Table 1.
Clinical features of four main categories of bone disease (renal osteodystrophy) in kidney transplant recipients (see also Figure 1)
Type | Histopathologic features | Biochemical abnormalities | Clinical consequences |
---|---|---|---|
Hyperactive (high turnover) bone disease (including osteitisfibrosa) | Marked increase in bone turnover, irregularly shaped trabecules displaying numerous abnormal remodeling sites, and an unusually high number of bone cells with irregular arrangement and shape |
|
|
Adynamic (low turnover) bone disease | Reduced bone volume and mineralization paralleled by a decrease in bone formation. It is also characterized by presence of few osteoid seams and few osteoblasts. Osteoclast number may be low, normal, or high. |
|
|
Mixed renal osteodystrophy | Defective mineralization with or without increased bone formation and increased PTH activity in bone. Increased numbers of heterogeneous remodeling sites and an increase in osteoclast number. Bone volume is variable and depends on a dominant pathogenic cause. |
|
|
Osteomalacia (may also be included under low-turnover category) | Accumulation of unmineralized matrix in which a decrease in mineralization precedes or is more pronounced than the inhibition of collagen deposition. |
|
|
Bone specific AlkPhos is preferred but total (non-specific) AlkPhos can be used after ruling out liver disease or other non-bone sources of circulating AlkPhos.