Key result
Well-controlled HIV infection on long-term antiretroviral therapy was not associated with abnormal left ventricular global longitudinal strain compared to HIV-negative controls.
Why the study?
Previous studies have reported impairment in systolic and diastolic function in people with HIV, but whether echocardiographically measured LV global longitudinal strain is abnormal in asymptomatic individuals remained to be determined.
Does well-controlled HIV on long-term ART impair left ventricular global longitudinal strain in asymptomatic individuals?
Cross-Sectional (n=148)
No
Does well-controlled HIV on long-term ART impair left ventricular global longitudinal strain in asymptomatic individuals?
Mean Difference: 0.65 (95% CI 0.21–1.5)
Absolute Event Rate: -20.3% vs -21%
p-value: p=0.137
Asymptomatic people with well-controlled HIV on long-term ART do not have clinically significant impairment of myocardial systolic function as measured by LV GLS compared to healthy controls.
Supports preserved LV GLS in well-controlled HIV; leaves open need for longitudinal outcome studies.
Background Previous studies have reported impairment in systolic and diastolic function in people with HIV (PWHIV). Our aim was to determine if echocardiographically measured left ventricular (LV) global longitudinal strain (GLS) is abnormal in asymptomatic PWHIV. Methods A cross-sectional study of PWHIV ( n = 98, 89% male, median age 53 years) and HIV-negative people ( n = 50, median age 53 years) without known cardiovascular disease were recruited from a single centre. All participants completed a health/lifestyle questionnaire, provided a fasting blood sample, and underwent a comprehensive echocardiogram for assessment of diastolic and systolic LV function, including measurement of GLS. Results All PWHIV were receiving antiretroviral therapy (ART) for a median of 12 years (IQR: 6.9, 22.4), the majority with good virological control (87% suppressed) and without immunological compromise (median CD4 598 cells/µl, IQR: 388, 841). Compared with controls of similar age and gender, there was no difference in GLS [mean GLS −20.3% (SD 2.5%) vs. −21.0% (SD 2.5%), p = 0.14] or left ventricular ejection fractions [65.3% (SD 6.3) vs. 64.8% (SD 4.8), p = 0.62]. Following adjustment for covariates (gender, heart rate, systolic and diastolic blood pressure, and fasting glucose), the difference in GLS remained non-significant. There were no differences in LV diastolic function between the groups. Exposure to at least one mitochondrially toxic ART drug (didanosine, stavudine, zidovudine, or zalcitabine) was not associated with impairment of LV systolic function. Conclusion No clinically significant impairment of myocardial systolic function, as measured by LV GLS, was detected in this predominantly Caucasian male population of PWHIV on long-term ART, with no history of cardiovascular disease.
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Hoy et al. (2023) conducted a cross-sectional in HIV infection (n=148). HIV infection (well-controlled on ART) vs. HIV-negative controls was evaluated on Left ventricular global longitudinal strain (LV GLS) (Mean difference 0.65, 95% CI 0.21-1.50, p=0.137). Well-controlled HIV infection on long-term antiretroviral therapy was not associated with abnormal left ventricular global longitudinal strain compared to HIV-negative controls.
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