Impact of heredity in myopia
- PMID: 1937488
- DOI: 10.1159/000153994
Impact of heredity in myopia
Abstract
A series of 109 like-sexed twin pairs in the age group 30-31 years (54 monozygotic and 55 dizygotic) with one or both members of the twins with myopia was found in the Finnish Twin Cohort. The series was based on a random sample of 1,200 twins in one age stratum of the cohort. The twins received a questionnaire on their health status with special reference to eye diseases and symptoms. The refractive status of the twin pairs was ascertained by asking the twins to send their latest prescription for glasses to the authors or the refraction was obtained from the ophthalmologists or opticians of the twins. The mean difference in refraction between the monozygotic twins was 1.19 dptr in the right eyes and 1.15 dptr in the left eyes. The difference between dizygotic pairs was 2.34 dptr in the right eyes and 2.47 dptr in the left eyes. Analysis of variance showed that the difference in refraction between the two eyes of a twin pair was not significant. The mean difference in refraction between the monozygotic twins was significantly lower than that between dizygotic twins (p less than or equal to 0.001). The intrapair variances were doubled among dizygotic twin pairs compared to monozygotic twin pairs in the male group. The intrapair variance in the female group was 4-fold among dizygotic twin pairs as compared to monozygotic twin pairs. Heritability of myopia was 0.58 (0.74 for males and 0.61 for females) when myopia was considered a dichotomous variable. This result suggests that inheritance has a substantial effect on the etiology of myopia.
Similar articles
-
Study of gene-environment effects on development of hyperopia: a study of 191 adult twin pairs from the Finnish Twin Cohort Study.Acta Genet Med Gemellol (Roma). 1990;39(1):133-6. doi: 10.1017/s0001566000005651. Acta Genet Med Gemellol (Roma). 1990. PMID: 2392890
-
Heritability of defects of far vision in young adults--a twin study.Scand J Soc Med. 1992 Jun;20(2):73-8. Scand J Soc Med. 1992. PMID: 1496333
-
Heritability estimate for refractive errors--a population-based sample of adult twins.Genet Epidemiol. 1988;5(3):171-81. doi: 10.1002/gepi.1370050304. Genet Epidemiol. 1988. PMID: 3049225 Review.
-
Testing protocol and recruitment in the genes in myopia twin study.Ophthalmic Epidemiol. 2008 May-Jun;15(3):140-7. doi: 10.1080/09286580801939338. Ophthalmic Epidemiol. 2008. PMID: 18569808
-
Heritability of myopic refractive errors in identical and fraternal twins.Graefes Arch Clin Exp Ophthalmol. 1993 Oct;231(10):580-5. doi: 10.1007/BF00936522. Graefes Arch Clin Exp Ophthalmol. 1993. PMID: 8224933 Review.
Cited by
-
Lack of association with high myopia and the MYP2 locus in the Japanese population by high resolution microsatellite analysis on chromosome 18.Clin Ophthalmol. 2007 Sep;1(3):311-6. Clin Ophthalmol. 2007. PMID: 19668486 Free PMC article.
-
Stopping the rise of myopia in Asia.Graefes Arch Clin Exp Ophthalmol. 2020 May;258(5):943-959. doi: 10.1007/s00417-019-04555-0. Epub 2019 Dec 23. Graefes Arch Clin Exp Ophthalmol. 2020. PMID: 31873785 Review.
-
Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family.Mol Vis. 2010 Oct 12;16:2043-54. Mol Vis. 2010. PMID: 21042559 Free PMC article.
-
Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia.PLoS Genet. 2013;9(2):e1003299. doi: 10.1371/journal.pgen.1003299. Epub 2013 Feb 28. PLoS Genet. 2013. PMID: 23468642 Free PMC article.
-
MYP2 locus genes: Sequence variations, genetic association studies and haplotypic association in patients with High Myopia.Int J Biochem Mol Biol. 2021 Feb 15;12(1):35-48. eCollection 2021. Int J Biochem Mol Biol. 2021. PMID: 33824778 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical