Skip to content
Gallery
Diosa Ara Research Database (Confidential)
Research Dashboard
Share
Explore
Literature

Untitled

Bibliography

Chan, D., Bennett, P. R., Lee, Y. S., Kundu, S., Teoh, T. G., Adan, M., Ahmed, S., Brown, R. G., David, A. L., Lewis, H. V., Gimeno-Molina, B., Norman, J. E., Stock, S. J., Terzidou, V., Kropf, P., Botto, M., MacIntyre, D. A., & Sykes, L. (2022). Microbial-driven preterm labour involves crosstalk between the innate and adaptive immune response. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-28620-1
Fettweis, J. M., Serrano, M. G., Brooks, J. P., Edwards, D. J., Girerd, P. H., Parikh, H. I., Huang, B., Arodz, T. J., Edupuganti, L., Glascock, A. L., Xu, J., Jimenez, N. R., Vivadelli, S. C., Fong, S. S., Sheth, N. U., Jean, S., Lee, V., Bokhari, Y. A., Lara, A. M., … Buck, G. A. (2019). The vaginal microbiome and preterm birth. Nature Medicine, 25(6), 1012–1021. https://doi.org/10.1038/s41591-019-0450-2
Kindschuh, W. F., Baldini, F., Liu, M. C., Liao, J., Meydan, Y., Lee, H. H., Heinken, A., Thiele, I., Thaiss, C. A., Levy, M., & Korem, T. (2023). Preterm birth is associated with xenobiotics and predicted by the vaginal metabolome. Nature Microbiology, 8(2), 246–259. https://doi.org/10.1038/s41564-022-01293-8
Liu, Y., & Gao, L. (2021). Preterm Labor, a Syndrome Attributed to the Combination of External and Internal Factors. Maternal-Fetal Medicine, 4(1), 61–71. https://doi.org/10.1097/fm9.0000000000000136
Kindschuh, W. F., Baldini, F., Liu, M. C., Liao, J., Meydan, Y., Lee, H. H., Heinken, A., Thiele, I., Thaiss, C. A., Levy, M., & Korem, T. (2023). Preterm birth is associated with xenobiotics and predicted by the vaginal metabolome. Nature Microbiology, 8(2), 246–259. https://doi.org/10.1038/s41564-022-01293-8
Gudnadottir, U., Debelius, J. W., Du, J., Hugerth, L. W., Danielsson, H., Schuppe-Koistinen, I., Fransson, E., & Brusselaers, N. (2022). The vaginal microbiome and the risk of preterm birth: a systematic review and network meta-analysis. Scientific Reports, 12(1). https://doi.org/10.1038/s41598-022-12007-9
Nadeem, L., Lye, S. J., & Shynlova, O. (2019). Genetics and Genomics of Preterm Birth. In Human Reproductive and Prenatal Genetics (pp. 335–360). Elsevier. https://doi.org/10.1016/b978-0-12-813570-9.00015-2
Gomez-Lopez, N., Galaz, J., Miller, D., Farias-Jofre, M., Liu, Z., Arenas-Hernandez, M., Garcia-Flores, V., Shaffer, Z., Greenberg, J. M., Theis, K. R., & Romero, R. (2022). The immunobiology of preterm labor and birth: intra-amniotic inflammation or breakdown of maternal–fetal homeostasis. Reproduction, 164(2), R11–R45. https://doi.org/10.1530/rep-22-0046
Green, E. S., & Arck, P. C. (2020). Pathogenesis of preterm birth: bidirectional inflammation in mother and fetus. Seminars in Immunopathology, 42(4), 413–429. https://doi.org/10.1007/s00281-020-00807-y
Green, E. S., & Arck, P. C. (2020). Pathogenesis of preterm birth: bidirectional inflammation in mother and fetus. Seminars in Immunopathology, 42(4), 413–429. https://doi.org/10.1007/s00281-020-00807-y
Areia, A. L., & Mota-Pinto, A. (2022). Inflammation and Preterm Birth: A Systematic Review. Reproductive Medicine, 3(2), 101–111. https://doi.org/10.3390/reprodmed3020009

The vaginal microbiome and the risk of preterm birth: a systematic review and network meta-analysis

Unnur Gudnadottir; Justine W. Debelius; Juan Du; Luisa W. Hugerth; Hanna Danielsson; Ina Schuppe-Koistinen; Emma Fransson; Nele Brusselaers
2022

Abstract

Preterm birth is a major cause of neonatal morbidity and mortality worldwide. Increasing evidence links the vaginal microbiome to the risk of spontaneous preterm labour that leads to preterm birth. The aim of this systematic review and network meta-analysis was to investigate the association between the vaginal microbiome, defined as community state types (CSTs, i.e. dominance of specific lactobacilli spp, or not (low-lactobacilli)), and the risk of preterm birth. Systematic review using PubMed, Web of Science, Embase and Cochrane library was performed. Longitudinal studies using culture-independent methods categorizing the vaginal microbiome in at least three different CSTs to assess the risk of preterm birth were included. A (network) meta-analysis was conducted, presenting pooled odds ratios (OR) and 95% confidence intervals (CI); and weighted proportions and 95% CI. All 17 studies were published between 2014 and 2021 and included 38–539 pregnancies and 8–107 preterm births. Women presenting with “low-lactobacilli” vaginal microbiome were at increased risk (OR 1.69, 95% CI 1.15–2.49) for delivering preterm compared to Lactobacillus crispatus dominant women. Our network meta-analysis supports the microbiome being predictive of preterm birth, where low abundance of lactobacilli is associated with the highest risk, and L. crispatus dominance the lowest.

Key points

● Preterm birth (< 37 completed gestation weeks), which accounts for over 10% of births worldwide, is a major cause of neonatal mortality and morbidity[1]
● Original studies were eligible if they reported the risk of preterm birth in at least three community state types (CSTs) or vaginal microbiome compositions[6], with sufficient data to report the risk per individual and not per number of samples if multiple samples were collected per woman
● In the final selection of studies, seven were excluded because a lack of CST grouping[11,21,22,23,24,25,26], all women receiving cervical cerclage[27], sampling after signs of labor[28], no information regarding preterm birth for current pregnancy[29], only the use of polymerase chain reaction (PCR) instead of sequencing[30] or multiple CSTs assigned to each woman because of multiple sampling points[31]
● The risk of preterm birth was higher among women presenting with “low-lactobacilli” compared to L. crispatus (Fig. 4)
● Ranking tests showed that the L. crispatus dominant group was most probable to be the “best” microbiome composition, and L. jensenii the most probably the “worst” group considering the association with preterm birth
● The diversity of the vaginal microbiome seems to play a part in the risk of preterm birth, where women with low abundance of lactobacilli were at greater risk of delivering preterm compared to women with L. crispatus dominant microbiome

Summary

Introduction Many factors can trigger premature labour onset, including preterm premature rupture of membranes (PPROM), infections (e.g. Trichomonas vaginalis and Chlamydia trachomatis2) and microbial invasion of the amniotic cavity[3,4].
The vaginal microbiome is thought to protect from such infections, with low diversity microbiome dominated by Lactobacillus species considered “healthy”.
A diverse microbiome with low abundance of lactobacilli and high amounts of anaerobic bacteria can cause dysbiosis, overlapping with the clinical bacterial vaginosis (BV) diagnosis[5,6,7].
It has been proposed that different Lactobacillus species may present different risk profiles for various adverse events[5,8].
Since vaginal dysbiosis affects millions of women, it is important to understand the role of the vaginal microbiome in preterm birth[5,11].
There are few studies available that assess the relationship between the vaginal microbiome and preterm birth, with conflicting findings on whether the vaginal microbiome can influence the risk of preterm birth[2,12]
Methods Longitudinal studies were considered, in which the vaginal microbiome was assessed clearly before the onset of labour, including premature rupture of membranes and other labour-associated complications; and in which all participants were followed up until delivery.
Studies exclusively including high risk pregnancies were excluded to minimize the effects of risk factors apart from the microbiome.
Original studies were eligible if they reported the risk of preterm birth in at least three CSTs or vaginal microbiome compositions[6], with sufficient data to report the risk per individual and not per number of samples if multiple samples were collected per woman.
The earliest pregnancy samples were used for the analysis if feasible.
As this study is based on aggregated data, the authors used the categorization of preterm and term delivery as reported in each paper, yet if possible, the categorization of the World Health Organization was used, defining preterm birth as birth before 37 completed weeks of gestation[1]
Results Out of 4321 unique articles, 17 cohort studies were included, all published in English between 2014 and 2021 (Fig. 1).
The number of pregnancies per study ranged between 38 and 539, with 8 and 107 preterm births.
In the final selection of studies, seven were excluded because a lack of CST grouping[11,21,22,23,24,25,26], all women receiving cervical cerclage[27], sampling after signs of labor[28], no information regarding preterm birth for current pregnancy[29], only the use of polymerase chain reaction (PCR) instead of sequencing[30] or multiple CSTs assigned to each woman because of multiple sampling points[31]
Conclusion This network meta-analysis suggests that women with a “low-lactobacilli” vaginal microbiome composition were at higher risk of preterm birth compared to women with L. crispatus dominant microbiome compositions. The authors' systematic review and network meta-analysis is the first of its kind, since only one meta-analysis had previously been done on this subject, which used individual level sequencing data[16].
CSTs are more complimentary to the current knowledge, and not ideal, are good for clinical uses and for identifying targets for future developments.
The authors see both meta-analysis approaches as complementary.
Most common were subgroups of the diverse non-lactobacilli dominant group, but there was not enough uniformity between those in the studies to use subgrouping for this analysis.
Despite these factors, the inconsistency tests gave robust results showing that the method is stable enough to use the results

Introduction

Preterm birth (< 37 completed gestation weeks), which accounts for over 10% of births worldwide, is a major cause of neonatal mortality and morbidity[1]. Many factors can trigger premature labour onset, including preterm premature rupture of membranes (PPROM), infections (e.g. Trichomonas vaginalis and Chlamydia trachomatis2) and microbial invasion of the amniotic cavity[3,4]. The vaginal microbiome is thought to protect from such infections, with low diversity microbiome dominated by Lactobacillus species considered “healthy”. In contrast, a diverse microbiome with low abundance of lactobacilli and high amounts of anaerobic bacteria can cause dysbiosis, overlapping with the clinical bacterial vaginosis (BV) diagnosis[5,6,7]. BV is often asymptomatic, yet has been associated with higher risks of genital infections and complications, including human papillomavirus (HPV) infections[8,9] and pelvic inflammatory disease[10]. It has also been proposed that different Lactobacillus species may present different risk profiles for various adverse events[5,8]. Since vaginal dysbiosis affects millions of women, it is important to understand the role of the vaginal microbiome in preterm birth[5,11]. Currently there are few studies available that assess the relationship between the vaginal microbiome and preterm birth, with conflicting findings on whether the vaginal microbiome can influence the risk of preterm birth[2,12].

Methods

Study selection and criteria Only longitudinal studies were considered, in which the vaginal microbiome was assessed clearly before the onset of labour, including premature rupture of membranes and other labour-associated complications; and in which all participants were followed up until delivery. Studies exclusively including high risk pregnancies were excluded to minimize the effects of risk factors apart from the microbiome (e.g., only women with prior preterm birth, cervical weakness). Original studies were eligible if they reported the risk of preterm birth in at least three CSTs or vaginal microbiome compositions[6], with sufficient data to report the risk per individual and not per number of samples if multiple samples were collected per woman. The earliest pregnancy samples were used for the analysis if feasible. To enable the identification of species without the need for culturing, 16S analysis of samples was preferred. Since 16S sequencing techniques have only been available recently, only studies published since 2010 were included. As this study is based on aggregated data, we used the categorization of preterm and term delivery as reported in each paper, yet if possible, the categorization of the World Health Organization was used, defining preterm birth as birth before 37 completed weeks of gestation[1].

Results

Study selection Out of 4321 unique articles, 17 cohort studies were included, all published in English between 2014 and 2021 (Fig. 1). None of the 79 retrieved studies in other languages were relevant. The number of pregnancies per study ranged between 38 and 539, with 8 and 107 preterm births. PRISMA flowchart of selection of articles included in the network meta-analysis. The most common exclusion criteria of otherwise eligible studies were the lack of CST grouping of results (Supplementary Table S3). In the final selection of studies, seven were excluded because a lack of CST grouping[11,21,22,23,24,25,26], all women receiving cervical cerclage[27], sampling after signs of labor[28], no information regarding preterm birth for current pregnancy[29], only the use of polymerase chain reaction (PCR) instead of sequencing[30] or multiple CSTs assigned to each woman because of multiple sampling points[31].

Discussion

This network meta-analysis suggests that women with a “low-lactobacilli” vaginal microbiome composition were at higher risk of preterm birth (spontaneous and overall) compared to women with L. crispatus dominant microbiome compositions. Our systematic review and network meta-analysis is the first of its kind, since only one meta-analysis had previously been done on this subject, which used individual level sequencing data[16]. We chose CSTs over individual sequencing data because there can be a lack of open access to the data leading to selection bias of studies, and updating the recently published individual patient data meta-analysis would not have contributed any new information to the field. Furthermore, CSTs are more complimentary to the current knowledge, and although not ideal, are good for clinical uses and for identifying targets for future developments. Therefore, we see both meta-analysis approaches as complementary. Although we also had to exclude six otherwise eligible studies because CSTs were not reported, we were able to include 17 studies, compared to the six studies of the previous meta-analysis[16] (only one study in common[4]). Authors of the excluded papers were contacted for data but never replied. As mentioned above, heterogeneity of methods may propose problems and decrease the number of studies which can be included in individual patient data meta-analyses. Nonetheless, by using CST categorization we were able to compare five different groups (CSTs) to each other in this network approach, instead of just using two groups as is common in classic meta-analyses. The use of CSTs was first described in a small cohort study from 20106 and has been widely used despite its challenges and limitations[47,48], but it is currently the best option in the field to categorize vaginal microbiome compositions. Many of the included studies used an adapted form of the original CSTs, using a range from 3 to 13 groups. Most common were subgroups of the diverse non-lactobacilli dominant group, but there was not enough uniformity between those in the studies to use subgrouping for this analysis. Despite these factors, our inconsistency tests gave robust results showing that the method is stable enough to use the results.

Conclusion

To conclude, the diversity of the vaginal microbiome seems to play a part in the risk of preterm birth, where women with low abundance of lactobacilli were at greater risk of delivering preterm compared to women with L. crispatus dominant microbiome.

Funding

Open access funding provided by Karolinska Institute. This work was supported by funding from Ferring Pharmaceuticals. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Participants and statistics

Among women who delivered preterm, the pooled proportion with “low-lactobacilli” was 0.41 (95% CI 0.30–0.53) compared to 0.29 (95% CI 0.20–0.38) of women with term deliveries (Fig. 2). Forest plots showing all 17 included studies and the pooled and weighted proportion of “low-lactobacilli” women who delivered (a) preterm and (b) at term. The network map (Fig. 3) indicates that direct evidence was available for the association between all five CST categories (at least eight studies reported on each CST category)
A (network) meta-analysis was conducted, presenting pooled odds ratios (OR) and 95% confidence intervals (CI); and weighted proportions and 95% CI. All 17 studies were published between 2014 and 2021 and included 38–539 pregnancies and 8–107 preterm births. Women presenting with “low-lactobacilli” vaginal microbiome were at increased risk (OR 1.69, 95% CI 1.15–2.49) for delivering preterm compared to Lactobacillus crispatus dominant women
The quality of included studies was assessed by a customized checklist by two authors (UG & NB) (see Supplementary Table S2). Data used for the meta-analysis was extracted in double (UG, NB) to ensure quality, and meta-analyses were only conducted if at least three studies reported the required data. We grouped the CSTs into five categories based on the dominating species: L. crispatus, L. gasseri, L. iners, “low-lactobacilli” and L. jensenii
The number of included studies was too low for constructing funnel plots (to assess bias by small study effects). In addition, average richness and diversity indices of each paper using either Chao[1], Evenness (Simpson or Pielou) or Shannon index were pooled if sufficient data were available (at least 3 studies with means and standard deviations for both term and preterm pregnancies).
The number of included studies was too low for constructing funnel plots (to assess bias by small study effects). In addition, average richness and diversity indices of each paper using either Chao[1], Evenness (Simpson or Pielou) or Shannon index were pooled if sufficient data were available (at least 3 studies with means and standard deviations for both term and preterm pregnancies). Out of 4321 unique articles, 17 cohort studies were included, all published in English between 2014 and 2021 (Fig. 1)
In addition, average richness and diversity indices of each paper using either Chao[1], Evenness (Simpson or Pielou) or Shannon index were pooled if sufficient data were available (at least 3 studies with means and standard deviations for both term and preterm pregnancies). Out of 4321 unique articles, 17 cohort studies were included, all published in English between 2014 and 2021 (Fig. 1). None of the 79 retrieved studies in other languages were relevant
Out of 4321 unique articles, 17 cohort studies were included, all published in English between 2014 and 2021 (Fig. 1). None of the 79 retrieved studies in other languages were relevant. The number of pregnancies per study ranged between 38 and 539, with 8 and 107 preterm births
Study characteristics and quality. Out of the 17 eligible studies, seven originated from North-America[4,5,32,33,34,35,36], three from Europe[37,38,39], two from South-America[40,41], three from Asia[42,43,44] and two from Africa45,46. Microbiome samples were taken before the third trimester in all studies
Five studies specified that women at high-risk of preterm birth were not excluded from the cohort[37,38,39,43,45], while others did not specify the risk profiles. Out of the five studies that included high risk women, one study included 29 HIV positive women[45], one included women diagnosed with preterm prelabour rupture of membranes (PPROM)[43] and three included unspecified high-risk women37,38,39. Preterm birth was defined as birth before 37 completed weeks of gestation for all studies except one, where it was defined as before 34 weeks of gestation[4]
Preterm birth was defined as birth before 37 completed weeks of gestation for all studies except one, where it was defined as before 34 weeks of gestation4. In twelve studies, a healthcare professional took the samples[4,5,32,37,38,39,41,42,43,44,45,46], while the other five had self-sampling33,34,35,36,40. Furthermore, all studies except for two reported that the onset of preterm birth was spontaneous (Supplementary Table S4)[45,46]
The test for inconsistency indicated overall consistency (p = 0.77), and so did all loop inconsistency tests (p > 0.05), indicating this method can be used to assess the associations between the different CSTs. Network map of all 17 included studies by vaginal microbiome composition, showing how many studies reported which community state types (CSTs). Legend: Each dot represents a CST, with the number indicating how many studies reported it
Therefore, we see both meta-analysis approaches as complementary. Although we also had to exclude six otherwise eligible studies because CSTs were not reported, we were able to include 17 studies, compared to the six studies of the previous meta-analysis[16] (only one study in common4). Authors of the excluded papers were contacted for data but never replied
[object Object]
[object Object]
[object Object]
The network map (Fig. 3) indicates that direct evidence was available for the association between all five CST categories (at least eight studies reported on each CST category). The test for inconsistency indicated overall consistency (p = 0.77), and so did all loop inconsistency tests (p > 0.05), indicating this method can be used to assess the associations between the different CSTs. Network map of all 17 included studies by vaginal microbiome composition, showing how many studies reported which community state types (CSTs)
[object Object]

References

1. (WHO) WHO. Preterm Birth. https://www.who.int/news-room/fact-sheets/detail/preterm-birth.
2. Bayar, E., Bennett, P. R., Chan, D., Sykes, L. & MacIntyre, D. A. The pregnancy microbiome and preterm birth. Semin. Immunopathol. 42(4), 487–499 (2020).
3. Baldwin, E. A. et al. Persistent microbial dysbiosis in preterm premature rupture of membranes from onset until delivery. PeerJ 3, e1398 (2015).
4. Romero, R. et al. The vaginal microbiota of pregnant women who subsequently have spontaneous preterm labor and delivery and those with a normal delivery at term. Microbiome 2, 1–15 (2014).
5. Fettweis, J. M. et al. The vaginal microbiome and preterm birth. Nat. Med. 25(6), 1012 (2019).
6. Ravel, J. et al. Vaginal microbiome of reproductive-age women. Proc. Natl. Acad. Sci. USA 15(108 Suppl 1), 4680–4687 (2011).
7. van de Wijgert, J. H. et al. The vaginal microbiota: What have we learned after a decade of molecular characterization?. PLoS ONE 9(8), e105998 (2014).
8. Norenhag, J. et al. The vaginal microbiota, human papillomavirus and cervical dysplasia: A systematic review and network meta-analysis. BJOG 127(2), 171–180 (2020).
9. Brusselaers, N., Shrestha, S., van de Wijgert, J. & Verstraelen, H. Vaginal dysbiosis and the risk of human papillomavirus and cervical cancer: Systematic review and meta-analysis. Am. J. Obstet. Gynecol. 221(1), 9–18 (2019).
10. Chen, X., Lu, Y., Chen, T. & Li, R. The female vaginal microbiome in health and bacterial vaginosis. Front. Cell. Infect. Microbiol. 11, 631972 (2021).
11. Hyman, R. W. et al. Diversity of the Vaginal Microbiome Correlates With Preterm Birth. Reprod Sci. 21(1), 32–40 (2014).
12. Tsonis, O. et al. Female genital tract microbiota affecting the risk of preterm birth: What do we know so far? A review. Eur. J. Obstet. Gynecol. Reprod. Biol. 245, 168–173 (2020).
13. Hugerth, L. W. & Andersson, A. F. Analysing microbial community composition through amplicon sequencing: From sampling to hypothesis testing. Front. Microbiol. 8, 1561 (2017).
14. Debelius, J. et al. Tiny microbes, enormous impacts: What matters in gut microbiome studies?. Genome Biol. 17(1), 217 (2016).
15. Peelen, M. et al. The influence of the vaginal microbiota on preterm birth: A systematic review and recommendations for a minimum dataset for future research. Placenta 79, 30–39 (2019).
16. Kosti, I., Lyalina, S., Pollard, K. S., Butte, A. J. & Sirota, M. Meta-analysis of vaginal microbiome data provides new insights into preterm birth. Front. Microbiol. 11, 476. https://doi.org/10.3389/fmicb.2020.00476 (2020).
17. Hutton, B. et al. The PRISMA extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: Checklist and explanations. Ann. Intern. Med. 162(11), 777–784 (2015).
18. Nyaga, V. N., Arbyn, M. & Aerts, M. Metaprop: A Stata command to perform meta-analysis of binomial data. Arch. Public Health. 72(1), 39 (2014).
19. Michael Borenstein L. H. Hannah Rothstein Meta-Analysis Fixed effect vs. random effects 2007. https://www.meta-analysis.com/downloads/M-a_f_e_v_r_e_sv.pdf.
20. Shim, S., Yoon, B. H., Shin, I. S. & Bae, J. M. Network meta-analysis: Application and practice using Stata. Epidemiol. Health. 39, e2017047 (2017).
21. Nasir, S. A., Mohammed, B. K. & Alabsi, S. G. J. Lactobacillus species detected by 16S rRNA gene sequence isolated from the vaginae of pregnant women and its relation to preterm labor. Int. J. Res. Pharm. Sci. 9(1), 160–164 (2018).
22. Stout, M. J. et al. Early pregnancy vaginal microbiome trends and preterm birth. Am. J. Obstet. Gynecol. 217(3), 326.e1-326.e18 (2017).
23. Subramaniam, A. et al. Vaginal microbiota in pregnancy: Evaluation based on vaginal flora, birth outcome, and race. Am. J. Perinatol. 33(4), 401–408 (2016).
24. Wheeler, S. et al. The relationship of cervical microbiota diversity with race and disparities in preterm birth. J. Neonatal-Perinatal Med. 11(3), 305–310 (2018).
25. Callahan, B. J. et al. Replication and refinement of a vaginal microbial signature of preterm birth in two racially distinct cohorts of US women. Proc. Natl. Acad. Sci. U.S.A. 114(37), 9966–9971 (2017).
26. de Freitas, A. S. et al. Defining microbial biomarkers for risk of preterm labor. Braz. J. Microbiol. 51(1), 151–159 (2020).
27. Kindinger, L. M. et al. Relationship between vaginal microbial dysbiosis, inflammation, and pregnancy outcomes in cervical cerclage. Sci. Transl. Med. 8(350), 350ra12 (2016).
28. Hocevar, K. et al. Vaginal microbiome signature is associated with spontaneous preterm delivery. Front. Med. https://doi.org/10.3389/fmed.2019.00201 (2019).
29. Nasioudis, D. et al. Influence of pregnancy history on the vaginal microbiome of pregnant women in their first trimester. Sci Rep. 7, 1–16 (2017).
30. Amabebe, E., Chapman, D. R., Stern, V. L., Stafford, G. & Anumba, D. O. C. Mid-gestational changes in cervicovaginal fluid cytokine levels in asymptomatic pregnant women are predictive markers of inflammation-associated spontaneous preterm birth. J. Reprod. Immunol. 126, 1–10 (2018).
31. DiGiulio, D. B. et al. Temporal and spatial variation of the human microbiota during pregnancy. Proc. Natl. Acad. Sci. U.S.A. 112(35), 11060–11065 (2015).
32. Freitas, A. C., Bocking, A., Hill, J. E. & Money, D. M. Increased richness and diversity of the vaginal microbiota and spontaneous preterm birth. Microbiome 6, 1–15 (2018).
33. Nelson, D. B., Shin, H., Wu, J. W. & Dominguez-Bello, M. G. The gestational vaginal microbiome and spontaneous preterm birth among nulliparous African American women. Am. J. Perinatol. 33(9), 887–893 (2016).
34. Tabatabaei, N. et al. Vaginal microbiome in early pregnancy and subsequent risk of spontaneous preterm birth: A case-control study. BJOG 126(3), 349–358 (2019).
35. Dunlop, A. L. et al. Vaginal microbiome composition in early pregnancy and risk of spontaneous preterm and early term birth among African American women. Front. Cell Infect. Microbiol. 11, 641005 (2021).
36. Elovitz, M. A., Brown, A. G. & Ravel, J. The cervicovaginal metabolomic signature is different among women with CST IV in the 2nd trimester who ultimately have a preterm birth. Reprod. Sci. 26, 302A-A303 (2019).
37. Feehily, C. et al. Shotgun sequencing of the vaginal microbiome reveals both a species and functional potential signature of preterm birth. NPJ Biofilms Microbiomes 6(1), 50 (2020).
38. Kindinger, L. M. et al. The interaction between vaginal microbiota, cervical length, and vaginal progesterone treatment for preterm birth risk. Microbiome 5, 1–14 (2017).
39. Stafford, G. P. et al. Spontaneous preterm birth is associated with differential expression of vaginal metabolites by lactobacilli-dominated microflora. Front. Physiol. 8, 615 (2017).
40. Blostein, F., Gelaye, B., Sanchez, S. E., Williams, M. A. & Foxman, B. Vaginal microbiome diversity and preterm birth: Results of a nested case-control study in Peru. Ann. Epidemiol. 41, 28–34 (2020).
41. Sarmento, S. G. P. et al. An exploratory study of associations with spontaneous preterm birth in primigravid pregnant women with a normal cervical length. J. Matern.-Fetal Neonatal Med. 1, 1–6 (2021).
42. Chang, D. H. et al. Vaginal microbiota profiles of native Korean Women and associations with high-risk pregnancy. J. Microbiol. Biotechnol. 30(2), 248–258 (2020).
43. You, Y. A. et al. Vaginal microbiome profiles of pregnant women in Korea using a 16S metagenomics approach. Am. J. Reprod. Immunol. 82(1), e13124 (2019).
44. Kumar, M. et al. Vaginal microbiota and cytokine levels predict preterm delivery in Asian women. Front. Cell Infect. Microbiol. 11, 639665 (2021).
45. Gudza-Mugabe, M. et al. Human immunodeficiency virus infection is associated with preterm delivery independent of vaginal microbiota in pregnant African women. J. Infect. Dis. 221(7), 1194–1203 (2020).
46. Odogwu, N. M. et al. Predominance of atopobium vaginae at midtrimester: A potential indicator of preterm birth risk in a Nigerian cohort. mSphere 6(1), e01261 (2021).
47. France, M. T. et al. VALENCIA: A nearest centroid classification method for vaginal microbial communities based on composition. Microbiome 8(1), 166 (2020).
48. Ma, Z. S. & Li, L. Quantifying the human vaginal community state types (CSTs) with the species specificity index. PeerJ 5, e3366 (2017).
49. Klindworth, A. et al. Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies. Nucleic Acids Res. 41(1), e1 (2013).

Full text

Front matter
Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.
Subjects
Abstract
Preterm birth is a major cause of neonatal morbidity and mortality worldwide. Increasing evidence links the vaginal microbiome to the risk of spontaneous preterm labour that leads to preterm birth. The aim of this systematic review and network meta-analysis was to investigate the association between the vaginal microbiome, defined as community state types (CSTs, i.e. dominance of specific lactobacilli spp, or not (low-lactobacilli)), and the risk of preterm birth. Systematic review using PubMed, Web of Science, Embase and Cochrane library was performed. Longitudinal studies using culture-independent methods categorizing the vaginal microbiome in at least three different CSTs to assess the risk of preterm birth were included. A (network) meta-analysis was conducted, presenting pooled odds ratios (OR) and 95% confidence intervals (CI); and weighted proportions and 95% CI. All 17 studies were published between 2014 and 2021 and included 38–539 pregnancies and 8–107 preterm births. Women presenting with “low-lactobacilli” vaginal microbiome were at increased risk (OR 1.69, 95% CI 1.15–2.49) for delivering preterm compared to Lactobacillus crispatus dominant women. Our network meta-analysis supports the microbiome being predictive of preterm birth, where low abundance of lactobacilli is associated with the highest risk, and L. crispatus dominance the lowest.
Introduction
Preterm birth (< 37 completed gestation weeks), which accounts for over 10% of births worldwide, is a major cause of neonatal mortality and morbidity[1]. Many factors can trigger premature labour onset, including preterm premature rupture of membranes (PPROM), infections (e.g. Trichomonas vaginalis and Chlamydia trachomatis2) and microbial invasion of the amniotic cavity[3,4]. The vaginal microbiome is thought to protect from such infections, with low diversity microbiome dominated by Lactobacillus species considered “healthy”. In contrast, a diverse microbiome with low abundance of lactobacilli and high amounts of anaerobic bacteria can cause dysbiosis, overlapping with the clinical bacterial vaginosis (BV) diagnosis[5,6,7]. BV is often asymptomatic, yet has been associated with higher risks of genital infections and complications, including human papillomavirus (HPV) infections[8,9] and pelvic inflammatory disease[10]. It has also been proposed that different Lactobacillus species may present different risk profiles for various adverse events[5,8]. Since vaginal dysbiosis affects millions of women, it is important to understand the role of the vaginal microbiome in preterm birth[5,11]. Currently there are few studies available that assess the relationship between the vaginal microbiome and preterm birth, with conflicting findings on whether the vaginal microbiome can influence the risk of preterm birth[2,12].
Although meta-analyses are a great tool to pool the results from different studies, common challenges are clinical and methodological heterogeneity. Meta-analysing microbiome studies is particularly difficult because of diverse study designs, limited power and a large variety in sampling and processing techniques, including different hypervariable regions targeted[13,14]. These challenges were described in a systematic review based on culture-independent methods to assess the vaginal microbiome and preterm birth, which included nine studies[15]. One systematic review included an individual-patient meta-analysis, yet only five cohorts had sequencing data publicly available[16].
Our group recently introduced a novel method into the microbiome meta-analysis field to assess the relationship between the vaginal microbiome and the risk of HPV infections[8]. This network meta-analysis approach is based on aggregated data; and can be used to compare different microbiome “categories” in the same statistical model, based on direct and indirect evidence. Although categorizing the vaginal microbiome has its challenges, community state types (CSTs)[6] are commonly used and easy to interpret.
We used this network-meta-analysis method to assess the association between the vaginal microbiome (as CSTs) and the risk of preterm birth, based on a comprehensive systematic review.
Methods
Want to print your doc?
This is not the way.
Try clicking the ⋯ next to your doc name or using a keyboard shortcut (
CtrlP
) instead.