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本文引用的文献

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C-Reactive Protein Levels at the Midpregnancy Can Predict Gestational Complications.中孕期 C 反应蛋白水平可预测妊娠并发症。
Biomed Res Int. 2018 Nov 7;2018:1070151. doi: 10.1155/2018/1070151. eCollection 2018.
2
Associations between repeated ultrasound measures of fetal growth and biomarkers of maternal oxidative stress and inflammation in pregnancy.孕期胎儿生长的重复超声测量与母体氧化应激和炎症生物标志物之间的关联。
Am J Reprod Immunol. 2018 Oct;80(4):e13017. doi: 10.1111/aji.13017. Epub 2018 Jul 8.
3
Inflammation-Induced Adverse Pregnancy and Neonatal Outcomes Can Be Improved by the Immunomodulatory Peptide Exendin-4.炎症引起的不良妊娠和新生儿结局可通过免疫调节肽 Exendin-4 得到改善。
Front Immunol. 2018 Jun 18;9:1291. doi: 10.3389/fimmu.2018.01291. eCollection 2018.
4
Plasma inflammatory and immune proteins as predictors of intra-amniotic infection and spontaneous preterm delivery in women with preterm labor: a retrospective study.血浆炎症和免疫蛋白作为早产妇女羊膜腔内感染和自发性早产的预测指标:一项回顾性研究
BMC Pregnancy Childbirth. 2018 May 9;18(1):146. doi: 10.1186/s12884-018-1780-7.
5
Maternal serum C-reactive protein concentration and intra-amniotic inflammation in women with preterm prelabor rupture of membranes.胎膜早破早产女性的母血C反应蛋白浓度与羊膜腔内炎症
PLoS One. 2017 Aug 16;12(8):e0182731. doi: 10.1371/journal.pone.0182731. eCollection 2017.
6
Maternal c-reactive protein and oxidative stress markers as predictors of delivery latency in patients experiencing preterm premature rupture of membranes.母体C反应蛋白和氧化应激标志物作为胎膜早破患者分娩延迟的预测指标。
Int J Gynaecol Obstet. 2017 Feb;136(2):145-150. doi: 10.1002/ijgo.12024. Epub 2016 Nov 18.
7
Pre-pregnancy maternal plasma cytokine levels and risks of small-for-gestational-age at birth.孕前母体血浆细胞因子水平与出生时小于胎龄儿的风险
J Matern Fetal Neonatal Med. 2016 Dec;29(24):4065-9. doi: 10.3109/14767058.2016.1156669. Epub 2016 Mar 24.
8
The use of maternal C-reactive protein in the predicting of preterm labor and tocolytic therapy in preterm labor women.母体C反应蛋白在预测早产及早产妇女的宫缩抑制剂治疗中的应用。
Adv Biomed Res. 2014 Jul 31;3:154. doi: 10.4103/2277-9175.137864. eCollection 2014.
9
Angiogenic and inflammatory biomarkers in midpregnancy and small-for-gestational-age outcomes in Tanzania.坦桑尼亚孕中期血管生成和炎症生物标志物与小于胎龄儿结局
Am J Obstet Gynecol. 2014 Nov;211(5):509.e1-8. doi: 10.1016/j.ajog.2014.05.032. Epub 2014 May 29.
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Longitudinal profiling of inflammatory cytokines and C-reactive protein during uncomplicated and preterm pregnancy.非复杂性妊娠和早产期间炎症细胞因子及C反应蛋白的纵向分析
Am J Reprod Immunol. 2014 Sep;72(3):326-36. doi: 10.1111/aji.12265. Epub 2014 May 8.

孕早期母体血清C反应蛋白水平预测胎儿生长受限和早产:一项前瞻性队列研究。

Maternal serum levels of C-reactive protein at early pregnancy to predict fetal growth restriction and preterm delivery: A prospective cohort study.

作者信息

Nikbakht Roshan, Moghadam Elham Karimi, Nasirkhani Zeinab

机构信息

Fertility Infertility and Perinatology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

Int J Reprod Biomed. 2020 Mar 29;18(3):157-164. doi: 10.18502/ijrm.v18i3.6710. eCollection 2020 Mar.

DOI:10.18502/ijrm.v18i3.6710
PMID:32309764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7142318/
Abstract

BACKGROUND

A considerable evidence suggests that maternal inflammation dysregulation may play as a risk factor for both maternal and neonatal outcomes. The study's objectives were designed to evaluate the correlation between serum C-reactive protein (CRP) levels, as an inflammation factor, preterm delivery, and small for gestational age (SGA) births.

MATERIALS AND METHODS

This prospective cohort study was conducted on 120 singleton pregnant women with gestational age less than 20 wk. Maternal CRP serum concentration was measured before 20 wk gestation. Patients were followed-up until the delivery and final outcomes of pregnancy were recorded in terms of preterm delivery and SGA births. : Serum CRP levels in participants with normal fetuses and SGA births were 4.09 1.35 mg/l and 6.04 3.29 mg/l, respectively (p = 0.19), while in cases of preterm delivery, it was 9.63 5.78 mg/l (p 0.001). By using receiver operating characteristic (ROC) curve, serum CRP levels (cut-off point 5.27 mg/l, area 0.836) had acceptable diagnostic accuracy value in distinguishing preterm delivery (sensitivity (75%), specificity (86.1%), positive predictive value (37.5%), negative predictive value (96.87%), accuracy (85%)) and serum CRP levels (cut-off point 6.67 mg/l, area 0.673) in distinguishing SGA births (sensitivity (50%), specificity (91.2%), positive predictive value (23.07%), and negative predictive value (97.19%), and accuracy (89.16 %)).

CONCLUSION

Higher maternal serum CRP levels measured early in pregnancy may associate with higher risk of preterm delivery and SGA.

摘要

背景

大量证据表明,母体炎症调节异常可能是影响母体和新生儿结局的一个危险因素。本研究旨在评估作为炎症因子的血清C反应蛋白(CRP)水平与早产及小于胎龄(SGA)儿出生之间的相关性。

材料与方法

本前瞻性队列研究对120名单胎妊娠且孕周小于20周的孕妇进行。在妊娠20周前测量母体血清CRP浓度。对患者进行随访直至分娩,并记录妊娠的最终结局,包括早产和SGA儿出生情况。正常胎儿组和SGA儿出生组参与者的血清CRP水平分别为4.09±1.35mg/L和6.04±3.29mg/L(p = 0.19),而早产组为9.63±5.78mg/L(p<0.001)。通过绘制受试者工作特征(ROC)曲线,血清CRP水平(截断点为5.27mg/L,曲线下面积为0.836)在区分早产方面具有可接受的诊断准确性(敏感性(75%)、特异性(86.1%)、阳性预测值(37.5%)、阴性预测值(96.87%)、准确性(85%));血清CRP水平(截断点为6.67mg/L,曲线下面积为0.673)在区分SGA儿出生方面(敏感性(50%)、特异性(91.2%)、阳性预测值(23.07%)、阴性预测值(97.19%)、准确性(89.16%))。

结论

妊娠早期测得的母体血清CRP水平较高可能与早产和SGA儿出生的较高风险相关。