Biochemical-clinical correlation in patients with different loads of the mitochondrial DNA T8993G mutation

Valerio Carelli, Alessandra Baracca, Silvia Barogi, Francesco Pallotti, Maria Lucia Valentino, Pasquale Montagna, Massimo Zeviani, Antonella Pini, Giorgio Lenaz, Agostino Baruzzi, Giancarlo Solaini

Research output: Contribution to journalArticlepeer-review


Objective: To investigate the correlation between biochemical and clinical phenotype in 6 patients from 3 unrelated families with different mutation loads (heteroplasmy) of the T8993G mitochondrial DNA mutation associated with neuropathy, ataxia, and retinitis pigmentosa-Leigh syndrome. Methods: We studied adenosine triphosphate (ATP) synthase activity (synthesis and hydrolysis) in platelet-derived submitochondrial particles and assessed mutant loads both in platelets used for biochemical analysis and in other available tissues. Biochemical and molecular results were correlated with clinical features. Results: The rate of ATP hydrolysis was normal, but ATP synthesis was severely impaired (30% to 4% of residual activity) in patients harboring 34% to 90% mutant mitochondrial DNA, without any evidence of a threshold for the expression of this defect. There was little variation in heteroplasmy among tissues from each patient, but wider variability was detected in 2 mothers. Correlation of heteroplasmy and clinical and biochemical features suggested that ATP synthesis is defective at mutant loads as low as 34% and is extremely reduced at mutant loads above 80% when the phenotype is neuropathy, ataxia, and retinitis pigmentosa-Leigh syndrome. Conclusions: This study indicates a close relationship between tissue heteroplasmy, expression of the biochemical defect in platelets, and clinical involvement. The biochemical defect was greater than previously reported, and we found no evidence of a biochemical threshold. The uniform distribution of high mutant loads among our patients' tissues suggests a differential tissue-specific reliance on mitochondrial ATP synthesis.

Original languageEnglish
Pages (from-to)264-270
Number of pages7
JournalArchives of Neurology
Issue number2
Publication statusPublished - 2002

ASJC Scopus subject areas

  • Neuroscience(all)


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