Literature DB >> 15223817

Localized retinal electrophysiological and fundus autofluorescence imaging abnormalities in maternal inherited diabetes and deafness.

Caren Bellmann1, Magella M Neveu, Hendrik P N Scholl, Chris R Hogg, Pamela P Rath, Sharon Jenkins, Alan C Bird, Graham E Holder.   

Abstract

PURPOSE: To investigate retinal function in patients with maternally inherited diabetes and deafness (MIDD) and to correlate the findings with fundus autofluorescence (FAF) imaging.
METHODS: FAF was imaged in five patients (age range, 49-60 years) confirmed to have the mitochondrial DNA nucleotide A3243G point mutation. Retinal function was measured by full-field (Ganzfeld) electroretinography (ERG) and pattern ERG, incorporating the International Society for Clinical Electrophysiology of Vision (ISCEV) standards. Multifocal ERG (mfERG) was also performed. For analysis of the mfERG data, five regional ring groups of equal eccentricity were formed. For each ring, the peak amplitude (defined as the difference between P1 and N1) and the implicit time of P1 were determined and compared with normative values.
RESULTS: Visual acuity in the patients was between 20/20 and 20/40 (Early Treatment Diabetic Retinopathy Study [ETDRS] chart). Irregular increased FAF signals were observed adjacent to and between areas of atrophy of the retinal pigment epithelium (RPE). Ganzfeld ERGs were within normal limits in three patients. Pattern ERG was abnormal in five eyes of three patients. mfERG peak amplitude abnormalities were particularly present in rings 2 and 3 and were consistent with the distribution of FAF abnormalities. In all but one eye, no implicit times changes were present.
CONCLUSIONS: Significant mfERG abnormalities with normal Ganzfeld ERG are consistent with nonuniform damage to the central retina in MIDD, in keeping with the FAF findings. Reduced peak amplitudes with normal implicit times in the mfERG suggest localized loss of function and may indicate damage to the cone photoreceptor outer segments or cone photoreceptor loss in MIDD.

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Year:  2004        PMID: 15223817     DOI: 10.1167/iovs.03-1090

Source DB:  PubMed          Journal:  Invest Ophthalmol Vis Sci        ISSN: 0146-0404            Impact factor:   4.799


  12 in total

1.  Cystoid macular changes on optical coherence tomography in a patient with maternally inherited diabetes and deafness (MIDD)-associated macular dystrophy.

Authors:  Cynthia X Qian; Kari Branham; Naheed Khan; Steven K Lundy; John R Heckenlively; Thiran Jayasundera
Journal:  Ophthalmic Genet       Date:  2017-01-31       Impact factor: 1.803

2.  Functional characterisation and serial imaging of abnormal fundus autofluorescence in patients with retinitis pigmentosa and normal visual acuity.

Authors:  A G Robson; Z Saihan; S A Jenkins; F W Fitzke; A C Bird; A R Webster; G E Holder
Journal:  Br J Ophthalmol       Date:  2006-04       Impact factor: 4.638

3.  Transitions of multifocal electroretinography following combined intravitreal bevacizumab and photodynamic therapy for polypoidal choroidal vasculopathy.

Authors:  Chengguo Zuo; Feng Wen; Jiaqing Li; Yan Liu; Meng Li
Journal:  Doc Ophthalmol       Date:  2009-01-31       Impact factor: 2.379

4.  The Tip of the Iceberg in Maternally Inherited Diabetes and Deafness.

Authors:  Josef Finsterer; Marlies Frank
Journal:  Oman Med J       Date:  2018-09

5.  Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome.

Authors:  Kenji Ozawa; Kiyofumi Mochizuki; Yusuke Manabe; Nobuaki Yoshikura; Takayoshi Shimohata; Ichizo Nishino; Yu-Ichi Goto
Journal:  Doc Ophthalmol       Date:  2019-01-30       Impact factor: 2.379

6.  [Retinal pigment epithelium atrophy and hypacousia in monozygotic twin sisters].

Authors:  T Oppermann; J Roider; J Hillenkamp
Journal:  Ophthalmologe       Date:  2010-01       Impact factor: 1.059

7.  Fundus Autofluorescence in Maternally Inherited Diabetes and Deafness: The Gold Standard for Monitoring Maculopathy?

Authors:  Christopher A Ovens; Kate Ahmad; Clare L Fraser
Journal:  Neuroophthalmology       Date:  2019-09-24

Review 8.  Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literature.

Authors:  Alejandra Daruich; Alexandre Matet; François-Xavier Borruat
Journal:  BMC Ophthalmol       Date:  2014-06-06       Impact factor: 2.209

Review 9.  Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update.

Authors:  Anthony G Robson; Michel Michaelides; Zubin Saihan; Alan C Bird; Andrew R Webster; Anthony T Moore; Fred W Fitzke; Graham E Holder
Journal:  Doc Ophthalmol       Date:  2007-11-06       Impact factor: 2.379

10.  Pigmentary retinopathy, rod-cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNALys (m.8340G>A) gene variant.

Authors:  Jaidip S Gill; Steven A Hardy; Emma L Blakely; Sila Hopton; Andrea H Nemeth; Carl Fratter; Joanna Poulton; Robert W Taylor; Susan M Downes
Journal:  Br J Ophthalmol       Date:  2017-07-20       Impact factor: 4.638

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