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孕早期筛查染色体异常中的尿高糖基化人绒毛膜促性腺激素

Urinary hyperglycosylated hCG in first trimester screening for chromosomal abnormalities.

作者信息

Weinans M J, Butler S A, Mantingh A, Cole L A

机构信息

Antenatal Diagnosis Unit, Department of Obstetrics and Gynaecology, University Hospital, Groningen, The Netherlands.

出版信息

Prenat Diagn. 2000 Dec;20(12):976-8. doi: 10.1002/1097-0223(200012)20:12<976::aid-pd962>3.0.co;2-2.

Abstract

Hyperglycosylated human chorionic gonadotrophin (H-hCG), also known as Invasive Trophoblast Antigen or ITA, is a unique metabolic variant of hCG with more complex oligosaccharide side chains. Concentrations are independent of regular hCG. Urine H-hCG has recently proved to be a highly sensitive marker for Down syndrome screening in the second trimester of pregnancy. We evaluated H-hCG as a potential marker in the first trimester of pregnancy. Maternal urine samples were collected from 10(+0) to 11(+6) weeks of gestation prior to genetic analysis and stored in frozen form. Samples from eight cases of Down syndrome, two cases of trisomy 13, one case of trisomy 18, and 55 control pregnancies were hand-carried frozen to the USA and tested blindly. Samples were tested in a specific H-hCG immunoassay and values were normalized to creatinine concentration. Values were plotted against gestational age, and multiples of control pregnancy median (MoM) calculated. The median level of the MoMs of the eight Down syndrome cases was 3.6 MoM. Five of the eight Down syndrome cases exceeded the 90th centile of the 55 unaffected cases. The MoMs of the trisomy 13 and 18 pregnancies were 0.2, 0.2 and 0.3. All three cases were under the 10th centile of unaffected pregnancies. The results of this study indicate that H-hCG testing may be useful in screening for Down syndrome in the first trimester of pregnancy. Further studies are needed to assess the potential screening values of urine H-hCG and the combination of this test with free beta-subunit, PAPP-A and other markers for Down syndrome in the first trimester of pregnancy.

摘要

高糖基化人绒毛膜促性腺激素(H-hCG),也称为侵袭性滋养层抗原或ITA,是hCG的一种独特代谢变体,具有更复杂的寡糖侧链。其浓度与常规hCG无关。最近已证明,尿H-hCG是孕中期唐氏综合征筛查的高灵敏度标志物。我们评估了H-hCG作为孕早期潜在标志物的情况。在进行基因分析之前,于妊娠10(+0)至11(+6)周收集孕妇尿液样本,并冷冻保存。将8例唐氏综合征、2例13三体、1例18三体病例以及55例对照妊娠的样本冷冻后专人送往美国进行盲法检测。采用特定的H-hCG免疫测定法对样本进行检测,并将数值标准化为肌酐浓度。将数值与孕周作图,并计算对照妊娠中位数的倍数(MoM)。8例唐氏综合征病例的MoM中位数为3.6 MoM。8例唐氏综合征病例中有5例超过了55例未受影响病例的第90百分位数。13三体和18三体妊娠的MoM分别为0.2、0.2和0.3。所有3例均低于未受影响妊娠的第10百分位数。本研究结果表明,H-hCG检测可能有助于孕早期唐氏综合征的筛查。需要进一步研究以评估尿H-hCG的潜在筛查价值,以及该检测与游离β亚基、妊娠相关血浆蛋白A和其他孕早期唐氏综合征标志物联合检测的价值。

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