Evidence map›Paper›PMID 40814060›Full record

ReviewJournal of ovarian research2025

Mitochondrial dysfunction in oocytes: implications for fertility and ageing.

Tong Wang, Peixin Xu, Jianlong Yuan, Hong Chen, Xin Guo, Jing Gao, Yurong Wang, Dongmei Yao, Xin Li, Bingchun Liu and 1 more

Abstract readReview
In one paragraph

Review in Journal of ovarian research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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  11. The role of mTOR signaling in regulating the quality of mammalian oocytes.Journal of assisted reproduction and genetics · 2026
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  13. Article
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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

11 authors.

Tong Wang *Department of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Peixin Xu *Department of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Jianlong YuanDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Hong ChenDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Xin GuoDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Jing GaoDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Yurong WangDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Dongmei YaoDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Xin LiDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China.
Bingchun LiuCentral Laboratory of Organ Transplantation/ Stem Cell Laboratory/ Inner Mongolia Autonomous Region Engineering Laboratory for Genetic Test and Research of Tumour Cells, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China. liubc@immu.edu.cn.ORCID http://orcid.org/0000-0002-4619-7625
Yang LiuDepartment of Clinical Laboratory, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, 010000, Inner Mongolia, China. liuyang@immu.edu.cn.

Funding

2024 Joint Fund for Research in Public Hospitals Science and Technology Projects 2024GLLH0298Affiliated Hospital of Inner Mongolia Medical University National Nature Cultivation Programme (2023NYFYPY006Central Guided Local Science and Technology Development Funds Project 2023ZY0004Inner Mongolia Autonomous Region Provincial Health Commission, Science and Technology Program for Building High-level Clinical Specialties in Public Hospitals in the Capital Region (2024SGGZ071National Natural Science Foundation of China 31960154Q2022085); Natural Science Foundation of Inner Mongolia 2023QN03047Science and Technology Project of the Scientific Research Joint Fund for Public Hospitals in Inner Mongolia Autonomous Region 2024GLLH0321Scientific Research Project of Inner Mongolia Autonomous Region Colleges and Universities NJZZ23017Youth Innovation Talents Training Program of the Inner Mongolia Autonomous Region"Prairie excellence"Project Q2022085
6 · The paper itself

Abstract

The impact of environmental pollution on fertility has become an essential issue in global public health. Maturation, fertilisation, and embryonic development of oocytes depend on the energy provided by mitochondria; however, with increased environmental pollution and ageing, mitochondrial dysfunction and its subsequent functional and metabolic abnormalities have become leading causes of female fertility decline. When mitochondrial dysfunction occurs in the oocyte, reduced metabolic efficiency leads to impaired nuclear and cytoplasmic maturation of the oocyte, affecting the quality of the oocyte, which further contributes to decreased female fertility and increased risk of infertility, miscarriage, and aneuploid foetuses due to ovarian dysfunction. Several factors affect mitochondrial function, including excess reactive oxygen species (ROS)-induced mutations in mitochondrial DNA (mtDNA), changes in mtDNA copy number, oxidative stress (OS), damage to key cellular components and organelles, and changes in metabolic intermediates and byproducts at the cellular level, further affecting oocyte developmental competence. Mitochondrial dysfunction leads to problems such as abnormal spindle formation and chromosome misalignment, reducing fertilisation potential and embryonic developmental capacity. Mitochondrial dysfunction plays a key role in oocyte ageing and the decline in germ cell function, and an in-depth study of its molecular mechanisms and intervention strategies is highly important for slowing oocyte ageing, increasing fertility, and improving the success rate of assisted reproduction techniques. Clinical trial numberNot applicable.

Indexed as

AgingFertilityMitochondriaOocytesAnimalsDNA, MitochondrialFemaleHumansOxidative StressReactive Oxygen SpeciesDNA, MitochondrialReactive Oxygen Species

Identifiers

PMID40814060
PMCPMC12355882

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.