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M

M. Daley

Researcher at Merck & Co.

Publications -  5
Citations -  1364

M. Daley is an academic researcher from Merck & Co.. The author has contributed to research in topics: Osteoporosis & Bone disease. The author has an hindex of 5, co-authored 5 publications receiving 1326 citations.

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Journal ArticleDOI

Prevention of bone loss with alendronate in postmenopausal women under 60 years of age. Early Postmenopausal Intervention Cohort Study Group.

TL;DR: Estrogen-replacement therapy prevents osteoporosis in postmenopausal women by inhibiting bone resorption, but the balance between its long-term risks and benefits remains unclear.
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Low Body Mass Index Is an Important Risk Factor for Low Bone Mass and Increased Bone Loss in Early Postmenopausal Women

TL;DR: Thinness is an important risk factor for low bone mass and increased bone loss in postmenopausal women and because the response to alendronate treatment is independent of fat mass parameters, prevention of post menopausal osteoporosis can be equally achieved in thinner and heavier women.
Journal ArticleDOI

Prevention of Bone Loss With Alendronate in Postmenopausal Women Under 60 Years of Age

TL;DR: Alendronate prevents bone loss in postmenopausal women under 60 years of age to nearly the same extent as estrogen-progestin and was well tolerated, with a safety profile similar to that of placebo or estrogen- Progestin.
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Alendronate and estrogen-progestin in the long-term prevention of bone loss: four-year results from the early postmenopausal intervention cohort study. A randomized, controlled trial.

TL;DR: In this article, four years of alendronate or estrogen-progestin therapy prevented postmenopausal bone loss and a residual effect was seen 2 years after alendralate therapy was stopped.
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Evidence that increased calcium intake does not prevent early postmenopausal bone loss

TL;DR: Investigation of the relation of calcium intake to bone loss in early postmenopausal women using data from the Early Postmenopausal Interventional Cohort study found more effective therapy appears to be required when the therapeutic goal is to increase or maintain BMD.