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The association of alcohol consumption with glaucoma and related traits: Findings from the UK Biobank

The association of alcohol consumption with glaucoma and related traits: Findings from the UK Biobank
The association of alcohol consumption with glaucoma and related traits: Findings from the UK Biobank

Purpose: To examine the associations of alcohol consumption with glaucoma and related traits, to assess whether a genetic predisposition to glaucoma modified these associations, and to perform Mendelian randomization (MR) experiments to probe causal effects. Design: Cross-sectional observational and gene–environment interaction analyses in the UK Biobank. Two-sample MR experiments using summary statistics from large genetic consortia. Participants: UK Biobank participants with data on intraocular pressure (IOP) (n = 109 097), OCT-derived macular inner retinal layer thickness measures (n = 46 236) and glaucoma status (n = 173 407). Methods: Participants were categorized according to self-reported drinking behaviors. Quantitative estimates of alcohol intake were derived from touchscreen questionnaires and food composition tables. We performed a 2-step analysis, first comparing categories of alcohol consumption (never, infrequent, regular, and former drinkers) before assessing for a dose-response effect in regular drinkers only. Multivariable linear, logistic, and restricted cubic spline regression, adjusted for key sociodemographic, medical, anthropometric, and lifestyle factors, were used to examine associations. We assessed whether any association was modified by a multitrait glaucoma polygenic risk score. The inverse-variance weighted method was used for the main MR analyses. Main Outcome Measures: Intraocular pressure, macular retinal nerve fiber layer (mRNFL) thickness, macular ganglion cell–inner plexiform layer (mGCIPL) thickness, and prevalent glaucoma. Results: Compared with infrequent drinkers, regular drinkers had higher IOP (+0.17 mmHg; P < 0.001) and thinner mGCIPL (-0.17 μm; P = 0.049), whereas former drinkers had a higher prevalence of glaucoma (odds ratio, 1.53; P = 0.002). In regular drinkers, alcohol intake was adversely associated with all outcomes in a dose-dependent manner (all P < 0.001). Restricted cubic spline regression analyses suggested nonlinear associations, with apparent threshold effects at approximately 50 g (∼6 UK or 4 US alcoholic units)/week for mRNFL and mGCIPL thickness. Significantly stronger alcohol–IOP associations were observed in participants at higher genetic susceptibility to glaucoma (Pinteraction < 0.001). Mendelian randomization analyses provided evidence for a causal association with mGCIPL thickness. Conclusions: Alcohol intake was consistently and adversely associated with glaucoma and related traits, and at levels below current United Kingdom (< 112 g/week) and United States (women, < 98 g/week; men, < 196 g/week) guidelines. Although we cannot infer causality definitively, these results will be of interest to people with or at risk of glaucoma and their advising physicians. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.

Alcohol, Glaucoma, Intraocular pressure, OCT, UK Biobank
2589-4234
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Modifiable Risk Factors for Glaucoma Collaboration, the UK Biobank Eye and Vision Consortium, and the International Glaucoma Genetics Consortium
Members of the Modifiable Risk Factors for Glaucoma Collaboration
Members of the UK Biobank Eye and Vision Consortium
Members of the International Glaucoma Genetics Consortium
Stuart, Kelsey
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Luben, Robert N.
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Warwick, Alasdair N.
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Madjedi, Kian
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Patel, Praveen J.
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Biradar, Mahantesh I.
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Sun, Zihan
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Chia, Mark
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Pasquale, Louis
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Wiggs, Janey
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Pasquale, Louis
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Wilson, James
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Modifiable Risk Factors for Glaucoma Collaboration, the UK Biobank Eye and Vision Consortium, and the International Glaucoma Genetics Consortium, Members of the Modifiable Risk Factors for Glaucoma Collaboration, Members of the UK Biobank Eye and Vision Consortium and Members of the International Glaucoma Genetics Consortium (2022) The association of alcohol consumption with glaucoma and related traits: Findings from the UK Biobank. Ophthalmology Glaucoma. (doi:10.1016/j.ogla.2022.11.008).

Record type: Article

Abstract

Purpose: To examine the associations of alcohol consumption with glaucoma and related traits, to assess whether a genetic predisposition to glaucoma modified these associations, and to perform Mendelian randomization (MR) experiments to probe causal effects. Design: Cross-sectional observational and gene–environment interaction analyses in the UK Biobank. Two-sample MR experiments using summary statistics from large genetic consortia. Participants: UK Biobank participants with data on intraocular pressure (IOP) (n = 109 097), OCT-derived macular inner retinal layer thickness measures (n = 46 236) and glaucoma status (n = 173 407). Methods: Participants were categorized according to self-reported drinking behaviors. Quantitative estimates of alcohol intake were derived from touchscreen questionnaires and food composition tables. We performed a 2-step analysis, first comparing categories of alcohol consumption (never, infrequent, regular, and former drinkers) before assessing for a dose-response effect in regular drinkers only. Multivariable linear, logistic, and restricted cubic spline regression, adjusted for key sociodemographic, medical, anthropometric, and lifestyle factors, were used to examine associations. We assessed whether any association was modified by a multitrait glaucoma polygenic risk score. The inverse-variance weighted method was used for the main MR analyses. Main Outcome Measures: Intraocular pressure, macular retinal nerve fiber layer (mRNFL) thickness, macular ganglion cell–inner plexiform layer (mGCIPL) thickness, and prevalent glaucoma. Results: Compared with infrequent drinkers, regular drinkers had higher IOP (+0.17 mmHg; P < 0.001) and thinner mGCIPL (-0.17 μm; P = 0.049), whereas former drinkers had a higher prevalence of glaucoma (odds ratio, 1.53; P = 0.002). In regular drinkers, alcohol intake was adversely associated with all outcomes in a dose-dependent manner (all P < 0.001). Restricted cubic spline regression analyses suggested nonlinear associations, with apparent threshold effects at approximately 50 g (∼6 UK or 4 US alcoholic units)/week for mRNFL and mGCIPL thickness. Significantly stronger alcohol–IOP associations were observed in participants at higher genetic susceptibility to glaucoma (Pinteraction < 0.001). Mendelian randomization analyses provided evidence for a causal association with mGCIPL thickness. Conclusions: Alcohol intake was consistently and adversely associated with glaucoma and related traits, and at levels below current United Kingdom (< 112 g/week) and United States (women, < 98 g/week; men, < 196 g/week) guidelines. Although we cannot infer causality definitively, these results will be of interest to people with or at risk of glaucoma and their advising physicians. Financial Disclosure(s): Proprietary or commercial disclosure may be found after the references.

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Accepted/In Press date: 30 November 2022
e-pub ahead of print date: 5 December 2022
Additional Information: Copyright © 2022 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.
Keywords: Alcohol, Glaucoma, Intraocular pressure, OCT, UK Biobank

Identifiers

Local EPrints ID: 475792
URI: http://eprints.soton.ac.uk/id/eprint/475792
ISSN: 2589-4234
PURE UUID: e2129763-bc11-44a1-ad5d-dfbb6546268a
ORCID for Roxana Carare: ORCID iD orcid.org/0000-0001-6458-3776
ORCID for Sarah Ennis: ORCID iD orcid.org/0000-0003-2648-0869
ORCID for Andrew Lotery: ORCID iD orcid.org/0000-0001-5541-4305
ORCID for Jay Self: ORCID iD orcid.org/0000-0002-1030-9963
ORCID for Irene Stratton: ORCID iD orcid.org/0000-0003-1172-7865
ORCID for Angela Cree: ORCID iD orcid.org/0000-0002-1987-8900

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Date deposited: 28 Mar 2023 18:18
Last modified: 18 Mar 2024 04:01

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Contributors

Author: Kelsey Stuart
Author: Robert N. Luben
Author: Alasdair N. Warwick
Author: Kian Madjedi
Author: Praveen J. Patel
Author: Mahantesh I. Biradar
Author: Zihan Sun
Author: Mark Chia
Author: Louis Pasquale
Author: Janey Wiggs
Author: Jae H. Kang
Author: Jihye Kim
Author: Hugues Aschard
Author: Jessica H. Tran
Author: Marleen Lentjes
Author: Paul J. Foster
Author: Anthony Khawaja
Author: Mark Chia
Author: Sharon Chua
Author: Ron Do
Author: Paul Foster
Author: Jae Kang
Author: Alan Kastner
Author: Anthony Khawaja
Author: Marleen Lentjes
Author: Robert Luben
Author: Kian Madjedi
Author: Giovanni Montesano
Author: Louis Pasquale
Author: Kelsey Stuart
Author: Alasdair Warwick
Author: Janey Wiggs
Author: Naomi Allen
Author: Tariq Aslam
Author: Denize Atan
Author: Sarah Barman
Author: Jenny Barrett
Author: Paul Bishop
Author: Graeme Black
Author: Roxana Carare ORCID iD
Author: Sarah Ennis ORCID iD
Author: Jane Gibson
Author: Andrew Lotery ORCID iD
Author: James Morgan
Author: Jay Self ORCID iD
Author: Irene Stratton ORCID iD
Author: Li Chen
Author: Ching Yu Cheng
Author: Angela Cree ORCID iD
Author: James Wilson
Corporate Author: Modifiable Risk Factors for Glaucoma Collaboration, the UK Biobank Eye and Vision Consortium, and the International Glaucoma Genetics Consortium
Corporate Author: Members of the Modifiable Risk Factors for Glaucoma Collaboration
Corporate Author: Members of the UK Biobank Eye and Vision Consortium
Corporate Author: Members of the International Glaucoma Genetics Consortium

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