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马凡综合征患儿及青年患者家族史及二叶式主动脉瓣的临床意义。

Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome.

机构信息

Inherited and Rare Cardiovascular Diseases, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Monaldi Hospital, Naples, Italy.

Department of Pediatrics, University of Naples "Federico II", Naples, Italy.

出版信息

Cardiol Young. 2020 May;30(5):663-667. doi: 10.1017/S1047951120000748. Epub 2020 Apr 15.

Abstract

BACKGROUND

Marfan syndrome is an autosomal dominant disorder of the connective tissue, whose cardinal features affect eyes, musculoskeletal, and cardiovascular system. Despite prevalence and natural history of cardiovascular manifestation are well known in adults, little is known about children and young adult patients. The aim of this study was to describe a well-characterised cohort of consecutive children and young patients with marfan syndrome, looking at the impact of family history and presence of bicuspid aortic valve on disease severity.

METHODS

A total of 30 consecutive children and young patients with Marfan syndrome were evaluated. All patients underwent a comprehensive clinical-instrumental-genetic evaluation. Particular attention was posed to identify differences in prevalence of cardiovascular abnormalities between patients with and without family history of Marfan syndrome or bicuspid aortic valve.

RESULTS

Of these 30 patients, family history of Marfan syndrome and bicuspid aortic valve were present in 76 and 13%, respectively. Compared to patients with family history of Marfan syndrome, those without showed higher prevalence of aortic sinus dilation (87 versus 32%, p-value = 0.009), greater aortic sinus diameters (4.2 ± 2.1 versus 1.9 ± 1.1 z score, p-value = 0.002), and higher rate of aortic surgery during follow-up (37 versus 0%, p-value = 0.002). Compared to patients with tricuspid aortic valve, those with bicuspid aortic valve were younger (3.2 ± 4.3 versus 10.7 ± 6.8 years old, p-value = 0.043), showed greater aortic sinus diameters (4.2 ± 0.9 versus 2.2 ± 1.6 z score, p-value = 0.033), and underwent more frequently aortic root replacement (50 versus 4%, p-value = 0.004).

CONCLUSIONS

In our cohort of patients with Marfan syndrome, the absence of family history and the presence of bicuspid aortic valve were associated to severe aortic phenotype and worse prognosis.

摘要

背景

马凡综合征是一种常染色体显性遗传性结缔组织疾病,其主要特征影响眼睛、肌肉骨骼和心血管系统。尽管成人的心血管表现的患病率和自然病史众所周知,但对儿童和年轻成年患者知之甚少。本研究旨在描述一组特征明确的连续儿童和年轻马凡综合征患者,研究家族史和二叶式主动脉瓣的存在对疾病严重程度的影响。

方法

共评估了 30 例连续的马凡综合征儿童和年轻患者。所有患者均接受了全面的临床-仪器-遗传评估。特别注意识别有或无马凡综合征家族史或二叶式主动脉瓣的患者心血管异常的患病率差异。

结果

30 例患者中,有马凡综合征家族史和二叶式主动脉瓣的分别为 76%和 13%。与有马凡综合征家族史的患者相比,无家族史的患者主动脉窦扩张的患病率更高(87%对 32%,p 值=0.009),主动脉窦直径更大(4.2±2.1 对 1.9±1.1 z 评分,p 值=0.002),随访期间主动脉手术的发生率更高(37%对 0%,p 值=0.002)。与三叶式主动脉瓣患者相比,二叶式主动脉瓣患者更年轻(3.2±4.3 对 10.7±6.8 岁,p 值=0.043),主动脉窦直径更大(4.2±0.9 对 2.2±1.6 z 评分,p 值=0.033),更频繁地行主动脉根部置换术(50%对 4%,p 值=0.004)。

结论

在我们的马凡综合征患者队列中,无家族史和二叶式主动脉瓣的存在与严重的主动脉表型和更差的预后相关。

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