Zoppi Maria A, Putzolu Monica, Ibba Rosa M, Floris Marcella, Monni Giovanni
Department of Obstetrics and Gynecology, Prenatal and Preimplantation Genetic Diagnosis and Fetal Therapy, Ospedale Microcitemico, Cagliari, Italy.
Fetal Diagn Ther. 2002 Jan-Feb;17(1):52-7. doi: 10.1159/000048007.
To evaluate first-trimester ductus venosus flow in relation to nuchal translucency (NT) and fetal karyotype.
Ductus venosus flow was measured in fetuses with NT greater than or equal to the 95th centile (group A) and in fetuses with NT less than the 95th centile (group B). The waveforms were classified as normal if the lowest forward velocity during atrial contraction (ACV) was positive and abnormal if it was absent or negative. The results were compared with the fetal karyotype.
Ductus venosus measurement was carried out in 330 fetuses. In group A, there were 156 fetuses: in 4 cases, it was not possible to obtain the measurement, and in the other 152 cases, 93 (61%) had a normal ACV and 59 (39%) an abnormal ACV. NT thickness was significantly greater in fetuses with abnormal ACV. In 34 out of 156 cases (22%), chromosomal abnormalities were found. Twenty-three chromosomopathies out of 33 (70%) had an abnormal ACV, and 10 (30%) had a normal ACV. A significant association between abnormal karyotype and abnormal ACV was found. Ductus venosus measurement was carried out in 174 fetuses of group B. In 1 case, it was not possible to obtain the measurement. One hundred and seventy-one (99%) cases had a normal ACV, and in 2 (1%) cases the ACV was abnormal. No chromosomal abnormalities were found in group B. Considering group A and group B, a significant association between the finding of an enlarged NT and abnormal ACV was detected (p < 0.05).
An abnormal ACV is more frequent in fetuses presenting enlarged NT than in those having normal NTs and in fetuses having the larger nuchal thickness. The probability of having a chromosomal abnormality in fetuses with enlarged NT is greater when an abnormal ACV is found.
评估孕早期静脉导管血流与颈项透明层(NT)及胎儿核型的关系。
对NT大于或等于第95百分位数的胎儿(A组)和NT小于第95百分位数的胎儿(B组)进行静脉导管血流测量。如果心房收缩期最低正向速度(ACV)为阳性,则波形分类为正常;如果ACV缺失或为阴性,则波形分类为异常。将结果与胎儿核型进行比较。
对330例胎儿进行了静脉导管测量。A组有156例胎儿:4例无法获得测量结果,在其他152例中,93例(61%)ACV正常,59例(39%)ACV异常。ACV异常的胎儿NT厚度明显更大。156例中有34例(22%)发现染色体异常。33例染色体病中有23例(70%)ACV异常,10例(30%)ACV正常。发现核型异常与ACV异常之间存在显著关联。对B组174例胎儿进行了静脉导管测量。1例无法获得测量结果。171例(99%)ACV正常,2例(1%)ACV异常。B组未发现染色体异常。综合A组和B组,发现NT增大与ACV异常之间存在显著关联(p<0.05)。
与NT正常的胎儿相比,NT增大的胎儿中ACV异常更为常见,且颈项厚度越大的胎儿ACV异常越常见。当发现ACV异常时,NT增大的胎儿出现染色体异常的可能性更大。