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Clinical value of fetal prenasal thickness examination with ultrasonograpy to scann Down syndrome |
YE Feng1, DONG Xueqin1, BAI Lili1, NI Jiana1, XU Xueqin2, CHEN Limin1. |
1.Department of Ultrosonograpy, Dingli Clinical Hospital of Wenzhou Medical University, Central Hospital of Wenzhou, Wenzhou, 325000; 2.Department of Clinical Laboratory, Dingli Clinical Hospital of Wenzhou Medical University, Central Hospital of Wenzhou, Wenzhou, 325000
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Cite this article: |
YE Feng,DONG Xueqin,BAI LilI, et al. Clinical value of fetal prenasal thickness examination with ultrasonograpy to scann Down syndrome[J]. JOURNAL OF WEZHOU MEDICAL UNIVERSITY, 2016, 46(2): 129-132.
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Abstract Objective: To construct a reference range for fetal prenasal thickness of second trimester fetuses with prenatal ultrasonograpy and to explore the relationship between the thickness in fetuses with Down syndrome. To evaluate the clinical value of prenasal thickness in scanning Down syndrome. Methods: The fetal profile was acquired from 597 normal fetuses and 46 fetuses with trisomy 21 at 16~25 weeks’ gestation between February 2012 and February 2014. Two-dimensional ultrasound was used to obtain the exact mid-sagittal plane and the prenasal thickness between the anterior edge of the lowest part of the frontal bone (at the junction with the nasal bone when present) and the skin anteriorly. Results: In the normal group prenasal thickness increased with gestation from a mean of (2.2± 0.4) mm at 16 weeks to (4.7±0.5) mm at 25 weeks (r=0.725, P<0.001). In 32 (69.6%) cases of the trisomy-21 fetuses the prenasal thickness was above the 95th centile of the normal range. When prenasal thickness above the 95th centile of the normal range was used as a cut-off, the sensitivity for Down syndrome. was 69.6%, the specificity was 96.3%, the positive predictive value was 64.0%, the negative predictive value was 97.1%, the positive likelihood ratio was 19.0, the negative likelihood ratio was 0.32. Conclusion: Increased prenasal thickness is a high risk for DS and can be used as a prenatal ultrasonographic mark in scanning Down syndrome.
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Received: 18 May 2015
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[1] 石晓梅, 方群, 陈宝江, 等. 超声软指标在筛查胎儿21三体综合征中的应用[J]. 中华妇产科杂志, 2013, 48(2): 81-85.
[2] AGATHOKLEOUS M, CHAVEEVA P, POON L C, et al.Meta-analysis of second-trimester markers for trisomy 21[J].Ultrasound Obset Gynecol, 2013, 41(3): 247-261.
[3] BENACERRAF B R. The role of the second trimester genetic sonogram in screening for fetal Down syndrome[J]. Semin Perinatol, 2005, 29(6): 386-394.
[4] SOUTER V L, NYBERG D A, BENN P A, et al. Correlation of second-trimester sonographic and biochemical markers[J]. J Ultrasound Med, 2004, 23(4): 505-511.
[5] MAYMON R, LEVINSOHN-TAVOR O, Cuckle H, et al. Second trimester ultrasound prenasal thickness combined with nasal bone length: a new method of Down syndrome screening[J]. Prenat Diagn, 2005, 25(10): 906-911.
[6] PERSICO N, BORENSTEIN M, MOLINA F, et al. Prenasal thickness in trisomy-21 fetuses at 16-24 weeks of gestation[J]. Ultrasound Obstet Gynecol, 2008, 32(6): 751-754.
[7] OZCAN T, ALLEN J, PETERSON J, et al. Prenatal prediction of Down syndrome using prenasal thickness on second trimester ultrasound[J]. Eur J Obstet Gynecol Reprod Biol, 2013, 171(2): 220-224.
[8] MAYMON R, MOSKOVITCH M, LEVINSOHN-TAVOR O, et al. Bedside estimation of Down syndrome risk from second-trimester ultrasound prenasal thickness[J]. Ultrasound Obstet Gynecol, 2009, 34(6): 629-633.
[9] VON KAISENBERG C S, KRENN V, LUDWIG M, et al. Morphological classification of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12-18 weeks and in a trisomy 16 mouse[J]. Anat Embryol, 1998, 197(2): 105-124.
[10] VON KAISENBERG C S, BRAND-SABERI B, CHRIST B, et al. Collagen type VI gene expression in the skin of trisomy 21 fetuses[J]. Obstet Gynecol, 1998, 91(3): 319-323.
[11] WEILL D, MATTEI M G, PASSAGE E, et al. Cloning and chromosomal localization of human genes encoding the three chains of typeVI collagen[J]. Am J Hum Genet, 1988, 42(3): 435-455.
[12] NICOLAIDES K H, SPENCER K, AVGIDOU K, et al. Multicenter study of first-trimester screening for trisomy 21 in 75821 pregnancies: results and estimation of the potential impact of individual risk-orientated two-stage first-trimester screening[J]. Ultrasound Obstet Gynecol, 2005,25(3): 221-226.
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