Calpainopathy

Disease severity varies greatly, even between family members with identical mutations.[1] Age of onset is highly variable, although symptoms usually appear between 8 and 15 years of age.[3] Patients usually lose the ability to ambulate 10 - 20 years after symptoms appear.[3] Milder forms present with symptoms other than weakness, such as muscle aches, cramps, or exercise intolerance, and people in this group can retain ambulation beyond age 60.[3] Weakness is symmetric, progressive, and proximal (on or close to the torso), usually affecting the hip girdle and shoulder girdle muscles.[1][3] Hip weakness can manifest as a waddling gate.[1] Shoulder weakness can manifest as winged scapulas.[1] Muscle contractures, especially of the Achilles tendon, and scoliosis can also occur.[1]

Heart function and intelligence are generally not affected.[1] Additionally, the muscles of the face, eye, tongue, and neck are spared.[1]

Mutation in the gene CAPN3, which encodes the protein calpain-3 (CAPN3), is the cause of calpainopathy.[1] As of 2019, more than 480 CAPN3 mutations have been reported, some of which can be associated with severe or benign disease course.[3] Usually, the disease follows an autosomal recessive inheritance pattern, requiring both CAPN3 alleles to be mutated for disease to occur.[1] However, there can be CAPN3 mutations that follow an autosomal dominant inheritance pattern.[1]

Diagram of calpainopathy pathophysiology, showing calcium dysregulation to play a central role.

Schematic representation of CAPN3 structure. Regions specific to CAPN3 are shown in blue (NS, IS1, and IS2). Regions shared with similar proteins are protease core domains (PC1 and PC2), a calpain-type β-sandwich domain (CBSW), and a penta E-F hand domain (PEF) that binds four calcium ions.

As of 2019, the pathophysiology is largely not understood, although it is increasingly becoming accepted that calcium dysregulation plays a role.[3]

Photomicrograph of muscle affected by calpainopathy. Seen in these views are endomysial fibrosis (black asterisks), central nuclei (black arrows), fiber splitting (yellow triangle), necrosis (black triangles), atrophic fibers (yellow arrows), and increased variation in size and shape. Scale bar: 25µm

Genetic testing is the most definitive test.[1]

If genetic testing is not available, a muscle biopsy with protein immunoanalysis can be used.[1] Biopsy shows general dystrophic features, such as areas of muscle death, variability in muscle size, nuclei in the center of muscle fibers, and disorganized muscle fibers within muscle cells.[3]

Serum creatine kinase, a nonspecific marker of muscle damage, can be elevated early in the disease.[3]

Facioscapulohumeral muscular dystrophy (FSHD) can present similarly, although facial weakness and asymetrical weakness is common in FSHD.

As of 2019, no disease modifying pharmaceuticals are known.[3]

Both strength and aerobic exercise have shown to be beneficial,[3] although strenuous and excessive exercise should be avoided.[1]

Physical therapy can address contractures.[1]

Orthopedic surgery address foot deformities, scoliosis, Achilles tendon contractures, and winged scapula. Winged scapula can be addressed with either scapulopexy or scapulothoracic fusion.[1]

Circumstances to avoid include extremes of body weight, bone fractures, and prolonged immobility.[1]

Prevalence ranges from 1 to 9 cases per 100,000 people.[3] LGMDR1 represents 30% of all LGMD cases.[3]

Research is being done to identify the proteins cleaved by calpain-3.[4]

Gene therapy is being studied to replace the function of the calpain-3. Injection of plasmids containing CAPN3 into mouse models resulted in increased levels of calpain-3.[5]