Evidence map›Paper›PMID 39741796›Full record

ArticleClinical ophthalmology (Auckland, N.Z.)2024

Corneal Alterations in Patients with Osteogenesis Imperfecta: An in vivo Corneal Confocal Microscopy Study.

Pietro Mangiantini, Fabiana Mallone, Mattia D'Andrea, Lorenzo Albanesi, Luca Lucchino, Luca Celli, Mauro Celli, Alessandro Lambiase, Antonietta Moramarco

Abstract read
In one paragraph

Article in Clinical ophthalmology (Auckland, N.Z.), 2024. 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

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

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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.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

9 authors.

Pietro Mangiantini *Department of Sense Organs, Sapienza University, Rome, Italy.
Fabiana Mallone *Department of Sense Organs, Sapienza University, Rome, Italy.ORCID 0000-0001-6274-015X
Mattia D'AndreaDepartment of Sense Organs, Sapienza University, Rome, Italy.ORCID 0000-0001-9074-3964
Lorenzo AlbanesiDepartment of Sense Organs, Sapienza University, Rome, Italy.
Luca LucchinoDepartment of Sense Organs, Sapienza University, Rome, Italy.
Luca CelliDepartment of Pediatrics, Center for Congenital Osteodystrophy, Sapienza University, Rome, Italy.
Mauro CelliDepartment of Pediatrics, Center for Congenital Osteodystrophy, Sapienza University, Rome, Italy.
Alessandro LambiaseDepartment of Sense Organs, Sapienza University, Rome, Italy.ORCID 0000-0002-8974-991X
Antonietta MoramarcoDepartment of Sense Organs, Sapienza University, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Osteogenesis imperfecta (OI) is a rare hereditary disorder of the connective tissue. Despite recent attention to corneal abnormalities in OI, understanding remains limited. This study aimed to comprehensively evaluate corneal changes in a large sample of OI patients compared to controls using in vivo confocal microscopy (IVCM). Patients and Methods: Nineteen OI patients (mean age: 34.0 ± 16.00 years; 9 females, 10 males) and 20 healthy controls (mean age: 35.5 ± 12.00; 12 females, 8 males) were included, matched for age and gender. The integrity of corneal cell layers, with a focus on Bowman's layer and sub-epithelial stroma, was evaluated. Additionally, we conducted a quantitative analysis of the corneal sub-basal nerve plexus (CSNP), measuring nerve fiber density (NFD), nerve branch density (NBD), nerve fiber length (NFL), and dendritic cells (DCs) density. Clinical parameters including blue discoloration of the sclera, corneal thickness and sensitivity were also evaluated. Results: Bowman's layer alterations were observed in 42.11% of OI patients. NFD was significantly reduced in OI patients (27,3±6.98 vs controls 37.85±13,74 fiber/mm2; p-value=0.005). NBD and NFL were lower in OI patients but did not reach statistical significance (p=0.650 and p=0.120, respectively). DCs density was higher in OI patients than controls (11,37 ± 12.79 vs 2.09±2,91 cells/mm2; p-value < 0.001). Corneal thickness and sensitivity were significantly reduced in OI patients compared to controls (p<0.001, p=0.001, respectively). OI patients with blue sclera or abnormal Bowman's layer exhibited even lower central corneal thickness (CCT) (p=0.010, p=0.005, respectively). Conclusion: OI patients demonstrated Bowman's layer abnormalities, neuropathic changes and higher inflammatory cell count. These results suggest potential corneal complications, and hold promise for diagnostic applications and intervention strategies in OI.

Indexed as

CSNP corneal nervesDCsdendritic cellsIVCM corneal sub-basal nerve plexusOI in vivo confocal microscopyosteogenesis imperfecta

Identifiers

PMID39741796
PMCPMC11687199

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