Visual evoked potentials findings in non-affected subjects from a large Brazilian pedigree of 11778 Leber's hereditary optic neuropathy

Paula Yuri Sacai, Solange Rios Salomão, Valerio Carelli, Josenilson Martins Pereira, Rubens Belfort, Alfredo Arrigo Sadun, Adriana Berezovsky

Research output: Contribution to journalArticlepeer-review

Abstract

To investigate pattern-reversal visual evoked potentials (PRVEP) in asymptomatic maternally and non-maternally related members from a large Brazilian 11778/ND4 LHON pedigree. Transient PRVEP for check sizes 15′ and 60′ were recorded from asymptomatic mutation carriers and non-mutant descendants of affected/non-affected males, all with best-corrected visual acuity of 20/20. A control group of spouses (off-pedigree) was also included. Parameters of N75, P100 and N135 latencies (ms) and N75-P100 peak-to-peak amplitude (μV) as well as temporal dispersion (latency of N135-latency of N75) were determined. Longitudinal testing was obtained in a subseries of carriers in three annual consecutive visits. We tested 48 asymptomatic mutation carriers, 19 descendants of affected males, 9 descendants of non-affected males and 27 off-pedigrees, all of the latter being non-mutant. All non-mutant male descendants did not differ from off-pedigree controls. Statistically prolonged P100 latencies were found in mutation carriers (P = 0.0143) when compared with off-pedigrees for check sizes 15′, as well as significantly larger temporal dispersions for both check size 15′ (P = 0.0012) and check size 60′ (P = 0.0271). Serial testing in 15 mutation carriers disclosed prolonged P100 latencies and larger temporal dispersion that did not change over time. Subclinical PRVEP abnormalities were detected in this large group of asymptomatic carriers of the 11778/ND4 LHON mutation from the same family, confirming and extending previous psychophysical and structural findings of a selective involvement of the parvocellular pathway. PRVEP is a useful test to characterize and monitor visual dysfunction in this devastating disease.

Original languageEnglish
Pages (from-to)147-154
Number of pages8
JournalDocumenta Ophthalmologica
Volume121
Issue number2
DOIs
Publication statusPublished - Oct 2010

Keywords

  • 11778 mutation
  • Leber hereditary optic neuropathy
  • Mitochondrial disease
  • Optic nerve
  • Visual evoked potentials

ASJC Scopus subject areas

  • Ophthalmology
  • Sensory Systems
  • Physiology (medical)

Fingerprint Dive into the research topics of 'Visual evoked potentials findings in non-affected subjects from a large Brazilian pedigree of 11778 Leber's hereditary optic neuropathy'. Together they form a unique fingerprint.

Cite this