Noticing a loss of muscle mass can be a distressing and disorienting experience. Muscle atrophy often creeps in slowly, making everyday tasks like lifting groceries, climbing stairs, or even standing up from a chair feel increasingly difficult. Whether it stems from a long period of bed rest, recovery from a cast, the natural aging process, or an underlying medical condition, the loss of strength affects independence and confidence. It is more than just a change in appearance; it is a change in how one interacts with the world.

Treatment is vital to halt the wasting process and, where possible, rebuild lost tissue. The primary objective is to restore function and prevent falls or injuries associated with weakness. Because muscle atrophy can result from diverse causes, ranging from nerve damage and malnutrition to chronic disease, treatment plans are not one-size-fits-all. While physical therapy is universal, medication choices depend entirely on the specific root cause, such as hormonal imbalances or genetic disorders (National Institute of Arthritis and Musculoskeletal and Skin Diseases, 2023).

Overview of treatment options for Muscle Atrophy

The management of muscle atrophy typically involves a combination of nutritional support, physical rehabilitation, and, when necessary, pharmacological intervention. While exercise remains the gold standard for reversing disuse atrophy (such as after a broken bone), medications are critical for addressing “pathological” atrophy caused by disease, hormonal deficiencies, or nerve disorders.

The main goal of medical treatment is to shift the body’s metabolism from a catabolic state (breaking down muscle) to an anabolic state (building muscle). For genetic forms of atrophy, such as Spinal Muscular Atrophy (SMA), specialized disease-modifying therapies are used. For wasting syndromes associated with chronic illness (cachexia), the focus is on appetite stimulation and preserving lean body mass.

Medications used for Muscle Atrophy

For muscle wasting related to severe illness, surgery, or trauma, doctors may prescribe anabolic steroids. Unlike performance-enhancing drugs used illicitly, medical-grade anabolic agents like oxandrolone are prescribed in controlled doses to help the body rebuild tissues lost to catabolic stress.

If atrophy is linked to natural hormonal decline or hypogonadism, Testosterone Replacement Therapy (TRT) is a common first-line approach. This can be administered via injections, gels, or patches. Clinical experience suggests that restoring testosterone levels to a normal range can improve muscle protein synthesis and strength in men with clinically low levels.

For atrophy caused by malnutrition or chronic conditions like cancer, appetite stimulants such as megestrol acetate or dronabinol may be prescribed to increase caloric intake and stabilize weight.

In the specific context of genetic atrophy (SMA), the FDA has approved groundbreaking therapies such as nusinersen and risdiplam. These are highly specialized drugs designed to target the genetic errors causing the muscle loss (FDA, 2023).

How these medications work

Anabolic agents and testosterone function by binding to androgen receptors in muscle tissue. This interaction stimulates the production of protein within the muscle cells and helps the body retain nitrogen, a building block essential for muscle growth. By flipping the metabolic switch, these drugs encourage the body to repair and enlarge muscle fibers rather than break them down for energy.

Appetite stimulants work on the central nervous system to trigger hunger signals, ensuring the body has enough fuel to maintain tissue. Disease-modifying drugs for genetic atrophy work at the molecular level. They help the body produce functional proteins that are necessary for the survival of motor neurons, the nerves that control muscle movement. When these nerves survive, the muscles stay active and do not waste away (MedlinePlus, 2021).

Side effects and safety considerations

Medications for muscle atrophy carry significant risks. Anabolic steroids and testosterone therapy can cause liver strain, fluid retention, cholesterol changes, and mood swings/aggression. Women require monitoring for virilization.

Appetite stimulants, like megestrol, increase the risk of blood clots. Specialized genetic drugs often necessitate regular kidney or liver monitoring. Since some anabolic agents impact cardiovascular function, patients must discuss heart health with a provider. Seek medical care for jaundice, severe leg swelling, or chest pain.

Since everyone’s experience with the condition and its treatments can vary, working closely with a qualified healthcare provider helps ensure safe and effective care.

References

  1. Food and Drug Administration. https://www.fda.gov
  2. MedlinePlus. https://medlineplus.gov
  3. National Institute of Arthritis and Musculoskeletal and Skin Diseases. https://www.niams.nih.gov
  4. Mayo Clinic. https://www.mayoclinic.org

Medications for Muscle Atrophy

These are drugs that have been approved by the US Food and Drug Administration (FDA), meaning they have been determined to be safe and effective for use in Muscle Atrophy.

Found 2 Approved Drugs for Muscle Atrophy

Spinraza

Generic Name
Nusinersen

Spinraza

Generic Name
Nusinersen
SPINRAZA is indicated for the treatment of spinal muscular atrophy (SMA) in pediatric and adult patients. SPINRAZA is a survival motor neuron-2 (SMN2)-directed antisense oligonucleotide indicated for the treatment of spinal muscular atrophy (SMA) in pediatric and adult patients ( 1 )

Zolgensma

Generic Name
Onasemnogene Abeparvovec-Xioi

Zolgensma

Generic Name
Onasemnogene Abeparvovec-Xioi
ZOLGENSMA is an adeno-associated virus (AAV) vector-based gene therapy indicated for the treatment of pediatric patients less than 2 years of age with spinal muscular atrophy (SMA) with bi-allelic mutations in the survival motor neuron 1 (SMN1) gene. Limitations of Use The safety and effectiveness of repeat administration of ZOLGENSMA have not been evaluated [see Adverse Reactions.
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