马凡氏综合征主动脉的异常力学特性

B. Sonesson , F. Hansen , T. Länne
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引用次数: 56

摘要

目的:主动脉扩张、夹层和破裂是马凡氏综合征患者死亡的主要原因。该研究的目的是调查这些受试者的主动脉力学特性或顺应性,并将其与年龄和性别匹配的健康参考人群进行比较。材料与方法:采用超声锁相回声跟踪系统测定9例马凡氏综合征患者的肾下主动脉内径及搏动内径变化,并与165例正常人进行比较。顺应性,定义为Ep(压力应变弹性模量)或刚度(β)的倒数,根据脉搏直径变化和用血压计听诊法获得的血压计算。统计分析采用健康对照的可信区间(95%)进行比较。对女性患者进行协方差分析(ANCOVA)。男性(n = 2)的样本量太小,无法进行后一种分析。结果:与正常人及其置信区间相比,马凡氏综合征患者的肾下主动脉Ep和僵硬度(β)升高,应变(分数直径变化)降低。此外,女性患者ANCOVA β升高(p <0.01)和Ep (p <0.01),应变减小(p <0.001)。两组的主动脉直径、MAP和脉压相似。结论:本研究表明马凡氏综合征主动脉力学特性的改变表现为主动脉壁硬度增加。这可能对主动脉夹层和破裂的发病机制有重要意义。
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Abnormal mechanical properties of the aorta in Marfan's syndrome

Objectives:

Aortic dilatation, dissection and rupture are among the major causes of death in subjects with Marfan's syndrome. The aim of the study was to investigate the mechanical properties or compliance of the aorta in these subjects and compare them with a healthy age- and sex-matched reference population.

Materials and methods:

An ultrasound phase-locked echo-tracking system was used to determine diameter and pulsatile diameter change of the infrarenal aorta in nine subjects with Marfan's syndrome which were then compared with the values for 165 healthy individuals. Compliance, defined as the inverse of Ep (pressure strain elastic modulus) or stiffness (β), was calculated from pulsatile diameter change and blood pressure obtained by the auscultatory method with a sphygmomanometer. For statistical analysis confidence intervals (95%) obtained from the healthy controls were used for comparison. Analysis of covariance (ANCOVA) was performed for the female patients. The sample size for males (n = 2) was too small for the latter analysis.

Results:

Compared with normal subjects and their confidence intervals, subjects with Marfan's syndrome had an increased Ep and stiffness (β) and decreased strain (fractional diameter change) in the infrarenal aorta. Furthermore, ANCOVA in the female patients showed increased β (p < 0.01) and Ep (p < 0.01) and a decreased strain (p < 0.001). Aortic diameters, MAP, as well as the pulse pressure, were similar in the two groups.

Conclusion:

This investigation demonstrates alterations in the mechanical properties of the aorta in Marfan's syndrome in the form of increased stiffness of the aortic wall. This may be of importance in the pathogenesis of aortic dissection and rupture.

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