Literature DB >> 23647424

Association of Mn-SOD mutation (c.47T > C) with various POAG clinical indices.

Khaled K Abu-Amero1, Altaf A Kondkar, Ahmed Mousa, Essam A Osman, Saleh A Al-Obeidan.   

Abstract

BACKGROUND: To investigate whether the c.47T > C mutation in the manganese superoxide dismutase gene (Mn-SOD) is a risk factor for primary open angle glaucoma (POAG) in the Saudi population.
MATERIALS AND METHODS: A cohort of 226 unrelated POAG patients and 403 unrelated control subjects from Saudi Arabia were genotyped for a single nucleotide polymorphism (SNP; rs4880; c.47T > C) utilizing Taq-Man® assay ID: C_8709053_10. The association between mutant genotypes and various clinical indices important for POAG was also investigated.
RESULTS: Among cases, the prevalence of the wildtype genotype (T/T) was 22.1% (50/226), while the heterozygous mutated genotype (T/C) was 50.9% (115/226) and the homozygous mutant genotype (C/C) was 27% (61/226). There were no statistically significant differences between cases and controls in terms of the genotype distribution on both heterozygous mutant (p = 0.916) and homozygous mutant (p = 0.988) genotypes. POAG patients with the mutant genotypes had slightly higher intraocular pressure (IOP) than controls. Additionally, patients with T/C genotype had slight elevation of the cup/disc ratio than the normal group. Additionally, the age at onset of disease showed an increasing trend with severity of mutation where it increases across groups T/T, T/C, and C/C being at [48.9 (±16.3), 51.4 (±12.2), and 56.5 (±13.9)] respectively and a p value of 0.028 for the C/C genotype.
CONCLUSIONS: This mutation could be associated with various clinical indices important for POAG. If similar findings were found in other populations and larger cohorts, then this SNP may be used as a marker for assessing the severity of the disease.

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Year:  2013        PMID: 23647424     DOI: 10.3109/13816810.2013.796390

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  7 in total

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Authors:  Shaoqing He; Dorota L Stankowska; Dorette Z Ellis; Raghu R Krishnamoorthy; Thomas Yorio
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Review 2.  An Updated Review on the Genetics of Primary Open Angle Glaucoma.

Authors:  Khaled Abu-Amero; Altaf A Kondkar; Kakarla V Chalam
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3.  Lack of association between polymorphism rs540782 and primary open angle glaucoma in Saudi patients.

Authors:  Altaf A Kondkar; Nikhil B Edward; Hatem Kalantan; Abdullah S Al-Kharashi; Saleh Altuwaijri; Gamal Mohamed; Tahira Sultan; Taif A Azad; Khaled K Abu-Amero
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4.  Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort.

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Journal:  BMC Res Notes       Date:  2017-11-29

5.  Polymorphism rs547984 on human chromosome 1q43 is not associated with primary open angle glaucoma in a Saudi cohort.

Authors:  Taif A Azad; Nikhil B Edward; Altaf A Kondkar; Hatem Kalantan; Saleh Altuwaijri; Tahira Sultan; Faisal A Al-Mobarak; Saleh A Al-Obeidan; Khaled K Abu-Amero
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Review 6.  The Role of Endogenous Neuroprotective Mechanisms in the Prevention of Retinal Ganglion Cells Degeneration.

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7.  Polymorphism rs7555523 in transmembrane and coiled-coil domain 1 (TMCO1) is not a risk factor for primary open angle glaucoma in a Saudi cohort.

Authors:  Altaf A Kondkar; Ahmed Mousa; Taif A Azad; Tahira Sultan; Abdullah Alawad; Saleh Altuwaijri; Saleh A Al-Obeidan; Khaled K Abu-Amero
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  7 in total

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