Evidence map›Paper›PMID 42094487›Full record

ArticlebioRxiv : the preprint server for biology2026

Characterization of the SKC mouse strain as a potential model for keratoconus.

Rachel Hadvina, Jingwen Cai, Hongfang Yu, Amy Estes, Yutao Liu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Rachel HadvinaCenter for Biotechnology and Genomic Medicine, Augusta University, Augusta, GA 30912, USA.ORCID 0009-0000-1940-0088
Jingwen CaiDepartment of Ophthalmology, Mayo Clinic, Rochester, MN 55905, USA.
Hongfang YuDepartment of Cellular Biology & Anatomy, Augusta University, Augusta, GA 30912, USA.
Amy EstesDepartment of Ophthalmology, Augusta University, Augusta, GA 30912, USA.
Yutao LiuCenter for Biotechnology and Genomic Medicine, Augusta University, Augusta, GA 30912, USA.

Funding

Module 3: Gene Expression/ProteomicsP30EY031631 · NEI · AUGUSTA UNIVERSITY · PI Xingjun Fan · 2020 to 2026
$3.6M
Gene Discovery in Familial KeratoconusR01EY023242 · NEI · DUKE UNIVERSITY · PI LIU, YUTAO · 2013 to 2023
$3.4M
Estrogen and its Receptor in Intraocular Pressure RegulationR01EY032960 · NEI · MAYO CLINIC ROCHESTER · PI Yutao Liu · 2023 to 2026
$1.6M
Long Noncoding RNA lncLOXL1 and Exfoliation Syndrome.R21EY028671 · NEI · AUGUSTA UNIVERSITY · PI LIU, YUTAO · 2018 to 2019
$467k
MIR182 and Ocular Hypertension.R21EY033961 · NEI · AUGUSTA UNIVERSITY · PI LIU, YUTAO · 2023 to 2024
$424k
Interaction of Genetic and Environmental Factors in KeratoconusF31EY036722 · NEI · AUGUSTA UNIVERSITY · PI HADVINA, RACHEL · 2024 to 2024
$49k
NEI NIH HHS F31 EY036722NEI NIH HHS P30 EY031631NEI NIH HHS R01 EY023242NEI NIH HHS R01 EY032960NEI NIH HHS R21 EY028671NEI NIH HHS R21 EY033961
6 · The paper itself

Abstract

Background: Keratoconus (KC) is a multifactorial disorder with unclear etiology, characterized by localized thinning and a cone-like protrusion of the cornea. The complex etiology of KC exacerbates the lack of an animal model. Previous studies by Tachibana et al. (2002) described an inbred mouse strain (SKC) with a spontaneous, androgen-dependent, cone-like corneal morphology. This study aimed to investigate the corneal phenotypes of SKC mice through an in-depth ophthalmic examination. Methods: Mice (n=53) were examined via slit lamp biomicroscopy with fluorescein staining. Spectral-domain optical coherence tomography (SD-OCT) enabled central corneal thickness (CCT) measurement in selected mice (n=26 eyes), and OCT-based pachymetry mapping (n=16 eyes). In vivo corneal confocal microscopy was conducted on eyes to assess cellular morphology (n= 9 eyes). Eyes were collected for histology analysis (n=22). Results: Lesions and epithelial breaks were present in ~95% of eyes (n=101). Neovascularization, perforation, scarring, and hydrops were seen primarily in males. An opaque, unilateral cone-like morphology was exclusive to males (n=11). Male and female corneas showed no significant difference in CCT, though pachymetry mapping revealed regional thinning patterns in both sexes. Loosened epithelial tight junctions, stromal fibrosis, vascularization, and inflammation of variable severity were identified in both sexes. Conclusion: This study identified previously unreported corneal phenotypes in SKC mice through ophthalmic examination. Unlike previous studies, gross and histological abnormalities were observed in female SKC mice. Our findings suggest a lower penetrance of the cone-like phenotype (~20%) than previously reported (~33%) and support that the conical phenotype in male mice may be secondary to keratitis.

Indexed as

corneaeye rubbinggeneticsinflammationkeratoconusmouse modelSKC mice

Identifiers

PMID42094487
PMCPMC13142376

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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.