Evidence map›Paper›PMID 42177482›Full record

ArticleReproductive biology and endocrinology : RB&E2026

Quantitative determination of vaginal diamines as a biomarker for vaginal dysbiosis and IVF-ET outcome.

Elisa Lazzeri, Simone Lucchesi, Kevin Mendonca, Stefano De Giorgi, Alice Luddi, Rosetta Ponchia, Giuseppe Morgante, Paola Piomboni, Francesco Santoro, Gianni Pozzi and 1 more

Abstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Elisa LazzeriDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy.
Simone LucchesiDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy.
Kevin MendoncaDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy.
Stefano De GiorgiDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy.
Alice LuddiDepartment of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Rosetta PonchiaMedically Assisted Reproduction Unit, Siena University Hospital, Siena, Italy.
Giuseppe MorganteDepartment of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Paola PiomboniDepartment of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Francesco SantoroDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy.
Gianni PozziDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy.
Susanna RicciDepartment of Medical Biotechnologies, Laboratory of Molecular Microbiology and Biotechnology (LA.M.M.B.), University of Siena, Siena, Italy. susanna.ricci@unisi.it.

Funding

Progetti di Rilevante Interesse Nazionale (PRIN) 2022 PNRR P202228W7E
6 · The paper itself

Abstract

backgroundLactobacillus species generally predominate in a healthy vaginal microbiota, and alterations of this population correlate with increased risk of genital infections and poor reproductive outcomes. Composition and functions of the vaginal microbiota are influenced by a variety of factors, among which hormones represent a major player. As therapy with gonadotropins is a key step in controlled ovarian hyperstimulation (COH) before in vitro fertilization and embryo transfer (IVF-ET), in this work the effect of hormone therapy for COH on the vaginal microbiota and embryo implantation outcome was evaluated in a cohort of women undergoing IVF-ET.

methodsA cohort of 108 infertile females were prospectively enrolled in the study. Hormone therapy consisted of recombinant follicle stimulating hormone and recombinant luteinizing hormone in a gonadotropin-releasing hormone antagonist regimen. Two vaginal swabs, before and after therapy, were collected from patients. Vaginal swabs were analyzed by microbiological standard culture methods for the presence of genital pathogens and lactobacilli. Changes in the vaginal microbiota were also assessed by using a vaginal diamine assay for the quantification of diamines, which are considered as a biomarker of the catabolic activity of bacteria involved in bacterial vaginosis.

resultsCOH significantly impacted on both vaginal diamine levels and microbiota composition. Median concentration of diamines in vaginal fluids increased from 0 µM (IQR = 0-8.96) to 21.86 µM (IQR = 5.11-46.74) before (pre-HT) and after (post-HT) hormone therapy, respectively (p < 0.0001). The diamine value of 9.5 µM was found to be the threshold between eubiotic and dysbiotic microbiota. Microbiological analysis of pre-HT and post-HT samples showed a post-HT enrichment of the vaginal population in streptococci, enterococci, enterobacteria, staphylococci and fungi, which are prevalent in aerobic vaginitis. The frequency of vaginal samples positive for genital pathogens and with elevated concentrations of diamines (> 9.5 µM) was significantly increased in post-HT compared to pre-HT specimens (p < 0.0001). Levels of diamines were significantly lower in patients with successful IVF-ET compared to those with failed implantation (p = 0.015), and 56.25% of patients who achieved embryo implantation had diamine levels below 9.5 µM. Finally, multivariate analysis of factors associated with implantation outcomes showed that younger maternal age, absence of genital pathogens and low levels of vaginal diamine post-HT were all associated with positive reproductive outcomes.

conclusionsThe data from this study demonstrate that, following COH, an increase in diamine levels and genital pathogens occurred, leading to vaginal dysbiosis. Diamine concentrations higher than 9.5 µM post-HT significantly correlated with embryo implantation failure and may be used as a predictive biomarker of vaginal dysbiosis and IVF-ET outcome.

Indexed as

DysbiosisEmbryo TransferFertilization in VitroInfertility, FemaleVaginaAdultBiomarkersEmbryo ImplantationFemaleHumansLactobacillusMicrobiotaOvulation InductionPregnancyProspective StudiesTreatment OutcomeBiomarkersBiomarkerControlled ovarian hyperstimulationGenital pathogensGonadotropin treatmentIn vitro fertilization and embryo transferLactobacilliVaginal diaminesVaginal dysbiosis

Identifiers

PMID42177482
PMCPMC13377824

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.