What Is Hypothyroid Myopathy? Symptoms and Treatment

Hypothyroid myopathy is a muscle disorder that develops as a complication of hypothyroidism, a condition where the thyroid gland fails to produce sufficient hormones essential for regulating the body’s metabolism. While hypothyroidism affects numerous bodily systems, the musculoskeletal system is frequently impacted. Hypothyroid myopathy is a common manifestation, affecting an estimated 30% to 80% of patients with low thyroid function. The condition is defined by muscle weakness and stiffness, which typically improve once the underlying hormonal imbalance is corrected.

The Link Between Thyroid Function and Muscle Health

Thyroid hormones, specifically thyroxine (T4) and triiodothyronine (T3), regulate energy production and consumption within skeletal muscles. T3 modulates gene expression within muscle cells, influencing protein turnover—the balance between building and breaking down muscle tissue. When thyroid hormone levels are low, this metabolic regulation is disrupted, leading to cellular changes that impair muscle function.

Low hormone levels reduce the overall metabolic rate in the muscle, resulting in impaired carbohydrate metabolism and reduced protein turnover. This diminished function affects the muscle’s machinery, particularly the mitochondria, which generate energy. Reduced mitochondrial oxidative capacity means muscle cells cannot efficiently produce the energy needed for normal contraction and relaxation.

Low T3 levels can also cause a shift in muscle fiber types, favoring slower-twitch fibers, which contributes to sluggish muscle movement. The ability of the muscle to relax is compromised due to delayed reuptake of calcium ions by the sarcoplasmic reticulum. These combined deficits ultimately lead to the characteristic weakness, stiffness, and slow reflexes seen in hypothyroid myopathy.

Recognizing the Signs of Muscle Involvement

The clinical presentation of hypothyroid myopathy involves symptoms noticeable during daily activities that range in severity. A hallmark sign is proximal muscle weakness, affecting muscles closest to the center of the body, such as those in the hips and shoulders. Patients often report difficulty performing tasks like climbing stairs, rising from a low chair, or lifting objects over their head.

In addition to weakness, many individuals experience myalgia, which is generalized muscle pain or aching, and muscle stiffness. These symptoms are often exacerbated by physical exertion, reflecting the underlying metabolic impairment. Muscle cramps are also common.

A physician may observe the delayed relaxation of deep tendon reflexes, sometimes called “hung-up” reflexes. This is a specific sign related to the slow calcium reuptake mechanism in the muscle.

Rare, specific forms of the condition involve muscle enlargement, or pseudohypertrophy, where the muscle appears large but is actually weak. Hoffman syndrome is one such form in adults, characterized by weak, enlarged muscles with spasms and stiffness. Kocher-Debré-Sémélaigne syndrome is the corresponding rare form seen in children, presenting alongside congenital hypothyroidism.

Diagnosing and Managing Hypothyroid Myopathy

Diagnosing hypothyroid myopathy requires confirming the underlying thyroid disorder, as the muscle symptoms are a consequence of low thyroid hormone levels. This involves blood tests to measure Thyroid-Stimulating Hormone (TSH) and free Thyroxine (free T4) levels. An elevated TSH level combined with a low free T4 level confirms the diagnosis of primary hypothyroidism.

A common finding is an elevated level of Creatine Kinase (CK), a muscle enzyme that leaks into the bloodstream when muscle tissue is stressed. While high CK levels are not specific to this condition, their presence alongside hypothyroidism strongly suggests muscle involvement. More invasive tests, such as electromyography or muscle biopsy, are generally reserved for cases where the diagnosis is uncertain or other muscle disorders need to be ruled out.

The management of hypothyroid myopathy is directly tied to treating the hypothyroidism itself. Treatment involves hormone replacement therapy, typically using a synthetic T4 medication such as levothyroxine. The goal is to restore thyroid hormone levels to a healthy range, which normalizes the metabolic processes in the muscle.

Patients often feel general improvements in their hypothyroid symptoms within a few weeks of starting treatment. The resolution of muscle-related symptoms, however, can be a slower process, sometimes taking several months to a year for complete recovery. Regular monitoring of TSH and free T4 levels is necessary to ensure the levothyroxine dosage remains optimal.