Abstract

Glaucoma is the leading cause of irreversible blindness worldwide, with elevated intraocular pressure (IOP) as the only known modifiable risk factor. Trabecular meshwork (TM)-inducible myocilin (the MYOC gene) was the first to be identified and linked to juvenile and primary open-angle glaucoma. It has been suggested that mutations in the MYOC gene and the aggregation of mutant myocilin in the endoplasmic reticulum (ER) of TM may cause ER stress, resulting in a reduced outflow of aqueous humor and an increase in IOP. We selected 20 MYOC mutations with experimentally determined melting temperatures of mutated myocilin proteins. We included 40 published studies with at least one glaucoma patient with one of these 20 MYOC mutations and information on age at glaucoma diagnosis. Based on data from 458 patients, we found that a statistically significant but weak correlation was present between age and melting temperature based on various assumptions for age. We therefore conclude that genetic analysis of MYOC mutations alone cannot be used to accurately predict age at glaucoma diagnosis. However, it might be an important prognostic factor combined with other clinical factors for critical and early detection of glaucoma.

Highlights

  • Glaucoma is the leading cause of irreversible blindness and is characterized by optic nerve damage and retinal ganglion cell loss [1,2]

  • endoplasmic reticulum (ER) stress implicated in ocular diseases including glaucoma and neurodegenerative diseases [17,72] can be induced by genetic mutations, overexpression of genes, or other pathophysiological processes that lead to protein aggregation in the ER lumen [73]

  • Our analysis shows there is a weak to moderate correlation between the stability of mutated myocilin and age at glaucoma diagnosis of those patients who have the mutations

Read more

Summary

Introduction

Glaucoma is the leading cause of irreversible blindness and is characterized by optic nerve damage and retinal ganglion cell loss [1,2]. Glaucoma affects approximately 70 million people worldwide, and is projected to affect 111.8 million people by 2040 [3]. Risk factors include a family history of glaucoma, age, chronic steroid use, myopia, diabetes, and hypertension [4]. IOP is a measurement of the aqueous humor produced by the ciliary bodies that is drained out through the trabecular meshwork (TM) and uveoscleral outflow [6]. Changes in the cellular signaling pathways and physical structure of TM may increase resistance to aqueous humor outflow, which can increase IOP [8]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call