Osteoporosis

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Osteoporosis

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
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Mitochondrial myopathy
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Spondylolysis
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Osteoarthritis
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Spinal cord reflexes
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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
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Osteosclerosis
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Clostridium perfringens
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Anatomy of the brachial plexus
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Somatosensory receptors
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Neuromuscular blockers
Myotonic dystrophy
Development of the axial skeleton
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Anatomy of the arm
Anatomy clinical correlates: Clavicle and shoulder

Transcript

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Osteo- refers to bones and -porosis means pores. So, osteoporosis is when there’s a higher breakdown of bone in comparison to the formation of new bone which results in porous bones, meaning a decrease in bone density to the point of potential fracture.

Looking at a cross-section of a bone, there’s a hard-external layer known as the cortical bone and a softer internal layer of spongy bone or trabecular bone that is composed of trabeculae. The trabeculae are like a framework of beams that give structural support to the spongy bone. The cortical bone, in turn, is made up of many functional, pipe-like units called osteons, which run through the length of the bone. In the center of these osteons, there are hollow spaces called Haversian canals, which contain the blood supply and innervation for the bone cells. Around the Haversian canals, there are concentric lamellae, which look a bit like tree rings. The lamellae have an organic part, which is mostly collagen, and an inorganic part called hydroxyapatite, which is mostly calcium phosphate. In between neighboring lamellae, there are spaces called lacunae, which contain bone cells called osteocytes.

At first glance, bone may appear inert and unchanging, but it’s actually a very dynamic tissue. In fact, spongy bone is replaced every 3 to 4 years and compact bone is replaced every 10 years, in a process called bone remodeling, which has two steps: bone resorption, when specialized cells called osteoclasts break down bone, and bone formation, which is when another type of cells called osteoblasts form new bone.

Bone remodeling as a whole is highly dependent on serum calcium levels, which, in turn, are kept in the normal range by a balance between parathyroid hormone, or PTH, calcitonin and vitamin D.

Parathyroid hormone is produced by the parathyroid glands in response to low serum calcium, and it increases bone resorption to release calcium into the bloodstream. On the other hand, calcitonin is produced by the thyroid gland in response to high serum calcium, so it opposes the action of PTH - therefore promoting bone formation and decreasing bone resorption. Finally, vitamin D promotes calcium absorption in the gut, so it increases serum calcium, promoting bone formation and decreasing bone resorption.

The balance between these regulatory factors results in a peak bone mass, usually by age 20 to 29 - and this usually occurs earlier in females than in males. Factors that determine the peak bone mass are genetics and nutrition (meaning adequate vitamin D intake increases bone peak mass). Finally, strength training increases peak bone mass, as well as hormones like estrogens and androgens that inhibit bone resorption.

Ok, now, when osteoclasts break down bone faster than the osteoblasts can rebuild, it results in the lowering of the bone mass and eventually in osteoporosis.

If we zoom into a cross-section of an osteoporotic bone, it will show normal cells with normal mineralization, which differentiates it from osteomalacia where there's lack of mineralization. So with osteoporosis, abnormal findings include fewer trabeculae in the spongy bone and thinning of the cortical bone, as well as the widening of the Haversian canals. These bone changes increase the risk of fracture, and they are known as fragility or pathologic fractures. Some bones like the vertebrae, shoulder blades, and ribs consist mainly of spongy bone, so they are at great risk of fragility fractures.

Factors that accelerate bone mass loss and increase the risk of osteoporosis are low estrogen levels, like after menopause, and low serum calcium. Additional factors include alcohol consumption, smoking, drugs like glucocorticoids, which decrease calcium absorption from the gut through antagonism of vitamin D, and drugs like heparin and L-thyroxine. Another factor is physical inactivity, as seen in astronauts in a zero-gravity environment where they just don't use their musculoskeletal system as hard as when they’re on earth. As a result, bone deposition decreases due to a lack of stress, while resorption increases. There are also diseases that can cause osteoporosis like Turner syndrome, hyperprolactinemia, Klinefelter syndrome, Cushing syndrome, and diabetes mellitus.

Key Takeaways

Osteoporosis refers to decreased bone density due to increased bone resorption compared to bone formation. Commonly affected bones include vertebrae, forearm, and hip. Osteoporosis is typically asymptomatic until a broken bone occurs; such breaks may occur spontaneously or with minor stress because of the disease's unremarkable progression. The treatment involves bisphosphonate drugs like alendronate and risedronate.

Sources

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  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
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  5. "Bone Resorption by Osteoclasts" Science (2000)
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  7. "Osteoporotic compression fractures of the spine; current options and considerations for treatment" The Spine Journal (2006)