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

Luigi Lovato MD , Mariano Cefarelli MD, PhD , Luca Di Marco MD, PhD , Daniel Arcioni MD , Giada Tortora MD, PhD , Ada Dormi Mth D Biostatistical , Nicolò Schicchi MD , Elisabetta Mariucci MD, PhD , Marco Di Eusanio MD, PhD , Davide Pacini MD, PhD , Rossella Fattori MD, PhD
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Abstract

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.

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Marfan 和 Loeys-Dietz 主动脉表型:诊断和管理的潜在工具
目的 在遗传性主动脉疾病中,可能会出现不同的血管受累情况,从而对主动脉扩张/离断风险产生潜在的不同影响。本研究旨在分析马凡氏综合征和洛伊-迪茨氏综合征患者的主动脉解剖结构,以确定可能存在的形态学差异。方法对 114 名马凡氏综合征和洛伊-迪茨氏综合征患者以及 20 名匹配的对照组受试者的胸腹主动脉(从近端主动脉上血管到股骨分叉水平)进行计算机断层扫描和磁共振成像检查。结果显示,马凡氏综合征患者的升主动脉和主动脉根部扩张率较高(P = .011),主动脉根部较大且较长(P = .013),呈梨形表型,峡部/降主动脉直径比较大(P = .015),肾上主动脉和髂动脉较大。Loeys-Dietz综合征患者的指数节段更长,弓明显更长(P = .006),2/3型弓的发病率更高(P = .097)。测量比率分析提供了临界值(主动脉根部至升主动脉长度/主动脉根部直径、主动脉根部/细支交界处、主动脉根部/升主动脉直径),可将马凡氏综合征患者与洛伊-狄茨综合征患者区分开来,即使在疾病的早期阶段也是如此。这些特征可能代表了不同基因突变对主动脉发育的影响,对预后有潜在影响,并可能有助于更好地治疗疾病。应始终考虑系统性地采用磁共振或计算机断层扫描进行全身成像,因为它们可以进行全面的血管评估,并提供实用的鉴别诊断指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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