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青光眼发病机制中基因、年龄和环境的相互作用。

The interactions of genes, age, and environment in glaucoma pathogenesis.

机构信息

Faculty of Medicine and Dentistry, Department of Medical Genetics, Edmonton, Alberta T6G 2H7, Canada.

Faculty of Medicine and Dentistry, Department of Medical Genetics, Edmonton, Alberta T6G 2H7, Canada.

出版信息

Surv Ophthalmol. 2015 Jul-Aug;60(4):310-26. doi: 10.1016/j.survophthal.2015.01.004. Epub 2015 Feb 4.

Abstract

Glaucoma, a progressive degenerative condition that results in the death of retinal ganglion cells, is one of the leading causes of blindness, affecting millions worldwide. The mechanisms underlying glaucoma are not well understood, although years of studies have shown that the largest risk factors are elevated intraocular pressure, age, and genetics. Eleven genes and multiple loci have been identified as contributing factors. These genes act by a number of mechanisms, including mechanical stress, ischemic/oxidative stress, and neurodegeneration. We summarize the recent advances in the understanding of glaucoma and propose a unified hypothesis for glaucoma pathogenesis. Glaucoma does not result from a single pathological mechanism, but rather a combination of pathways that are influenced by genes, age, and environment. In particular, we hypothesize that, in the presence of genetic risk factors, exposure to environment stresses results in an earlier age of onset for glaucoma. This hypothesis is based upon the overlap of the molecular pathways in which glaucoma genes are involved. Because of the interactions between these processes, it is likely that there are common therapies that may be effective for different subtypes of glaucoma.

摘要

青光眼是一种进行性退行性疾病,可导致视网膜神经节细胞死亡,是全球数百万人失明的主要原因之一。尽管多年的研究表明,眼压升高、年龄和遗传是最大的风险因素,但青光眼的发病机制仍不清楚。已经确定了 11 个基因和多个基因座作为致病因素。这些基因通过多种机制起作用,包括机械应激、缺血/氧化应激和神经退行性变。我们总结了对青光眼发病机制的理解的最新进展,并提出了一个统一的假说。青光眼不是由单一的病理机制引起的,而是受基因、年龄和环境影响的多种途径的组合。特别是,我们假设在存在遗传风险因素的情况下,暴露于环境应激会导致青光眼的发病年龄更早。这一假说基于青光眼基因参与的分子途径的重叠。由于这些过程之间的相互作用,很可能存在对不同亚型青光眼有效的共同治疗方法。

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