Why the study?
Autonomic dysfunction has been detected in early HIV infection and in AIDS patients with advanced cardiomyopathy, but detailed heart rate variability analysis is needed.
Does HAART preserve or restore autonomic function (measured by heart rate variability) in HIV/AIDS patients compared to HAART-naïve patients and healthy controls?
Cross-Sectional (n=120)
Does HAART preserve or restore autonomic function (measured by heart rate variability) in HIV/AIDS patients compared to HAART-naïve patients and healthy controls?
Answers are grounded in this paper and cite their sources.
HAART may protect against or reverse the autonomic dysfunction commonly seen in HIV infection, as measured by heart rate variability.
BACKGROUND: In HIV-infected patients the risks for cardiovascular disease are multifactorial. Autonomic dysfunction has been detected in the early phase of HIV infection as well as in AIDS patients with advanced cardiomyopathy. METHODS: Forty AIDS patients receiving highly active antiretroviral therapy (HAART), 40 HIV+ naïve of HAART, and 40 control subjects were studied. Computerized analysis of heart rate variability was performed using an analog to digital converter. R-R intervals were obtained from a standard ECG, recorded in DII lead in supine rest and after the cold-face and tilt tests. The series of R-R intervals were assessed in time and frequency domains using an autoregressive algorithm. RESULTS: There was no difference regarding to mean values of R-R intervals and variance in baseline. The normalized power of the low-frequency (LF) component and the low-frequency/high-frequency (HF) ratio (LF/HF) was significantly decreased in the HIV group. Responses of normalized HF and LF/HF ratio during the cold-face test were significantly decreased in the HIV group, as compared to the control. During the tilt test, a higher augmentation of normalized LF and the LF/HF ratio was observed in the HIV group compared with the control. The AIDS group was similar to the control in baseline and after cold-face and tilt tests. CONCLUSION: The HIV group presented in baseline conditions, a shift of cardiac sympathovagal balance, an exacerbated response of the LF component during the tilt test, and an ineffective cardiac vagal response to the cold-face test suggesting sympathetic and parasympathetic dysfunction. AIDS patients receiving HAART did not present these autonomic alterations.
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Correia et al. (2006) conducted a cross-sectional in HIV infection and AIDS (n=120). HIV infection and HAART status vs. Control subjects was evaluated on Heart rate variability (normalized LF, HF, and LF/HF ratio) at baseline and during cold-face and tilt tests.
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