Artículos de revistas
Biomarkers and Bacterial Pneumonia Risk in Patients with Treated HIV Infection: A Case-Control Study
Fecha
2013-02Registro en:
Plos One, v. 8. n.2, p. e56249 (8p.), 2013.
10.1371/journal.pone.0056249
Autor
Bjerk, Sonja M.
Baker, Jason V.
Emery, Sean
Neuhaus, Jacqueline
Angus, Brian
Gordin, Fred M.
Pett, Sarah L.
Stephan, Christoph
Kunisaki, Ken M.
INSIGHT SMART Study Group
Casseb, Jorge Simão do Rosário
Institución
Resumen
Background: Despite advances in HIV treatment, bacterial pneumonia continues to cause considerable morbidity and
mortality in patients with HIV infection. Studies of biomarker associations with bacterial pneumonia risk in treated HIVinfected
patients do not currently exist.
Methods: We performed a nested, matched, case-control study among participants randomized to continuous combination
antiretroviral therapy (cART) in the Strategies for Management of Antiretroviral Therapy trial. Patients who developed
bacterial pneumonia (cases) and patients without bacterial pneumonia (controls) were matched 1:1 on clinical center,
smoking status, age, and baseline cART use. Baseline levels of Club Cell Secretory Protein 16 (CC16), Surfactant Protein D
(SP-D), C-reactive protein (hsCRP), interleukin-6 (IL-6), and d-dimer were compared between cases and controls.
Results: Cases (n = 72) and controls (n = 72) were 25.7% female, 51.4% black, 65.3% current smokers, 9.7% diabetic, 36.1%
co-infected with Hepatitis B/C, and 75.0% were on cART at baseline. Median (IQR) age was 45 (41, 51) years with CD4+ count
of 553 (436, 690) cells/mm3. Baseline CC16 and SP-D were similar between cases and controls, but hsCRP was significantly
higher in cases than controls (2.94 mg/mL in cases vs. 1.93 mg/mL in controls; p = 0.02). IL-6 and d-dimer levels were also
higher in cases compared to controls, though differences were not statistically significant (p-value 0.06 and 0.10,
respectively).
Conclusions: In patients with cART-treated HIV infection, higher levels of systemic inflammatory markers were associated
with increased bacterial pneumonia risk, while two pulmonary-specific inflammatory biomarkers, CC16 and SP-D, were not
associated with bacterial pneumonia risk.