Key result
Blood stasis syndrome was significantly associated with vascular endothelial dysfunction evaluated through flow-mediated dilation (OR 6.26; p=0.03).
Why the study?
The association between Kampo medicine blood stasis syndrome and vascular endothelial dysfunction, as determined using flow-mediated dilation, had not been reported.
Is blood stasis syndrome associated with vascular endothelial dysfunction in patients with normal or impaired glucose tolerance?
Cross-Sectional (n=41)
Is blood stasis syndrome associated with vascular endothelial dysfunction in patients with normal or impaired glucose tolerance?
Odds Ratio: 6.26
p-value: p=0.03
Blood stasis syndrome in Kampo medicine is significantly associated with vascular endothelial dysfunction, suggesting its potential utility in detecting early pathogenic stages of atherosclerosis.
Should not yet change practice; hypothesis-generating for BS syndrome as endothelial dysfunction marker in glucose tolerance disorders.
In Kampo medicine, blood stasis (BS) syndrome is strongly associated with microangiopathy and can lead to atherosclerosis. Vascular endothelial dysfunction (VED), evaluated through flow-mediated dilation (FMD), plays an important role in the early stages of atherosclerosis. However, the association of BS syndrome with VED, as determined using FMD, has not been reported. This study investigated the association between BS syndrome and VED using FMD. Forty-one patients with normal glucose tolerance or impaired glucose tolerance (IGT) and without macrovascular complications were evaluated using FMD from May 2017 to August 2017. Based on the BS score, the patients were divided into the non-BS (n = 19) and BS syndrome (n = 22) groups. Physical and background characteristics, physiological function test results, and laboratory data were compared. Univariate analysis revealed that FMD and a history of dyslipidemia/IGT were significantly different between the two groups ( p < 0.05 ). Multiple logistic regression analysis showed that BS syndrome was significantly associated with FMD (odds ratio: 6.26; p = 0.03 ) after adjusting for the history of dyslipidemia/IGT. The receiver operating characteristic curve showed that the area under the curve for BS syndrome (0.74; p < 0.001 ) and history of IGT ( p < 0.007 ) provided good diagnostic accuracy for FMD. The area under the curve for “BS syndrome + IGT” showed very good accuracy (0.80; p < 0.0001 ) and was higher than that for BS syndrome or IGT alone. In conclusion, the results of this study suggest that the BS score in Kampo medicine could be a useful tool for detecting the early pathogenic stages of atherosclerosis.
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Morita et al. (2021) conducted a cross-sectional in Vascular endothelial dysfunction / Atherosclerosis (n=41). Blood stasis (BS) syndrome vs. Non-BS syndrome was evaluated on Vascular endothelial dysfunction evaluated through flow-mediated dilation (FMD) (OR 6.26, p=0.03). Blood stasis syndrome was significantly associated with vascular endothelial dysfunction evaluated through flow-mediated dilation (OR 6.26; p=0.03).
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