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妊娠中期血清标志物对染色体正常和无脑儿畸形胎儿心脏缺陷的预测价值。

Second trimester serum predictors of congenital heart defects in pregnancies without chromosomal or neural tube defects.

机构信息

California Department of Public Health, Genetic Disease Screening Program, Richmond, CA, USA.

出版信息

Prenat Diagn. 2011 May;31(5):466-72. doi: 10.1002/pd.2720. Epub 2011 Feb 24.

Abstract

OBJECTIVE

To compare euploid pregnancies with congenital heart defects (CHDs) to similar pregnancies without CHDs on typically collected second trimester biomarker measurements.

METHOD

Second trimester serum levels of alpha-fetoprotein (AFP), human chorionic gonadotrophin (hCG), and unconjugated estriol were compared for 306 CHD cases and 1224 no-CHD controls drawn from a sample of singleton pregnancies without chromosomal or neural tube defects (NTDs). Logistic regression models were built comparing biomarkers for cases and controls.

RESULTS

Regardless of the severity of defect, CHD cases were more likely to have unusually high AFP and/or hCG levels and/or unusually low hCG and/or uE3 levels [odds ratio (OR) 1.8-2.4, 95% confidence intervals (CIs) 1.2-4.0]. Cases with critical CHDs were more than twice as likely to have an AFP multiple of the median (MoM) ≥ the 95th percentile and/or an hCG and/uE3 MoM ≤ the 5th percentile (OR 2.1-3.9, 95% CIs 1.1-7.8).

CONCLUSION

Abnormal levels of specific second trimester maternal serum biomarkers indicated an increased risk for CHDs among this sample of low risk pregnancies. Our data suggest that future efforts aimed at improving CHD detection in low risk pregnancies may benefit from considering serum biomarkers.

摘要

目的

比较患有先天性心脏病(CHD)的正常二倍体妊娠与无 CHD 的类似妊娠在通常收集的中期二联生物标志物测量值方面的差异。

方法

从无染色体或神经管缺陷(NTD)的单胎妊娠样本中抽取了 306 例 CHD 病例和 1224 例无 CHD 对照,比较了这些病例和对照的血清中甲胎蛋白(AFP)、人绒毛膜促性腺激素(hCG)和未结合雌三醇的水平。构建了比较病例和对照生物标志物的逻辑回归模型。

结果

无论缺陷的严重程度如何,CHD 病例均更有可能出现异常高的 AFP 和/或 hCG 水平和/或异常低的 hCG 和/或 uE3 水平[比值比(OR)为 1.8-2.4,95%置信区间(CI)为 1.2-4.0]。患有严重 CHD 的病例 AFP 中位数倍数(MoM)≥第 95 百分位和/或 hCG 和/uE3 MoM≤第 5 百分位的可能性高出两倍以上(OR 2.1-3.9,95%CI 为 1.1-7.8)。

结论

特定中期母体血清生物标志物的异常水平表明,该低风险妊娠样本中 CHD 的风险增加。我们的数据表明,未来旨在提高低风险妊娠中 CHD 检出率的努力可能受益于考虑血清生物标志物。

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