益生菌对先兆早产孕妇早产率的影响(PROPEV试验)

The Effect of Probiotics on Preterm Birth Rates in Pregnant Women After a Threatened Preterm Birth Episode (The PROPEV Trial).

作者信息

Del Barco Ester, Molano Leidy-Alejandra G, Vargas Mireia, Miserachs Marta, Puerto Linda, Garrido-Giménez Carmen, Soler Zaida, Muñoz Begoña, Pratcorona Laia, Rimbaut Sonia, Vidal Mercè, Dalmau Marta, Casellas Alba, Carreras Elena, Manichanh Chaysavanh, Goya Maria

机构信息

Maternal-Fetal Medicine Unit, Department of Obstetrics, Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain.

Microbiome Lab, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron, 08035 Barcelona, Spain.

出版信息

Biomedicines. 2025 May 8;13(5):1141. doi: 10.3390/biomedicines13051141.

Abstract

: Preterm birth is the leading cause of perinatal mortality worldwide, with prevalence rates showing little reduction. Although mortality rates have decreased, morbidity rates remain concerningly high. In recent years, there has been a surge in studies examining the etiology, risk factors, and management of preterm birth. The use of vaginal probiotics in pregnant women at risk of preterm birth has garnered attention as a potential approach for improving perinatal outcomes and modulating the vaginal microbiota. However, the efficacy of this intervention remains unclear. Therefore, this study explored the impact of vaginal probiotics on perinatal outcomes and vaginal microbiota composition in pregnant women at risk of preterm birth. : This was a randomized, prospective, longitudinal, double-blind, placebo-controlled, multicentric trial conducted across seven maternities in Spain from October 2017 to August 2022 in pregnant women at risk of preterm birth. Participants were randomly assigned to receive vaginal probiotics containing four lactobacilli strains or a placebo. The primary outcome was to explore a potential correlation between probiotic use among pregnant women at risk of preterm birth and the actual rate of preterm birth before 37 gestational weeks. Secondary outcomes included an evaluation of preterm birth rates, neonatal morbidity, the vaginal microbiota, and changes in the vaginal microbiota after receiving probiotics. Other secondary outcomes were identifying vaginal microbiota patterns associated with preterm birth and exploring potential therapeutic mechanisms involving probiotics. Trial registration: Clinicaltrials.gov, identifier: NCT03689166. : A total of 200 participants were included. Of those, birth data were obtained for 181 women. Demographics were similar between both groups. An analysis of perinatal outcomes found no significant differences in preterm birth rates, prematurity rates, gestational weeks at delivery, neonatal complications, time to birth, or latency time to delivery. Microbiota analysis showed no significant differences in vaginal microbiota changes between groups. No serious or unexpected adverse reactions were reported. : There were no statistically significant differences for spontaneous preterm birth between pregnant women receiving probiotics and pregnant women receiving the placebo.

摘要

早产是全球围产期死亡的主要原因,其患病率几乎没有下降。尽管死亡率有所降低,但发病率仍然高得令人担忧。近年来,研究早产的病因、风险因素和管理的研究激增。在有早产风险的孕妇中使用阴道益生菌作为改善围产期结局和调节阴道微生物群的一种潜在方法已引起关注。然而,这种干预措施的疗效仍不明确。因此,本研究探讨了阴道益生菌对有早产风险的孕妇围产期结局和阴道微生物群组成的影响。

这是一项随机、前瞻性、纵向、双盲、安慰剂对照、多中心试验,于2017年10月至2022年8月在西班牙的七个产科对有早产风险的孕妇进行。参与者被随机分配接受含有四种乳酸杆菌菌株的阴道益生菌或安慰剂。主要结果是探讨有早产风险的孕妇使用益生菌与妊娠37周前实际早产率之间的潜在相关性。次要结果包括评估早产率、新生儿发病率、阴道微生物群以及接受益生菌后阴道微生物群的变化。其他次要结果是确定与早产相关的阴道微生物群模式,并探索涉及益生菌的潜在治疗机制。试验注册:Clinicaltrials.gov,标识符:NCT03689166。

总共纳入了200名参与者。其中,获得了181名女性的分娩数据。两组的人口统计学特征相似。围产期结局分析发现,早产率、早产发生率、分娩孕周、新生儿并发症、分娩时间或分娩潜伏期没有显著差异。微生物群分析显示,两组之间阴道微生物群变化没有显著差异。未报告严重或意外的不良反应。

接受益生菌的孕妇与接受安慰剂的孕妇在自然早产方面没有统计学上的显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7963/12109440/cba8884d2c19/biomedicines-13-01141-ch001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索