DiMaio M S, Baumgarten A, Greenstein R M, Saal H M, Mahoney M J
N Engl J Med. 1987 Aug 6;317(6):342-6. doi: 10.1056/NEJM198708063170603.
Although the risk of Down's syndrome increases with maternal age, women under 35 bear about 80 percent of the infants born with this condition. We prospectively investigated the utility of measuring maternal serum alpha-fetoprotein during the second trimester in women under 35 in order to identify pregnancies in which the fetus was affected with Down's syndrome. Over a two-year period, 34,354 women in this age group were screened. Amniocentesis was offered when the risk of Down's syndrome, calculated as a function of maternal age and maternal serum alpha-fetoprotein concentration adjusted for maternal weight and race, was 1:270 or higher, the risk for a 35-year-old woman. This threshold was exceeded in 1451 women in whom gestational age was confirmed by ultrasound; 9 women in this group had a fetus with the syndrome. In three women whose fetuses had trisomy 18 and one whose fetus had trisomy 13, the calculated risk of Down's syndrome was 1:270 or higher. Thus, among women in whom the risk exceeded our cutoff point, 1 in 161 were found to have a pregnancy in which the fetus was affected with Down's syndrome; the figure was 1 in 112 for all autosomal trisomies. Eighteen pregnancies involving Down's syndrome, three involving trisomy 18, and two involving trisomy 13 were not associated with a calculated risk above the cutoff point. The available data indicate that in our population, using a cutoff for risk at which 5 percent of women under 35 are offered amniocentesis, we will detect one quarter to one third of pregnancies in which the fetus has Down's syndrome.
尽管唐氏综合征的风险会随着母亲年龄的增长而增加,但35岁以下的女性所生育的患有该疾病的婴儿约占80%。我们前瞻性地研究了在孕中期测量35岁以下女性血清甲胎蛋白的作用,以识别胎儿患有唐氏综合征的妊娠情况。在两年的时间里,对该年龄组的34354名女性进行了筛查。当根据母亲年龄、经母亲体重和种族校正后的母亲血清甲胎蛋白浓度计算出的唐氏综合征风险达到或高于1:270(即35岁女性的风险水平)时,建议进行羊水穿刺。在1451名经超声确认孕周的女性中,该阈值被超过;该组中有9名女性的胎儿患有该综合征。在3名胎儿为18三体和1名胎儿为13三体的女性中,计算出的唐氏综合征风险为1:270或更高。因此,在风险超过我们设定切点的女性中,发现每161名中有1名的胎儿患有唐氏综合征;对于所有常染色体三体而言,这一数字为每112名中有1名。18例涉及唐氏综合征的妊娠、3例涉及18三体的妊娠和2例涉及13三体的妊娠,其计算出的风险并未高于切点。现有数据表明,在我们的人群中,使用5%的35岁以下女性接受羊水穿刺的风险切点,我们将检测出四分之一至三分之一的胎儿患有唐氏综合征的妊娠。