Literature DB >> 12876828

Interactions of genes and environment in myopia.

Marita Feldkämper1, Frank Schaeffel.   

Abstract

Myopia is a condition in which the eye is too long for the focal length of cornea and lens, and the plane of sharp focus ends up in front of the retina. Given that the growth of the length of the eye is normally controlled with extreme precision by an image-processing feedback mechanism in the retina, myopia can either be the result of inappropriate visual stimulation, genetically determined changes in the gain or offset of the feedback loops or of inappropriate responses of the target tissues. There is no doubt that an environmental component is involved and extended near work appears to be the major risk factor. However, there is also no doubt that myopia is inherited since myopic parents are much more likely to have myopic children, and myopia is far more frequent in Asian populations than in the USA or Europe, even if groups are compared that have performed similar amounts of near work. A number of systemic or ophthalmic diseases are associated with myopia, indicating that metabolic conditions may interfere either with the gains of the feedback loops or the responses of the target tissue, the sclera. Since there is still no therapy against myopia development, research is directed toward the identification of genes that control the axial elongation of the eye.

Entities:  

Mesh:

Year:  2003        PMID: 12876828     DOI: 10.1159/000072037

Source DB:  PubMed          Journal:  Dev Ophthalmol        ISSN: 0250-3751


  34 in total

1.  High myopia caused by a mutation in LEPREL1, encoding prolyl 3-hydroxylase 2.

Authors:  Shikma Mordechai; Libe Gradstein; Annika Pasanen; Rivka Ofir; Khalil El Amour; Jaime Levy; Nadav Belfair; Tova Lifshitz; Sara Joshua; Ginat Narkis; Khalil Elbedour; Johanna Myllyharju; Ohad S Birk
Journal:  Am J Hum Genet       Date:  2011-09-01       Impact factor: 11.025

2.  Three-dimensional MRI study of the relationship between eye dimensions, retinal shape and myopia.

Authors:  James M Pope; Pavan K Verkicharla; Farshid Sepehrband; Marwan Suheimat; Katrina L Schmid; David A Atchison
Journal:  Biomed Opt Express       Date:  2017-04-05       Impact factor: 3.732

3.  Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.

Authors:  Christina Zeitz; Samuel G Jacobson; Christian P Hamel; Kinga Bujakowska; Marion Neuillé; Elise Orhan; Xavier Zanlonghi; Marie-Elise Lancelot; Christelle Michiels; Sharon B Schwartz; Béatrice Bocquet; Aline Antonio; Claire Audier; Mélanie Letexier; Jean-Paul Saraiva; Tien D Luu; Florian Sennlaub; Hoan Nguyen; Olivier Poch; Hélène Dollfus; Odile Lecompte; Susanne Kohl; José-Alain Sahel; Shomi S Bhattacharya; Isabelle Audo
Journal:  Am J Hum Genet       Date:  2012-12-13       Impact factor: 11.025

4.  Identification of a locus for autosomal dominant high myopia on chromosome 5p13.3-p15.1 in a Chinese family.

Authors:  Jun-Hua Ma; Shu-Hong Shen; Guo-Wei Zhang; Dong-Sheng Zhao; Chao Xu; Chun-Ming Pan; He Jiang; Zhi-Quan Wang; Huai-Dong Song
Journal:  Mol Vis       Date:  2010-10-12       Impact factor: 2.367

5.  Familial aggregation of myopia in the Tehran eye study: estimation of the sibling and parent offspring recurrence risk ratios.

Authors:  Akbar Fotouhi; Arash Etemadi; Hassan Hashemi; Hojjat Zeraati; Joan E Bailey-Wilson; Kazem Mohammad
Journal:  Br J Ophthalmol       Date:  2007-05-10       Impact factor: 4.638

6.  Clinical and linkage study on a consanguineous Chinese family with autosomal recessive high myopia.

Authors:  Zhikuan Yang; Xueshan Xiao; Shiqiang Li; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-02-09       Impact factor: 2.367

7.  Sequence variations of GRM6 in patients with high myopia.

Authors:  Xiaoyu Xu; Shiqiang Li; Xueshan Xiao; Panfeng Wang; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-10-19       Impact factor: 2.367

8.  Muscarinic acetylcholine receptor 1 gene polymorphisms associated with high myopia.

Authors:  Hui-Ju Lin; Lei Wan; Yuhsin Tsai; Wen-Chi Chen; Shih-Wei Tsai; Fuu-Jen Tsai
Journal:  Mol Vis       Date:  2009-09-04       Impact factor: 2.367

9.  Sclera-related gene polymorphisms in high myopia.

Authors:  Hui-Ju Lin; Lei Wan; Yuhsin Tsai; Su-Ching Liu; Wen-Chi Chen; Shih-Wei Tsai; Fuu-Jen Tsai
Journal:  Mol Vis       Date:  2009-08-20       Impact factor: 2.367

10.  An evaluation of OPTC and EPYC as candidate genes for high myopia.

Authors:  Panfeng Wang; Shiqiang Li; Xueshan Xiao; Xiangming Guo; Qingjiong Zhang
Journal:  Mol Vis       Date:  2009-10-15       Impact factor: 2.367

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