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阴道微生物失调会增加早产胎膜破裂、新生儿败血症的风险,并且会因红霉素而加剧。

Vaginal dysbiosis increases risk of preterm fetal membrane rupture, neonatal sepsis and is exacerbated by erythromycin.

作者信息

Brown Richard G, Marchesi Julian R, Lee Yun S, Smith Ann, Lehne Benjamin, Kindinger Lindsay M, Terzidou Vasso, Holmes Elaine, Nicholson Jeremy K, Bennett Phillip R, MacIntyre David A

机构信息

Imperial College Parturition Research Group, Division of the Institute of Reproductive and Developmental Biology, Imperial College London, London, W12 0NN, UK.

Centre for Digestive and Gut Health, Imperial College London, London, W2 1NY, UK.

出版信息

BMC Med. 2018 Jan 24;16(1):9. doi: 10.1186/s12916-017-0999-x.

Abstract

BACKGROUND

Preterm prelabour rupture of the fetal membranes (PPROM) precedes 30% of preterm births and is a risk factor for early onset neonatal sepsis. As PPROM is strongly associated with ascending vaginal infection, prophylactic antibiotics are widely used. The evolution of vaginal microbiota compositions associated with PPROM and the impact of antibiotics on bacterial compositions are unknown.

METHODS

We prospectively assessed vaginal microbiota prior to and following PPROM using MiSeq-based sequencing of 16S rRNA gene amplicons and examined the impact of erythromycin prophylaxis on bacterial load and community structures.

RESULTS

In contrast to pregnancies delivering at term, vaginal dysbiosis characterised by Lactobacillus spp. depletion was present prior to the rupture of fetal membranes in approximately a third of cases (0% vs. 27%, P = 0.026) and persisted following membrane rupture (31%, P = 0.005). Vaginal dysbiosis was exacerbated by erythromycin treatment (47%, P = 0.00009) particularly in women initially colonised by Lactobacillus spp. Lactobacillus depletion and increased relative abundance of Sneathia spp. were associated with subsequent funisitis and early onset neonatal sepsis.

CONCLUSIONS

Our data show that vaginal microbiota composition is a risk factor for subsequent PPROM and is associated with adverse short-term maternal and neonatal outcomes. This highlights vaginal microbiota as a potentially modifiable antenatal risk factor for PPROM and suggests that routine use of erythromycin for PPROM be re-examined.

摘要

背景

胎膜早破(PPROM)发生在30%的早产之前,是早发性新生儿败血症的一个危险因素。由于PPROM与阴道上行感染密切相关,预防性使用抗生素被广泛应用。与PPROM相关的阴道微生物群组成的演变以及抗生素对细菌组成的影响尚不清楚。

方法

我们使用基于MiSeq的16S rRNA基因扩增子测序对PPROM前后的阴道微生物群进行前瞻性评估,并研究红霉素预防对细菌载量和群落结构的影响。

结果

与足月分娩的妊娠相比,约三分之一的病例在胎膜破裂前存在以乳酸杆菌属缺失为特征的阴道生态失调(0%对27%,P = 0.026),且在胎膜破裂后持续存在(31%,P = 0.005)。红霉素治疗会加剧阴道生态失调(47%,P = 0.00009),尤其是在最初由乳酸杆菌属定殖的女性中。乳酸杆菌缺失和斯奈氏菌属相对丰度增加与随后的脐带炎和早发性新生儿败血症有关。

结论

我们的数据表明,阴道微生物群组成是随后发生PPROM的一个危险因素,并与不良的短期母婴结局相关。这突出了阴道微生物群作为PPROM一个潜在可改变的产前危险因素,并建议重新审视红霉素在PPROM中的常规使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37e3/5782380/36b6294ca5bd/12916_2017_999_Fig1_HTML.jpg

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