Evidence map›Paper›PMID 32045599›Full record

ArticleExperimental eye research2020

Morphological ciliary muscle changes associated with form deprivation-induced myopia.

Andrew D Pucker, Ashley R Jackson, Kirk M McHugh, Donald O Mutti

Open access · greenAbstract read
In one paragraph

Article in Experimental eye research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Retinoscopes: Past and present.World journal of methodology · 2024
    Article
  3. Article
  4. Mutational screening ofMolecular vision · 2021
    Article
  5. Article
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 3 institutions in 1 country.

Andrew D PuckerUniversity of Alabama at Birmingham, School of Optometry, 1716 University Blvd, Birmingham, AL, USA. Electronic address: apucker@uab.edu.
Ashley R JacksonNationwide Children's Hospital, Center for Clinical and Translational Research, 700 Childrens Drive, Columbus, OH, USA. Electronic address: ashley.jackson@nationwidechildrens.org.
Kirk M McHughNationwide Children's Hospital, Center for Clinical and Translational Research, 700 Childrens Drive, Columbus, OH, USA. Electronic address: kirk.mchugh@osumc.edu.
Donald O MuttiThe Ohio State University, College of Optometry, 338 W 10th Ave, Columbus, OH, USA. Electronic address: mutti.2@osu.edu.
Nationwide Children's Hospital · USThe Ohio State University · USUniversity of Alabama at Birmingham · US

Funding

Visual Phenotyping CoreP30EY003039 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul Douglas Gamlin · 1985 to 2026
$16.9M
Mechanotransduction in the Ciliary MuscleK08EY023264 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PUCKER, ANDREW D · 2013 to 2017
$689k
NEI NIH HHS K08 EY023264NEI NIH HHS P30 EY003039
6 · The paper itself

Abstract

Myopic children have larger ciliary muscles than non-myopic children, suggesting that the ciliary muscle may have an impact on or be affected by refractive error development. The guinea pig represents an attractive model organism for myopia development research. The purpose of the study was to investigate whether form deprivation-induced myopia in one or more strains of guinea pig causes thickening of the ciliary muscle as seen in human myopia. Thirty-nine guinea pigs were bred from in-house progenitors obtained from Cincinnati Children's Hospital (Cincinnati) and the United States Army (Strain 13). At 2-4 days of age the right eyes of animals were exposed to form deprivation for 7 days while the fellow eyes served as controls. Refractive error was determined with retinoscopy while vitreous chamber depth (VCD) and axial length (AL) were determined with A-scan ultrasound. Ciliary muscle characteristics (ciliary muscle length, cross-sectional area, volume, cell number, cell size, and smooth muscle actin concentration) were determined histologically with antibody labeling and analyzed according to whether the animal developed axial myopia (anisometropia > -2.00 D with VCD and/or AL differences > 0.1 mm) or was unresponsive. This analysis method yielded four groups with Group 1 having no induced myopia but with axial elongation (n = 11), Group 2 having myopia without vitreous or axial elongation (n = 8), Group 3 having myopia with either vitreous or axial elongation (n = 11), and Group 4 having myopia with both vitreous and axial elongation (n = 8). There were no post-treatment inter-ocular differences between strains or for the overall group of animals for any ciliary muscle variable; however, a higher response group number in multivariate ordinal regression was related to having a treated compared to fellow eye that had a lower smooth muscle actin concentration (p = 0.006), with a shorter ciliary muscle length (p = 0.042), and a less oblate eye shape (p = 0.010). Guinea pig ciliary muscle length and smooth muscle actin concentration were significantly less in the treated eyes of axially myopic animals suggesting that 7 days of form deprivation induced ciliary muscle cellular atrophy or inhibited ciliary muscle growth. Form deprivation myopia in the guinea pig does not result in the increase in ciliary muscle thickness associated with human juvenile and adult myopia.

Indexed as

AnimalsCiliary BodyDisease Models, AnimalGuinea PigsMyopiaRefraction, OcularRetinoscopySensory DeprivationCiliary muscleDevelopmentGuinea pigsHistologyMyopiaRefractive error

Identifiers

PMID32045599
PMCPMC7113096
OpenAlexW3004772567

What OpenQuestion holds

Textmetadata
LicenceTDM
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.