Leber’s hereditary optic neuropathy (LHON) in an Apulian cohort of subjects

Angelica Bianco1 ¹, Luigi Bisceglia ², Paolo Trerotoli ³, Luciana Russo ¹, Leonardo D’Agruma ², Silvana Guerriero ¹ and Vittoria Petruzzella ¹

¹Dipartimento di Scienze Mediche di Base, Neuroscienze e Organi di Senso, Università degli Studi Aldo Moro, Bari, Italia; ² Ospedale Casa Sollievo della Sofferenza IRCCS, UOC Genetica Medica, San Giovanni Rotondo, Foggia, Italia; ³Dipartimento di Scienze Biomediche ed Oncologia Umana, Università degli Studi Aldo Moro, Bari, Italia

Leber’s hereditary optic neuropathy (LHON) is a maternally inherited disorder that causes severe loss of sight in young adults, and is typically associated to mitochondrial DNA (mtDNA) mutations. Heteroplasmy of primary LHON mutations, presence of ‘ancillary’ mtDNA mutations, and mtDNA copy number are probably correlated with the penetrance and the severity of the disease. In this study, we performed a mutational screening in an Apulian cohort of LHON patients and we found that 41 out of 54 subjects harbored the m.11778G>A mutation, and 13 harbored the m.3460G>A mutation. Whole mtDNA sequencing was performed in three affected subjects belonging to three unrelated m.11778G>A pedigrees to evaluate the putative synergistic role of additional mtDNA mutations in determining the phenotype. Our study suggests to include haplogroup T as a possible genetic background influencing LHON penetrance and to consider the increase of mtDNA copy number as a protective factor from vision loss regardless the hetero/homoplasmic status of LHON primary mutations.

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