Literature DB >> 25603773

Electrophysiological testing as a method of cone-rod and cone dystrophy diagnoses and prediction of disease progression.

Ewa Langwińska-Wośko1, Kamil Szulborski, Anna Zaleska-Żmijewska, Jerzy Szaflik.   

Abstract

PURPOSE: To determine the characteristics of patients with cone (CD) and cone-rod dystrophies (CRD) and to evaluate the changes in flash electroretinograms in both groups.
METHODS: The retrospective study involved 48 patients-34 with CRD and 14 with CD. The patients underwent full ophthalmological examination, including Goldmann perimetry and full-field flash electroretinogram (FERG) within the initial examination. These examinations were then repeated seven, or more, years later. The longest follow-up period was 10 years, with the mean at 8.2 years. During both examinations, we assessed the amplitudes of the b wave in the scotopic ERG test 0.01 (which reflects rod response), the maximal scotopic ERG test 3.0 (which reflects cone and rod response) and the photopic 3.0 ERG test (which reflects cone response). The results were then compared against normal values.
RESULTS: The progression over time of ERG b wave amplitudes in the scotopic ERG 0.01, maximal scotopic ERG 3.0 and photopic ERG tests was assessed. There were significant differences in rod, maximal and cone responses, between CD and CRD patients. While rod responses were markedly decreased in CRD patients during their initial examination, the decrease in the rod function in both CD and CRD patients was similar in their follow-up examination (p = 0.2398). Moreover, during initial examination, maximal responses were less common amongst CRD patients, over those with CD. Following the observation period, patients suffering from CRD exhibited a significant decrease in both maximal (p = 0.0125) and cone (p = 0.0046) responses.
CONCLUSION: The clinical course of CRD and CD may vary; however, the latter appears to have a more favourable course than former. Although, at initial examination, the cone function was more diminished in CD patients, the final examinations reveal a more significant drop for CRD patients. Consequently, a differential diagnosis is essential for treating patients and forecasting their disease progression.

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Year:  2015        PMID: 25603773     DOI: 10.1007/s10633-015-9479-9

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  15 in total

Review 1.  Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis.

Authors:  Michel Michaelides; Alison J Hardcastle; David M Hunt; Anthony T Moore
Journal:  Surv Ophthalmol       Date:  2006 May-Jun       Impact factor: 6.048

2.  ISCEV Standard for full-field clinical electroretinography (2008 update).

Authors:  M F Marmor; A B Fulton; G E Holder; Y Miyake; M Brigell; M Bach
Journal:  Doc Ophthalmol       Date:  2008-11-22       Impact factor: 2.379

3.  Cone and rod function in cone degenerations.

Authors:  B Sadowski; E Zrenner
Journal:  Vision Res       Date:  1997-08       Impact factor: 1.886

4.  Clinical course, genetic etiology, and visual outcome in cone and cone-rod dystrophy.

Authors:  Alberta A H J Thiadens; T My Lan Phan; Renate C Zekveld-Vroon; Bart P Leroy; L Ingeborgh van den Born; Carel B Hoyng; Caroline C W Klaver; Susanne Roosing; Jan-Willem R Pott; Mary J van Schooneveld; Norka van Moll-Ramirez; Maria M van Genderen; Camiel J F Boon; Anneke I den Hollander; Arthur A B Bergen; Elfride De Baere; Frans P M Cremers; Andrew J Lotery
Journal:  Ophthalmology       Date:  2012-01-20       Impact factor: 12.079

Review 5.  The cone dysfunction syndromes.

Authors:  M Michaelides; D M Hunt; A T Moore
Journal:  Br J Ophthalmol       Date:  2004-02       Impact factor: 4.638

6.  Abnormal cone synapses in human cone-rod dystrophy.

Authors:  K Gregory-Evans; R N Fariss; D E Possin; C Y Gregory-Evans; A H Milam
Journal:  Ophthalmology       Date:  1998-12       Impact factor: 12.079

7.  Late onset cone dystrophy.

Authors:  Ewa Langwińska-Wośko; Kamil Szulborski; Karina Broniek-Kowalik
Journal:  Doc Ophthalmol       Date:  2010-01-13       Impact factor: 2.379

Review 8.  Cone rod dystrophies.

Authors:  Christian P Hamel
Journal:  Orphanet J Rare Dis       Date:  2007-02-01       Impact factor: 4.123

9.  Novel GUCA1A mutations suggesting possible mechanisms of pathogenesis in cone, cone-rod, and macular dystrophy patients.

Authors:  Kunka Kamenarova; Marta Corton; Blanca García-Sandoval; Patricia Fernández-San Jose; Valentin Panchev; Almudena Avila-Fernández; Maria Isabel López-Molina; Christina Chakarova; Carmen Ayuso; Shomi S Bhattacharya
Journal:  Biomed Res Int       Date:  2013-08-14       Impact factor: 3.411

10.  Inverse pattern of photoreceptor abnormalities in retinitis pigmentosa and cone-rod dystrophy.

Authors:  Midori Yokochi; Danjie Li; Masayuki Horiguchi; Shoji Kishi
Journal:  Doc Ophthalmol       Date:  2012-08-05       Impact factor: 2.379

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  2 in total

1.  Cerebral malaria induces electrophysiological and neurochemical impairment in mice retinal tissue: possible effect on glutathione and glutamatergic system.

Authors:  Karen R H M Oliveira; Nayara Kauffmann; Luana K R Leão; Adelaide C F Passos; Fernando A F Rocha; Anderson M Herculano; José L M do Nascimento
Journal:  Malar J       Date:  2017-11-02       Impact factor: 2.979

2.  A Case Presentation Emphasizing the Value of Full-field ERG in Retinal Dystrophies.

Authors:  A C Corici; D O Alexandru; O M Corici; M Iancău
Journal:  Curr Health Sci J       Date:  2015-03-15
  2 in total

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