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Evidence that increased calcium intake does not prevent early postmenopausal bone loss
D J Hosking1, P D Ross, D E Thompson
1Division of Mineral Metabolism, City Hospital, Nottingham, United Kingdom.
Clinical Therapeutics
|November 26, 1998
Summary
Adequate calcium intake alone does not prevent bone loss in early postmenopausal women. Even with increased intake, bone mineral density (BMD) declined, suggesting other therapies are needed to maintain bone health.
Area of Science:
- Bone Metabolism and Endocrinology
- Postmenopausal Health
- Nutritional Science
Background:
- The role of calcium in preventing bone loss among early postmenopausal women remains debated.
- Previous research has yielded conflicting results regarding calcium's efficacy in bone health maintenance.
Purpose of the Study:
- To investigate the relationship between calcium intake and bone loss in early postmenopausal women.
- To determine if varying levels of calcium intake influence bone mineral density (BMD) and bone turnover markers.
Main Methods:
- Analysis of data from 394 women in the placebo group of the Early Postmenopausal Interventional Cohort study.
- Measurement of calcium intake, BMD (lumbar spine, total body, forearm, hip), and biochemical bone turnover markers over 24 months.
- Intervention included advising women with low baseline calcium intake (<500 mg/d) to increase consumption.
Main Results:
- Mean BMD decreased by approximately 1.9% at the lumbar spine and 1.6% at the hip over 24 months.
- No significant association was found between baseline or changed calcium intake and BMD or bone turnover markers.
- Even women in the highest tertile of calcium intake (>1333 mg/d) experienced BMD declines similar to those in lower intake groups.
Conclusions:
- Calcium intake alone, even when increased, did not demonstrate a protective effect against bone loss in this cohort.
- Significant declines in BMD occurred despite variations in calcium consumption.
- More potent therapeutic strategies are necessary to effectively increase or maintain BMD in early postmenopausal women.