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马凡综合征患者的主动脉根部不对称性;磁共振成像评估及与标准超声心动图的比较

Aortic root asymmetry in marfan patients; evaluation by magnetic resonance imaging and comparison with standard echocardiography.

作者信息

Meijboom L J, Groenink M, van der Wall E E, Romkes H, Stoker J, Mulder B J

机构信息

Department of Cardiology, Academic Medical Center, Amsterdam, The Netherlands.

出版信息

Int J Card Imaging. 2000 Jun;16(3):161-8. doi: 10.1023/a:1006429603062.

DOI:10.1023/a:1006429603062
PMID:11144769
Abstract

BACKGROUND

Patients with Marfan syndrome may develop aortic root dissection despite only mild aortic root dilation as shown by standard echocardiography, which may be due to aortic root asymmetry. Purpose of the present study was to investigate aortic root asymmetry by magnetic resonance (MR) imaging in patients with Marfan syndrome and to compare these measurements with standardly performed echocardiography.

METHODS

Eighty-seven Marfan patients (mean age 31 +/- 8 years) underwent MR imaging. From this population, 15 patients (mean age 29 +/- 3 years) were selected in whom both echocardiography and MR imaging had been performed within 3 months. With echocardiography, the aortic root was measured according to the recommendations of the American Society of Echocardiography. With MR imaging, a short axis view of the aortic root was obtained to measure distances between the noncoronary, right coronary and left coronary cusps and the aortic root area. Correlations between aortic root area and diameters were assessed, and 95% confidence intervals (95% CIs) calculated.

RESULTS

No difference in the standardly measured noncoronary to right coronary cusp diameter between MR imaging and echocardiography was shown (42 +/- 6 mm). Largest aortic root diameter on the MR images was the right to left coronary cusp diameter (46 +/- 7 mm, p < 0.02). For a given noncoronary to right coronary cusp diameter, 95% confidence intervals revealed a variation of -20 to +20% in the aortic root area.

CONCLUSIONS

The majority of Marfan patients show asymmetric dilation of the aortic root by MR imaging. This phenomenon may go unnoticed when standard echocardiography is performed. The asymmetry of the aortic root might be of clinical importance in unexpected aortic root dissection.

摘要

背景

马凡综合征患者可能会发生主动脉根部夹层,尽管标准超声心动图显示主动脉根部仅轻度扩张,这可能是由于主动脉根部不对称所致。本研究的目的是通过磁共振成像(MR)研究马凡综合征患者的主动脉根部不对称性,并将这些测量结果与常规进行的超声心动图检查结果进行比较。

方法

87例马凡综合征患者(平均年龄31±8岁)接受了磁共振成像检查。从该人群中选取了15例患者(平均年龄29±3岁),这些患者在3个月内同时进行了超声心动图和磁共振成像检查。超声心动图检查时,根据美国超声心动图学会的建议测量主动脉根部。磁共振成像检查时,获取主动脉根部的短轴视图,以测量无冠瓣、右冠瓣和左冠瓣之间的距离以及主动脉根部面积。评估主动脉根部面积与直径之间的相关性,并计算95%置信区间(95%CI)。

结果

磁共振成像和超声心动图检查在常规测量的无冠瓣至右冠瓣直径方面未显示差异(42±6mm)。磁共振图像上最大的主动脉根部直径是右冠瓣至左冠瓣直径(46±7mm,p<0.02)。对于给定的无冠瓣至右冠瓣直径,95%置信区间显示主动脉根部面积的变化范围为-20%至+20%。

结论

大多数马凡综合征患者通过磁共振成像显示主动脉根部不对称扩张。当进行标准超声心动图检查时,这种现象可能未被注意到。主动脉根部的不对称性在意外的主动脉根部夹层中可能具有临床重要性。

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本文引用的文献

1
Survival and complication free survival in Marfan's syndrome: implications of current guidelines.马凡综合征的生存及无并发症生存情况:现行指南的意义
Heart. 1999 Oct;82(4):499-504. doi: 10.1136/hrt.82.4.499.
2
Replacement of the aortic root in patients with Marfan's syndrome.马凡综合征患者主动脉根部置换术。
N Engl J Med. 1999 Apr 29;340(17):1307-13. doi: 10.1056/NEJM199904293401702.
3
Color flow and conventional echocardiography of the Marfan syndrome.马凡综合征的彩色血流及传统超声心动图检查
磁共振血管造影预测马凡综合征主动脉根部进行性扩张和手术的指标。
PLoS One. 2022 Feb 3;17(2):e0262826. doi: 10.1371/journal.pone.0262826. eCollection 2022.
4
No beneficial effect of general and specific anti-inflammatory therapies on aortic dilatation in Marfan mice.一般和特异性抗炎疗法对马凡综合征小鼠主动脉扩张无有益作用。
PLoS One. 2014 Sep 19;9(9):e107221. doi: 10.1371/journal.pone.0107221. eCollection 2014.
5
Cardiovascular magnetic resonance in Marfan syndrome.马凡综合征的心血管磁共振成像。
J Cardiovasc Magn Reson. 2013 Apr 15;15(1):33. doi: 10.1186/1532-429X-15-33.
6
Marfan's syndrome: an overview.马凡综合征概述
Sao Paulo Med J. 2010 Dec;128(6):360-6. doi: 10.1590/s1516-31802010000600009.
7
Quantitative assessment of the entire thoracic aorta from magnetic resonance images.基于磁共振图像对整个胸主动脉进行定量评估。
Cardiol Young. 2011 Apr;21(2):170-7. doi: 10.1017/S1047951110001678. Epub 2010 Dec 22.
8
Automated analysis of four-dimensional magnetic resonance images of the human aorta.人体主动脉四维磁共振图像的自动分析。
Int J Cardiovasc Imaging. 2010 Jun;26(5):571-8. doi: 10.1007/s10554-010-9592-5. Epub 2010 Feb 10.
9
Cardiovascular dynamics in ischemic cardiomyopathy during exercise.运动期间缺血性心肌病的心血管动力学
Int J Cardiovasc Imaging. 2010 Feb;26(2):161-4. doi: 10.1007/s10554-009-9533-3.
10
The distal aorta in the Marfan syndrome.马凡综合征的主动脉远端。
Neth Heart J. 2008 Nov;16(11):382-6. doi: 10.1007/BF03086183.
Echocardiography. 1992 Nov;9(6):627-36. doi: 10.1111/j.1540-8175.1992.tb00508.x.
4
Stress variations in the human aortic root and valve: the role of anatomic asymmetry.
Ann Biomed Eng. 1998 Jul-Aug;26(4):534-45. doi: 10.1114/1.122.
5
A comparison of adult pulmonary autograft diameter measurements with echocardiography and magnetic resonance imaging.
Eur Heart J. 1998 Feb;19(2):301-9. doi: 10.1053/euhj.1997.0745.
6
Marfan syndrome in children and adolescents: an adjusted nomogram for screening aortic root dilatation.儿童和青少年马凡综合征:用于筛查主动脉根部扩张的校正列线图。
Heart. 1998 Jan;79(1):69-72. doi: 10.1136/hrt.79.1.69.
7
Aortic root complications in Marfan's syndrome: identification of a lower risk group.马凡综合征的主动脉根部并发症:低风险组的识别。
Heart. 1996 Apr;75(4):389-95. doi: 10.1136/hrt.75.4.389.
8
Cardiovascular manifestations of Marfan's syndrome: improved evaluation by transoesophageal echocardiography.马凡综合征的心血管表现:经食管超声心动图评估的改进
Br Heart J. 1993 Feb;69(2):104-8. doi: 10.1136/hrt.69.2.104.
9
Prognostic significance of the pattern of aortic root dilation in the Marfan syndrome.马凡综合征中主动脉根部扩张模式的预后意义。
J Am Coll Cardiol. 1993 Nov 1;22(5):1470-6. doi: 10.1016/0735-1097(93)90559-j.
10
Life expectancy in the Marfan syndrome.马凡综合征患者的预期寿命。
Am J Cardiol. 1995 Jan 15;75(2):157-60. doi: 10.1016/s0002-9149(00)80066-1.