Evidence map›Paper›PMID 35212880›Full record

ReviewJournal of assisted reproduction and genetics2022

Oocyte aging: looking beyond chromosome segregation errors.

Daniela Bebbere, Giovanni Coticchio, Andrea Borini, Sergio Ledda

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of assisted reproduction and genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
14.2field-weighted citation impact, top 1% of its field
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

23 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
  2. Article
  3. From Cytoskeletal Remodeling to Oocyte Quality: The Emerging Role of Mechanics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

4 authors at 1 institution in 1 country.

Daniela BebbereDepartment of Veterinary Medicine, University of Sassari, Sassari, Italy. dbebbere@uniss.it.ORCID http://orcid.org/0000-0002-5277-5698
Giovanni Coticchio9.Baby, Family and Fertility Center, Bologna, Italy.ORCID http://orcid.org/0000-0003-1635-9205
Andrea Borini9.Baby, Family and Fertility Center, Bologna, Italy.ORCID http://orcid.org/0000-0001-9049-0020
Sergio LeddaDepartment of Veterinary Medicine, University of Sassari, Sassari, Italy.ORCID http://orcid.org/0000-0002-9779-5684
University of Sassari · IT

Funding

Fondazione Banco di Sardegna 2017 CUP J85F21000740005.
6 · The paper itself

Abstract

The age-associated decline in female fertility is largely ascribable to a decrease in oocyte quality. This phenomenon is multifaceted and influenced by numerous interconnected maternal and environmental factors. An increase in the rate of meiotic errors is the major cause of the decline in oocyte developmental competence. However, abnormalities in the ooplasm accumulating with age - including altered metabolism, organelle dysfunction, and aberrant gene regulation - progressively undermine oocyte quality. Stockpiling of maternal macromolecules during folliculogenesis is crucial, as oocyte competence to achieve maturation, fertilization, and the earliest phases of embryo development occur in absence of transcription. At the same time, crucial remodeling of oocyte epigenetics during oogenesis is potentially exposed to interfering factors, such as assisted reproduction technologies (ARTs) or environmental changes, whose impact may be enhanced by reproductive aging. As the effects of maternal aging on molecular mechanisms governing the function of the human oocyte remain poorly understood, studies in animal models are essential to deepen current understanding, with translational implications for human ARTs. The present mini review aims at offering an updated and consistent view of cytoplasmic alterations occurring in oocytes during aging, focusing particularly on gene and epigenetic regulation. Appreciation of these mechanisms could inspire solutions to mitigate/control the phenomenon, and thus benefit modern ARTs.

Indexed as

Chromosome SegregationEpigenesis, GeneticAnimalsEmbryonic DevelopmentFemaleHumansOocytesOogenesisCytoplasmic deteriorationGene and epigenetic dysregulationReproductive aging

Identifiers

PMID35212880
PMCPMC9051005
OpenAlexW4214595215

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.