Key result
HAART is linked to ~21% lower hyperemic forearm blood flow response in HIV.
Why the study?
Differences in vascular microcirculatory function between HIV-1 infected patients receiving HAART and those never treated were investigated.
Does highly active antiretroviral therapy (HAART) impair vascular microcirculatory function in HIV-1 infected patients?
Cross-Sectional (n=60)
Does highly active antiretroviral therapy (HAART) impair vascular microcirculatory function in HIV-1 infected patients?
Absolute Event Rate: 714% vs 907%
p-value: p=0.01
HAART in HIV-1 infected patients is associated with abnormalities in arterial microcirculation and higher cholesterol levels compared to treatment-naive patients.
HAART may impair microvascular reactivity in HIV; hypothesis-generating for CV risk, needs prospective confirmation.
OBJECTIVES: We investigated whether HIV-1 infected patients receiving highly active antiretroviral therapy (HAART) and HIV-1 infected patients who had never received HAART had differences in their vascular microcirculatory function. METHODS: We assessed the forearm blood flow before and after four minutes of ischemic occlusion of the brachial artery using venous occlusion strain gauge plethysmography. The hyperaemic forearm blood flow was recorded for three minutes at 15 second intervals. We calculated the maximal percent increase of the forearm blood flow during hyperemia. Forty HIV-infected male patients receiving HAART were compared to 20 age- and BMI- matched, male HIV-infected patients who had never received HAART (control group). RESULTS: Patients on HAART had similar baseline forearm blood flow but lower maximal and percentage (%) change in forearm blood flow than control patients (4.2 +/- 1.7 vs. 4.1 +/- 1.7 l/ 100mL/min P = 0.8, 32 +/- 11.2 vs. 38.9 +/- 10.5 l/100 mL/min. P = 0.04 and 714 +/- 255 vs. 907 +/- 325%, P = 0.01, respectively). Patients receiving HAART had higher cholesterol than control patients (221 +/- 58 vs. 163 +/- 38 mg/dL, P = 0.001). HAART was associated with the percentage change in the blood flow during hyperemia (coefficient regression B = -0.32, P = 0.02) after adjustment for age, cholesterol and viral load. CONCLUSIONS: HIV-infected patients receiving HAART present abnormalities of arterial microcirculation in comparison with never-treated patients.
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Palios et al. (2010) conducted a cross-sectional in HIV-1 infection (n=60). Highly active antiretroviral therapy (HAART) vs. Never received HAART was evaluated on Percentage change in forearm blood flow during hyperemia (p=0.01). HIV-1 infected men receiving HAART exhibited a significantly lower percentage increase in hyperemic forearm blood flow compared to HAART-naive controls (714% vs 907%, P=0.01).
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