ObjectiveTo study the relationship between antiretroviral (ARV) treatment and abnormal ankle-branch index (ABI) and to compare the risk factors for altered ABI.
MethodsPatients coming to the office from April 2007 until July 2007 were offered the chance to take part in the study. ABI was obtained by the standard technique. Those 0.9 or 1.3 were considered altered ABI. Clinical reports were reviewed to examine traditional vascular risk factors, coinfection with hepatitis C virus and/or hepatitis B virus, tobacco use, highly active antiretroviral therapy use and its components and length of use of each ARV drug.Results ABI was measured in 147 patients, 82.3% males. Thirty-three patients (22.45%) had an altered ABI, and it was related to CD4 cell nadir, dyslipidaemia and protease inhibitor (PI) use. When logistic regression was carried out, only dyslipidaemia (OR 2.68, CI 95%: 1.06-6.91) and PI use (OR 2.79, CI 95%: 1.15-6.54) remained in the model.
ConclusionsAltered ABI is associated with PI use independently of dyslipidaemia. Probably, it marks patients with high vascular risk not identified with traditional scales.Keywords: ankle-branch index, HAART, HIV, protease inhibitors, vascular risk
IntroductionSince the introduction of highly active antiretroviral therapy (HAART) in the management of infection by HIV, patients' life expectancy has increased spectacularly [1,2]. Some cohort studies even compare the survival rates of lesser immunosuppressed HIV patients with those of the general population [3].However, some observational studies published over the last few years support the idea that HIV, and above all HAART, increase the risk of major vascular events [4,5]. Clinical evidence suggests that protease inhibitors (PIs) are mainly responsible for most of these events [6]. PI implication in changes to the lipid profile [7,8] [decreasing high-density lipoproteins (HDL) and increasing low-density lipoproteins (LDL) as well as triglycerides], insulin resistance [9,10] and lowering of the peripheral arterial vasodilation response [11] have been proved.In addition, hepatitis C virus (HCV) co-infection increases insulin resistance [12,13], and HIV infection chronic immune activation causes deterioration in the lipid profile [14,15]. Patients' mean age has also increased. All these factors make an early diagnosis and treatment of vascular disease necessary.Because there are no reliable scores to evaluate the vascular risk of the HIV-infected population other than clinical history (past medical history and family history), physical exploration and blood tests (renal function, lipid profile, glycaemia, etc) it would be most desirable to have a test to determine early vascular risk in HIV patients that is simple, affordable and easy to perform.Ankle-brachial index (ABI) meets these criteria. It is a non-invasive diagnostic test of peripheral arterial disease and a marker of vascular morbimortality. An altered ABI is associated with cardiovascular and cerebrovascular disease. If lower than 0.9, ABI has been related to hi...