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. Author manuscript; available in PMC: 2013 Sep 1.
Published in final edited form as: Endocrinol Metab Clin North Am. 2012 May 23;41(3):595–611. doi: 10.1016/j.ecl.2012.04.004

Table 2.

Treatment of Glucocorticoid-Induced Osteoporosis.

Intervention Advantages Disadvantages
Alendronate (oral;
10 mg/d or 70
mg/wk), risedronate
(5 mg/d or 35
mg/wk)
Osteoclast inhibition reduces
   bone loss. Alendronate also
   prevents glucocorticoid-
   induced osteocyte apoptosis.
   If glucocorticoids are
   discontinued, these drugs can
   be stopped.
Antiresorptive agents do not directly
   address the decreased bone
   formation characteristic of
   glucocorticoid-induced bone
   disease. Additional problems
   include gastrointestinal side
   effects, rare uveitis, poor
   compliance with oral therapy, and
   the time required to obtain skeletal
   protection. Avoid in patients with
   a creatinine clearance less than 30
   mL/min.
Zoledronic acid (5
mg IV/yr)
Osteoclast inhibition reduces
   bone loss. Increased
   compliance compared with
   oral treatment and rapid onset
   of skeletal effects.
   Gastrointestinal side effects
   are unlikely.
Does not address the reduced bone
   formation caused by glucocorticoid
   excess. Avoid in patients with a
   creatinine clearance less than 30
   mL/min.
Teriparatide (20 µg
subcut/d)
Directly addresses the
   pathogenesis of GIO.
   Reduces vertebral fractures.
Cost, daily injections are required,
   reduced response with high dose
   glucocorticoids. Not studied in
   patients with elevated parathyroid
   hormone levels. Adverse effects:
   mild hypercalcemia, headache,
   nausea, leg cramps, dizziness.
   Caution with pre-existing
   nephrolithiasis. Check serum
   calcium at least once ≥16 hours
   after injection and adjust oral
   calcium intake as needed (54).
Denosumab (60 mg
subcut every 6 mo)
Potent inhibitor of osteoclasts
   with ease of administration.
   Can be stopped if
   glucocorticoids are
   discontinued. Useful in renal
   insufficiency.
Does not address the reduced bone
   formation caused by glucocorticoid
   excess. Not yet approved for GIO.
Vertebroplasty,
kyphoplasty
Commonly used to treat recent
   painful vertebral fractures.
Beneficial effects similar to sham
   procedures. Dangers of cement
   leakage. Increased incidence of
   additional fractures in patients
   receiving glucocorticoids (58).