Summers Anne M, Huang Tianhua, Meier Chris, Wyatt Philip R
Department of Genetics, North York General Hospital, Toronto, Ontario, Canada.
Obstet Gynecol. 2003 Jun;101(6):1301-6. doi: 10.1016/s0029-7844(03)00235-7.
To investigate the genetic and obstetric implications of false positive Down syndrome serum screening results.
The study population comprised 162774 women underwent triple marker screening in the Ontario Maternal Serum Screening program between October 1995 and September 1998, with outcomes obtained from the Canadian Institute of Health Information. The study compares the incidence of chromosomal abnormalities other than Down syndrome in screen positive women with background incidence from the literature. It also compares the risks of having a fetus with congenital abnormalities or of developing obstetric complications in 11549 screen positive women with their matched controls.
A higher incidence of trisomy 13 (12.4 per 10000) was seen in screen positive women; the incidence of other chromosomal abnormalities in screen positive women was not increased relative to the general population. The higher incidence of trisomy 13 may have been biased by the selective uptake of amniocentesis in women who had high risks for Down syndrome or abnormal ultrasound findings. Incidences of fetal congenital abnormality in screen positive and negative women were similar. Women who screened positive for Down syndrome had increased risk of spontaneous fetal loss (odds ratio 1.80; 95% confidence interval 1.54, 2.07) but no other obstetric complications.
Among women who screened positive for Down syndrome, we found a higher number of spontaneous fetal losses and a possibly higher risk of having a fetus with trisomy 13. We did not find an increased risk for other chromosomal abnormalities, congenital abnormalities, or other adverse obstetric outcomes.
探讨唐氏综合征血清筛查结果假阳性的遗传学及产科意义。
研究人群包括1995年10月至1998年9月在安大略省孕产妇血清筛查项目中接受三联筛查的162774名妇女,结局数据来自加拿大卫生信息研究所。该研究将筛查阳性妇女中除唐氏综合征外的染色体异常发生率与文献中的背景发生率进行比较。还比较了11549名筛查阳性妇女及其匹配对照者怀有先天性异常胎儿或发生产科并发症的风险。
筛查阳性妇女中13三体的发生率较高(每10000例中有12.4例);筛查阳性妇女中其他染色体异常的发生率相对于普通人群并未增加。13三体较高的发生率可能因唐氏综合征高危或超声检查异常的妇女选择性接受羊膜腔穿刺而存在偏差。筛查阳性和阴性妇女中胎儿先天性异常的发生率相似。唐氏综合征筛查阳性的妇女自然流产风险增加(比值比1.80;95%置信区间1.54, 2.07),但无其他产科并发症。
在唐氏综合征筛查阳性的妇女中,我们发现自然流产的数量较多,怀有13三体胎儿的风险可能更高。我们未发现其他染色体异常、先天性异常或其他不良产科结局的风险增加。