Potential underlying genetic associations between keratoconus and diabetes mellitus

被引:8
|
作者
Ates, Kristin M. [1 ,2 ]
Estes, Amy J. [2 ,3 ]
Liu, Yutao [1 ,3 ,4 ]
机构
[1] Augusta Univ, Med Coll Georgia, Dept Cellular Biol & Anat, Augusta, GA USA
[2] Augusta Univ, Med Coll Georgia, Dept Ophthalmol, Augusta, GA USA
[3] Augusta Univ, James & Jean Culver Vis Discovery Inst, Med Coll Georgia, Augusta, GA USA
[4] Augusta Univ, Med Coll Georgia, Ctr Biotechnol & Genom Med, Augusta, GA USA
来源
ADVANCES IN OPHTHALMOLOGY PRACTICE AND RESEARCH | 2021年 / 1卷 / 01期
基金
美国国家卫生研究院;
关键词
Keratoconus; Genetics; Diabetes; Collagen crosslinking; Oxidative stress; CENTRAL CORNEAL THICKNESS; HEPATOCYTE GROWTH-FACTOR; GENOME-WIDE ASSOCIATION; GLYCATION END-PRODUCTS; EPITHELIAL-MESENCHYMAL TRANSITION; MATRIX PROTEIN BETA-IG-H3; EHLERS-DANLOS-SYNDROME; BETA-CELL DESTRUCTION; DISMUTASE-1; SOD1; GENE; CALPASTATIN CAST GENE;
D O I
10.1016/j.aopr.2021.100005
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background: Keratoconus (KC) is the most common ectatic corneal disease, characterized by significantly localized thinning of the corneal stroma. Genetic, environmental, hormonal, and metabolic factors contribute to the pathogenesis of KC. Additionally, multiple comorbidities, such as diabetes mellitus, may affect the risk of KC. Main Text: Patients with diabetes mellitus (DM) have been reported to have lower risk of developing KC by way of increased endogenous collagen crosslinking in response to chronic hyperglycemia. However, this remains a debated topic as other studies have suggested either a positive association or no association between DM and KC. To gain further insight into the underlying genetic components of these two diseases, we reviewed candidate genes associated with KC and central corneal thickness in the literature. We then explored how these genes may be regulated similarly or differentially under hyperglycemic conditions and the role they play in the systemic complications associated with DM. Conclusions: Our comprehensive review of potential genetic factors underlying KC and DM provides a direction for future studies to further determine the genetic etiology of KC and how it is influenced by systemic diseases such as diabetes.
引用
收藏
页数:17
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