Exploring ethnic and racial differences in intraocular pressure and glaucoma: The Canadian Longitudinal Study on aging.


Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
15 Apr 2024
Historique:
received: 17 08 2023
revised: 20 03 2024
accepted: 21 03 2024
medline: 8 4 2024
pubmed: 8 4 2024
entrez: 8 4 2024
Statut: epublish

Résumé

To determine whether self-reported race/ethnicity is associated with intraocular pressure (IOP) and glaucoma and to explore whether any associations are due to social, behavioral, genetic, or health differences. Cross-sectional analysis of population-based data. We used the Canadian Longitudinal Study on Aging Comprehensive Cohort, which consists of 30,097 adults aged 45-85 years. Race/ethnicity was self-reported. Corneal-compensated intraocular pressure (IOP) was measured in mmHg using the Reichert Ocular Response Analyzer. Participants were asked to report if they have ever had a diagnosis of glaucoma and whether they used eye care in the past year. A glaucoma polygenic risk score (PRS) was calculated. Logistic and linear regression models were used. Black individuals had higher mean IOP levels (beta coefficient (β) = 1.46; 95% confidence interval [CI], 0.62, 2.30) while Chinese, Japanese and Korean (β = -1.00; 95% CI, -1.63, -0.38) and Southeast Asian and Filipino individuals (β = -1.56; 95% CI, -2.68, -0.43) had lower mean IOP levels as compared to White individuals after adjustment for sociodemographic, behavioral, genetic, and health-related variables. Black people were more likely to report glaucoma as compared to White people after adjustment (odds ratio [OR] = 2.43; 95% CI, 1.27, 4.64). Racial and ethnic differences in IOP and glaucoma were identified. Adjusting for sociodemographic, behavioral, genetic, and health-related variables did not fully explain these differences. Longitudinal research is needed to further explore the reasons for these differences and to understand their relevance to disease pathogenesis and progression.

Identifiants

pubmed: 38586381
doi: 10.1016/j.heliyon.2024.e28611
pii: S2405-8440(24)04642-5
pmc: PMC10998131
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e28611

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Marie-Helene Roy-Gagnon reports financial support was provided by Canadian Institutes of Health Research.

Auteurs

Alyssa Grant (A)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.

Marie-Hélène Roy-Gagnon (MH)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.

Joseph Bastasic (J)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.

Akshay Talekar (A)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.

Garfield Miller (G)

Ottawa Eye Institute, The Ottawa Hospital, Ottawa, Canada.
Department of Ophthalmology, University of Ottawa, Ottawa, Canada.

Gisele Li (G)

Maisonneuve-Rosemont Hospital, Montreal, Canada.

Ellen E Freeman (EE)

School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.
Ottawa Hospital Research Institute, Canada.
Bruyère Research Institute, Ottawa, Canada.

Classifications MeSH