Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies
Chin-Chang Huang1, Hung-Chou Kuo, Chen-Che Chu
1Department of Neurology, Chang Gung Memorial Hospital and University, Taipei, Taiwan, ROC. cch0537@adm.cgmh.org.tw
Abstract:
We studied 42 individuals, including 8 patients with either complete or partial syndrome of mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS), 8 patients with either complete or partial syndrome of myoclonic epilepsy with ragged-red fibers (MERRF) and 26 maternal family members who carried either the A3243G or A8344G mutation of mitochondrial DNA (mtDNA). Clinical manifestations and prognosis were followed up in the patients harboring the A3243G or A8344G mutation. The relationship between clinical features and proportions of mutant mtDNAs in muscle biopsies, blood cells and/or hair follicles was studied. In the 8 regularly followed patients with the A3243G mutation, 4 died within 1 month to 7 years due to status epilepticus and/or recurrent stroke-like episodes. Two patients developed marked mental deterioration and 2 remained stationary. All of the patients harboring the A8344G mutation were stable or deteriorated slightly, except for 1 patient who died due to brain herniation after putaminal hemorrhage. The A3243G and A8344G mtDNA mutations were heteroplasmic in the muscle biopsies, blood cells and hair follicles of both the probands and their maternal family members. The mean proportion of A3243G mutant mtDNA in the muscle biopsies of the patients with MELAS syndrome (68.5 +/- 21.3%, range 33-92%) was significantly higher than that of the asymptomatic family members (37.1 +/- 12.6%, range 0-51%). The average proportions of A8344G mutant mtDNA in the muscle biopsies (90.1 +/- 3.9%, range 89-95%) and hair follicles (93.9 +/- 6.4%, range 84-99%) of the patients with MERRF syndrome were also significantly higher than those of the asymptomatic family members (muscle: 40.3 +/- 39.5%, range 1-80%; hair follicles: 51.0 +/- 44.5%, range 0.1-82%). We concluded that measurement of the proportion of mutant mtDNA in muscle biopsies may provide useful information in the identification of symptomatic patients with mitochondrial encephalomyopathies. For patients with the A3243G mutation, the prognosis was related to status epilepticus and the number of recurrent stroke-like episodes and was much worse than for patients with the A8344G mutation of mtDNA, who had stable or slowly deteriorating clinical courses.
Insights
Mitochondrial DNA mutations A3243G and A8344G cause MELAS and MERRF syndromes. Higher mutant mtDNA levels in muscle biopsies indicate symptomatic disease, with A3243G mutations having a worse prognosis.
Area of Science:
- Genetics
- Neurology
- Mitochondrial Diseases
Background:
- Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and myoclonic epilepsy with ragged-red fibers (MERRF) are debilitating mitochondrial diseases.
- Specific mitochondrial DNA (mtDNA) mutations, A3243G and A8344G, are implicated in these syndromes.
- Understanding the correlation between mutation load and clinical presentation is crucial for diagnosis and prognosis.
Purpose of the Study:
- To investigate the relationship between mutant mtDNA proportions and clinical manifestations in patients with MELAS and MERRF syndromes.
- To compare the clinical outcomes and prognosis of patients carrying the A3243G mutation versus the A8344G mutation.
- To determine if mutant mtDNA levels in accessible tissues can aid in identifying symptomatic individuals.
Main Methods:
- Studied 42 individuals: 8 MELAS patients, 8 MERRF patients, and 26 asymptomatic maternal family members.
- Analyzed mutant mtDNA proportions (A3243G and A8344G) in muscle biopsies, blood cells, and hair follicles.
- Correlated mutation load with clinical features, disease severity, and patient prognosis over time.
Main Results:
- Significantly higher mean proportions of A3243G mutant mtDNA in muscle biopsies of MELAS patients (68.5%) compared to asymptomatic family members (37.1%).
- Significantly higher mean proportions of A8344G mutant mtDNA in muscle (90.1%) and hair follicles (93.9%) of MERRF patients versus asymptomatic family members (muscle: 40.3%, hair: 51.0%).
- Patients with A3243G mutations had a poorer prognosis, with higher mortality due to stroke-like episodes and status epilepticus, while A8344G patients showed stable or slowly deteriorating courses.
Conclusions:
- Measurement of mutant mtDNA proportion in muscle biopsies is a valuable tool for identifying symptomatic patients with mitochondrial encephalomyopathies.
- The A3243G mutation is associated with a significantly worse prognosis compared to the A8344G mutation, primarily due to neurological complications.
- Heteroplasmy levels in accessible tissues like blood and hair may also provide insights into disease status, though muscle biopsy shows stronger correlation for symptomatic identification.
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