Acquired Diseases of Bone Flashcards
Primary osteoporosis
Typically postmenopausal, following andropause, age-related in men and women (more prevalent in women), low bone mass (low BMD), microarchitecture disruption, fracture with minimal trauma, tends to be in trabecular bone
Secondary osteoporosis
Quantitative and qualitative changes in bone structure as the result of disease (such as hyperparathyroidism), medications (excess use of glucocorticoids), deficiencies (vitamin D deficiency), or other (alcoholism, tobacco use)
Phases in the development of Paget’s disease
Osteoclastic (lytic), mixed osteoclastic-osteoblastic, osteoblastic
Osteomalacia
Deficient mineralization of bone and cartilage that occurs after the epiphyseal plates have closed in adults and is due to many secondary causes such as vitamin D deficiency or tumor induced
Rickets
Deficient mineralization of bone and cartilage that occurs in growing bones of children. It can be caused by deficiencies, insensitivity to or derangement of metabolism of vitamin D, calcium or phosphorus. Can result in profusion of disorganized, nonmineralized, degenerating cartilage, widening of the epiphyseal plate, rachitic rosary, swelling at the ends of long bones, growth retardation
Hyperparathyroidism changes
Hypercalcemia, elevated bone turnover, subperiosteal resorption of cortical bone in phalanges, salt and pepper appearance of skull, bone cysts, osteoporosis
Biochemical markers of bone formation
Type I collagen propeptides (P1NP in serum), bone specific alkaline phosphatase (bAP in serum), osteocalcin (in serum)
Biochemical markers of bone resorption
Type I collagen telopeptides (NTx or CTx in serum or urine), pyridinoline/hydroxypyridinoline (in urine)
Antiresorptive agents
Bisphosphate, denosumab, nasal calcitonin, sclerostin inhibitors
Bone-forming agents
Parathyroid hormone