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1.
BMJ ; 361: k2022, 2018 06 06.
Artigo em Inglês | MEDLINE | ID: mdl-29875094

RESUMO

OBJECTIVES: To determine whether more years spent in education is a causal risk factor for myopia, or whether myopia is a causal risk factor for more years in education. DESIGN: Bidirectional, two sample mendelian randomisation study. SETTING: Publically available genetic data from two consortiums applied to a large, independent population cohort. Genetic variants used as proxies for myopia and years of education were derived from two large genome wide association studies: 23andMe and Social Science Genetic Association Consortium (SSGAC), respectively. PARTICIPANTS: 67 798 men and women from England, Scotland, and Wales in the UK Biobank cohort with available information for years of completed education and refractive error. MAIN OUTCOME MEASURES: Mendelian randomisation analyses were performed in two directions: the first exposure was the genetic predisposition to myopia, measured with 44 genetic variants strongly associated with myopia in 23andMe, and the outcome was years in education; and the second exposure was the genetic predisposition to higher levels of education, measured with 69 genetic variants from SSGAC, and the outcome was refractive error. RESULTS: Conventional regression analyses of the observational data suggested that every additional year of education was associated with a more myopic refractive error of -0.18 dioptres/y (95% confidence interval -0.19 to -0.17; P<2e-16). Mendelian randomisation analyses suggested the true causal effect was even stronger: -0.27 dioptres/y (-0.37 to -0.17; P=4e-8). By contrast, there was little evidence to suggest myopia affected education (years in education per dioptre of refractive error -0.008 y/dioptre, 95% confidence interval -0.041 to 0.025, P=0.6). Thus, the cumulative effect of more years in education on refractive error means that a university graduate from the United Kingdom with 17 years of education would, on average, be at least -1 dioptre more myopic than someone who left school at age 16 (with 12 years of education). Myopia of this magnitude would be sufficient to necessitate the use of glasses for driving. Sensitivity analyses showed minimal evidence for genetic confounding that could have biased the causal effect estimates. CONCLUSIONS: This study shows that exposure to more years in education contributes to the rising prevalence of myopia. Increasing the length of time spent in education may inadvertently increase the prevalence of myopia and potential future visual disability.


Assuntos
Escolaridade , Miopia/etiologia , Adulto , Feminino , Humanos , Masculino , Análise da Randomização Mendeliana/métodos , Miopia/epidemiologia , Prevalência , Erros de Refração/etiologia , Fatores de Risco , Reino Unido/epidemiologia
2.
Syst Rev ; 5(1): 144, 2016 08 31.
Artigo em Inglês | MEDLINE | ID: mdl-27577553

RESUMO

BACKGROUND: The parameters of the optic disc and peripapillary retinal nerve fibre layer (pRNFL) in premature children may vary with disease processes that contribute to visual impairment and blindness and so could be useful as an objective measure in at-risk children. METHODS: A systematic review of current literature on the range of pRNFL and optic disc parameters in children aged less than 18 years, who were born before 37 weeks gestation, will be performed. The bibliographic databases MEDLINE, CINAHL, EMBASE, Scopus and Web of Science will be systematically searched. Where possible and appropriate, study-specific estimates will be combined using meta-analysis to obtain an overall summary estimate of pRNFL thickness and cup-disc ratio across studies, and results will be presented by age of population. DISCUSSION: This review aims to improve understanding of what might be considered within/outside the range of normality for this high-risk group. SYSTEMATIC REVIEW REGISTRATION: The review is registered on PROSPERO: CRD42016037933.


Assuntos
Disco Óptico/anatomia & histologia , Disco Óptico/diagnóstico por imagem , Nascimento Prematuro , Retina/anatomia & histologia , Retina/diagnóstico por imagem , Tomografia de Coerência Óptica , Humanos , Fibras Nervosas , Valores de Referência , Revisões Sistemáticas como Assunto
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