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Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men

BACKGROUND: We aimed to determine whether late adolescent visual impairment is associated with later psychosis. METHODS: We conducted a longitudinal cohort study of Swedish male military conscripts aged 18 or 19 years from January 1, 1974, through December 31, 1997 (N = 1140710). At conscription, un...

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Autores principales: Hayes, Joseph F, Picot, Suzanne, Osborn, David P J, Lewis, Glyn, Dalman, Christina, Lundin, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483575/
https://www.ncbi.nlm.nih.gov/pubmed/29901774
http://dx.doi.org/10.1093/schbul/sby084
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author Hayes, Joseph F
Picot, Suzanne
Osborn, David P J
Lewis, Glyn
Dalman, Christina
Lundin, Andreas
author_facet Hayes, Joseph F
Picot, Suzanne
Osborn, David P J
Lewis, Glyn
Dalman, Christina
Lundin, Andreas
author_sort Hayes, Joseph F
collection PubMed
description BACKGROUND: We aimed to determine whether late adolescent visual impairment is associated with later psychosis. METHODS: We conducted a longitudinal cohort study of Swedish male military conscripts aged 18 or 19 years from January 1, 1974, through December 31, 1997 (N = 1140710). At conscription, uncorrected and optometry-lens-corrected distance visual acuity was measured. Participants were then followed up to see if they received an inpatient diagnosis of non-affective psychotic disorder, including schizophrenia (N = 10769). Multivariable Cox modeling was used to estimate differences between groups. RESULTS: After adjustment for confounders, those with severe impairment before optical correction in their best eye (decimal fraction <0.3) had an increased psychosis rate compared to those with normal uncorrected vision (decimal fraction 1.0) (hazard ratio [HR] 1.26, 95% CI 1.16–1.37). Larger interocular visual acuity difference was associated with an increased psychosis rate (adjusted HR 1.49, 95% CI 1.37–1.63 in those with differences >0.5 compared to those with no between eye acuity difference). Individuals with impaired vision that could not be corrected to normal with lenses had highest rates of psychosis (best eye adjusted HR 1.56; 95% CI 1.33–1.82), those with imperfect, but correctable vision also had elevated rates (best eye adjusted HR 1.21; 95% CI 1.15–1.28). Individuals with visual impairment had higher rates of psychosis than their full siblings with normal vision (adjusted HR 1.20, 95% CI 1.07–1.35). CONCLUSIONS: Impaired visual acuity is associated with non-affective psychosis. Visual impairment as a phenotype in psychosis requires further consideration.
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spelling pubmed-64835752019-04-30 Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men Hayes, Joseph F Picot, Suzanne Osborn, David P J Lewis, Glyn Dalman, Christina Lundin, Andreas Schizophr Bull Regular Articles BACKGROUND: We aimed to determine whether late adolescent visual impairment is associated with later psychosis. METHODS: We conducted a longitudinal cohort study of Swedish male military conscripts aged 18 or 19 years from January 1, 1974, through December 31, 1997 (N = 1140710). At conscription, uncorrected and optometry-lens-corrected distance visual acuity was measured. Participants were then followed up to see if they received an inpatient diagnosis of non-affective psychotic disorder, including schizophrenia (N = 10769). Multivariable Cox modeling was used to estimate differences between groups. RESULTS: After adjustment for confounders, those with severe impairment before optical correction in their best eye (decimal fraction <0.3) had an increased psychosis rate compared to those with normal uncorrected vision (decimal fraction 1.0) (hazard ratio [HR] 1.26, 95% CI 1.16–1.37). Larger interocular visual acuity difference was associated with an increased psychosis rate (adjusted HR 1.49, 95% CI 1.37–1.63 in those with differences >0.5 compared to those with no between eye acuity difference). Individuals with impaired vision that could not be corrected to normal with lenses had highest rates of psychosis (best eye adjusted HR 1.56; 95% CI 1.33–1.82), those with imperfect, but correctable vision also had elevated rates (best eye adjusted HR 1.21; 95% CI 1.15–1.28). Individuals with visual impairment had higher rates of psychosis than their full siblings with normal vision (adjusted HR 1.20, 95% CI 1.07–1.35). CONCLUSIONS: Impaired visual acuity is associated with non-affective psychosis. Visual impairment as a phenotype in psychosis requires further consideration. Oxford University Press 2019-04 2018-06-12 /pmc/articles/PMC6483575/ /pubmed/29901774 http://dx.doi.org/10.1093/schbul/sby084 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Articles
Hayes, Joseph F
Picot, Suzanne
Osborn, David P J
Lewis, Glyn
Dalman, Christina
Lundin, Andreas
Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men
title Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men
title_full Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men
title_fullStr Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men
title_full_unstemmed Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men
title_short Visual Acuity in Late Adolescence and Future Psychosis Risk in a Cohort of 1 Million Men
title_sort visual acuity in late adolescence and future psychosis risk in a cohort of 1 million men
topic Regular Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483575/
https://www.ncbi.nlm.nih.gov/pubmed/29901774
http://dx.doi.org/10.1093/schbul/sby084
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