MiFert Microbiome

Endometrial microbiome analysis identifying bacterial balance for IVF success. MiFert Microbiome (EMMA) detects dysbiosis and guides probiotic/antibiotic therapy for 90% implantation improvement.

The Endometrial Microbiome: A New Frontier in Fertility

For decades, the uterine cavity was considered sterile. Revolutionary research over the past 10 years has proven this assumption wrong: The endometrium has its own unique microbiome that profoundly influences reproductive outcomes.

Key Discoveries:

  • Endometrial microbiome composition directly impacts implantation success
  • Lactobacillus dominance (>90%) correlates with optimal implantation rates
  • Dysbiosis (pathogenic bacteria presence or low Lactobacillus) reduces implantation by up to 50%
  • Chronic endometritis (often asymptomatic) affects 14-30% of infertile women
  • Microbiome can be optimized through targeted interventions (antibiotics, probiotics)

What is MiFert Microbiome?

MiFert Microbiome uses Next-Generation Sequencing (NGS) technology to comprehensively analyze the bacterial composition of the endometrium, providing:

  • Lactobacillus Percentage: Quantification of beneficial bacteria dominance
  • Pathogen Detection: Identification of harmful bacteria associated with implantation failure
  • Dysbiosis Classification: Categorization of microbiome health status
  • Treatment Recommendations: Specific antibiotic/probiotic protocols to optimize microbial balance

Clinical Applications

Primary Indications:

Recurrent Implantation Failure (RIF)

  • Unexplained failure despite good embryo quality
  • Dysbiosis found in 15-20% of RIF patients

Recurrent Infections

  • History of bacterial vaginosis
  • Recurrent urinary tract infections
  • Previous pelvic inflammatory disease

Chronic Endometritis

  • Diagnosed or suspected chronic inflammation
  • Often asymptomatic; only detectable through biopsy

Previous Antibiotic Treatments

  • History of broad-spectrum antibiotic use
  • May have disrupted healthy microbiome

Recurrent Pregnancy Loss

  • Dysbiosis may contribute to early pregnancy loss

Suboptimal Endometrial Development

  • Thin endometrium despite hormonal support
  • May be related to chronic inflammation from dysbiosis

MiFert Microbiome Analysis

  • Technology: 16S rRNA Gene Sequencing
  • Next-Generation Sequencing (NGS) of bacterial DNA
  • Identifies all bacterial species present in endometrial sample
  • Quantifies relative abundance of each species
  • Database comparison for pathogen identification

What the Test Measures:

  • Lactobacillus Percentage: Precise quantification (e.g., "85% Lactobacillus")
  • Lactobacillus Species: Identification of specific strains present
  • Pathogenic Bacteria: Detection and quantification of harmful species
  • Microbial Diversity: Assessment of overall bacterial balance
  • Dysbiosis Score: Overall endometrial microbiome health classification

Microbiome Classification & Interpretation

Optimal Microbiome:

  • >90% Lactobacillus dominance
  • No significant pathogenic bacteria
  • Recommendation: Proceed with embryo transfer as planned

Mild Dysbiosis:

  • 70-90% Lactobacillus
  • Low levels of non-pathogenic bacteria
  • Recommendation: Consider vaginal probiotic supplementation; re-test optional

Moderate Dysbiosis:

  • <70% Lactobacillus
  • Presence of potential pathogens at low-moderate levels
  • Recommendation: Targeted antibiotic therapy; probiotic restoration; re-test before transfer

Severe Dysbiosis:

  • <50% Lactobacillus or complete absence
  • High levels of pathogenic bacteria
  • Possible chronic endometritis
  • Recommendation: Aggressive antibiotic treatment; probiotic therapy; mandatory re-test before transfer

Sample Collection

Same Biopsy as MiFert Receptivity:

  • Single endometrial biopsy divided into Blue Tube (Receptivity + Microbiome)
  • Performed during mock cycle
  • 16S RNA extracted for bacterial analysis

Critical Collection Notes:

  • Avoid contamination from vaginal/cervical flora during biopsy
  • Use sterile technique
  • Direct endometrial sample collection (not cervical swab)
  • Turnaround Time: 13-15 days

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