Association Between CD4+, Viral Load, and Pulmonary Function in HIV.
Marjan Islam1,2, Navitha Ramesh3, Samuel Kolman4
1Department of Internal Medicine, Mount Sinai Beth Israel, Icahn School of Medicine at Mount Sinai, New York, NY, USA. marjan.islam@mountsinai.org.
Lung
|June 26, 2017
Summary
High viral load (VL) in HIV patients significantly impairs lung diffusing capacity (DLCO). Suppressing VL may improve lung function over time, but further research is needed to confirm this recovery.
Area of Science:
- Pulmonary Medicine
- Infectious Diseases
- HIV Research
Background:
- The advent of antiretroviral therapy has altered HIV epidemiology, highlighting non-infectious pulmonary complications.
- Understanding the relationship between HIV disease parameters and lung function is crucial for patient management.
Purpose of the Study:
- To investigate the association between CD4+ cell count, viral load (VL), and pulmonary function in individuals with uncontrolled HIV.
- To determine the longitudinal impact of changes in CD4+ count and VL on pulmonary function.
Main Methods:
- Retrospective observational study of 146 individuals with HIV undergoing pulmonary function testing.
- Analysis of CD4+ count, VL, and pulmonary function parameters including DLCO, FEV1, FEV1/FVC, and TLC.
- Statistical analysis including univariate and multivariate correlations, and Spearman's Rank correlation for longitudinal changes.
Main Results:
- Lower CD4+ count (<200 cells/μl) and higher VL (≥75 copies/ml) were independently associated with significantly impaired DLCO.
- VL ≥75 copies/ml correlated with an 11.2 decrease in DLCO after adjusting for confounders.
- A negative correlation was observed between changes in VL and changes in DLCO over time, suggesting potential for recovery with VL suppression.
Conclusions:
- Viremia in HIV-positive individuals is independently linked to reduced diffusing capacity (DLCO).
- Suppression of HIV viral load may lead to improvements in lung diffusing capacity over time.
- Further investigation is warranted to quantify the extent of DLCO recovery following viral load suppression.
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