1992
DOI: 10.1016/0169-6009(92)90866-c
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Ipriflavone and low doses of estrogens in the prevention of bone mineral loss in climacterium

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Cited by 28 publications
(4 citation statements)
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“…30 Combinations included ipriflavone 600 mg/day with either CEE 0.625 mg/day, 28 CEE 0.3 mg/day, 27,29 or CEE 0.15 mg/day. 29 Although the study populations varied (early postoopherectomy in one, healthy postmenopausal in another, and postmenopausal with osteoporosis risk factors in the third), all three trials suggested a benefit of the combination treatment over CEE 0.3-0.625 mg/day alone. Additionally, two other recent trials suggest a preventive benefit of CEE combined with either calcitriol or risedronate.…”
Section: Discussionmentioning
confidence: 99%
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“…30 Combinations included ipriflavone 600 mg/day with either CEE 0.625 mg/day, 28 CEE 0.3 mg/day, 27,29 or CEE 0.15 mg/day. 29 Although the study populations varied (early postoopherectomy in one, healthy postmenopausal in another, and postmenopausal with osteoporosis risk factors in the third), all three trials suggested a benefit of the combination treatment over CEE 0.3-0.625 mg/day alone. Additionally, two other recent trials suggest a preventive benefit of CEE combined with either calcitriol or risedronate.…”
Section: Discussionmentioning
confidence: 99%
“…For example, ipriflavone is a synthetic isoflavone that has been combined with estrogen replacement in three trials. [27][28][29] Isoflavones are the principal phytoestrogens (plant estrogens) of soy and have weak estrogenic activity. 30 Combinations included ipriflavone 600 mg/day with either CEE 0.625 mg/day, 28 CEE 0.3 mg/day, 27,29 or CEE 0.15 mg/day.…”
Section: Discussionmentioning
confidence: 99%
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“…Numerous clinical trials have demonstrated IP's ability to slow the continual decline in bone mineral density (BMD) commonly observed after menopause. [1][2][3][4][5][6][7] Melis et al 8 demonstrated that IP may be as effective as estrogen in its ability to prevent bone loss, and a combination of the two treatments may improve the effects of hormone replacement therapy (HRT). IP has been shown to reduce the rate of bone breakdown by inhibiting osteoclast and stimulating osteoblast activity while apparently having no effect on breast or reproductive tissue.…”
Section: Introductionmentioning
confidence: 98%