EVIDENCE THAT INCREASED CALCIUM INTAKE DOES NOT PREVENT EARLY POSTMENOPAUSAL BONE LOSS

Citation
Dj. Hosking et al., EVIDENCE THAT INCREASED CALCIUM INTAKE DOES NOT PREVENT EARLY POSTMENOPAUSAL BONE LOSS, Clinical therapeutics, 20(5), 1998, pp. 933-944
Citations number
22
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
01492918
Volume
20
Issue
5
Year of publication
1998
Pages
933 - 944
Database
ISI
SICI code
0149-2918(1998)20:5<933:ETICID>2.0.ZU;2-X
Abstract
Calcium's ability to prevent bone loss in early postmenopausal women i s controversial. We used data on 394 women from the placebo group of t he Early Postmenopausal Interventional Cohort study, a clinical trial of alendronate, to investigate the relation of calcium intake to bone loss. Calcium intake was recorded, and bone mineral density (BMD) (in the lumbar spine, total body, forearm, and hip) and biochemical marker s of bone turnover (serum total alkaline phosphatase, serum osteocalci n, and urinary N-telopeptide crosslink levels) were measured at baseli ne and annually thereafter. Women whose baseline calcium intake was <5 00 mg/d were advised to increase their calcium intake. Mean (+/- SE) B MD decreased by 1.9% +/- 0.16% at the lumbar spine and 1.6% +/- 0.14% at the hip over the 24-month period. Despite wide variations in baseli ne calcium intake and changes in calcium intake, these measures were n ot significantly associated with changes in BMD or bone turnover. Even women whose total calcium intake was >1333 mg/d (the highest tertile of total calcium intake) showed a decline in BMD of almost 2%, similar to declines in the lower two tertiles of total calcium intake (<869 a nd 869-1333 mg/d, respectively). Increased calcium intake resulted in modest mean increases of approximately 200 mg/d. We were unable to dem onstrate that increases of this magnitude or much greater(1 g/d) were protective against declines in BMD at any site, even in women who had the lowest calcium intake at baseline. In addition to adequate calcium intake, more effective therapy appears to be required when the therap eutic goal is to increase or maintain BMD.