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用于描述鼻骨发育不全和预测21三体综合征的鼻骨至鼻尖长度比值

Nasal bone to nasal tip length ratio for describing nasal bone hypoplasia and predicting trisomy 21.

作者信息

Ekmekci Emre, Demirel Emine, Kelekci Sefa

机构信息

Maternal-Fetal Medicine Unit, Obstetrics and Gynecology Department, Sanliurfa Education and Research Hospital, Sanliurfa, Turkey.

Maternal-Fetal Medicine Unit, Obstetrics and Gynecology Department, Faculty of Medicine, Izmir Katip Celebi University, Izmir, Turkey.

出版信息

Arch Med Sci. 2019 Jun 6;18(2):395-399. doi: 10.5114/aoms.2019.85655. eCollection 2022.

Abstract

INTRODUCTION

Fetal nasal bone hypoplasia has been proven to be a strong marker for trisomy 21 during second trimester ultrasonography. Rather than evaluating the nasal bone hypoplasia according to the nomograms, it may be possible to evaluate it with a more practical and specific method.

MATERIAL AND METHODS

Retrospectively collected data were provided from the saved and stored patient data between 2012 and 2017. Nasal bone length and nasal tip length were measured and the ratio was calculated. The ratio ≤ 1/3 was defined as the threshold ratio for the definition of the marker. Nasal bone nasal tip length (NB/NL) ratio values were compared among groups with trisomy 21 and euploid fetuses.

RESULTS

A total of 59 fetuses had trisomy 21 and 2304 euploid fetuses were included in the study. The ratio of nasal bone to nasal tip length was 1/3 and below in 21/59 (35.5%) of fetuses with trisomy 21 whereas this ratio was 31/2304 (1.3%) in euploid fetuses. The difference was statistically significant ( < 0.001). Sensitivity, specificity, positive likelihood ratio and negative likelihood ratio of nasal bone/nasal tip ratio ≤ 1/3 were 35.5%, 98.6%, 26.4 and 0.6 for Down syndrome, respectively.

CONCLUSIONS

This study suggested that the nasal bone to nasal tip length ratio may be a new promising and practical sonographic marker in the second trimester genetic sonography. Although its sensitivity is not high, it seems to be more practical and specific than the evaluation of fetal nasal bone length.

摘要

引言

胎儿鼻骨发育不全已被证实在孕中期超声检查中是21三体综合征的一个有力标志物。与其根据列线图评估鼻骨发育不全,或许可以用一种更实用、更具特异性的方法来评估。

材料与方法

回顾性收集2012年至2017年间保存和存储的患者数据。测量鼻骨长度和鼻尖长度并计算比值。将该比值≤1/3定义为标志物定义的阈值比值。比较21三体胎儿组和整倍体胎儿组的鼻骨鼻尖长度(NB/NL)比值。

结果

本研究共纳入59例21三体胎儿和2304例整倍体胎儿。21三体胎儿中21/59(35.5%)的鼻骨与鼻尖长度比值为1/3及以下,而整倍体胎儿中该比值为31/2304(1.3%)。差异具有统计学意义(<0.001)。鼻骨/鼻尖比值≤1/3对唐氏综合征的敏感度、特异度、阳性似然比和阴性似然比分别为35.5%、98.6%、26.4和0.6。

结论

本研究表明,鼻骨与鼻尖长度比值可能是孕中期遗传学超声检查中一个新的有前景且实用的超声标志物。尽管其敏感度不高,但似乎比评估胎儿鼻骨长度更实用、更具特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/8924847/be551c94c863/AMS-18-2-109116-g001.jpg

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