Inclusion body myopathy

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Inclusion body myopathy

MSK Module Content

MSK Module Content

Resting membrane potential
Action potentials in myocytes
Neuron action potential
Neuromuscular junction and motor unit
Sliding filament model of muscle contraction
Cholinergic receptors
Lambert-Eaton myasthenic syndrome
Neuromuscular junction disorders: Pathology review
Myasthenia gravis
Myalgias and myositis: Pathology review
Pediatric orthopedic conditions: Clinical
Muscle weakness: Clinical
Slow twitch and fast twitch muscle fibers
Muscle spindles and golgi tendon organs
Muscle contraction
Skeletal muscle histology
Muscular system anatomy and physiology
Lower back pain: Clinical
Back pain: Pathology review
Systemic lupus erythematosus (SLE): Clinical
Osteoporosis
Child abuse: Clinical
Non-steroidal anti-inflammatory drugs
Rheumatoid arthritis
Physiological changes during exercise
Polymyositis
Lordosis, kyphosis, and scoliosis
Spinal disc herniation
Acetaminophen (Paracetamol)
Osteochondroma
Scleroderma
Skeletal system anatomy and physiology
Bone remodeling and repair
Legg-Calve-Perthes disease
Genu varum
Inflammatory myopathies: Clinical
Muscular dystrophies and mitochondrial myopathies: Pathology review
Mitochondrial myopathy
Inclusion body myopathy
Monoclonal antibodies
Spondylolysis
Spondylosis
Spondylitis
Bone disorders: Pathology review
Muscular dystrophy
Mixed connective tissue disease
Cartilage histology
Raynaud phenomenon
Scleroderma: Pathology review
Osteoarthritis
Cartilage structure and growth
Fibrous, cartilage, and synovial joints
Septic arthritis
Slipped capital femoral epiphysis
Bone tumors
Osgood-Schlatter disease (traction apophysitis)
Achondroplasia
Rheumatoid arthritis: Clinical
Developmental dysplasia of the hip
Bone tumors: Pathology review
Neck trauma: Clinical
Spinal cord reflexes
Pediatric bone and joint infections: Clinical
Paget disease of bone
Bone histology
Pediatric bone tumors: Clinical
Anatomy clinical correlates: Bones, joints and muscles of the back
Joints of the wrist and hand
Osteomalacia and rickets
Osteomalacia
Osteopetrosis
Osteoporosis medications
Osteosclerosis
Osteogenesis imperfecta
Osteomyelitis
Clostridium perfringens
Necrotizing fasciitis
Skin and soft tissue infections: Clinical
Brachial plexus
Anatomy of the brachial plexus
Klumpke paralysis
Anatomy clinical correlates: Wrist and hand
Muscles of the hand
Achilles tendon rupture
Rotator cuff tear
Somatosensory receptors
Carpal tunnel syndrome
Patellar tendon rupture
Ankylosing spondylitis
Marfan syndrome
Polymyalgia rheumatica
Reactive arthritis
Seronegative arthritis: Clinical
Psoriatic arthritis
Juvenile idiopathic arthritis
Seronegative and septic arthritis: Pathology review
Rheumatoid arthritis and osteoarthritis: Pathology review
Ehlers-Danlos syndrome
Alport syndrome
Gout
Gout and pseudogout: Pathology review
Antigout medications
Nucleotide metabolism
Joint pain: Clinical
Lesch-Nyhan syndrome
Thoracic outlet syndrome
Introduction to the muscular system
Introduction to the skeletal system
Development of the muscular system
Torticollis
Pigeon toe
Neuromuscular blockers
Myotonic dystrophy
Development of the axial skeleton
Development of the limbs
Muscles of the back
Anatomy of the arm
Anatomy clinical correlates: Clavicle and shoulder

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Inclusion body myopathy

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In inclusion body myopathy, “myopathy” refers to muscle disease and “inclusion body” refers to the presence of inclusions, or vacuoles, formed by clumps of protein that collect within the muscle fibers.

There’s a sporadic form, sporadic meaning that it strikes at random, which is the most common and is also called inclusion body myositis - because it causes muscle inflammation.

There’s also a rare hereditary form, that causes no muscle inflammation.

Normally, the cells of the immune system are ready to spot and destroy anything foreign that could cause the body harm.

To help with this, most cells in the body have a set of proteins that come together to form a major histocompatibility complex, or MHC, class I proteins which sits on the surface of their cell membrane.

These surface proteins act kind of like a serving platter, presenting molecules from within the cell for the immune system, so that it can have a way of performing ongoing surveillance.

Normally the MHC class I proteins serves up a normal harmless molecule from the cell - a self-antigen, and there’s no response.

But if a cell is invaded by a pathogen like a virus, then viral proteins are served upon on the MHC class I proteins.

When these viral antigens are displayed on the cell surface, it sparks an immune response.

Specifically, a type of T-lymphocyte, called a CD8+ T-cell or a cytotoxic T-cell, will bind to the antigen presented by the MHC class I proteins.

If the cytotoxic T-cell binds strongly, than the antigen is recognized as foreign, and the cytotoxic T-cell secretes inflammatory molecules and enzymes - like perforin and granzymes.

Perforin is able to form holes in the infected cell and that allows the granzymes to enter the cell.

Once inside, the granzymes induce apoptosis, or programmed cell death - which destroys the cell.

And as if that weren’t enough, the cytotoxic T-cells have a protein called Fas ligand on their surface.

Fas ligand binds to a protein called Fas on the surface of the infected cell.

And when these two combine, it triggers a cascade of signaling events inside the target cell that also leads to apoptosis.

So either way - the infected cell is doomed.

Okay, now, in sporadic inclusion body myositis there are features of inflammation and degeneration.

The exact mechanism is unclear, but one thought is that the trigger may be a virus that infects and damages myocytes.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "GNE myopathy: from clinics and genetics to pathology and research strategies" Orphanet Journal of Rare Diseases (2018)
  6. "Hereditary inclusion-body myopathies" Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2015)
  7. "GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges" Neurotherapeutics (2018)