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Ultrasound Assessment of Endothelial-Dependent Flow-Mediated Vasodilation of the Brachial Artery in Clinical Research
Published on: October 22, 2014
Ankle-brachial pressure index: a simple tool for assessing cardiovascular risk in patients with systemic vasculitis
S R Sangle1, R J Davies, M Mora
1The Lupus Research Unit, The Rayne Institute, St Thomas' Hospital, London, UK.
Insights
Patients with systemic vasculitides (SV) have a higher prevalence of abnormal Ankle-Brachial Pressure Index (ABPI), indicating increased cardiovascular disease risk. This simple test can identify SV patients at risk for atherosclerosis.
Area of Science:
- Cardiology
- Rheumatology
- Vascular Medicine
Background:
- Systemic vasculitides (SV) are associated with increased cardiovascular disease (CVD) risk.
- The Ankle-Brachial Pressure Index (ABPI) is a non-invasive measure of peripheral artery disease and cardiovascular risk.
Purpose of the Study:
- To determine the prevalence of abnormal ABPI in patients with SV compared to healthy controls.
- To correlate ABPI findings with clinical and serological parameters in SV patients.
Main Methods:
- A cross-sectional study involving 54 SV patients and 49 healthy controls.
- Patients were classified using established criteria (ACR 1990, Chapel Hill Consensus).
- ABPI was measured, and traditional CVD risk factors, glucose, lipids, CRP, hsCRP, ANCA, and aPL were assessed.
Main Results:
- Abnormal ABPI was found in 20.4% of SV patients versus 4% in controls (P < 0.03).
- Cardiovascular events were significantly more common in SV patients with abnormal ABPI (45.5% vs 11.6%, P < 0.01).
Conclusions:
- Systemic vasculitis patients exhibit a higher prevalence of abnormal ABPI, suggesting elevated cardiovascular risk.
- ABPI is a valuable, simple tool for identifying SV patients at risk of accelerated atherosclerosis.
Objective:
Cardiovascular disease may be increased in patients with systemic vasculitides (SV). The Ankle-Brachial Pressure Index (ABPI) is a non-invasive tool for the assessment of cardiovascular risk (CV). Our aim was to determine the prevalence of an abnormal ABPI in patients with SV and healthy controls and to correlate with clinical and serological parameters.
Methods:
We studied 54 consecutive vasculitis patients (20 males) attending the vasculitis clinic and 49 healthy subjects. Patients were classified according to the ACR 1990 criteria and the Chapel Hill Consensus definitions. There were 18 patients with Wegener's granulomatosis, eight with Behcet's disease, seven with Churg-Strauss Syndrome, three with Henoch-Schonlein purpura, three with polyarteritis nodosa, three with Takayasu's disease, three with p-ANCA associated vasculitis, three with urticarial vasculitis, two with cutaneous leucocytoclastic angiitis, one with microscopic polyangiitis, one with primary central nervous system angiitis, one giant cell arteritis and one with cutaneous vasculitis secondary to Sjogren's syndrome. Traditional risk factors as well as glucose, lipid profile, CRP, hsCRP, ANCA and aPL were assessed. ABPI was measured according to a consensus statement on the methodology.
Results:
The ABPI was abnormal in 11/54 (20.4%) of SV patients and 2/49 (4%) of the control group (chi(2) with Yates correction = 4.8, P
Conclusions:
There is an increased prevalence of an abnormal ABPI in patients with systemic vasculitides implying an increased risk of cardiovascular disease. This simple tool may be clinically useful in identifying systemic vasculitis patients at risk of accelerated atherosclerosis.
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Preparation:
