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Медицинская библиотека · Transactions of the American Ophthalmological Society · 2006

Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study.

Sadun Alfredo A, Salomao Solange R, Berezovsky Adriana, Sadun Federico, Denegri Anna Maria, Quiros Peter A, Chicani Filipe, Ventura Dora, Barboni Piero, Sherman Jerome, Sutter Erich, Belfort Rubens, Carelli Valerio

Клинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

PURPOSE: The authors previously presented the results of their 2001 field investigation to rural Brazil to investigate a 336-member pedigree of Leber hereditary optic neuropathy (LHON). The present work describes the yearly field investigations 2001 to 2005, utilizing a variety of highly sophisticated psychophysical and electrophysiologic procedures, in asymptomatic LHON carriers, some of whom converted to affected status.

METHODS

Careful, repeated examinations of 75 carriers of homoplasmic 11778 LHON mtDNA J-haplogroup mutants were performed as part of the field investigation of this pedigree. All subjects underwent a detailed neuro-ophthalmologic investigation, including formal visual fields (Humphrey; HVF) and fundus photography. In addition, many subjects underwent rigorous psychophysical examination, including Cambridge Research Systems color vision and contrast sensitivity testing, OCT, GDx, and multifocal visual evoked response (mfVER) and multifocal electroretinogram (mfERG). Two patients followed as nonsymptomatic LHON carriers converted to affected status.

RESULTS

Many LHON carriers did, in fact, show subclinical or occult abnormalities. Focal edema was often seen involving the arcuate nerve fiber bundles, and this corresponded with areas of relative paracentral or arcuate scotomas on HVF testing. Compared to controls, LHON carriers had significant losses in color vision affecting mostly the red-green system and reduction in spatial but not temporal contrast sensitivity. The mfVER and mfERG data showed that most carriers had depressed central responses and abnormal interocular asymmetries.

CONCLUSIONS

In this very large pedigree of 11778 LHON, the carriers frequently showed manifestations of optic nerve impairments. Their occult disease reflected low-grade compromise that waxed and waned. In two cases, these changes led to a crescendo of dramatic impairments that characterize conversion to affected status.

Для цитирования: Sadun Alfredo A, Salomao Solange R, Berezovsky Adriana, Sadun Federico, Denegri Anna Maria, Quiros Peter A, Chicani Filipe, Ventura Dora, Barboni Piero, Sherman Jerome, Sutter Erich, Belfort Rubens, Carelli Valerio. Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study.. Transactions of the American Ophthalmological Society. 2006.

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