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首页> 外文期刊>The Annals of Thoracic Surgery: Official Journal of the Society of Thoracic Surgeons and the Southern Thoracic Surgical Association >Distal Transverse Arch to Left Carotid Artery Ratio?Helps to Identify Infants With Aortic Arch?Hypoplasia
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Distal Transverse Arch to Left Carotid Artery Ratio?Helps to Identify Infants With Aortic Arch?Hypoplasia

机译:远端横弓对左颈动脉比率有助于鉴别婴儿主动脉弓发育不足

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Patient RecruitmentEchocardiographic MeasurementsSurgical ApproachTissue PreparationMicroarrayReverse Transcriptase Polymerase Chain ReactionOutcome MethodsStatistical AnalysesResultsMicroarray AnalysisReverse Transcriptase Polymerase Chain ReactionOutcomesCommentDefining CoA With AAHGenetics Involved in CoA With AAHOutcomesStudy LimitationsSupplementary DataDiscussionReferencesAortic coarctation (CoA) with concomitant aortic arch hypoplasia (AAH) is associated with an increased risk of hypertension after surgical repair. The differentiation of CoA with or without AAH may be critical to delineate the ideal surgical approach that best ameliorates postoperative hypertension. Since 2000, we have defined CoA with AAH when the diameter of the distal transverse aortic arch is equal to or less than the diameter of the left carotid artery. We hypothesized that, based on our definition, aortic tissue from infants having CoA with AAH would demonstrate distinct genetic expression patterns as compared with infants having CoA alone.MethodsFrom 6 infants (AAH, 3; CoA, 3), an Affymetrix 1.0 genome array identified genes in the coarctation/arch region that were differentially expressed between infants having CoA with AAH versus CoA alone. Reverse transcription polymerase chain reaction validated genetic differences from a cohort of 21 infants (CoA with AAH, 10; CoA, 11). To evaluate the clinical outcomes based on our definition of CoA with AAH, we reviewed infants repaired using this algorithm from 2000 to?2010.ResultsMicroarray data demonstrated genes differentially expressed between groups. Reverse transcription polymerase chain reaction confirmed that CoA with AAH was associated with an increased expression of genes involved in cardiac and vascular development and growth, including hepsin, fibroblast growth factor-18, and T-box 2. The clinical outcomes of 79 infants (AAH, 26; CoA, 53) demonstrated that 90.1% were free of hypertension at 13 years when managed with this surgical strategy.ConclusionsThese findings provide evidence that the ratio of the diameter of the distal transverse arch to the left carotid artery may be helpful to identify CoA with AAH and, when used to delineate the surgical approach, may minimize hypertension.The AppendixAppendix can be viewed in the online version of this article [http://dx.doi.org/10.1016/j.athoracsur.2015.04.107] on http://www.annalsthoracicsurgery.orgCompared with simple coarctation of the aorta (CoA), coarctation with concomitant aortic arch hypoplasia (AAH) is associated with an increased risk of reintervention, reoperation, and lifelong hypertension [
机译:患者招聘超声心动图测量手术方法组织准备微阵列逆转录酶聚合酶链反应结果方法统计分析结果微阵列分析逆转录酶聚合酶链反应结果评论定义CoA与AAH遗传学涉及CoA与AAH结局研究限度低度与合并症相关性动脉粥样硬化与合并症的关系伴或不伴AAH的CoA的差异可能对于描绘最能改善术后高血压的理想手术方法至关重要。自2000年以来,当远侧主动脉弓的直径等于或小于左颈动脉的直径时,我们用AAH定义了CoA。我们假设,根据我们的定义,与仅具有CoA的婴儿相比,患有CoA和AAH的婴儿的主动脉组织将表现出独特的基因表达模式。缩窄/弓形区域中的基因在具有CoA和AAH的婴儿与单独的CoA之间差异表达。逆转录聚合酶链反应证实了21名婴儿的遗传差异(CoA与AAH,10; CoA,11)。为了根据我们用AAH进行CoA的定义来评估临床结局,我们回顾了使用该算法修复的2000年至2010年的婴儿。结果微阵列数据显示了两组之间差异表达的基因。逆转录聚合酶链反应证实,伴有AAH的CoA与参与心脏和血管发育和生长的基因(包括肝素,成纤维细胞生长因子18和T-box 2)的表达增加有关。79例婴儿(AAH)的临床结局(26; CoA,53)证明,采用这种手术策略后,在13岁时90.1%的人无高血压。结论这些发现提供了证据,表明远端横弓与左颈动脉直径的比值可能有助于确定CoA与AAH结合使用,当用于描述外科手术方法时,可以最大程度地减少高血压。可以在本文的在线版本中查看附录附录[http://dx.doi.org/10.1016/j.athoracsur.2015.04.107]与单纯主动脉缩窄(CoA)相比,缩窄伴有主动脉弓发育不全(AAH)与再次介入,再次手术和终生高血压[

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