Evidence map›Paper›PMID 41137995›Full record

ArticleJournal of assisted reproduction and genetics2026

Age-related changes in mitochondrial markers and telomere dynamics during initial growth of human preantral follicles.

Luciana Cacciottola, Manyu Zhang, Lara Houeis, Caroline Bouzin, Marie-Astrid van Dievoet, Mathieu Luyckx, Jacques Donnez, Marie-Madeleine Dolmans

Abstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

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4 · The record

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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

8 authors.

Luciana CacciottolaGynecology Research Unit, Institut de Recherche Expérimentale Et Clinique, Université Catholique de Louvain, Avenue Mounier 52, Bte. B1.52.02, Brussels, 1200, Belgium.ORCID http://orcid.org/0000-0001-6738-289X
Manyu ZhangGynecology Research Unit, Institut de Recherche Expérimentale Et Clinique, Université Catholique de Louvain, Avenue Mounier 52, Bte. B1.52.02, Brussels, 1200, Belgium.
Lara HoueisGynecology Research Unit, Institut de Recherche Expérimentale Et Clinique, Université Catholique de Louvain, Avenue Mounier 52, Bte. B1.52.02, Brussels, 1200, Belgium.ORCID http://orcid.org/0009-0002-9276-5600
Caroline Bouzin2IP-IREC Imaging Platform (RRID:SCR_023378), Institute of Experimental and Clinical Research, Université Catholique de Louvain, Brussels, Belgium.ORCID http://orcid.org/0000-0003-0694-1947
Marie-Astrid van DievoetHematology Department of Laboratory Medicine, Cliniques Universitaires Saint-Luc, Brussels, Belgium.ORCID http://orcid.org/0000-0001-7056-7123
Mathieu LuyckxGynecology Department, Cliniques Universitaires Saint-Luc, Brussels, Belgium.ORCID http://orcid.org/0000-0002-3687-3001
Jacques DonnezSociety for Research Into Infertility, Brussels, Belgium.ORCID http://orcid.org/0000-0003-2528-206X
Marie-Madeleine DolmansGynecology Research Unit, Institut de Recherche Expérimentale Et Clinique, Université Catholique de Louvain, Avenue Mounier 52, Bte. B1.52.02, Brussels, 1200, Belgium. marie-madeleine.dolmans@uclouvain.be.ORCID http://orcid.org/0000-0002-6331-3026

Funding

China Scholarship Council CSCNO.202308530003Fonds De La Recherche Scientifique - FNRS scientific collaborator mandateFonds De La Recherche Scientifique - FNRS T.0064.22-PDR
6 · The paper itself

Abstract

purposeTo investigate how mitochondria and telomeres evolve during early follicle growth in human preantral follicles, and how these changes relate to reproductive age.

methodsThis prospective study included ovarian cortex and peripheral blood samples from 21 women, categorized into young (20-26, n = 7), mid (27-36, n = 6) and advanced (37-46, n = 8) reproductive age groups. Ovarian biopsies were processed for (i) follicle isolation for mitochondrial marker assessment (MitoTracker Deep Red and MitoSOX live staining) and telomerase subunit expression (hTERT, hTERC) by droplet digital PCR; and (ii) histological evaluation of the ovarian follicle pool, mitochondrial mass (TOMM20) and telomere length in different ovarian compartments (oocytes, granulosa cells and stroma) by fluorescence in situ hybridization (FISH). Leukocyte telomere length was measured by flow-FISH.

resultsMitochondrial mass (TOMM20) in the follicle pool was stable across age groups, but increased significantly during early follicle growth in younger patients (p < 0.01). Active mitochondria did not decline with age, but reactive oxygen species (ROS) generation showed complex age-related patterns, with younger subjects exhibiting lower ROS levels during follicle growth (p < 0.01) than other age groups. Telomere length was stable in granulosa cells and oocytes within primordial follicles, but increased during growth in younger age groups. Telomerase subunit expression was detected in preantral follicles without any significant age or size differences.

conclusionsThese results point to greater mitochondrial mass, mitochondrial ability to limit ROS generation, and telomere dynamics changing with increasing age in early growing follicles, potentially guiding the development of strategies to enhance fertility outcomes during the early stages of folliculogenesis.

Indexed as

AgingMitochondriaOvarian FollicleTelomereAdultBiomarkersFemaleGranulosa CellsHumansMiddle AgedOocytesProspective StudiesReactive Oxygen SpeciesTelomeraseTelomere HomeostasisYoung AdultBiomarkersReactive Oxygen SpeciesTelomeraseFertilityFollicle isolationMitochondriaOvarian agingTelomeraseTelomere length

Identifiers

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Textmetadata
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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 Socratic graph.