Marfan and Loeys-Dietz aortic phenotype: A potential tool for diagnosis and management

被引:1
|
作者
Lovato, Luigi [1 ]
Cefarelli, Mariano [2 ,3 ]
Di Marco, Luca [4 ]
Arcioni, Daniel [5 ]
Tortora, Giada [6 ]
Dormi, Ada [7 ]
Schicchi, Nicolo [8 ]
Mariucci, Elisabetta [9 ]
Di Eusanio, Marco [2 ,3 ]
Pacini, Davide [4 ]
Fattori, Rossella [10 ]
机构
[1] IRCCS Azienda Osped Univ Bologna, Pediat & Adult Cardiothorac & Vasc, Oncohematol & Emergency Radiol Unit, Via Massarenti 9, I-40138 Bologna, Italy
[2] Polytech Univ Marche, Lancisi Cardiovasc Ctr, Cardiac Surg Unit, Ancona, Italy
[3] Polytech Univ Marche, Marfan Ctr, Lancisi Cardiovasc Ctr, Ancona, Italy
[4] IRCCS Azienda Osped Univ Bologna, Cardiac Surg Unit, Bologna, Italy
[5] IRCCS Univ Cattolica Sacro Cuore, Fdn Policlin Univ Agostino Gemelli, Rome, Italy
[6] Azienda Osped Univ Marche, Med Genet Unit, Ancona, Italy
[7] Alma Mater Studiorum Univ Bologna, Dept Med & Surg Sci, Bologna, Italy
[8] Azienda Osped Univ Marche, Dept Radiol, Cardiovasc Radiol Unit, Ancona, Italy
[9] IRCCS Azienda Osped Univ Bologna, Pediat Cardiol & Adult Congenital Heart Dis Progra, Bologna, Italy
[10] Azienda Osped Univ Marche, Lancisi Cardiovasc Ctr, Ctr Sindrome Marfan & Aortopatie Ereditaria, Ancona, Italy
来源
JTCVS OPEN | 2024年 / 19卷
关键词
aortic anatomy; aortic root; computed tomog- raphy; Loeys-Dietz syndrome; magnetic resonance angiography; Marfan syndrome; MANIFESTATIONS; MUTATIONS; FBN1; ROOT;
D O I
10.1016/j.xjon.2024.03.015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: In heritable aortic diseases, different vascular involvement may occur with potential variable implications in aortic dilation/dissection risk. This study aimed to analyze the aortic anatomy of individuals with Marfan syndrome and Loeys-Dietz syndrome to identify possible morphological differences. Methods: Computed tomography and magnetic resonance imaging of the thoracoabdominal aorta from the proximal supra-aortic vessels to the femoral bifurcation level of 114 patients with Marfan and Loeys-Dietz syndromes and 20 matched control subjects were examined. Aortic diameters, areas, length, and tortuosity were measured in different aortic segments using specific vessel analysis software. Results: Patients with Marfan syndrome showed a higher prevalence of ascending aorta and aortic root dilation (P = .011), larger and longer aortic roots (P = .013) with pear-shaped phenotype, larger isthmus/descending aorta diameter ratio (P = .015), and larger suprarenal aorta and iliac arteries. Patients with Loeys-Dietz syndrome showed longer indexed segments and a significantly longer arch (P = .006) with type 2/3 arch prevalence (P = .097). Measurement ratios analysis provided cut-off values (aortic root to ascending aorta length/aortic root diameter, aortic root/sinotubular junction, aortic root/ascending aorta diameter) differentiating patients with Marfan syndrome from patients with Loeys-Dietz syndrome, even in the early stage of the disease. Conclusions: Both syndromes show peculiar anatomic patterns at different aortic levels irrespective of aortic dilation and disease severity. These features may represent the expression of different genetic mutations on aortic development, with a potential impact on prognosis and possibly contributing to better management of the diseases. The systematic adoption of whole body imaging with magnetic resonance or computed tomography should always be considered, because they allow a complete vascular assessment with practical indicators of differential diagnosis.
引用
收藏
页码:223 / 240
页数:18
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