Szymczyk Konrad, Polguj Michał, Szymczyk Ewa, Bakoń Leopold, Pacho Ryszard, Stefańczyk Ludomir
Department of Radiology, Barlicki University Hospital, Medical University of Lodz, ul. Kopcińskiego 22, 90-153, Lodz, Poland.
Department of Angiology, Medical University of Lodz, Narutowicza 60, Łódź, 90-136, Poland.
BMC Cardiovasc Disord. 2016 May 10;16:89. doi: 10.1186/s12872-016-0261-z.
Bicuspid aortic valve (BAV) is the most common congenital cardiac anomaly. Other aortic valve variants are rare but are associated with an increased incidence of various pathologies of the aortic valve (AV). The aim of this study was to assess the AV function in regard to its anatomical variants morphology in patients who underwent 64-slice coronary computed tomography angiography (CCTA) for suspected or known coronary artery disease.
The results of 64-detector retrospective ECG-gated CCTA of 2053 patients (mean age 58 years; 1265 males) were analyzed retrospectively by experienced cardiovascular radiologist. Coronary anatomy (with coronary artery dominance) and the extent of occlusion in the coronary arteries were assessed. Furthermore morphological and functional status of AV variants were analyzed. Among measured parameters were area at the level of AV annulus, orifice and tubular portion of the ascending aorta.
The AV was visualized in all CCTA studies and the analysis of its morphology and function was done in all patients. BAV was found in 19 patients (0.9 %), from which type 0 was diagnosed in five patients (0.2 %) and type 1 in 14 patients (0.7 %) - there was no patient with BAV type 2. Unicuspid (UAV) and quadricuspid (QAV) variant were both observed each in one patient (0.05 %). In rest of the patients from the study group tricuspid AV variant was recognized. Function of AV variants was mostly affected in BAV0 and UAV. Among patients with BAV1 there were patients with normal and abnormal function of AV. QAV variant did not deteriorate AV function. There was no difference in coronary artery disease and dominancy between different anatomical variants of AV.
During CCTA different valve variants can be detected and detailed analysis of valvular function can be proceeded. Larger values of annulus area, wider diameters of ascending aorta and more stenotic profile were observed in BAV 0, BAV 1 and UAV. Among AV variants morphology and function was mostly affected in patients with BAV 0 and UAV variants, while subjects with BAV1 had normal or abnormal function of the AV. Moreover, we noticed that QAV variant did not deteriorate AV function.
二叶式主动脉瓣(BAV)是最常见的先天性心脏异常。其他主动脉瓣变异罕见,但与主动脉瓣(AV)各种病变的发生率增加相关。本研究的目的是在因疑似或已知冠状动脉疾病而接受64层冠状动脉计算机断层扫描血管造影(CCTA)的患者中,评估AV功能及其解剖变异形态。
由经验丰富的心血管放射科医生对2053例患者(平均年龄58岁;1265例男性)的64探测器回顾性心电图门控CCTA结果进行回顾性分析。评估冠状动脉解剖结构(包括冠状动脉优势)和冠状动脉闭塞程度。此外,分析AV变异的形态和功能状态。测量参数包括AV瓣环水平面积、升主动脉口和管状部分。
所有CCTA研究均能显示AV,并对所有患者进行了其形态和功能分析。19例患者(0.9%)发现BAV,其中5例(0.2%)诊断为0型,14例(0.7%)为1型——无2型BAV患者。单叶式(UAV)和四叶式(QAV)变异各在1例患者中观察到(0.05%)。研究组其余患者为三叶式AV变异。AV变异功能大多在BAV0和UAV中受影响。BAV1患者中,有AV功能正常和异常的患者。QAV变异未使AV功能恶化。不同AV解剖变异之间在冠状动脉疾病和优势方面无差异。
在CCTA期间可检测到不同的瓣膜变异,并可对瓣膜功能进行详细分析。在BAV 0、BAV 1和UAV中观察到瓣环面积更大、升主动脉直径更宽和狭窄程度更高的情况。在AV变异中,BAV 0和UAV变异患者的形态和功能受影响最大,而BAV1患者的AV功能正常或异常。此外,我们注意到QAV变异未使AV功能恶化。