Evidence map›Paper›PMID 42418469›Full record

ArticlePloS one2026

Visualization of the microstructure and distribution of follicles in deep human ovaries using speckle-modulated optical coherence microscopy.

Koichiro Ito, Momoko Kanaya, Seido Takae, Nao Suzuki, Kosuke Tsukada

Abstract read
In one paragraph

Article in PloS one, 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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Koichiro ItoCenter for Applied Physics and Physico-Informatics, Graduate School of Mathematical and Physical Sciences, Keio University, Yokohama, Japan.
Momoko KanayaCenter for Applied Physics and Physico-Informatics, Graduate School of Mathematical and Physical Sciences, Keio University, Yokohama, Japan.
Seido TakaeDepartment of Obstetrics and Gynecology, St. Marianna University School of Medicine, Kawasaki, Japan.
Nao SuzukiDepartment of Obstetrics and Gynecology, St. Marianna University School of Medicine, Kawasaki, Japan.
Kosuke TsukadaCenter for Applied Physics and Physico-Informatics, Graduate School of Mathematical and Physical Sciences, Keio University, Yokohama, Japan.ORCID https://orcid.org/0000-0003-1463-2204

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian tissue cryopreservation and transplantation remain important fertility preservation options for children, adolescents, and young adults requiring immediate treatment for their primary disease. Reliable visualization of follicle-containing regions may provide useful information for future ovarian tissue assessment. Despite its potential as a noninvasive follicle visualization method, optical coherence microscopy (OCM) remains limited by spatial resolution, imaging depth, and speckle noise when resolving fine follicular structures in deep ovarian tissue. In this study, we applied speckle modulation to a near-infrared wavelength-swept OCM system to visualize follicular microstructures in deep ovarian tissue. OCM images of 4-day-old mouse ovaries revealed dense superficial distributions of primordial follicles, which were distinguishable from primary follicles surrounded by a single layer of granulosa cells. Secondary follicles were predominantly observed in 14-day-old mouse ovarian tissue, and their internal microstructures were visualized. The proposed OCM approach visualized primordial follicular microstructures to depths of approximately 300 and 500 μm in ovarian tissues from a 15-year-old patient with acute myeloid leukemia and a 14-year-old patient with acute lymphoblastic leukemia, respectively. In the examined specimens, follicle localization varied with imaging location and depth, and similar structural features were also observed in HE-stained sections. Although challenges remain regarding imaging depth, acquisition time, and safety validation, these findings demonstrate the technical feasibility of visualizing follicular microstructures in human ovarian tissue and support future studies on ovarian tissue assessment.

Indexed as

MicroscopyOvarian FollicleOvaryTomography, Optical CoherenceAdolescentAnimalsFemaleHumansMice

Identifiers

PMID42418469
PMCPMC13345261

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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.