Morphological variants of meibomian glands: correlation of meibography features with histopathology findings.


Journal

The British journal of ophthalmology
ISSN: 1468-2079
Titre abrégé: Br J Ophthalmol
Pays: England
ID NLM: 0421041

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 12 03 2021
accepted: 02 08 2021
pubmed: 22 8 2021
medline: 25 1 2023
entrez: 21 8 2021
Statut: ppublish

Résumé

This study describes the histopathological features of different morphological variants of human meibomian glands (MGs) seen on infrared imaging. Tarsal plates dissected from seven cadaveric upper eyelids were imaged using infrared meibography, and then studied histopathologically using H&E, peroxisome proliferator-activated receptor gamma (PPARγ, meibocyte differentiation marker) and Ki-67 (cellular proliferation marker) antibody staining. The different morphological characteristics (varying size and shape) of MGs on meibography were correlated with histopathology findings using image analysis software. Of the total 127 glands, the morphological variants observed on meibography based on size were: normal (n=62), short (n=18), severely short (n=6) and dropout (n=12) glands, and on shape were: hooked (n=2), tortuous (n=5), overlapping (n=1), thick (n=15) and fluffy (n=6) glands. Short, hooked, tortuous and overlapping glands had similar acinar and ductal histology as seen in normal glands whereas thick, and fluffy glands had increased acinar diameter. All glands except the severely short type demonstrated normal signs of holocrine secretory activity and normal nuclear and cytoplasmic PPARγ expression. Severely short glands had nil while short glands had reduced Ki-67 proliferation index (3%±1%) as compared with normal and other variants (8%±5.2%). Gland dropout areas showed no evidence of any glandular tissue on histology. Hooked, tortuous and overlapping glands had completely normal glandular histology, whereas severely short glands showed atrophic changes with loss of meibocyte differentiation and cellular proliferation. Dropout areas showed total loss of glandular elements. Further studies are needed to validate and to explore the clinical implications of these findings.

Identifiants

pubmed: 34417185
pii: bjophthalmol-2021-318876
doi: 10.1136/bjophthalmol-2021-318876
doi:

Substances chimiques

PPAR gamma 0
Ki-67 Antigen 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

195-200

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Swati Singh (S)

Ophthalmic Plastic Surgery Services, LV Prasad Eye Institute, Hyderabad, Telangana, India.

Gorrepati C Naidu (GC)

Ophthalmic Pathology Laboratory, LV Prasad Eye Institute, Hyderabad, Telangana, India.

Geeta Vemuganti (G)

School of Medical Sciences, University of Hyderabad, Hyderabad, Telangana, India.

Sayan Basu (S)

Prof. Brien Holden Eye Research Centre (BHERC), LV Prasad Eye Institute, Hyderabad, Telangana, India sayanbasu@lvpei.org.
The Cornea Institute, LV Prasad Eye Institute, Hyderabad, Telangana, India.

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Classifications MeSH