Redox state as assessed using the measurement of human non-mercaptalbumin in embryo culture media is associated with successful embryo development in human in vitro fertilization.

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This study found that lower levels of oxidative stress, indicated by reduced human non-mercaptalbumin in embryo culture media, are associated with successful blastocyst formation in human in vitro fertilization.

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Abstract

The role of oxidative stress in the pathogenesis of various diseases has been attracting attention. We speculated as to whether the redox state of treatment solutions used for various diseases may play a role in treatment success. In the current study, we focused on the human embryo culture medium used for in vitro fertilization (IVF). A total of 173 oocytes from a total of 91 patients treated with IVF were enrolled. The redox state was assessed by measuring the levels of human non-mercaptalbumin (HNA). We analyzed factors related to blastocyst formation on day 5 or 6 after insemination. We also developed a random forest (RF) model for the prediction of blastocyst formation. The variable importance in the predictive model was assessed using the mean decrease in the Gini impurity. Blastocyst formation was observed in 41.04% (71/173) of the oocytes and was associated with a lower %HNA in the culture medium, a younger patient age, and the fertilization method (standard IVF or intracytoplasmic sperm injection). The RF model developed using these factors and 70% of the samples (training set, n = 121) was validated in the remaining testing set (n = 52) and produced an area under the curve of 0.761, where the %HNA in the culture medium was the most important variable for predicting blastocyst formation. In conclusion, lower levels of oxidative stress in embryo culture media were associated with the success of IVF treatment. The redox state of treatment solutions should be considered to support treatment success.
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The seven authors are justifiably credited with authorship, according to the authorship criteria. In detail: YK–conception, design, analysis and interpretation of data, data collection, drafting of the manuscript, final approval given; MS–design, analysis and interpretation of data, drafting of the manuscript, final approval given; HI–supervision of research, critical revision of manuscript, final approval given; KY–HNA measurement, interpretation of data, critical revision of manuscript, final approval given; XT–data collection, critical revision of manuscript, final approval given; YY–supervision of research, critical revision of manuscript, final approval given.

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europepmc
last seen: 2026-08-23T09:30:01.253652+00:00
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License: CC-BY-NC-ND-4.0