CAV3

At least two CAV3 gene mutations have been identified in people with distal myopathy, a disorder characterized by weakness and loss of function mainly affecting the muscles farthest from the center of the body (distal muscles), such as those of the hands and feet. Mutations that cause CAV3-related distal myopathy result in a shortage of caveolin-3 protein in the muscle cell membrane and a reduction in the number of caveolae. Researchers suggest that a shortage of caveolae impairs the structural integrity of muscle cells, interferes with cell signaling, and causes the self-destruction of cells (apoptosis). The resulting breakdown of muscle tissue leads to the signs and symptoms of CAV3-related distal myopathy.

At least four CAV3 gene mutations have been identified in individuals with isolated hyperCKemia. People with this condition have elevated levels of an enzyme called creatine kinase in the blood. Creatine kinase is released into the blood when muscle cells are damaged; however, people with isolated hyperCKemia have no muscle weakness or other symptoms of muscle disease. CAV3 gene mutations that cause isolated hyperCKemia lead to a caveolin-3 shortage that likely damages muscle cells. Although the damage is not severe enough to cause noticeable symptoms, it may lead to the elevated blood levels of creatine kinase that characterize isolated hyperCKemia.

At least 12 CAV3 gene mutations have been identified in people with rippling muscle disease, a condition in which the muscles are unusually sensitive to movement or pressure (irritable). Affected individuals may have muscle cramps, stiffness, and muscles that appear to ripple when they are stretched.

CAV3 gene mutations that cause rippling muscle disease result in a shortage of caveolin-3 protein in the muscle cell membrane. Researchers suggest that reduced caveolin-3 levels may impair the control of calcium levels in muscle cells, leading to abnormal muscle contractions in response to stimulation.

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CAV3 gene mutations also can cause hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy is a thickening of the heart (cardiac) muscle that forces the heart to work harder to pump blood. This condition can lead to heart failure.

When caused by CAV3 gene mutations, hypertrophic cardiomyopathy as well as limb-girdle muscular dystrophy, isolated hyperCKemia, rippling muscle disease, and distal myopathy (all described above) are classified as caveolinopathies. Several CAV3 gene mutations have been found to cause different caveolinopathies in different individuals. It is unclear why a particular CAV3 gene mutation may cause different patterns of signs and symptoms, even within the same family.

Mutations in the CAV3 gene have also been identified in people with long QT syndrome, which is a heart condition that causes the cardiac muscle to take longer than usual to recharge between beats. The irregular heartbeats (arrhythmia) can lead to fainting (syncope) or cardiac arrest and sudden death. Researchers suggest that CAV3 gene mutations may disrupt ion transport through sodium channels located in the caveolae. A disruption in ion transport may alter the way the heart beats, leading to the abnormal heart rhythm characteristic of long QT syndrome.