events, compared with control patients (P = .004), but similar HIV RNA levels at baseline. Pre-ART and 1-month C-reactive protein (CRP), D-dimer, and interleukin 6 (IL-6) levels and pre-ART hyaluronic acid (HA) levels were associated with new AIDS events or death (P <= .01). Patients who experienced immune reconstitution inflammatory syndrome (IRIS) events had higher pre-ART tumor necrosis factor alpha (TNF-alpha) and HIV RNA levels and significant 1-month increases in CRP, D-dimer, IL-6, interleukin 8, CXCL10, TNF-alpha, and interferon-gamma levels, compared with patients who experienced non-IRIS events (P <= .03). Individuals with baseline CRP and HA levels above the cohort median (>2.1 mg/L and >50.0 ng/mL, respectively) had increased risk of AIDS or death (OR, 4.6 [95% CI, 2.0-10.3]; P < .001) and IRIS (OR, 8.7 [95% CI, 2.2-34.8] P = .002). Conclusions. Biomarkers of Inflammation (CRP, IL-6), coagulation (D-dimer), and tissue fibrosis (HA) measured pre-ART and at 1 month are associated with higher risk of AIDS events, IRIS, or death, warranting additional study as risk stratification strategies.

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