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本文引用的文献

1
Angiogenic factors combined with clinical risk factors to predict preterm pre-eclampsia in nulliparous women: a predictive test accuracy study.将血管生成因子与临床危险因素相结合预测初产妇早产子痫前期:一项预测试验准确性研究。
BJOG. 2013 Sep;120(10):1215-23. doi: 10.1111/1471-0528.12195. Epub 2013 Mar 21.
2
Integrated proteomics pipeline yields novel biomarkers for predicting preeclampsia.综合蛋白质组学分析流程为预测子痫前期提供了新的生物标志物。
Hypertension. 2013 Jun;61(6):1281-8. doi: 10.1161/HYPERTENSIONAHA.113.01168. Epub 2013 Apr 1.
3
First-trimester prediction of preeclampsia in nulliparous women at low risk.早孕期预测低危初产妇子痫前期。
Obstet Gynecol. 2012 Jun;119(6):1234-42. doi: 10.1097/AOG.0b013e3182571669.
4
Sex-specific basis of severe placental dysfunction leading to extreme preterm delivery.导致极早产的严重胎盘功能障碍的性别特异性基础。
Placenta. 2012 Jul;33(7):568-71. doi: 10.1016/j.placenta.2012.03.011. Epub 2012 Apr 17.
5
The value of early second trimester PAPP-A and ADAM12 in screening for pre-eclampsia.早孕期 PAPP-A 和 ADAM12 在子痫前期筛查中的价值。
J Med Screen. 2012 Mar;19(1):51-4. doi: 10.1258/jms.2012.011085. Epub 2012 Feb 22.
6
The secretion of PAPP-A, ADAM12, and PP13 correlates with the size of the placenta for the first month of pregnancy.妊娠第一个月时,PAPP-A、ADAM12 和 PP13 的分泌与胎盘的大小相关。
Placenta. 2011 Dec;32(12):999-1003. doi: 10.1016/j.placenta.2011.10.005. Epub 2011 Oct 19.
7
Clinical risk prediction for pre-eclampsia in nulliparous women: development of model in international prospective cohort.国际前瞻性队列研究中对初产妇先兆子痫的临床风险预测:模型的建立。
BMJ. 2011 Apr 7;342:d1875. doi: 10.1136/bmj.d1875.
8
Prediction of early, intermediate and late pre-eclampsia from maternal factors, biophysical and biochemical markers at 11-13 weeks.从 11-13 周的母体因素、生物物理和生化标志物预测早发型、中间型和晚发型子痫前期。
Prenat Diagn. 2011 Jan;31(1):66-74. doi: 10.1002/pd.2660.
9
Acid-labile subunit (ALS) gene expression and protein content in human placentas: differences according to birth weight.人胎盘酸不稳定亚基(ALS)基因表达和蛋白含量:按出生体重的差异。
J Clin Endocrinol Metab. 2011 Jan;96(1):187-91. doi: 10.1210/jc.2010-0244. Epub 2010 Oct 13.
10
Robust early pregnancy prediction of later preeclampsia using metabolomic biomarkers.利用代谢组学生物标志物进行稳健的早期妊娠子痫前期预测。
Hypertension. 2010 Oct;56(4):741-9. doi: 10.1161/HYPERTENSIONAHA.110.157297.

中孕期母体 ADAM12 水平在子痫前期合并妊娠中根据胎儿性别而有所不同。

Mid-trimester maternal ADAM12 levels differ according to fetal gender in pregnancies complicated by preeclampsia.

机构信息

Maternal & Fetal Heath Research Centre, Manchester Academic Health Science Centre, University of Manchester, Central Manchester NHS Trust, Manchester, United Kingdom

Pronota, Zwijnaarde, Belgium.

出版信息

Reprod Sci. 2015 Feb;22(2):235-41. doi: 10.1177/1933719114537713. Epub 2014 Jun 4.

DOI:10.1177/1933719114537713
PMID:24899472
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4287597/
Abstract

An overrepresentation of adverse pregnancy outcomes has been observed in pregnancies associated with a male fetus. We investigated the association between fetal gender and candidate biomarkers for preeclampsia. Proteins were quantified in samples taken at 20 weeks from women recruited to the SCreening fOr Pregnancy Endpoints (SCOPE) study (preeclampsia n = 150; no preeclampsia n = 450). In contrast to placental growth factor, soluble endoglin, and insulin-like growth factor acid labile subunit, levels of metallopeptidase domain 12 (ADAM12) at 20 weeks were dependent on fetal gender in pregnancies complicated by preeclampsia, for male (n = 73) fetuses the multiples of the median (MoM; interquartile range [IQR] 1.1-1.5) was 1.3, whereas for female fetuses (n = 75) MoM was 1.1 (1.0-1.3); P < .01. Prediction of preeclampsia using ADAM12 levels was improved for pregnancies associated with a male fetus (area under receiver-operator curve [AUC] 0.73 [95% confidence interval [CI] 0.67-0.80]) than that of a female fetus (AUC 0.62 [0.55-0.70]); P = .03. The data presented here fit a contemporary hypothesis that there is a difference between the genders in response to an adverse maternal environment and suggest that an alteration in ADAM12 may reflect an altered placental response in pregnancies subsequently complicated by preeclampsia.

摘要

已有研究观察到,与男性胎儿相关的妊娠中不良妊娠结局的发生率更高。我们研究了胎儿性别与子痫前期候选生物标志物之间的关系。我们在 20 周时,从参加 SCreening fOr Pregnancy Endpoints(SCOPE)研究的女性(子痫前期患者 n = 150;无子痫前期患者 n = 450)中采集样本,定量检测了蛋白水平。与胎盘生长因子、可溶性内皮糖蛋白和胰岛素样生长因子酸不稳定亚基不同,在伴有子痫前期的妊娠中,20 周时金属肽酶结构域 12(ADAM12)的水平取决于胎儿性别,男性(n = 73)胎儿的倍数中位数(MoM;四分位距 [IQR] 1.1-1.5)为 1.3,而女性胎儿(n = 75)MoM 为 1.1(1.0-1.3);P <.01。使用 ADAM12 水平预测子痫前期,对于与男性胎儿相关的妊娠,其曲线下面积(AUC)为 0.73(95%置信区间 [CI] 0.67-0.80),优于女性胎儿(AUC 0.62 [0.55-0.70]);P =.03。这里呈现的数据符合一种现代假说,即女性对不良母体环境的反应存在性别差异,并表明 ADAM12 的改变可能反映了随后子痫前期妊娠中胎盘反应的改变。