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Maternal urinary beta-core fragment of hCG/creatinine ratios and fetal chromosomal abnormalities in the second trimester of pregnancy.

机译:孕中期孕妇的hCG /肌酐比值和胎儿染色体异常的尿β-核心片段。

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Our aim was to evaluate the potential value of the ratio of the maternal urinary beta-core fragment of human chorionic gonadotropin (beta C-hCG) to creatinine (Cr) in discriminating between normal pregnancies and pregnancies associated with fetal chromosomal abnormalities. We hypothesized that pregnancies with fetal chromosomal abnormalities had abnormal quantities of beta C-hCG in the urine. The aims of the present study were to investigate retrospectively whether maternal urinary ratios of beta C-hCG/Cr are abnormal in women carrying fetuses with chromosome aberrations and to determine normative median values and a reference range for beta C-hCG/Cr between 14 and 19 weeks' gestation. Maternal urinary beta C-hCG and Cr concentrations were measured in 150 healthy women from 14 to 19 weeks and compared with ten cases of fetal chromosomal abnormalities matched for gestational age. The preliminary cut-off points corresponded to 0.29 multiple of the normal median (MOM) and 2.83 MOM, which were equivalent to the tenth and 90th centiles of the normal range. Of ten cases of fetal chromosomal abnormalities, one out of one (100 per cent) case with trisomy 18 and three of four (75 per cent) cases of variant 9 chromosomes had low beta C-hCG/Cr (< or = 0.29 MOM). One of five (20 per cent) cases with Down syndrome had elevated beta C-hCG/Cr (> or = 2.83 MOM). Urinary beta C-hCG/Cr ratios obtained in the second trimester may be useful for improved detection efficiency of Down syndrome, trisomy 18, and inversion of chromosome 9. Second-trimester maternal urinary beta C-hCG/Cr should be investigated further as a potential marker for fetal chromosome anomalies.
机译:我们的目的是评估人绒毛膜促性腺激素(βC-hCG)与肌酐(Cr)的母体尿β-核心片段之比在区分正常妊娠和与胎儿染色体异常相关的妊娠中的潜在价值。我们假设,胎儿染色体异常的孕妇尿液中的βC-hCG含量异常。本研究的目的是回顾性研究携带染色体畸变胎儿的妇女的母体尿中βC-hCG / Cr的尿比是否异常,并确定βC-hCG / Cr的标准中位数和参考范围在14至怀孕19周。在150例14至19周的健康妇女中测量了母体尿中βC-hCG和Cr的浓度,并与10例与胎龄相匹配的胎儿染色体异常进行了比较。初始截止点对应于正常中位数(MOM)的0.29倍和2.83 MOM,分别相当于正常范围的十分之一和90百分位数。在10例胎儿染色体异常病例中,三分之一(18%的三分之一)(100%)和9号变体染色体的四分之三(75%)中的三例具有低βC-hCG / Cr(<或= 0.29 MOM) 。唐氏综合症的五分之一(20%)病例的βC-hCG / Cr升高(≥或等于2.83 MOM)。在妊娠中期获得的尿中βC-hCG / Cr比率可能有助于提高唐氏综合症,18三体性和9号染色体倒置的检测效率。妊娠中期,孕妇应进一步研究孕中期βC-hCG / Cr。胎儿染色体异常的潜在标志。

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