Bahado-Singh R O, Lynch L, Deren O, Morroti R, Copel J A, Mahoney M J, Williams J
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, CT 06520-8063, USA.
Am J Obstet Gynecol. 1997 May;176(5):976-80. doi: 10.1016/s0002-9378(97)70388-0.
Our purpose was to determine the effect of type of aneuploidy and gestational age on first-trimester fetal growth.
Crown-rump length measurement was obtained in pregnancies undergoing chorionic villus sampling in three large prenatal diagnosis centers. One hundred forty-four aneuploid fetuses, from 9 to 13 weeks' gestation, were compared with 440 matched control fetuses for evidence of crown-rump length shortening. Shortening was defined by the observed/expected crown-rump length. Expected values of crown-rump length based on last menstrual period were obtained from regression equations generated from a separate normal group. Threshold values for aneuploidy screening were determined on the basis of receiver-operator characteristic curves.
There was significant crown-rump length shortening in trisomy 18 compared with normal fetuses, with observed/expected values < or = 0.80 (odds ratio 13.78, 95% confidence interval 5.64 to 33.88, p < 0.000001); for trisomy 13 the observed/expected crown-rump length was < or = 0.90 (odds ratio 3.64, 95% confidence interval 1.08 to 12.96, p < 0.03). There was no significant shortening of crown-rump length in Down syndrome, with observed/expected values < or = 0.92 (odds ratio 0.86, 95% confidence interval 0.50 to 1.47, p = 0.6). With shortened crown-rump length (observed/expected value < 0.86) the risk of any aneuploidy is increased (odds ratio 2.52, 95% confidence interval 1.6 to 3.96, p < 0.0001). When the first-trimester crown-rump length was shortened by > or = 14 mm, the aneuploidy risk was high (odds ratio 9.04, 95% confidence interval 3.26 to 28.67, p < 0.00001).
In the first trimester fetuses with trisomy 18 and 13 appear to be growth restricted, in contrast to fetuses with trisomy 21. In at-risk pregnancies crown-length that is shorter than expected significantly increase the odds that aneuploidy is present.
我们的目的是确定非整倍体类型和孕周对孕早期胎儿生长的影响。
在三个大型产前诊断中心,对接受绒毛取样的孕妇进行头臀长度测量。将144例孕9至13周的非整倍体胎儿与440例匹配的对照胎儿进行比较,以寻找头臀长度缩短的证据。缩短定义为观察到的/预期的头臀长度。根据末次月经计算的头臀长度预期值来自于一个单独的正常组生成的回归方程。根据受试者工作特征曲线确定非整倍体筛查的阈值。
与正常胎儿相比,18三体胎儿的头臀长度显著缩短,观察到的/预期的值≤0.80(优势比13.78,95%置信区间5.64至33.88,p<0.000001);13三体胎儿的观察到的/预期的头臀长度≤0.90(优势比3.64,95%置信区间1.08至12.96,p<0.03)。唐氏综合征胎儿的头臀长度没有显著缩短,观察到的/预期的值≤0.92(优势比0.86,95%置信区间0.50至1.47,p=0.6)。当头臀长度缩短(观察到的/预期的值<0.86)时,任何非整倍体的风险都会增加(优势比2.52,95%置信区间1.6至3.96,p<0.0001)。当孕早期头臀长度缩短≥14mm时,非整倍体风险很高(优势比9.04,95%置信区间3.26至28.67,p<0.00001)。
在孕早期,18三体和13三体胎儿似乎生长受限,这与21三体胎儿不同。在高危妊娠中,头臀长度短于预期会显著增加存在非整倍体的几率。