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赖氨酸氧化酶在圆锥角膜和圆锥角膜相关疾病中的作用缺失。

The impairment of lysyl oxidase in keratoconus and in keratoconus-associated disorders.

机构信息

Laboratory of Biology and Pathology of Eye, First Faculty of Medicine, Institute of Inherited Metabolic Disorders, Charles University and General University Hospital, Prague, Czech Republic.

出版信息

J Neural Transm (Vienna). 2013 Jun;120(6):977-82. doi: 10.1007/s00702-013-0993-1. Epub 2013 Feb 20.

Abstract

Keratoconus (KC) is an eye disease characterized by the progressive thinning and protrusion of the cornea, which results in the loss of visual acuity. This disorder remains poorly understood, although recent studies indicate the involvement of genetic and environmental factors. Recently, we have found that the distribution of the cross-linking enzyme lysyl oxidase (LOX) is markedly decreased in about 63 % of keratoconic specimens. Similarly, LOX activity is significantly reduced by 38 % compared to control tissue. Nearly 70 systemic disorders have been reported in association with KC, most of them affecting the extracellular matrix. In this review we attempted to ascertain whether any KC-associated diseases exhibit signs that may reflect LOX impairment. We hypothesized that very similar changes in the extracellular matrix, particularly at the level of collagen metabolism, including LOX impairment in mitral leaflets, may reflect an association between KC and mitral valve prolapse. Moreover, this putative association is supported by the high frequency of Down syndrome in both diseases. Among other disorders that have been found to coincide with KC, we did not find any in which the LOX enzyme may be directly or indirectly impaired. On the other hand, in cases where KC is present along with other connective tissue disorders (Marfan syndrome, Ehlers-Danlos syndrome and others), KC may not arise as a localized manifestation, but rather may be induced as the result of a more complex connective tissue disorder.

摘要

圆锥角膜(KC)是一种以角膜进行性变薄和突出为特征的眼部疾病,可导致视力丧失。尽管最近的研究表明遗传和环境因素的参与,但这种疾病仍然知之甚少。最近,我们发现交联酶赖氨酰氧化酶(LOX)的分布在大约 63%的圆锥角膜标本中明显减少。同样,与对照组织相比,LOX 活性降低了 38%。已有近 70 种系统性疾病与 KC 相关,其中大多数影响细胞外基质。在这篇综述中,我们试图确定任何与 KC 相关的疾病是否表现出可能反映 LOX 损伤的迹象。我们假设细胞外基质,特别是在胶原代谢水平上,非常相似的变化,包括二尖瓣叶 LOX 损伤,可能反映了 KC 与二尖瓣脱垂之间的关联。此外,这一假设的关联得到了这两种疾病中唐氏综合征高发病率的支持。在与 KC 同时存在的其他疾病中,我们没有发现任何 LOX 酶可能直接或间接受损的疾病。另一方面,在 KC 与其他结缔组织疾病(马凡综合征、埃勒斯-当洛斯综合征等)同时存在的情况下,KC 可能不会作为局部表现出现,而可能是由于更复杂的结缔组织疾病引起的。

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