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A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.

Publication ,  Conference
Sadun, AA; Carelli, V; Salomao, SR; Berezovsky, A; Quiros, P; Sadun, F; DeNegri, A-M; Andrade, R; Schein, S; Belfort, R
Published in: Trans Am Ophthalmol Soc
2002

PURPOSE: We conducted extensive epidemiological, neuro-ophthalmological, psychophysical, and blood examinations on a newly discovered, very large pedigree with molecular analysis showing mtDNA mutation for Leber's hereditary optic neuropathy (LHON). METHODS: Four patients representing four index cases from a remote area of Brazil were sent to Sao Paulo, where complete ophthalmological examinations strongly suggested LHON. Molecular analysis of their blood demonstrated that they were LHON, homoplasmic 11778, J-haplogroup. They had an extensive family that all lived in one rural area in Brazil. To investigate this family, we drew on a number of international experts to form a team that traveled to Brazil. This field team also included several members of the Federal University of Sao Paulo, and together we evaluated 273 of the 295 family members that were still alive. We conducted epidemiological interviews emphasizing possible environmental risk factors, comprehensive neuro-ophthalmological examinations, psychophysical tests, Humphrey visual field studies, fundus photography, and blood testing for both mitochondrial genetic analysis and nuclear gene linkage analysis. RESULTS: The person representing the first-generation case immigrated from Verona, Italy, to Colatina. Subsequent generations demonstrated penetrance rates of 71%, 60%, 34%, 15%, and 9%. The percentages of males were 60%, 50%, 64%, 100%, and 100%. Age at onset varied from 10 to 64 years, and current visual acuities varied from LP to 20/400. CONCLUSIONS: Almost 95% of a nearly 300-member pedigree with LHON 11778 were comprehensively studied. Analysis of environmental risk factors and a nuclear modifying factor from this group may help address the perplexing mystery of LHON: Why do only some of the genetically affected individuals manifest the disease? This fully described database may also provide an excellent opportunity for future clinical trials of any purported neuroprotective agent.

Duke Scholars

Published In

Trans Am Ophthalmol Soc

ISSN

0065-9533

Publication Date

2002

Volume

100

Start / End Page

169 / 178

Location

United States

Related Subject Headings

  • Visual Fields
  • Visual Acuity
  • Risk Factors
  • Polymerase Chain Reaction
  • Point Mutation
  • Pedigree
  • Optic Atrophy, Hereditary, Leber
  • Ophthalmology & Optometry
  • Middle Aged
  • Male
 

Citation

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Sadun, A. A., Carelli, V., Salomao, S. R., Berezovsky, A., Quiros, P., Sadun, F., … Belfort, R. (2002). A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy. In Trans Am Ophthalmol Soc (Vol. 100, pp. 169–178). United States.
Sadun, Alfredo A., Valerio Carelli, Solange R. Salomao, Adriana Berezovsky, Peter Quiros, Federico Sadun, Anna-Maria DeNegri, Rafael Andrade, Stan Schein, and Rubens Belfort. “A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.” In Trans Am Ophthalmol Soc, 100:169–78, 2002.
Sadun AA, Carelli V, Salomao SR, Berezovsky A, Quiros P, Sadun F, et al. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy. In: Trans Am Ophthalmol Soc. 2002. p. 169–78.
Sadun, Alfredo A., et al. “A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy.Trans Am Ophthalmol Soc, vol. 100, 2002, pp. 169–78.
Sadun AA, Carelli V, Salomao SR, Berezovsky A, Quiros P, Sadun F, DeNegri A-M, Andrade R, Schein S, Belfort R. A very large Brazilian pedigree with 11778 Leber's hereditary optic neuropathy. Trans Am Ophthalmol Soc. 2002. p. 169–178.

Published In

Trans Am Ophthalmol Soc

ISSN

0065-9533

Publication Date

2002

Volume

100

Start / End Page

169 / 178

Location

United States

Related Subject Headings

  • Visual Fields
  • Visual Acuity
  • Risk Factors
  • Polymerase Chain Reaction
  • Point Mutation
  • Pedigree
  • Optic Atrophy, Hereditary, Leber
  • Ophthalmology & Optometry
  • Middle Aged
  • Male