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Progression of cardiac structure and function in people with human immunodeficiency virus
Gerald S Bloomfield1,2,3, Fawaz Alenezi1, Karen Chiswell2
1Division of Cardiology, Department of Medicine, Duke University, Durham, North Carolina, USA.
Insights
HIV viral suppression improves cardiac function in people living with HIV (PLWH). Echocardiographic measures show lasting gains in cardiac function for over 5 years with sustained HIV disease control.
Area of Science:
- Cardiology
- Infectious Diseases
- Public Health
Background:
- People living with HIV (PLWH) face elevated risks of cardiac dysfunction.
- Longitudinal changes in cardiac structure and function in PLWH remain under-characterized.
Purpose of the Study:
- To investigate the long-term trends in cardiac structure and function among PLWH.
- To assess the impact of CD4+ T cell count and HIV RNA suppression on cardiac indices over time.
Main Methods:
- Retrospective analysis of transthoracic echocardiograms (TTEs) from 150 PLWH between 2001 and 2012.
- Hierarchical mixed model analysis to evaluate progression of global longitudinal strain (GLS), LV mass, E/e' ratio, and LV volumes.
- Models adjusted for CD4+ T cell counts, HIV viral suppression, and clinical/demographic factors.
Main Results:
- Over a median of 5 years, left ventricular (LV) mass index increased in PLWH, irrespective of CD4+ counts or viral suppression.
- PLWH with baseline viral suppression maintained more normal GLS throughout follow-up.
- No significant longitudinal trends were observed in LV end-systolic/diastolic volumes or E/e' ratio.
Conclusions:
- HIV viral suppression is linked to sustained improvements in echocardiographic measures of cardiac function in PLWH.
- Effective HIV disease management positively influences cardiac health indicators with long-term prognostic implications.
Objective:
People living with HIV (PLWH) are at increased risk for cardiac dysfunction. It is unknown how their global longitudinal cardiac function, cardiac structure, and other indices of function progress over time. We aimed to characterize the longitudinal trend in cardiac structure and function in PLWH.
Design:
Retrospective study of PLWH with clinically obtained echocardiograms at an academic medical center.
Methods:
We reviewed archived transthoracic echocardiograms (TTEs) performed between 2001 and 2012 on PLWH. The primary outcome measures were progression of global longitudinal strain (GLS, left and right ventricles), LV mass, E/e' ratio, LV end-systolic, and -diastolic volumes using hierarchical mixed model analysis as a function of CD4+ T cell count and HIV RNA suppression. Models were adjusted for clinical and demographic characteristics.
Results:
We analyzed 469 TTEs from 150 individuals (median age 46 years, 58% male). Median CD4+ T cell counts at nadir and proximal to first echocardiogram were 85 and 222 cells/mm3 , respectively. Over a median of 5 years, LV mass index increased regardless of nadir or proximal CD4+ T cell count or viral suppression status. PLWH with viral suppression at baseline had more normal GLS throughout the follow-up period. There were no significant trends in LV end-systolic volume index or E/e'.
Conclusions:
In PLWH, HIV viral suppression is associated with early gains in echocardiographic indices of cardiac function that persist for up to >5 years. HIV disease control impacts routine echocardiographic measures with known impacts on long-term prognosis.
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