Key result
Systemic Lupus Erythematosus was associated with significantly impaired flow-mediated dilation compared to controls (median 2.4% vs 5.8%, P<0.001), driven by reduced diastolic shear stress.
Why the study?
Is flow-mediated dilation and forearm microcirculation impaired in patients with systemic lupus erythematosus compared to controls?
Case-Control (n=51)
Is flow-mediated dilation and forearm microcirculation impaired in patients with systemic lupus erythematosus compared to controls?
Absolute Event Rate: 2.4% vs 5.8%
p-value: p=<0.001
In patients with SLE, impaired flow-mediated dilation is associated with reduced diastolic shear stress, suggesting altered forearm microcirculation contributes to endothelial dysfunction.
Impaired FMD in SLE may reflect microcirculatory changes; hypothesis-generating and should not yet alter practice.
OBJECTIVE: Impaired flow-mediated dilation (FMD) occurs in disease states associated with atherosclerosis, including SLE. The primary hemodynamic determinant of FMD is wall shear stress, which is critically dependent on the forearm microcirculation. We explored the relationship between FMD, diastolic shear stress (DSS), and the forearm microcirculation in 32 patients with SLE and 19 controls. METHODS AND RESULTS: DSS was calculated using (mean diastolic velocity x 8 x blood viscosity)/baseline brachial artery diameter. Doppler velocity envelopes from the first 15 seconds of reactive hyperemia were analyzed for resistive index (RI), and interrogated in the frequency domain to assess forearm microvascular hemodynamics. FMD was significantly impaired in SLE patients (median, 2.4%; range, -2.1% to 10.7% versus median 5.8%; range, 1.9% to 14%; P<0.001). DSS (dyne/cm2) was significantly reduced in SLE patients (median, 18.5; range, 3.9 to 34.0 versus median 21.8; range, 14.1 to 58.7; P=0.037). A strong correlation between FMD and DSS, r(s)=0.65, P=0.01 was found. Postischemic RI was not significantly different between the 2 groups; however, there were significant differences in the power-frequency spectrums of the Doppler velocity envelopes (P<0.05). CONCLUSIONS: These data suggest that in SLE, altered structure and function of the forearm microcirculation contributes to impaired FMD through a reduction in shear stress stimulus.
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Wright et al. (2006) conducted a case-control in Systemic Lupus Erythematosus (n=51). Systemic Lupus Erythematosus (Exposure) vs. Controls was evaluated on Flow-mediated dilation (FMD) (p=<0.001). Systemic Lupus Erythematosus was associated with significantly impaired flow-mediated dilation compared to controls (median 2.4% vs 5.8%, P<0.001), driven by reduced diastolic shear stress.
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