Dudakova L, Liskova P, Jirsova K
Laboratory of the Biology and Pathology of the Eye, Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic.
Laboratory of the Biology and Pathology of the Eye, Institute of Inherited Metabolic Disorders, First Faculty of Medicine, Charles University and General University Hospital in Prague, Prague, Czech Republic; Department of Ophthalmology, General Teaching Hospital and First Faculty of Medicine, Charles University, Prague, Czech Republic.
Med Hypotheses. 2015 May;84(5):518-24. doi: 10.1016/j.mehy.2015.02.017. Epub 2015 Mar 2.
Keratoconus is a bilateral disease characterized by progressive corneal thinning leading to irregular astigmatism that results in significant visual impairment. Despite extensive research, the exact etiopathogenesis of keratoconus remains unknown. Many copper-dependent enzymes such as superoxide dismutases, cytochrome c oxidase and lysyl oxidase have been shown to be altered in keratoconic corneas, and a decrease of copper levels in the diseased tissue has been reported as well. We propose a hypothesis linking all the putative pathways of keratoconus development and suggest that copper imbalance in corneal tissue may be an independent risk factor for the disease. The assessment of copper levels and its distribution in keratoconic corneas warrants further investigation.
圆锥角膜是一种双侧性疾病,其特征是角膜逐渐变薄,导致不规则散光,进而造成严重视力损害。尽管进行了广泛研究,但圆锥角膜的确切病因仍不清楚。许多依赖铜的酶,如超氧化物歧化酶、细胞色素c氧化酶和赖氨酰氧化酶,已被证实在圆锥角膜中发生改变,并且有报道称患病组织中的铜水平降低。我们提出一个假说,将圆锥角膜发展的所有假定途径联系起来,并认为角膜组织中的铜失衡可能是该疾病的一个独立危险因素。评估圆锥角膜中铜的水平及其分布值得进一步研究。