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患有ACTA2基因突变的女性孕期急性主动脉夹层。

Acute aortic dissections with pregnancy in women with ACTA2 mutations.

作者信息

Regalado Ellen S, Guo Dong-chuan, Estrera Anthony L, Buja L Maximilian, Milewicz Dianna M

机构信息

Department of Internal Medicine, University of Texas Health Science Center at Houston, Houston, Texas.

出版信息

Am J Med Genet A. 2014 Jan;164A(1):106-12. doi: 10.1002/ajmg.a.36208. Epub 2013 Nov 15.

Abstract

Mutations in ACTA2 predispose to thoracic aortic aneurysms and dissection as well as coronary artery and cerebrovascular disease. Here we examined the risk of aortic dissections, stroke and myocardial infarct with pregnancy in women with ACTA2 mutations. Of the 53 women who had a total of 137 pregnancies, eight had aortic dissections in the third trimester or the postpartum period (6% of pregnancies). One woman also had a myocardial infarct that occurred during pregnancy that was independent of her aortic dissection. Compared to the population-based frequency of peripartum aortic dissections of 0.6%, the rate of peripartum aortic dissections in women with ACTA2 mutations is much higher (8 out of 39; 20%). Six of these dissections initiated in the ascending aorta (Stanford type A), three were fatal. Three women had ascending aortic dissections at diameters less that 5.0 cm (range 3.8-4.7 cm). Aortic pathology showed mild to moderate medial degeneration of the aorta in three women. Of note, five of the women had hypertension either during or before the pregnancy. In summary, the majority of women with ACTA2 mutations did not have aortic or other vascular complications with pregnancy. However, these findings show that pregnancy is associated with significant risk for aortic dissection in women with ACTA2 mutations. Women with ACTA2 mutations who are planning to get pregnant should be counseled about this risk of aortic dissection, and proper clinical management should be initiated to reduce this risk.

摘要

ACTA2基因的突变易引发胸主动脉瘤、主动脉夹层,以及冠状动脉和脑血管疾病。在此,我们研究了携带ACTA2基因突变的女性在孕期发生主动脉夹层、中风和心肌梗死的风险。在53名共有137次妊娠的女性中,有8名在妊娠晚期或产后发生了主动脉夹层(占妊娠次数的6%)。有一名女性在孕期还发生了与主动脉夹层无关的心肌梗死。与基于人群的围产期主动脉夹层发生率0.6%相比,携带ACTA2基因突变的女性围产期主动脉夹层发生率要高得多(39例中有8例;20%)。其中6例夹层起源于升主动脉(斯坦福A型),3例死亡。3名女性在升主动脉直径小于5.0 cm(范围3.8 - 4.7 cm)时发生了夹层。主动脉病理检查显示3名女性的主动脉有轻度至中度的中层退变。值得注意的是,其中5名女性在孕期或孕前患有高血压。总之,大多数携带ACTA2基因突变的女性在孕期没有发生主动脉或其他血管并发症。然而,这些研究结果表明,妊娠与携带ACTA2基因突变的女性发生主动脉夹层的显著风险相关。计划怀孕的携带ACTA2基因突变的女性应被告知主动脉夹层的这种风险,并应启动适当的临床管理以降低这种风险。

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