Occurrence of MYOC and CYP1B1 variants in juvenile open angle glaucoma Brazilian patients

ABSTRACT

Background: The purpose of this study was to screen juvenile open angle glaucoma (JOAG) patients from Brazil for variants within the MYOC and CYP1B1 genes.

Material and Methods: In this study, we evaluated the coding regions of MYOC and CYP1B1 genes in 100 non-related patients with JOAG and 200 controls through Sanger sequencing. We also tested the most frequent single nucleotide variants of CYP1B1 for association with JOAG.

Results: Sixteen different sequence variants in the MYOC gene were observed in JOAG patients: eight variants were described as neutral and eight were identified in 34 out of 100 patients with JOAG and no controls, thus being considered damaging. In the CYP1B1 gene, nine neutral variants and two damaging alterations were found among JOAG patients. No association between CYP1B1 variants and JOAG was detected.

Conclusion: While MYOC damaging alterations were highly prevalent (34%), CYP1B1 damaging variants were less frequent (2%) in this cohort of Brazilian JOAG patients.

KEYWORDS:

• Glaucoma
• MYOC
• CYP1B1
• JOAG
• variants

Acknowledgments

We thank the patients for their valuable collaboration and São Paulo Research Foundation, FAPESP) for the financial support.

Disclosure statement

No potential conflict of interest was reported by the author.

Additional information

Funding

This work received financial support from the São Paulo Research Foundation, FAPESP (grants 2002/11575-0, 2009/15223-0, 2010/18353-9 and 2013/17958-2).