Methods for treating heart disease in a subject with Friedreich's ataxia by an aromatic-cationic peptide
The disclosure provides methods of preventing or treating Friedreich's ataxia in a mammalian subject, reducing risk factors, signs and/or symptoms associated with Friedreich's ataxia, and/or reducing the likelihood or severity of Friedreich's ataxia. The methods comprise administering to the subject an effective amount of an aromatic-cationic peptide to e.g., reduce oxidative stress, increase mitochondrial metabolism, or a combination thereof.
1. A method for treating heart disease in a subject having Friedreich's ataxia, comprising administering to the subject a therapeutically effective amount of the peptide D-Arg-2′,6′-Dmt-Lys-Phe-NH 2 or a pharmaceutically acceptable salt thereof.
2. The method of claim 1 , wherein the peptide is administered daily for 6 weeks or more.
3. The method of claim 1 , wherein the peptide is administered daily for 12 weeks or more.
4. The method of claim 1 , wherein the heart disease comprises a condition selected from the group consisting of hypertrophic cardiomyopathy, myocardial fibrosis, and cardiac failure.
5. The method of claim 1 , wherein the heart disease comprises hypertrophic cardiomyopathy.
6. The method of claim 1 , wherein the heart disease comprises myocardial fibrosis.
7. The method of claim 1 , wherein the heart disease comprises cardiac failure.
8. The method of claim 1 , wherein the heart disease comprises a heart rhythm abnormality condition selected from the group consisting of tachycardia and heart block.
9. The method of claim 1 , wherein the subject suffers symptoms selected from the group consisting of chest pain, shortness of breath, and heart palpitations.
10. The method of claim 1 , wherein the subject is human.
11. The method of claim 1 , wherein the peptide is administered orally, topically, systemically, intravenously, subcutaneously, intraperitoneally, or intramuscularly.
12. The method of claim 1 , further comprising separately, sequentially or simultaneously administering to the subject one or more additional therapeutic agents selected from the group consisting of ACE inhibitors, digoxin, enalapril, or lisinopril, diuretics, beta blockers, idebenone, deferiprone, and insulin.
13. The method of claim 1 , wherein the pharmaceutically acceptable salt comprises acetate or trifluoroacetate salt.
14. The method of claim 12 , wherein administering the peptide and the additional therapeutic agent has a synergistic effect in the treatment of Friedreich's ataxia.