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Intramuscular clodronate therapy in postmenopausal osteoporosis
Bone
|February 10, 1999
Summary
Intramuscular clodronate injections improved bone mineral density in postmenopausal osteoporosis. However, injection site pain limited patient compliance and widespread use of this bisphosphonate therapy.
Area of Science:
- Endocrinology
- Orthopedics
- Pharmacology
Background:
- Oral bisphosphonates are effective for postmenopausal osteoporosis but may have compliance issues.
- Intramuscular (i.m.) clodronate offers an alternative administration route for osteoporosis treatment.
Purpose of the Study:
- To evaluate the efficacy of intermittent i.m. clodronate in treating postmenopausal osteoporosis.
- To compare weekly versus bi-weekly i.m. clodronate administration for bone mineral density (BMD) changes.
Main Methods:
- A 3-year randomized controlled study involving 90 osteoporotic postmenopausal women.
- Patients received calcium supplementation and were randomized to no therapy, 100 mg i.m. clodronate weekly, or 100 mg i.m. clodronate every two weeks.
- Bone mineral density (BMD) and biochemical markers of bone turnover were monitored.
Main Results:
- Intramuscular clodronate significantly increased spinal BMD compared to controls, with greater gains in the weekly group (4.5% over 3 years).
- Significant increases in trochanter and Ward's triangle BMD were observed with weekly injections at 12 months.
- Hip BMD changes differed significantly from controls in both i.m. clodronate groups; however, femoral neck BMD did not change significantly.
- Biochemical markers of bone turnover were suppressed in both clodronate treatment groups.
- Nearly 50% of patients on weekly i.m. clodronate withdrew due to injection site pain.
Conclusions:
- Intermittent i.m. clodronate administration demonstrates clinically relevant benefits for skeletal bone density in postmenopausal osteoporosis.
- The significant pain associated with i.m. injections may restrict the extensive clinical application of this bisphosphonate therapy.