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Targeting Myotonic Dystrophy Type 1 with Metformin.
García-Puga, Mikel; Saenz-Antoñanzas, Ander; Matheu, Ander; López de Munain, Adolfo.
Afiliação
  • García-Puga M; Neuromuscular Diseases Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
  • Saenz-Antoñanzas A; Cellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
  • Matheu A; Network Center for Biomedical Research in Neurodegenerative Diseases (CIBERNED-CIBER), Carlos III Institute, 28031 Madrid, Spain.
  • López de Munain A; Cellular Oncology Group, Biodonostia Health Research Institute, 20014 San Sebastian, Spain.
Int J Mol Sci ; 23(5)2022 Mar 07.
Article em En | MEDLINE | ID: mdl-35270043
ABSTRACT
Myotonic dystrophy type 1 (DM1) is a multisystemic disorder of genetic origin. Progressive muscular weakness, atrophy and myotonia are its most prominent neuromuscular features, while additional clinical manifestations in multiple organs are also common. Overall, DM1 features resemble accelerated aging. There is currently no cure or specific treatment for myotonic dystrophy patients. However, in recent years a great effort has been made to identify potential new therapeutic strategies for DM1 patients. Metformin is a biguanide antidiabetic drug, with potential to delay aging at cellular and organismal levels. In DM1, different studies revealed that metformin rescues multiple phenotypes of the disease. This review provides an overview of recent findings describing metformin as a novel therapy to combat DM1 and their link with aging.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metformina / Distrofia Miotônica Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metformina / Distrofia Miotônica Idioma: En Ano de publicação: 2022 Tipo de documento: Article