Mitochondrial A3243G mutation results in corneal endothelial polymegathism
| Autor: | Mathieu F. Bakhoum, Wei-Pu Wu, Eugenia C. White, Jesse D. Sengillo, Christian Sanfilippo, Marcelle M. Morcos, K. Bailey Freund, Henry D. Perry, David Sarraf, Stephen H. Tsang |
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| Rok vydání: | 2018 |
| Předmět: |
Mitochondrial Diseases
genetic structures Reverse Transcriptase Polymerase Chain Reaction DNA Mutational Analysis 05 social sciences Epithelium Corneal Microscopy Acoustic DNA Mitochondrial eye diseases Article Sensory Systems 03 medical and health sciences Cellular and Molecular Neuroscience Ophthalmology 0302 clinical medicine 0502 economics and business 030221 ophthalmology & optometry Humans Point Mutation sense organs Iridocorneal Endothelial Syndrome 050203 business & management |
| Zdroj: | Graefe's Archive for Clinical and Experimental Ophthalmology. 256:583-588 |
| ISSN: | 1435-702X 0721-832X |
| Popis: | PURPOSE: The mitochondrial DNA point mutation A3243G leads to a spectrum of syndromes ranging from MIDD to MELAS. Ocular manifestations include pattern macular dystrophy and concentric perifoveal atrophy. Given the high metabolic demand of corneal endothelial cells, we performed specular biomicroscopy analysis in patients harboring the mitochondrial DNA point mutation A3243G to assess for the associated presence of corneal endothelial abnormalities. METHODS: We present a case series with participants from two institutions. Patients diagnosed with macular dystrophy associated with MIDD, or MELAS and the mitochondrial DNA point mutation A3243G were recruited. Exclusion criteria included a prior diagnosis, or a positive family history, of endothelial corneal dystrophy. Slit-lamp corneal examination and specular biomicroscopy were performed. Corneal endothelial cell count, cell size and polymegathism, and central corneal thickness were assessed. Patients diagnosed with MIDD or MELAS based on clinical history and examination were genetically tested for the mitochondrial DNA point mutation A3243G using pyrosequencing. RESULTS: Five patients (two male and three female participants), from five different families, and with different ethnic backgrounds met the inclusion criteria. Their ages ranged from 41 to 60 years. Corneal endothelial changes observed using slit-lamp examination were primarily mild to rare guttata. Specular biomicroscopy displayed mainly polymegathism associated with guttata. The average endothelial cell count was 2358 ± 456 cells per mm(2), the average endothelial cell size was 442 ± 103 μm(2) and the average central corneal thickness (CCT) was 551 ± 33 μm. These values were similar to that of the average population. The average coefficient of variation (COV), an index of heterogeneity in cell size, was 42.0 ± 4.1%. When compared to the average population, the average COV was significantly higher than predicted for the patients’ age. None of the patients had signs of corneal edema. One patient had a pre-descemet’s opacity. CONCLUSIONS: In patients with the mitochondrial DNA point mutation A3243G, corneal endothelial polymegathism is present. This is mainly associated with mild guttata. The findings of corneal endothelial cell polymegathism may be a biomarker of mitochondrial disease, specifically in patients with the mitochondrial DNA A3243G mutation. |
| Databáze: | OpenAIRE |
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