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Clinical experience with etidronate in osteoporosis
1Department of Nuclear Medicine, Guy's Hospital, London.
Clinical Rheumatology
|September 1, 1994
Summary
Cyclical etidronate therapy effectively increases bone mineral density (BMD) in most osteoporosis patients, particularly in the lumbar spine and Ward's triangle, over one year. However, responses vary, with some patients showing no increase in bone mass.
Area of Science:
- Bone Biology and Metabolism
- Pharmacology and Therapeutics
Background:
- Osteoporosis is a significant public health concern characterized by low bone mass and microarchitectural deterioration.
- Bisphosphonates, such as etidronate, are a cornerstone in osteoporosis management.
Purpose of the Study:
- To evaluate the clinical efficacy and patient response to cyclical etidronate therapy for osteoporosis.
- To assess changes in bone mineral density (BMD) at various skeletal sites.
Main Methods:
- Retrospective review of 69 consecutive patients treated with cyclical etidronate.
- Bone mineral density (BMD) measurements using dual-energy X-ray absorptiometry (DXA) before and after 1 year of treatment.
- Analysis of BMD changes in subgroups with osteoporotic fractures and osteopenia.
Main Results:
- BMD increased by 4.50% in the lumbar spine (p < 0.001) and 5.5% at Ward's triangle (p < 0.01) after 1 year.
- No significant BMD changes were observed at the femoral neck or greater trochanter.
- 83% of patients showed increased lumbar spine BMD, and 55% had increased femoral neck BMD after 1 year.
Conclusions:
- Cyclical etidronate therapy demonstrates efficacy in preserving and increasing bone mass in the majority of osteoporosis patients.
- A wide variation in BMD response exists, with a minority of patients not experiencing bone mass increase.
- The therapy is generally well-tolerated, with few discontinuations due to adverse effects.