Evidence map›Paper›PMID 26817690›Full record

ReviewBMC ophthalmology2015

Meibomian gland dysfunction: hyperkeratinization or atrophy?

James V Jester, Geraint J Parfitt, Donald J Brown

Open access · goldAbstract readReview
In one paragraph

Review in BMC ophthalmology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

54 citing papers in PubMed, 101 citations in OpenAlex.

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  14. Crosslinking of tarsal collagen as a hypothetical therapy for dry eye disease.Medical hypothesis, discovery & innovation ophthalmology journal · 2025
    Article
  15. Article
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  19. Alkali burn injury model of meibomian gland dysfunction in mice.International journal of ophthalmology · 2024
    Article
  20. Review
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

3 authors at 1 institution in 1 country.

James V JesterGavin Herbert Eye Institute, University of California, Irvine, CA, USA. JJester@uci.edu.
Geraint J ParfittGavin Herbert Eye Institute, University of California, Irvine, CA, USA. gparfitt@uci.edu.
Donald J BrownGavin Herbert Eye Institute, University of California, Irvine, CA, USA. dbrown@uci.edu.
University of California, Irvine · US

Funding

Age-Related Meibomian Gland DysfunctionR01EY021510 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI James V Jester · 2011 to 2026
$4.8M
Structure and Biomechanics of the Human Optic Nerve HeadR01EY019719 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI BROWN, DONALD J · 2010 to 2013
$1.5M
NEI NIH HHS NEI EY019719NEI NIH HHS NEI EY021510NEI NIH HHS R01 EY019719NEI NIH HHS R01 EY021510
6 · The paper itself

Abstract

Meibomian gland dysfunction (MGD) is the major cause of evaporative dry eye disease (EDED) and dysfunction is widely thought to mechanistically involve ductal hyperkeratinization, plugging and obstruction. This review re-evaluates the role of hyperkeratinization in MGD based on more recent findings from mouse models. In these studies, eyelids from normal young and old mice or mice exposed to desiccating stress were evaluated by immunofluorescent tomography and 3-dimensional reconstruction to evaluate gland volume, expression of hyperkeratinization markers and cell proliferation or stimulated Raman scattering (SRS) microscopy to assess lipid quality. Results indicate that aging mice show dropout of meibomian glands with loss of gland volume and a forward migration of the mucocutaneous junction anterior to the gland orifice; similar age-related changes that are detected in human subjects. Atrophic glands also showed evidence of epithelial plugging of the orifice without the presence of hyperkeratinization. Mice exposed to desiccating stress showed hyperproliferation of the meibomian gland and ductal dilation suggesting a marked increase in lipid synthesis. Lipid quality was also affected in EDED mice with an increase in the protein content of lipid within the duct of the gland. Overall, age-related changes in the mouse show similar structural and functional correlates with that observed in clinical MGD without evidence of hyperkeratinization suggesting that gland atrophy may be a major cause of EDED. The response of the meibomian gland to desiccating stress also suggest that environmental conditions may accelerate or potentiate age-related changes.

Indexed as

AnimalsAtrophyDry Eye SyndromesEyelid DiseasesEye ProteinsHumansKeratinsMeibomian GlandsMiceEye ProteinsKeratins

Identifiers

PMID26817690
PMCPMC4895318
OpenAlexW2223338173

What OpenQuestion holds

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LicenceCC BY
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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.