Molecular genetics has been expanding greatly in different medicine fields (spheres), including ART. A good progress in reprogenetics in past few decades made it necessary to renew our knowledge in infertility etiology (factors, courses), unexplained infertility in particular.
OBJECTIVES
Causative Factors determination of ART failures during unexplained infertility treatment
MATERIALS AND METHODS
58 female unexplained infertility patients participated in the study (study group). 945 patients of the same age with well-established different diagnosis comprised the control group. ART treatment outcomes were evaluated in both groups. Next-generation sequencing (NGS) was used to determine the impact of genetics in (on) infertility etiology in 34 unexplained infertility women vs 50 controls.
RESULTS
Our data showed a significant decrease in average number of retrieved «mature» oocytes (MII), fertilization rate, and embryo transfer rate, accompanied by an essential increase in embryo segmentation and early (biochemical) pregnancy failure rate in unexplained infertility patients. NGS revealed genetic disturbances including point mutations — transitions and microdeletions in 19 of 34 (56%) patients of the study group.
CONCLUSION
According to the data obtained unexplained infertility prevalence appeared to be as low as 5.8% of total infertility group. Whereas clinical pregnancy rate was found to be extremely law among unexplained infertility patients. It could be probably (partly) explained by genetic disturbances (single nucleotide mutations, defects) affecting oocyte maturation and early embryo development. Thus low efficiency of ART (IVF) in unexplained infertility females at least (in more than a half) in a half of the patients could be due to genetic abnormalities. It seems reasonable to use individualized (case-by-case) approach to improve the situation of the low efficacy in IVF treatment among idiopathic infertility patient group.