Long-term metabolic complications of highly active antiretroviral therapy (HAART)
have been reported in general human immunodeficiency virus (HIV)-infected patients.
We sought to determine whether patients with pre-existing heart failure (HF) using
HAART are at high risk of subsequent metabolic syndrome (MetS) and cardiovascular
complications, compared with HIV-infected patients without pre-existing HF. This is
a prospective cohort study of 5 years of follow-up, in which 172 HIV-infected patients
were recruited for the comparison of Data Collection on Adverse Effects of Anti-HIV
Drugs (D:A:D), a cardiovascular disease (CVD) risk score for HAART, and lab data,
between HF patients and age- and gender-matched non-HF patients. HAART was effective
for both HIV-infected patients with or without HF, with a similar plasma viral load
(PVL) of HIV (r=0.001, P=0.69) and CD4 count for HF patients (r=-0.06, P=0.48). HAART
did not increase the risk of CVDs for patients with HF, with comparable D:A:D (R)
(r=0.002, P=0.97) and D:A:D (F) (r=0.04, P=0.62) scores. HF patients presented with
higher risk of T2DM (r = 0.24, P=0.01), increased total cholesterol (CHO) (r=0.23,
P=0.006), compared to baseline. Moreover, patients with HF presented with significantly
higher risk of increased LDL (r=0.18, P=0.04) and increased uric acid (r=0.35, P=0.004)
in HF patients. In conclusion, HAART was equally effective for HF and non-HF patients,
and did not result in more subsequent CVDs or renal toxicities, when compared with
patients without HF; however, increased risk of metabolic complications, including
T2DM, and increased levels of CHO, LDL, and uric acid, during follow-ups, were present.
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