Goodburn S F, Yates J R, Raggatt P R, Carr C, Ferguson-Smith M E, Kershaw A J, Milton P J, Ferguson-Smith M A
Department of Clinical Genetics, Addenbrooke's Hospital, Cambridge, U.K.
Prenat Diagn. 1994 May;14(5):391-402. doi: 10.1002/pd.1970140509.
Over a 2-year period from January 1991 to December 1992, second-trimester maternal serum screening for Down's syndrome using alpha-fetoprotein (alpha FP), human chorionic gonadotrophin (hCG), and unconjugated oestriol (uE3) was made available to five health districts in East Anglia, with a total population of 1.2 million. Amniocentesis was offered when the risk of Down's syndrome at term was 1:200 or greater. 25,359 singleton pregnancies were screened, representing an uptake of 77 per cent. The recall rate for the 24 per cent of women who had not had a dating scan prior to the test was 9.4 per cent compared with 3.9 per cent for those who had been scanned (P < 0.0005). Seventy-five per cent (36/48) of Down's syndrome pregnancies were detected for a false-positive rate of 4.0 per cent. Twenty-five out of 36 of detected Down's syndrome pregnancies were dated by scan prior to sampling, and in the 11 remaining cases, the dates were confirmed by scan after a high-risk result was obtained. The exclusion of uE3 from the screening protocol would have reduced the detection rate to 52 per cent (25/48) for the same false-positive rate. Eighty-five per cent of women identified at high risk accepted the offer of an amniocentesis. Other fetal abnormalities detected were trisomy 18 (3), trisomy 13 (2), 45,X (6), 69,XXX (5), other chromosome abnormalities (9), open neural tube defects (26), hydrocephalus (7), abdominal wall defects (4), and steroid sulphatase deficiency (6).
在1991年1月至1992年12月的两年期间,东盎格利亚的五个卫生区为120万总人口提供了孕中期唐氏综合征母体血清筛查,检测指标包括甲胎蛋白(αFP)、人绒毛膜促性腺激素(hCG)和未结合雌三醇(uE3)。当足月时唐氏综合征风险为1:200或更高时,会建议进行羊膜穿刺术。对25359例单胎妊娠进行了筛查,接受率为77%。检测前未进行孕周扫描的24%的女性召回率为9.4%,而进行过扫描的女性召回率为3.9%(P<0.0005)。75%(36/48)的唐氏综合征妊娠被检测出,假阳性率为4.0%。36例被检测出的唐氏综合征妊娠中有25例在采样前通过扫描确定了孕周,其余11例在获得高危结果后通过扫描确认了孕周。在相同假阳性率的情况下,从筛查方案中排除uE3会使检测率降至52%(25/48)。85%被确定为高危的女性接受了羊膜穿刺术的建议。检测出的其他胎儿异常包括18三体(3例)、13三体(2例)、45,X(6例)、69,XXX(5例)、其他染色体异常(9例)、开放性神经管缺陷(26例)、脑积水(7例)、腹壁缺陷(4例)和类固醇硫酸酯酶缺乏症(6例)。