Granese Roberta, Coco Claudio, Jeanty Philippe
Department of Obstetrics and Gynaecology, University of Messina, Messina, Italy.
Ultrasound Q. 2007 Jun;23(2):117-21. doi: 10.1097/01.ruq.0000263848.07808.02.
To assess the risk of the association of single umbilical artery and aneuploidies.
In a general unselected obstetric population of 12,672 singleton pregnant women from January 1998 to December 2002, we detected 61 fetuses (prevalence, 0.48%) with single umbilical artery (SUA) on prenatal ultrasound at 16 to 23 menstrual weeks.
Among the 61 fetuses with 2-vessel cord, 39 (64%) had SUA as an isolated finding, and 22 (36%) had additional findings, either minor or major. One (2.56%) of the 39 fetuses with SUA as an isolated finding had aneuploidy (trisomy 21 at maternal age of 32 years), whereas 5 (41.6%) of the 12 fetuses with SUA concomitant with major anomalies were aneuploid. None of the 10 fetuses with SUA and minor anomalies had aneuploidy. Among the 12,611 women with 3-vessel cord, we instead found 8 cases of trisomy 21 (0.06%), 1 case of translocation 14-21 (0.007%), 5 cases of trisomy 18 (0.04%), 1 case of trisomy 13 (0.007%), 1 case of 47,XXX (0.007%), and 2 cases of monosomy X (0.01%).
In an unselected population, second trimester sonographic detection of SUA and major fetal anomalies indicate increased risk for fetal aneuploidy. However, even if this study is based on a large population, the only 1 case of trisomy 21 among the fetuses with SUA as an isolated finding is not sufficient to draw a conclusion, and larger studies are needed to confirm or infirm this single case.
评估单脐动脉与非整倍体关联的风险。
在1998年1月至2002年12月期间,对12672名单胎孕妇的普通未筛选产科人群进行研究,我们在孕16至23周的产前超声检查中检测出61例胎儿(患病率为0.48%)存在单脐动脉(SUA)。
在61例双血管脐带胎儿中,39例(64%)的SUA为孤立发现,22例(36%)有其他轻微或严重的发现。39例孤立性SUA胎儿中有1例(2.56%)存在非整倍体(32岁孕妇的21三体),而12例伴有严重异常的SUA胎儿中有5例(41.6%)为非整倍体。10例伴有轻微异常的SUA胎儿均无非整倍体。在12611例三血管脐带的孕妇中,我们发现了8例21三体(0.06%)、1例14 - 21易位(0.007%)、5例18三体(0.04%)、1例13三体(0.007%)、1例47,XXX(0.007%)和2例X单体(0.01%)。
在未筛选人群中,孕中期超声检测到SUA和严重胎儿异常提示胎儿非整倍体风险增加。然而,即使本研究基于大量人群,孤立性SUA胎儿中仅1例21三体不足以得出结论,需要更大规模的研究来证实或否定这一单例情况。