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Lookup NU author(s): Dr Patrick Yu Wai Man, Joanna Stewart, Professor Gavin Hudson, Dr Richard Andrews, Philip Griffiths, Michael Birch, Professor Patrick Chinnery
Background Primary open angle glaucoma is a progressive optic neuropathy characterised by the selective loss of retinal ganglion cells, pathological optic disc cupping and visual field defects. The OPA1 gene encodes an inner mitochondrial membrane protein crucial for normal mitochondrial function, and pathogenic mutations cause autosomal dominant optic atrophy by specifically targeting retinal ganglion cells. This raises the distinct possibility that more subtle genetic variations in OPA1 could alter the risk of developing glaucoma. Methods 137 patients with primary open angle glaucoma (67 patients with high-tension glaucoma (HTG), 70 patients with normal-tension glaucoma (NTG)) and 75 controls from the North East of England were studied. Three single-nucleotide polymorphisms in intron 8 (IVS8+4c -> t and IVS8+32t -> c) and exon 4 (c.473A -> G) of the OPA1 gene were genotyped in the study group. In addition, the entire OPA1 coding region was sequenced in 24 individuals with the CT/TT compound genotype using standard BigDye chemistries. Results There was no difference in either allele or genotype frequency for the IVS8+32t -> c single-nucleotide polymorphisms between patients and controls, but there was a significant association between the T allele at IVS8+4c -> t and the risk of developing NTG (OR-2.04, 95% CI-1.10 to 3.81, p-0.004), but not HTG. Logistic regression analysis also confirmed a strong association between the CT/TT compound genotype at IVS8+4 and IVS8+32 with NTG (OR=29.75, 95% CI=3.83 to 231.21, p=0.001). Conclusions The CT/TT compound genotype at IVS8+4 and IVS8+32 is a strong genetic risk determinant for NTG but not HTG.
Author(s): Yu Wai Man P, Stewart JD, Hudson G, Andrews RM, Griffiths PG, Birch MK, Chinnery PF
Publication type: Article
Publication status: Published
Journal: Journal of Medical Genetics
Year: 2010
Volume: 47
Issue: 2
Pages: 120-125
Print publication date: 05/07/2010
Date deposited: 21/05/2010
ISSN (print): 0022-2593
ISSN (electronic): 1468-6244
Publisher: BMJ Group
URL: http://dx.doi.org/10.1136/jmg.2009.067512
DOI: 10.1136/jmg.2009.067512
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