首页> 外文期刊>Ultrasound in obstetrics & gynecology: the official journal of the International Society of Ultrasound in Obstetrics and Gynecology >Reliability of fetal thymus measurement in prediction of 22q11.2 deletion: a retrospective study using four-dimensional spatiotemporal image correlation volumes.
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Reliability of fetal thymus measurement in prediction of 22q11.2 deletion: a retrospective study using four-dimensional spatiotemporal image correlation volumes.

机译:胎儿胸腺测量值在预测22q11.2缺失中的可靠性:一项使用四时空图像相关量的回顾性研究。

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To evaluate the thymic-thoracic ratio (TT-ratio) method in assessment of the fetal thymus in normal fetuses and in those with cardiac abnormalities, in the presence or absence of 22q11.2 deletion.Database records were reviewed for cases of conotruncal and arch abnormalities found on fetal echocardiography between January 2007 and September 2011. The 22q11.2 deletion status was retrieved and cases in which this was not known were excluded from the analysis, as were fetuses with aneuploidy or other genetic disorders. An additional 55 normal fetuses were analyzed as a control group. The TT-ratio was measured retrospectively using stored spatiotemporal image correlation (STIC) volume datasets.Sixty-nine fetuses with relevant cardiac diagnoses were identified and, of these, 18 (26%) had 22q11.2 deletion. The mean gestational age at diagnosis was 22 weeks. Significant pairwise differences, but also overlap, were observed between all three groups (i.e. fetuses with heart defects with and without the 22q11.2 deletion and controls). The mean TT-ratio was 0.44 in our normal control group and was significantly smaller in fetuses with 22q11.2 deletion, corresponding to previously published data. However, the mean TT-ratio in the group with conotruncal anomalies but without the 22q11.2 deletion was also smaller than that in controls, in contrast to previously published data. The TT-ratio was above the normal mean, regardless of fetal karyotype, in all cases of interrupted aortic arch.The TT-ratio method is a feasible and potentially useful tool during detailed fetal heart assessment. However, the absolute measurement is not reliable for prediction of 22q11.2 deletion and the obtained results should therefore be interpreted with caution. Fetal karyotyping should be recommended in cases with conotruncal heart abnormalities, irrespective of the TT-ratio.
机译:为了评估胸腺胸比(TT-比率)方法在评估正常胎儿和心脏异常胎儿是否存在22q11.2缺失的情况下评估其胸腺的能力。在2007年1月至2011年9月期间在胎儿超声心动图上发现异常。分析中发现了22q11.2缺失状态,并且将不明原因的病例以及具有非整倍性或其他遗传疾病的胎儿排除在分析之外。分析另外55名正常胎儿作为对照组。使用存储的时空图像相关(STIC)体积数据集对TT比率进行回顾性测量,共鉴定出69例具有相关心脏诊断的胎儿,其中18例(26%)缺失22q11.2。诊断时的平均胎龄为22周。在所有三个组之间(即具有和不具有22q11.2缺失和对照组的有心脏缺陷的胎儿)均观察到了显着的成对差异,但也有重叠。在我们的正常对照组中,平均TT比率为0.44,在22q11.2缺失的胎儿中,平均TT比率显着较小,与先前发表的数据相对应。然而,与先前发表的数据相比,具有锥鼻异常但没有22q11.2缺失的组的平均TT比值也小于对照组。在所有主动脉弓中断的情况下,无论胎儿核型如何,TT比值均高于正常平均值.TT比值法在详细的胎儿心脏评估中是一种可行且潜在有用的工具。但是,绝对测量值对于22q11.2缺失的预测并不可靠,因此应谨慎解释所获得的结果。无论伴有TT比率如何,在圆锥锥性心脏异常的情况下均应建议进行胎儿核型分析。

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