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Title:Atypical Leber Hereditary Optic Neuropathy (LHON) associated with a novel MT-CYB:m.15309T>C(Ile188Thr) variant
Authors:ID Petrović Pajić, Sanja (Author)
ID Fakin, Ana (Author)
ID Jarc-Vidmar, Martina (Author)
ID Šuštar Habjan, Maja (Author)
ID Malinar, Lucija (Author)
ID Pavlovic, Kasja (Author)
ID Krako Jakovljevic, Nina (Author)
ID Volk, Marija (Author)
ID Maver, Aleš (Author)
ID Jezernik, Gregor (Author)
ID Glavač, Damjan (Author)
ID Peterlin, Borut (Author)
ID Hawlina, Marko (Author), et al.
Files:.pdf PDF - Presentation file, download (3,70 MB)
MD5: 3C00D0233976B2D04AE9EE2EE4D01B21
 
URL URL - Source URL, visit https://www.mdpi.com/2073-4425/16/1/108
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo UKC LJ - Ljubljana University Medical Centre
Abstract:Background: The study presents a detailed examination and follow-up of a Slovenian patient with an Leber Hereditary Optic Neuropathy (LHON)-like phenotype and bilateral optic neuropathy in whom genetic analysis identified a novel variant MT-CYB:m.15309T>C (Ile188Thr). Methods: We provide detailed analysis of the clinical examinations of a male patient with bilateral optic neuropathy from the acute stage to 8 years of follow-up. Complete ophthalmological exam, electrophysiology and optical coherence tomography (OCT) segmentation were performed. The genotype analysis was performed with a complete screening of the mitochondrial genome. Furthermore, proteomic analysis of the protein structure and function was performed to assess the pathogenicity of a novel variant of unknown significance. Mitochondrial function analysis of the patient’s peripheral blood mononuclear cells (PBMCs) was performed with the objective of evaluating the mutation effect on mitochondrial function using flow cytometry and high-resolution respirometry. Results: The patient had a profound consecutive bilateral visual loss at 19 years of age due to optic neuropathy with characteristics of LHON; however, unlike patients with typical LHON, the patient experienced a fluctuation in visual function and significant late recovery. He had a total of three visual acuity deteriorations and improvements in the left eye, with concomitant visual loss in the right eye and a final visual acuity drop reaching nadir 9 months after onset. The visual loss was characterized by centrocecal scotoma, abnormal color vision and abnormal VEP, while deterioration of PERG N95 followed with a lag of several months. The OCT examination showed retinal nerve fiber layer thinning matching disease progression. Following a two-year period of legal blindness, the patient’s visual function started to improve, and over the course of 5 years, it reached 0.5 and 0.7 Snellen (0.3 and 0.15 LogMAR) visual acuity (VA). Mitochondrial sequencing identified a presumably pathogenic variant m.15309T>C in the MT-CYB gene at 65% heteroplasmy, belonging to haplogroup K. Mitochondrial function assessment of the patient’s PBMCs showed a lower respiration rate, an increase in reactive oxygen species production and the presence of mitochondrial depolarization, compared to an age- and sex-matched healthy control’s PBMCs. Conclusions: A novel variant in the MT-CYB:m.15309T>C (Ile188Thr) gene was identified in a patient with optic nerve damage and the LHON phenotype without any additional systemic features and atypical presentation of the disease with late onset of visual function recovery. The pathogenicity of the variant is supported by proteomic analysis and the mitochondrial dysfunction observed in the patient’s PBMCs.
Keywords:LHON, gene, electrophysiology, retinal segmentation, VA improvement, mitochondrial disfunction, proteomic analysis
Publication status:Published
Publication version:Version of Record
Year of publishing:2025
Number of pages:str. 1-17
Numbering:Vol. 16, iss. 1, [article no.] 108
PID:20.500.12556/DiRROS-24062 New window
UDC:61:575
ISSN on article:2073-4425
DOI:10.3390/genes16010108 New window
COBISS.SI-ID:239673347 New window
Note:Nasl. z nasl. zaslona; Opis vira z dne 17. 6. 2025;
Publication date in DiRROS:10.11.2025
Views:136
Downloads:57
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Record is a part of a journal

Title:Genes
Shortened title:Genes
Publisher:Multidisciplinary Digital Publishing Institute (MDPI)
ISSN:2073-4425
COBISS.SI-ID:523100185 New window

Document is financed by a project

Funder:ARIS - Slovenian Research and Innovation Agency
Project number:P3-0333-2019
Name:Očesne bolezni odraslih in otrok

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License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

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