Key result
FMD-AUC and NMD-AUC are linked to aneurysm diameter in AAA and disease severity in PAD.
Why the study?
Parameters of time-course analysis for vascular function have been proposed but their correlation with vascular endothelial damage in AAA and PAD and their clinical applicability remain unclear.
Do time-course analysis parameters (FMD-AUC and NMD-AUC) correlate better with disease severity in AAA and PAD compared to standard peak diameter changes?
Observational (n=200)
Do time-course analysis parameters (FMD-AUC and NMD-AUC) correlate better with disease severity in AAA and PAD compared to standard peak diameter changes?
FMD-AUC and NMD-AUC are useful supplementary markers for estimating vascular endothelial and smooth muscle dysfunction in patients with PAD and AAA.
BACKGROUND: Abdominal aortic aneurysm (AAA) and peripheral artery disease (PAD) are associated with vascular endothelial dysfunction. To date, flow-mediated vasodilatation (FMD) and nitroglycerin-mediated vasodilatation (NMD) have been used to evaluate vascular function. Recently, parameters of time-course analysis have been proposed as useful evaluations for arteriosclerotic diseases. In this study, the correlation between the parameters of time-course analysis, to the degree of vascular endothelial damage in AAA and PAD, together with their applicability as a vascular function test, was investigated. METHODS: Brachial artery vasoreactivity was assessed in male patients with AAA (n = 150) and PAD (n = 50). The percentage change in peak diameters (ΔFMD and ΔNMD), the time to diameter change, the time to peak diameter from the diameter change, the blood flow decay time constant, the area under the curve (AUC), the maximum dilation rate and the extended time constant were measured. RESULTS: Among the groups of aneurysm diameter in AAA, the FMD-AUC was highly different (p = .01), while the ΔFMD was not significantly different (p = .36). Among the Fontaine stages in PAD, the FMD-AUC was inversely associated with severity (p = .01) although the ΔFMD was not significantly different (p = .71). Among the Fontaine stages, the NMD-AUC was also inversely associated with severity (p = .03) although the ΔNMD was not significantly different (p = .11). CONCLUSION: This study suggests that FMD-AUC and NMD-AUC are useful for estimating vascular endothelial and vascular smooth muscle dysfunction, serving as supplementary markers for the diagnosis and evaluation of PAD and AAA.
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Konno et al. (2021) conducted an observational in Abdominal aortic aneurysm and peripheral artery disease (n=200). Time-course analysis parameters (FMD-AUC and NMD-AUC) was evaluated on Association of FMD-AUC and NMD-AUC with aneurysm diameter in AAA and Fontaine stages in PAD (p=0.01). FMD-AUC and NMD-AUC were significantly associated with aneurysm diameter in AAA (p=0.01) and disease severity in PAD (p=0.01 and p=0.03, respectively).
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