Publications

Detailed Information

Comparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber`s hereditary optic neuropathy

DC Field Value Language
dc.contributor.authorSeo, J. H.-
dc.contributor.authorHwang, J-M-
dc.contributor.authorPark, S. S.-
dc.date.accessioned2012-05-22T08:55:09Z-
dc.date.available2012-05-22T08:55:09Z-
dc.date.issued2010-01-
dc.identifier.citationEYE; Vol.24 1; 107-111ko_KR
dc.identifier.issn0950-222X-
dc.identifier.urihttps://hdl.handle.net/10371/76259-
dc.description.abstractPurpose To compare retinal nerve fibre layer (RNFL) thickness changes between mitochondrial DNA (mtDNA) mutations at nucleotides 11778 and 14484 in Leber`s hereditary optic neuropathy (LHON) using optical coherence tomography (OCT). Methods Thirty LHON patients with mtDNA mutations at nucleotides 11778 or 14484 underwent full ophthalmologic examinations including Stratus OCT. Patients were divided into four groups according to disease duration (early <= 6 months, late >6 months) and mtDNA mutation type (11778 and 14484), and their RNFL thicknesses were compared. Results Average RNFL thickness in the early 11778 group was significantly greater than that in the early 14484 group (P = 0.04). Average RNFL thickness in the late 11778 group was significantly less than that in the late 14484 group (P = 0.02). Quadrant analysis of the superior, nasal, and inferior quadrant RNFL thickness in the late 11778 group showed more severe RNFL atrophy than in the late 14484 group (P = 0.023, 0.015, 0.003, respectively). Conclusions RNFL thickness was significantly increased in the early stage and decreased in the late stage in the 11778 group than in the 14484 group. Eye (2010) 24, 107-111; doi: 10.1038/eye.2009.36; published online 27 February 2009ko_KR
dc.language.isoenko_KR
dc.publisherNATURE PUBLISHING GROUPko_KR
dc.subjectLeber`s hereditary optic neuropathyko_KR
dc.subjectretinal nerve fibre layer thicknessko_KR
dc.subjectoptical coherence tomographyko_KR
dc.titleComparison of retinal nerve fibre layers between 11778 and 14484 mutations in Leber`s hereditary optic neuropathyko_KR
dc.typeArticleko_KR
dc.identifier.doi10.1038/eye.2009.36-
dc.citation.journaltitleEYE-
dc.description.citedreferenceNIKOSKELAINEN E, 1983, ARCH OPHTHALMOL-CHIC, V101, P1059-
dc.description.citedreferenceWALLACE DC, 1988, SCIENCE, V242, P1427-
dc.description.citedreferenceHUOPONEN K, 1991, AM J HUM GENET, V48, P1147-
dc.description.citedreferenceMACKEY D, 1992, AM J HUM GENET, V51, P1218-
dc.description.citedreferenceNEWMAN NJ, 1998, WALSH HOYTS CLIN NEU, P742-
dc.description.citedreferenceBlumenthal EZ, 2000, OPHTHALMOLOGY, V107, P2278-
dc.description.citedreferenceCarelli V, 2004, PROG RETIN EYE RES, V23, P53, DOI 10.1016/j.preteyeres.2003.10.003-
dc.description.citedreferenceBRUDENZ DL, 2005, OPHTHALMOLOGY, V112, P3-
dc.description.citedreferenceSavini G, 2005, OPHTHALMOLOGY, V112, P127, DOI 10.1016/j.ophtha.2004.09.033-
dc.description.citedreferencePro MJ, 2006, J NEUROL SCI, V250, P114, DOI 10.1016/j.jns.2006.08.012-
dc.description.citedreferenceBarboni P, 2006, INVEST OPHTH VIS SCI, V47, P5303, DOI 10.1167/iovs.06-0520-
dc.description.citedreferenceSavini G, 2006, ARCH OPHTHALMOL-CHIC, V124, P1111-
dc.description.citedreferenceBarboni P, 2005, OPHTHALMOLOGY, V112, P120, DOI 10.1016/j.ophtha.2004.06.034-
dc.description.citedreferenceMenke MN, 2005, INVEST OPHTH VIS SCI, V46, P3807, DOI 10.1167/iovs.05-0352-
dc.description.citedreferenceNIKOSKELAINEN E, 1982, ARCH OPHTHALMOL-CHIC, V100, P1597-
dc.description.tc2-
Appears in Collections:
Files in This Item:
There are no files associated with this item.

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share