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Association between 10-Year Atherosclerotic Cardiovascular Disease Risk and Vascular Endothelial Function in Patients with Vasospastic Angina.
Park, Kyoung-Ha; Park, Woo Jung; Kim, Hyun-Sook; Jo, Sang Ho; Kim, Sung-Ai; Choi, Hong-Mi; Suh, Sang Won.
Afiliação
  • Park KH; Division of Cardiovacular Disease, Hallym University Medical Center, Anyang, Republic of Korea.
  • Park WJ; Division of Cardiovacular Disease, Hallym University Medical Center, Anyang, Republic of Korea.
  • Kim HS; Division of Cardiovacular Disease, Hallym University Medical Center, Anyang, Republic of Korea.
  • Jo SH; Division of Cardiovacular Disease, Hallym University Medical Center, Anyang, Republic of Korea.
  • Kim SA; Division of Cardiovacular Disease, Hallym University Medical Center, Anyang, Republic of Korea.
  • Choi HM; Division of Cardiovacular Disease, Hallym University Medical Center, Anyang, Republic of Korea.
  • Suh SW; Department of Physiology, College of Medicine, Hallym University, Chuncheon, Republic of Korea.
Cardiology ; 146(3): 281-287, 2021.
Article em En | MEDLINE | ID: mdl-33849014
BACKGROUND: Endothelial dysfunction is a predictor of atherosclerotic cardiovascular disease (ASCVD) and plays an important role in vasospastic angina (VA). OBJECTIVES: This study evaluated whether flow-mediated dilation (FMD) is also a good marker of 10-year ASCVD risk (10Y-ASCVDR) in patients with VA. METHODS: Based on their clinical history and coronary artery diameter stenosis (DS), patients were retrospectively enrolled into VA (DS <50% and positive ergonovine provocation), minor coronary artery disease (mCAD, DS <30%), and significant coronary artery disease (sCAD, DS ≥50%) groups. Endothelial function was evaluated by FMD. RESULTS: Each group contained 50 patients. The 10Y-ASCVDR was significantly higher in the sCAD group than in the VA and mCAD groups (10.86 ± 7.30, 4.71 ± 4.04, and 4.77 ± 4.30, respectively, p < 0.001). The FMD was significantly higher in the mCAD group than in the VA and sCAD groups (6.37 ± 4.25, 3.10 ± 2.23, and 3.07 ± 1.89, respectively, p < 0.001). A significant correlation was found between the FMD and 10Y-ASCVD in the mCAD group (r = -0.622, p < 0.001) and the sCAD group (r = -0.557, p < 0.001) but not in the VA group (r = -0.193, p = 0.179). After adjusting for potential confounders such as BMI, C-reactive protein, maximal coronary stenosis, and brachial-ankle pulse wave velocity, multivariate analysis showed that FMD was independently associated with 10Y-ASCVDR in all patients. However, when looking only at the VA group, FMD did not correlate independently with 10Y-ASCVDR. CONCLUSIONS: Unlike mCAD and sCAD, we found no correlation between 10Y-ASCVDR and endothelial function in VA. Thus, our results support that FMD is not a good marker of atherosclerotic cardiovascular risk in VA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Vasoespasmo Coronário Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Vasoespasmo Coronário Idioma: En Ano de publicação: 2021 Tipo de documento: Article