Evidence map›Paper›PMID 41255002›Full record

ArticleMolecular reproduction and development2025

Extended In Vitro Maturation Enhances Oocyte Developmental Competence but Alters Gene Expression in Bovine Embryos Derived From Oocytes With Slow-Predicted Nuclear Maturation Speed.

Thomas Chia-Tang Ho, Takashi Tanida, Takashi Fujii, Keisuke Koyama

Abstract read
In one paragraph

Article in Molecular reproduction and development, 2025. 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

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Thomas Chia-Tang HoLaboratory of Theriogenology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, Japan.ORCID 0000-0002-0521-1507
Takashi TanidaLaboratory of Veterinary Anatomy, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, Japan.
Takashi FujiiFaculty of Agriculture, Iwate University, Iwate, Japan.ORCID 0000-0002-6532-6605
Keisuke KoyamaLaboratory of Theriogenology, Graduate School of Veterinary Science, Osaka Metropolitan University, Izumisano, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To identify the optimal in vitro maturation (IVM) duration for bovine oocytes with different nuclear maturation speeds (NMS), this study assessed how varying IVM durations (24, 28, and 32 h) affect developmental competence and embryo quality in oocytes with fast- or slow-predicted NMS classified via machine learning. Developmental competence was evaluated through cleavage rates, first cleavage timing and patterns, and blastocyst formation under individual culture. Embryo quality was assessed via differential staining of inner cell mass and trophectoderm and expression analysis of quality-related genes in formed blastocysts. For oocytes with slow-predicted NMS, extending IVM to 28 h increased cleavage rates and accelerated first cleavage timing (p < 0.01). The lower blastocyst formation rates of oocytes with slow-predicted NMS matured for 24 h improved when IVM reached 28 h, becoming comparable to fast-predicted NMS oocytes. However, extended IVM decreased expression of pluripotency-related genes (e.g., NANOG and OCT4; p < 0.01) regardless of predicted NMS. In conclusion, extending IVM duration to 28 h improved developmental competence of slow-predicted NMS oocytes, highlighting the importance of fertilization timing relative to nuclear maturation completion, though it reduced expression of key pluripotency genes. Individualized IVM protocols based on predicted NMS can enhance bovine embryo production efficiency.

Indexed as

BlastocystCell NucleusEmbryonic DevelopmentGene Expression Regulation, DevelopmentalIn Vitro Oocyte Maturation TechniquesOocytesAnimalsCattleFemalefertilization timingindividual culturemachine learningoocyte maturationtime‐lapse monitoring

Identifiers

PMID41255002
PMCPMC12627932

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Registered trials

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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.