Aims/hypothesis. We studied 76 patients with Type II (non-insulin-dependent) diabetes mellitus and 16 age-matched non-diabetic subjects (control
group) to clarify qualitative and quantitative abnormalities of waveform and flow volume of the popliteal artery.
Methods. The 76 diabetic patients comprised 16 patients with occlusive arterial disease in the lower extremities [arteriosclerosis
obliterans (ASO) group] and 60 patients free from this disease (non-ASO group). We flow analysed the popliteal artery and
measured the phosphocreatine to inorganic phosphate ratio of resting plantar muscles to identify risk factors for foot lesions
using gated magnetic resonance two-dimensional cine-mode phase-contrast imaging and
31P spectroscopy.
Results. The control and non-ASO groups had a triphasic waveform with systolic, early and late diastolic components. All ASO patients
had an abnormal monophasic waveform and a lower ankle brachial index than that of the control and non-ASO groups. To clarify
the mechanism of reduced flow volume of lower extremities, we assigned the 60 patients of the non-ASO group to the three subgroups
based on their levels of total flow volume of the popliteal artery. The lowest group showed an abnormal triphasic waveform
with lower amplitudes of systolic and late diastolic components and flow velocities in foot arteries than those of the highest
group although ABI was similar. From stepwise multiple regression analysis, late diastolic flow volume was identified as an
independent determinant for the phosphocreatine to inorganic phosphate ratio (
r
2 = 0.484,
p < 0.001).
Conclusion/interpretation. Waveform analysis of popliteal artery provides a powerful tool for identifying impaired peripheral circulation caused by
either occlusive arterial disease or increased arterial resistance in diabetic patients. [Diabetologia (2000) 43: 1031–1038]
Keywords Magnetic resonance - popliteal artery - waveform - flow volume - occlusive arterial disease - arterial resistance - plantar muscle - high energy phosphate content.
Received: 24 January 2000 and in revised form: 31 March 2000