PUMA
Istituto di Fisiologia Clinica     
Siciliano G., Monzani F., Manca M. L., Tessa A., Caraccio N., Tozzi G., Piemonte F., Mancuso M., Santarelli F. M., Ferrannini E., Murri L. Human mitochondrial transcription factor a reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathy. In: Molecular medicine, vol. 08 pp. 326 - 333. Feinstein, 2002.
 
 
Abstract
(English)
Background: Mitochondrial changes have been described in muscle tissue in acquired hypothyroidism. Among the molecular mechanisms by which thyroid hormones regulate expression of nuclear genes encoding for regulatory proteins of mitochondrial respiratory function, the mitochondrial transcription factor A (h-mtTFA) has been proposed to be a target of thyroid hormone action. The aim of this study has been to relate h-mtTFA levels in the skeletal muscle of patients affected by Hashimoto's hypothyroidism and myopathy (HHM) to muscle disease and thyroid status. Patients and Methods: Eleven HHM patients underwent complete thyroid status and neurologic assessment, along with determination of exercise lactate anaerobic threshold (LT) and muscle biopsy in which h-mtTFA levels were measured and mtDNA was analyzed. Correspondence and reprint requests should be addressed to: Dr Gabriele Siciliano, Department of Neuroscience, Neurological Clinics, University of Pisa, Via Roma 67, 56126 Pisa (I), Italy. Phone: =39-050-993046; fax: =39-050-554808; e-mail: gsicilia@neuro.med.unipi.it. Results: Decreased exercise lactate threshold, presence of cytochrome c oxidase negative fibers, reduction of cytochrome c oxidase activity, and mitochondrial DNA copy number at muscle biopsy were indicative of mitochondrial involvement in these patients. Furthermore, muscle h-mtTFA levels were reduced to a variable extent in comparison with a group of euthyroid controls. The h-mtTFA levels were inversely correlated with TSH and LT lactate, and positively correlated with FT4. Conclusions: These results indicate that low levels of the h-mtTFA occur in skeletal muscle of HHM and suggest that abnormal h-mtTFA turnover may be implicated in the pathogenesis of mitochondrial alterations in this disease.
URL: http://molmed.org/content/2002/326.pdf
Subject Human
Mitochondrial
Hypothyroid


Icona documento 1) Download Document PDF


Icona documento Open access Icona documento Restricted Icona documento Private

 


Per ulteriori informazioni, contattare: Librarian http://puma.isti.cnr.it

Valid HTML 4.0 Transitional