Purpose: To verify the frequencies of T34T, E50K, M98K, 691_692insAG, and R545Q variants in the optineurin (OPTN) gene in Brazilian subjects with primary open-angle glaucoma (POAG) and controls.
Patients And Methods: Ninety-nine patients with POAG and 100 normal controls were enrolled in this study. The frequency of alterations in the OPTN gene was analyzed by direct sequencing and enzymatic digestion of PCR products.
Results: None of the five alterations evaluated was significantly associated with POAG when compared to controls. However, the T34T silent change was present in greater frequency in POAG patients (37.37% vs. 23.00% in controls), while the R545Q change was more prevalent in controls (23.00% vs. 10.10% in POAG). The M98K and 691_692insAG presented with low frequencies in POAG patients (1.01% and 2.02%, respectively) and controls (2.00% and 2.00%, respectively). The E50K substitution was not observed.
Conclusion: Our data show no association between the five evaluated variants and POAG in the Brazilian population.
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http://dx.doi.org/10.1080/13816810802502970 | DOI Listing |
Dis Markers
November 2019
Department of Ophthalmology & Visual Sciences, The Chinese University of Hong Kong, Hong Kong.
Purpose: To study the roles of sequence alterations in the optineurin () gene-coding region in normal-tension glaucoma (NTG) among Chinese patients.
Methods: Genomic DNA was extracted from 190 NTG patients and 201 control subjects. The thirteen exons of were amplified by polymerase chain reaction and analyzed by direct sequencing.
Ophthalmic Genet
March 2009
Department of Ophthalmology, Faculty of Medical Sciences, Glaucoma Service, Irmandade da Santa Casa de Misericordia de Sao Paulo, Sao Paulo, Brazil.
Purpose: To verify the frequencies of T34T, E50K, M98K, 691_692insAG, and R545Q variants in the optineurin (OPTN) gene in Brazilian subjects with primary open-angle glaucoma (POAG) and controls.
Patients And Methods: Ninety-nine patients with POAG and 100 normal controls were enrolled in this study. The frequency of alterations in the OPTN gene was analyzed by direct sequencing and enzymatic digestion of PCR products.
Mol Vis
February 2007
Department of Ophthalmology and Visual Sciences, The University of Michigan, Ann Arbor, MI, uSA.
Purpose: To evaluate the extent to which mutations in the optineurin (OPTN) glaucoma gene play a role in glaucoma in different populations.
Methods: Case-controlled study of OPTN sequence variants in individuals with or without glaucoma in populations of different ancestral origins and evaluate previous OPTN reports. We analyzed 314 subjects with African, Asian, Caucasian and Hispanic ancestries included 229 cases of primary open-angle glaucoma, 51 cases of juvenile-onset open-angle glaucoma, 33 cases of normal tension glaucoma, and 371 controls.
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