Genetic modifiers of rodent animal models: the role in cataractogenesis

Visual impairment leads to a decrease in quality of life. Cataract is the most commonly observed ocular disease in humans that causes vision disorders. The risk factors associated with cataract development include aging, infections, eye injuries, environmental causes, such as radiation and exposure...

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Bibliographic Details
Published inExperimental Animals Vol. 68; no. 4; pp. 397 - 406
Main Authors Wada, Kenta, Yasuda, Shumpei P., Kikkawa, Yoshiaki
Format Journal Article
LanguageEnglish
Published Japan Japanese Association for Laboratory Animal Science 01.01.2019
Japan Science and Technology Agency
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Summary:Visual impairment leads to a decrease in quality of life. Cataract is the most commonly observed ocular disease in humans that causes vision disorders. The risk factors associated with cataract development include aging, infections, eye injuries, environmental causes, such as radiation and exposure to ultraviolet rays in sunlight, and genetic mutations. Additionally, several cataract patients display phenotypic heterogeneity, suggesting the role of genetic modifiers in the modulation of severity and onset time of cataractogenesis. However, the genetic modifiers associated with cataract have not been identified in humans yet. In contrast, the identification and mapping of genetic modifiers have been successfully carried out in mice and rats. In this review, we focus on the genetic modifiers of cataract in the rodent models.
ISSN:1341-1357
1881-7122
DOI:10.1538/expanim.19-0020