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本文引用的文献

1
Pathogenesis of preterm birth: bidirectional inflammation in mother and fetus.早产的发病机制:母婴双向炎症反应。
Semin Immunopathol. 2020 Aug;42(4):413-429. doi: 10.1007/s00281-020-00807-y. Epub 2020 Sep 7.
2
Novel pathways of inflammation in human fetal membranes associated with preterm birth and preterm pre-labor rupture of the membranes.与早产和胎膜早破相关的人胎膜炎症新途径。
Semin Immunopathol. 2020 Aug;42(4):431-450. doi: 10.1007/s00281-020-00808-x. Epub 2020 Aug 12.
3
Barriers to Accessing Maternal Care in Low Income Countries in Africa: A Systematic Review.非洲低收入国家获取孕产妇保健服务的障碍:系统评价。
Int J Environ Res Public Health. 2020 Jun 16;17(12):4292. doi: 10.3390/ijerph17124292.
4
Global burden of preterm birth.全球早产儿负担。
Int J Gynaecol Obstet. 2020 Jul;150(1):31-33. doi: 10.1002/ijgo.13195.
5
Low-dose aspirin for the prevention of preterm delivery in nulliparous women with a singleton pregnancy (ASPIRIN): a randomised, double-blind, placebo-controlled trial.低剂量阿司匹林用于预防初产妇单胎妊娠的早产(ASPIRIN):一项随机、双盲、安慰剂对照试验。
Lancet. 2020 Jan 25;395(10220):285-293. doi: 10.1016/S0140-6736(19)32973-3.
6
Air pollution and inflammation: Findings from concurrent repeated measures of systemic and reproductive tract cytokines during term pregnancy in Mexico City.空气污染与炎症:来自墨西哥城足月妊娠期间系统性和生殖道细胞因子同步重复测量的结果。
Sci Total Environ. 2019 Sep 1;681:235-241. doi: 10.1016/j.scitotenv.2019.05.041. Epub 2019 May 5.
7
Inflammation induced preterm labor and birth.炎症引起的早产和分娩。
J Reprod Immunol. 2018 Sep;129:53-58. doi: 10.1016/j.jri.2018.06.029. Epub 2018 Jun 30.
8
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.
9
Low-dose aspirin for prevention of morbidity and mortality from preeclampsia: a systematic evidence review for the U.S. Preventive Services Task Force.低剂量阿司匹林用于预防子痫前期的发病和死亡:美国预防服务工作组的系统证据回顾。
Ann Intern Med. 2014 May 20;160(10):695-703. doi: 10.7326/M13-2844.
10
Maternity waiting homes and traditional midwives in rural Liberia.利比里亚农村的母婴等候之家和传统助产士。
Int J Gynaecol Obstet. 2013 Nov;123(2):114-8. doi: 10.1016/j.ijgo.2013.05.024. Epub 2013 Aug 14.

孕期宫颈阴道细胞因子采集时间与早产:PRINCESA 队列的对比分析。

Timing of Cervico-Vaginal Cytokine Collection during Pregnancy and Preterm Birth: A Comparative Analysis in the PRINCESA Cohort.

机构信息

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.

Unidad de Vinculación Científica de la Facultad de Medicina, Universidad Nacional Autónoma de México en el Instituto Nacional de Medicina Genómica, Mexico City 14610, Mexico.

出版信息

Int J Environ Res Public Health. 2021 Mar 26;18(7):3436. doi: 10.3390/ijerph18073436.

DOI:10.3390/ijerph18073436
PMID:33810264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8036528/
Abstract

Preterm birth (PTB), defined as birth before 37 completed weeks of gestation, is a major cause of infant morbidity and mortality. Inflammation is an important component in the physiopathologic pathway leading to PTB but results from cross-sectional studies on associations between inflammation, as measured by cytokines, and PTB are inconsistent. Timing of cytokine measurement during pregnancy varies between studies and may contribute to inconsistent findings. We investigated the effects of timing on associations between 16 cervico-vaginal cytokines (Eotaxin, IL-10, IL-12p40, IL-17, IL-1RA, sIL-2rα, IL-1a, IL-1β, IL-2, IL-6, IP-10, MCP-1, MIP-1α, MIP-1β, TNFα, and VEGF) and PTB among 90 women throughout pregnancy. We used logistic regression to compare associations between concentrations of cervico-vaginal cytokines from periods in pregnancy and PTB. Trimester 1 cytokines had the strongest positive associations with PTB; for example, OR = 1.76 (95% confidence interval: 1.28, 2.42) for IL-6. Second and third trimester associations were weaker but largely positive. IL-1α was the only cytokine with a negative association (trimesters 2, 3 and overall pregnancy). Strong first trimester associations between cytokines and PTB suggest that measuring cytokines early in pregnancy may hold promise for early identification of PTB risk. Variations in cytokine measurement during pregnancy may contribute to inconsistencies among studies.

摘要

早产(PTB)定义为妊娠 37 周前分娩,是婴儿发病率和死亡率的主要原因。炎症是导致 PTB 的病理生理途径的重要组成部分,但来自炎症与 PTB 之间关联的横断面研究结果不一致,这些炎症是通过细胞因子来衡量的。怀孕期间细胞因子测量的时间在不同的研究中有所不同,这可能导致研究结果不一致。我们研究了在整个怀孕期间对 90 名女性的 16 种宫颈阴道细胞因子(Eotaxin、IL-10、IL-12p40、IL-17、IL-1RA、sIL-2rα、IL-1a、IL-1β、IL-2、IL-6、IP-10、MCP-1、MIP-1α、MIP-1β、TNFα和 VEGF)与 PTB 之间的关联随时间的变化。我们使用逻辑回归比较了怀孕期间宫颈阴道细胞因子浓度与 PTB 之间的关联。第一孕期细胞因子与 PTB 的正相关最强;例如,IL-6 的比值比(OR)为 1.76(95%置信区间:1.28,2.42)。第二和第三孕期的关联较弱,但大多为阳性。IL-1α 是唯一与 PTB 呈负相关的细胞因子(第二和第三孕期以及整个孕期)。细胞因子与 PTB 之间在第一孕期的强烈关联表明,在妊娠早期测量细胞因子可能有助于早期识别 PTB 风险。怀孕期间细胞因子测量的变化可能导致研究结果不一致。