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Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction

PURPOSE: To determine whether reliance on eyelid margin vascularization as a diagnostic criterion for meibomian gland dysfunction (MGD) results in underdiagnosis of MGD in individuals with dark skin pigmentation. PATIENTS AND METHODS: This cross-sectional study enrolled consecutive cornea clinic pat...

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Autores principales: Blumberg, Max J, Millen, Amy E, Patel, Sangita P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756854/
https://www.ncbi.nlm.nih.gov/pubmed/31571820
http://dx.doi.org/10.2147/OPTH.S222451
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author Blumberg, Max J
Millen, Amy E
Patel, Sangita P
author_facet Blumberg, Max J
Millen, Amy E
Patel, Sangita P
author_sort Blumberg, Max J
collection PubMed
description PURPOSE: To determine whether reliance on eyelid margin vascularization as a diagnostic criterion for meibomian gland dysfunction (MGD) results in underdiagnosis of MGD in individuals with dark skin pigmentation. PATIENTS AND METHODS: This cross-sectional study enrolled consecutive cornea clinic patients in Buffalo, New York. Eyelid margin vascularization was graded qualitatively from slit-lamp photos. Skin pigmentation was quantified from digital photos using red/green/blue (RGB) pixel analysis and dichotomized using the RGB median. MGD was defined as abnormal quantity or quality of meibum or increased pressure required to express meibum. Additional testing included infrared meibography, Schirmer’s testing, and a dry eye questionnaire. Sensitivity of MGD diagnosis by visualization of vascularization, compared to diagnosis by expression of meibum, was estimated with and without stratification by skin pigmentation. RESULTS: Among 47 participants, 15–79 years old, meibomian gland truncation/dropout, abnormal tear production, and dry eye symptoms affected individuals of all skin pigmentations. Eyelid margin vascularization was less common in subjects with dark (n=21%) compared to light pigmentation (65%; p=0.002), although the prevalence of MGD assessed via clinical evaluation did not vary significantly between those groups. Use of eyelid margin vascularization alone was not sensitive (33%) for MGD diagnosis. The sensitivity was 17% when limited to those with dark pigmentation. CONCLUSION: Our findings highlight the importance of gland expression and suggest limiting reliance on eyelid margin vascularization for MGD diagnosis, especially in those with dark eyelid skin pigmentation.
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spelling pubmed-67568542019-09-30 Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction Blumberg, Max J Millen, Amy E Patel, Sangita P Clin Ophthalmol Original Research PURPOSE: To determine whether reliance on eyelid margin vascularization as a diagnostic criterion for meibomian gland dysfunction (MGD) results in underdiagnosis of MGD in individuals with dark skin pigmentation. PATIENTS AND METHODS: This cross-sectional study enrolled consecutive cornea clinic patients in Buffalo, New York. Eyelid margin vascularization was graded qualitatively from slit-lamp photos. Skin pigmentation was quantified from digital photos using red/green/blue (RGB) pixel analysis and dichotomized using the RGB median. MGD was defined as abnormal quantity or quality of meibum or increased pressure required to express meibum. Additional testing included infrared meibography, Schirmer’s testing, and a dry eye questionnaire. Sensitivity of MGD diagnosis by visualization of vascularization, compared to diagnosis by expression of meibum, was estimated with and without stratification by skin pigmentation. RESULTS: Among 47 participants, 15–79 years old, meibomian gland truncation/dropout, abnormal tear production, and dry eye symptoms affected individuals of all skin pigmentations. Eyelid margin vascularization was less common in subjects with dark (n=21%) compared to light pigmentation (65%; p=0.002), although the prevalence of MGD assessed via clinical evaluation did not vary significantly between those groups. Use of eyelid margin vascularization alone was not sensitive (33%) for MGD diagnosis. The sensitivity was 17% when limited to those with dark pigmentation. CONCLUSION: Our findings highlight the importance of gland expression and suggest limiting reliance on eyelid margin vascularization for MGD diagnosis, especially in those with dark eyelid skin pigmentation. Dove 2019-09-19 /pmc/articles/PMC6756854/ /pubmed/31571820 http://dx.doi.org/10.2147/OPTH.S222451 Text en © 2019 Blumberg et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Blumberg, Max J
Millen, Amy E
Patel, Sangita P
Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
title Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
title_full Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
title_fullStr Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
title_full_unstemmed Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
title_short Influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
title_sort influence of eyelid pigmentation on the diagnosis of meibomian gland dysfunction
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756854/
https://www.ncbi.nlm.nih.gov/pubmed/31571820
http://dx.doi.org/10.2147/OPTH.S222451
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