Methods for diagnosing, prognosing and treating muscular dystrophy
Disclosed herein are methods for diagnosing, prognosing and treating muscular dystrophy. Also disclosed are methods of determining the effectiveness of an agent for the treatment of muscular dystrophy. Provided are methods of enhancing muscle regeneration, repair, or maintenance in a subject by administering galectin, such as Galectin-1 and/or Galectin-3 to a subject in need thereof. Also disclosed are methods of increasing or maintaining muscle strength and/or bone density in a subject by administering an effective amount of a Galectin-1 composition, Galectin-3 composition or a combination thereof to the subject in need thereof. Methods of preventing, inhibiting and/or reducing muscle loss and/or bone loss in a subject by administering an effective amount of a Galectin-1 composition, Galectin-3 composition or a combination thereof to the subject in need thereof are disclosed.
1. A method of increasing sarcolemmal stabilizing dystroglycan complex for increasing or maintaining muscle strength, muscle density, and/or bone density in a subject suffering from Duchenne muscular dystrophy (DMD), merosin deficient congenital muscular dystrophy Type 1A (MDC1A), limb-girdle muscular dystrophy (LGMD), facioscapulohumeral muscular dystrophy (FHMD), or Beckers muscular dystrophy (BMD), the method comprising systemically administering an effective amount of a Galectin-1 composition comprising a native mammalian Galectin-1 protein or a recombinant Galectin-1 protein having a full-length wild-type amino acid sequence, to the subject with DMD, MDC1A, LGMD, FHMD, or BMD and in need thereof, wherein the effective amount increases sarcolemmal stabilizing dystroglycan complex, thereby increasing or maintaining muscle strength, muscle density, and/or bone density.
2. The method of claim 1 , wherein the subject has Duchenne muscular dystrophy.
3. The method of claim 1 , wherein the Galectin-1 composition comprises a native mammalian Galectin-1 protein or a recombinant Galectin-1 protein having a full-length wild-type amino acid sequence and a carrier.
4. The method of claim 3 , wherein the Galectin-1 composition is administered intramuscularly.
5. The method of claim 3 , wherein the Galectin-1 composition is administered intraperitoneally.
6. The method of claim 3 , wherein systemic administration is intravenous.
7. The method of claim 1 , wherein the effective amount is systemically administered at least once daily.
8. The method of claim 7 , wherein at least 1 mg of the Galectin-1 composition is administered systemically at least once daily.
9. A method of increasing sarcolemmal stabilizing dystroglycan complex for preventing, inhibiting and/or reducing muscle loss and/or bone loss in a subject suffering from Duchenne muscular dystrophy (DMD), merosin deficient congenital muscular dystrophy Type 1A (MDC1 A), limb-girdle muscular dystrophy (LGMD), facioscapulohumeral muscular dystrophy (FHMD), or Beckers muscular dystrophy (BMD), the method comprising systemically administering an effective amount of a Galectin-1 composition comprising a native mammalian Galectin-1 protein or a recombinant Galectin-1 protein having a full-length wild-type amino acid sequence, to the subject with DMD, MDC1A, LGMD, FHMD, or BMD and in need thereof, wherein the effective amount increases sarcolemmal stabilizing dystroglycan complex, thereby preventing, inhibiting and/or reducing muscle loss and/or bone loss.
10. The method of claim 9 , wherein the subject has Duchenne muscular dystrophy.
11. The method of claim 9 , wherein the Galectin-1 composition comprises a native mammalian Galectin-1 protein or a recombinant Galectin-1 protein having a full-length wild-type amino acid sequence and a carrier.
12. The method of claim 11 , wherein the Galectin-1 composition is administered by intramuscular or intraperitoneal administration.
13. The method of claim 11 , wherein systemic administration is intravenous.
14. The method of claim 9 , wherein the effective amount is systemically administered at least once daily.
15. The method of claim 14 , wherein at least 1 mg of the Galectin-1 composition is administered systemically at least once daily.