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Peptide-based Identification of Functional Motifs and their Binding Partners
Published on: June 30, 2013
Elevated NT-pro-BNP levels are associated with comorbidities among HIV-infected women
Ather Mansoor1, Keri Althoff, Stephen Gange
1Division of Cardiology, Department of Medicine, SUNY Downstate Medical Center, Brooklyn, NY 11203, USA.
Insights
HIV infection is linked to higher natriuretic peptide levels, but this is primarily due to co-existing conditions like anemia and kidney disease, not the virus itself. These peptides signal overall comorbidity in HIV-infected individuals.
Area of Science:
- Cardiology
- Infectious Diseases
- Nephrology
Background:
- HIV infection is associated with left ventricular dysfunction and accelerated atherosclerosis, leading to elevated plasma natriuretic peptide (NP) levels.
- Natriuretic peptides, such as N-terminal-pro-BNP (NT-pro-BNP), are biomarkers of cardiac stress and dysfunction.
Purpose of the Study:
- To compare NT-pro-BNP levels in HIV-infected and HIV-uninfected women.
- To identify factors influencing NT-pro-BNP levels in HIV-infected women.
Main Methods:
- A cross-sectional study involving 454 HIV-infected and 200 HIV-uninfected women from the Women's Interagency HIV Study (WIHS).
- NT-pro-BNP levels were measured and compared using age-stratified cut-off values.
- Statistical analyses, including univariate and multivariate models, were used to identify associated factors.
Main Results:
- HIV-infected women had significantly higher NT-pro-BNP levels and a higher prevalence of elevated levels compared to HIV-uninfected women.
- Elevated NT-pro-BNP was significantly associated with anemia, kidney dysfunction, and Hepatitis C Virus (HCV) seropositivity in multivariate analysis.
- In HIV-infected women, NT-pro-BNP levels were not independently associated with HIV severity or HAART use.
Conclusions:
- Elevated NT-pro-BNP levels in HIV-infected women are primarily driven by non-HIV-related comorbidities such as anemia, kidney disease, and HCV coinfection.
- NT-pro-BNP serves as a global marker of comorbidity in the context of HIV infection.
- These findings underscore the importance of managing comorbidities in HIV-infected individuals to improve cardiovascular outcomes.
Abstract:
HIV infection is associated with left ventricular (LV) dysfunction and accelerated atherosclerosis. These conditions result in elevation of plasma natriuretic peptide (NP) levels. The present study compares N-terminal-pro-BNP (NT-pro-BNP) levels in HIV-infected and -uninfected women and identifies factors influencing NT-pro-BNP levels in HIV-infected women. A total of 454 HIV-infected and 200 HIV-uninfected participants from the Women's Interagency HIV Study (WIHS) had NT-pro-BNP determination. Elevated NT-pro-BNP level was defined using previously determined age stratified cut-off values of >164 ng/liter (age <60 years) and >225 (age > or = 60 years). HIV-infected women were older (41.6 +/- 8.9 vs. 38.9 +/- 10.5 years, p < 0.01) and were more likely to have anemia, hepatitis C virus (HCV) antibodies, and kidney dysfunction than HIV-uninfected women. HIV-infected women had significantly higher NT-pro-BNP levels (142.4 +/- 524.8 vs. 73.6 +/- 115.1 ng/liter, p = 0.01) and a higher prevalence of elevated NT-pro-BNP (12.1% vs. 7.5%; p = 0.08). In univariate analyses, elevated NT-pro-BNP was significantly associated with age, systolic BP, hypertension, anemia, triglyceride levels, kidney disease, and HCV seropositivity, but not HIV infection. In multivariate analysis, elevated NT-pro-BNP levels were significantly associated with anemia and kidney function, and had a borderline association with the presence of HCV antibodies. Among HIV-infected women, NT-pro-BNP levels were not independently associated with measures of severity of infection or with HAART use. Although HIV-infected women have higher NT-pro-BNP levels than HIV-uninfected women, the differences are due to non-HIV factors such as anemia, kidney disease, and HCV coinfection. These findings suggest that natriuretic peptide levels are a global marker of comorbidity in the setting of HIV infection.
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