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陈益明, 卢莎, 张闻, 王姗, 顾琳媛, 窦琳琳, 李慧, 何海雅. 胎儿神经管畸形中孕期母血清AFP和游离β-HCG筛查结果分析[J]. 中国公共卫生, 2018, 34(6): 854-857. DOI: 10.11847/zgggws1116096
引用本文: 陈益明, 卢莎, 张闻, 王姗, 顾琳媛, 窦琳琳, 李慧, 何海雅. 胎儿神经管畸形中孕期母血清AFP和游离β-HCG筛查结果分析[J]. 中国公共卫生, 2018, 34(6): 854-857. DOI: 10.11847/zgggws1116096
Yi-ming CHEN, Sha LU, Wen ZHANG, . Maternal serum AFP and free β-HCG detection during second trimester for screening of fetal neural tube defects: a retrospective multicenter study[J]. Chinese Journal of Public Health, 2018, 34(6): 854-857. DOI: 10.11847/zgggws1116096
Citation: Yi-ming CHEN, Sha LU, Wen ZHANG, . Maternal serum AFP and free β-HCG detection during second trimester for screening of fetal neural tube defects: a retrospective multicenter study[J]. Chinese Journal of Public Health, 2018, 34(6): 854-857. DOI: 10.11847/zgggws1116096

胎儿神经管畸形中孕期母血清AFP和游离β-HCG筛查结果分析

Maternal serum AFP and free β-HCG detection during second trimester for screening of fetal neural tube defects: a retrospective multicenter study

  • 摘要:
      目的  评价中孕母血清甲胎蛋白(AFP)和游离人绒毛膜促性腺激素 β 亚基(free β-HCG)二联法产前筛查胎儿神经管畸形(neural tube defects,NTD)的筛查效果。
      方法  采用多中心回顾性研究方法,分析2007年10月 —2014年9月在杭州市5家产前筛查中心自愿接受产前筛查的437 438名孕妇的出生缺陷监测资料及杭州市各区、县妇幼保健院上报的产前筛查随访结果资料,应用Risks 2T产筛分析软件,评估NTD的风险值。
      结果  筛查高风险孕妇中确诊无脑儿10例、脊柱裂32例、脑膨出9例,在随访筛查低风险孕妇中确诊新生儿无脑儿9例、脊柱裂28例、脑膨出14例,产前筛查的灵敏度分别为52.63 %(10/19)、53.33 %(32/60)、39.13 %(9/23);假阳性率分别为0.38 %(1 676/437 419)、0.38 %(1 654/437 378)、0.38 %(1 677/437 415);随访的高风险孕妇中无脑儿、脊柱裂、脑膨出的检出率分别为0.59 %、1.90 %和0.53 %,在随访的低风险孕妇中三者的检出率分别为0.02 ‰、0.07 ‰和0.03 ‰,筛查结果为高风险者,其检出NTD患儿的概率高于低风险者,两者差异均有统计学意义(均P < 0.001)。
      结论  血清学AFP、游离 β-HCG二联产前筛查不仅能筛查唐氏综合征、18三体综合征,还能筛查无脑儿、脊柱裂、脑膨出,后期应结合三维B超等产前诊断技术,做好对NTD产前筛查质量控制和后续诊断随访工作,减少先天性缺陷患儿出生。

     

    Abstract:
      Objective  To evaluate the efficiency of maternal serum alpha-fetoprotein (AFP) and free beta human chorionic gonadotrophin (free β-HCG) detection during second-trimester for screening of fetal neural tube defects (NTD).
      Methods  We collected data on 437 438 pregnant women who voluntarily received prenatal screening for fetal birth defects in 5 prenatal diagnosis centers in Hangzhou city during the period from October 2007 through September 2014. We also collected monitoring data on follow-up screening for birth defect reported by maternal and child health care hospitals in all counties or districts of Hangzhou municipality. Risks 2T Prenatal Screening Analyzing Software was adopted to assess NTD risk.
      Results  During the 8-year period, totally 10 anencephalus, 32 rachischisis, and 9 encephalocele cases were diagnosed among the pregnant women at high risk of having a baby with birth defect based on AFP and free β-HCG screening; another 9 anencephalus, 28 rachischisis, and 14 encephalocele cases were ascertained during follow-up surveys among the pregnant women at the low risk. The sensitivity of AFP and free β-HCG prenatal screening were 52.63% (10/19) for anencephalus, 53.33% (32/60) for rachischisis, and 39.13% (9/23) for encephalocele, respectively. The false positive rate of AFP and free β-HCG prenatal screening for anencephalus, rachischisis, and encephalocele were 0.38% (1 676/437 419), 0.38% (1 654/437 378), and 0.38% (1 677/437 415). The detection rate of anencephalus, rachischisis and encephalocele were 0.59%, 1.90%, and 0.53% among the pregnant women at high risk based on AFP and free β-HCG prenatal screening, which were significantly higher than those (0.02‰, 0.07‰, and 0.03‰) among the pregnant women at the low risk (P < 0.001 for all).
      Conclusion  The prenatal screening based on maternal serum AFP and free β-HCG measurement can detect not only Down′s syndrome and trisomy 18 syndrome, but also anencephalus, rachischisis, and encephalocele. Maternal serum AFP and free β-HCG detection combined with other prenatal screening technique and procedures is helpful to reduce the incidence of congenital defects.

     

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