The Association between Vaginal Dysbiosis and Reproductive Outcomes in Sub-Fertile Women Undergoing IVF-Treatment: A Systematic PRISMA Review and Meta-Analysis.
Axel Skafte-HolmPeter HumaidanAndrea BernabeuBelen LledoJorgen Skov JensenThor HaahrPublished in: Pathogens (Basel, Switzerland) (2021)
Recent advances in molecular microbiology have enabled refined studies of the genital tract microbiota. This constitutes the basis of the present updated systematic review and meta-analysis which investigate vaginal dysbiosis (VD) as defined by either microscopy (e.g., Nugent score for bacterial vaginosis) or molecular methods (qPCR and Next Generation Sequencing) to evaluate the impact of VD on the reproductive outcomes in women undergoing IVF-treatment. A total of 17 studies were included, comprising 3543 patients and with a VD prevalence of 18% (95%CI 17-19). Across all methods, VD is a significant risk factor for early pregnancy loss in IVF (Relative risk (RR) = 1.71 95%CI 1.29-2.27). Moreover, a predefined sub-analysis of studies using molecular methods for VD diagnosis showed a significant reduction in the clinical pregnancy rate when compared to normal vaginal microbiota patients (RR = 0.55 95%CI 0.32-0.93). However, regardless of diagnostic methodology, VD did not significantly influence live birth rate (LBR). In conclusion, molecular tools have provided a more detailed insight into the vaginal microbiota, which may be the reason for the increased adverse effect estimates in IVF patients with molecularly defined VD. However, the quality of evidence was very low across all outcomes according to GRADE and thus, more studies are warranted to understand the impact of VD in IVF.
Keyphrases
- pregnancy outcomes
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- single molecule
- peritoneal dialysis
- pregnant women
- risk factors
- prognostic factors
- type diabetes
- systematic review
- high throughput
- randomized controlled trial
- quality improvement
- high resolution
- optical coherence tomography
- gene expression
- copy number
- skeletal muscle
- cell free
- circulating tumor
- genome wide