
What is it?
Ipriflavone is a synthetic flavonoid
(isoflavone) derived from the soya compound
daidzein.
Ipriflavone promotes the incorporation of
calcium into bone. It also inhibits bone breakdown. Many clinical studies, including
numerous double-blind studies, have clearly shown that long-term treatment with ipriflavone
(along with 1,000 mg supplemental calcium per day) is both safe and effective in halting bone
loss in postmenopausal women or in women who
have had their ovaries removed. Ipriflavone has also been found to improve bone density in
cases of osteoporosis.1
2 3 4 5 6
In one study demonstrating that ipriflavone prevents bone loss, 56 recently post-menopausal
women with low bone density were assigned to receive either ipriflavone (200 mg three times
per day) or a placebo for two years.7 Consistent with most other studies with
ipriflavone, all women also received 1,000 mg of elemental calcium daily. While vertebral
(spine) bone density declined by 4.9% after two years in women taking only calcium, there was
no change in bone density among woman taking ipriflavone supplementation.
Double-blind studies in women with osteoporosis have also shown positive effects. The most
significant studies were performed in elderly women with a history of vertebral fractures due
to osteoporosis.8 9 10 Ipriflavone therapy not only stopped
bone loss, it actually increased bone density and significantly eliminated or improved
vertebral fractures and bone pain.
One double-blind study has failed to confirm the beneficial effect of ipriflavone. In that
study, ipriflavone was no more effective than a placebo for preventing bone loss in
postmenopausal women with osteoporosis.11 The women in this negative study were
older (average age, 63.3 years) than those in most other ipriflavone studies and had
relatively severe osteoporosis. It is possible that ipriflavone works only in younger women or
in those with less severe osteoporosis.
Where is it found?
Ipriflavone does occur naturally in food but only in trace amounts. It is available as a
nutritional supplement.
Ipriflavone has been used
in connection with the following conditions (refer to the individual
health concern for complete information):
Who is likely to be deficient?
As ipriflavone is not an essential nutrient, no deficiency state exists.
How much is usually taken?
The typical supplemental amount of ipriflavone is 200 mg three times daily. Taking 300 mg
twice daily has been reported to be just as effective as 200 mg three times per
day.12
Are there any side effects or interactions?
In a trial of ipriflavone for osteoporosis, 29 of the 132 women in the ipriflavone group
completing the three-year trial developed a clinically significant drop in
lymphocytes.13 These cells, which make up approximately 22 to 28% of the white
blood cells in the normal adult, are critical components of the immune system and its ability
to respond to viral infections. In some of these women, a return to normal levels took almost
two years after they had stopped the ipriflavone. Since this finding has been reported in one
other smaller clinical trial,14 it suggests that women choosing to take ipriflavone
should have their lymphocytes measured regularly by their doctor.
In double-blind studies, the frequency of perceived side effects in ipriflavone-treated
people (14.5%) was actually less than that observed in people receiving the placebo
(16.1%).15 Side effects were mainly mild stomach upset. Researchers recommend that patients
with severe kidney disease take a lower amount of ipriflavone (200 to 400 mg
daily).16
Are there any drug
interactions?
Certain medicines may interact with ipriflavone. Refer to drug interactions for a list of those medicines.
References
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1. Agnusdei D, Bufalino L. Efficacy of ipriflavone in established
osteoporosis and long-term safety. Calcif Tissue Int 199:61:S23–7 [includes
review].
2. Head KA. Ipriflavone: an important bone-building isoflavone.
Altern Med Rev 1999;4:10–22 [review].
3. Avioli LV. The future of ipriflavone in the management of osteoporotic
syndromes. Calcif Tissue Int 1997;61 Suppl 1:S33–5 [review].
4. Adami S, Bufalino L, Cervetti R, et al. Ipriflavone prevents radial
bone loss in postmenopausal women with low bone mass over 2 years. Osteoporos Int
1997;7:119–25.
5. Nozaki M, Hashimoto K, Inoue Y, et al. Treatment of bone loss in
oophorectomized women with a combination of ipriflavone and conjugated equine estrogen.
Int J Gynaecol Obstet 1998;62:69–75.
6. Gennari C, Adami S, Agnusdei D, et al. Effect of chronic treatment
with ipriflavone in postmenopausal women with low bone mass. Calcif Tissue Int
1997;61:S19–22.
7. Gennari C, Agnusdei D, Crepaldi G, et al. Effect of
ipriflavone—a synthetic derivative of natural isoflavones—on bone mass loss in the
early years after menopause. Menopause 1998;5:9–15.
8. Agnusdei D, Buffalino L. Efficacy of ipriflavone in established
osteoporosis and long-term safety. Calcif Tissue Int 1997;61 Suppl 1:S23–7.
9. Passeri M, Biondi M, Costi D, et al. Effects of 2-year therapy with
ipriflavone in elderly women with established osteoporosis. Ital J Mineral Electrolyte
Metabol 1995;9:137–44.
10. Kovacs AB. Efficacy of ipriflavone in the prevention and treatment of
postmenopausal osteoporosis. Agents Actions 1994;41(1–2):86–7.
11. Alexandersen P, Toussaint A, Christiansen C, et al. Ipriflavone in
the treatment of postmenopausal osteoporosis: a randomized controlled trial. JAMA
2001;285:1482–8.
12. Acerbi D, Poli G, Ventura P. Comparative bioavailability of two oral
formulations of ipriflavone in healthy volunteers at steady-state. Evaluation of two different
dosage schemes. Eur J Drug Metabol Pharmacokinet 1998,23:172–7.
13. Alexandersen P, Toussaint A, Christiansen C, et al. Ipriflavone in
the treatment of postmenopausal osteoporosis. JAMA 2001;285:1482–8.
14. Agnusdei D, Bufalino L. Efficacy of ipriflavone in established
osteoporosis and long-term safety. Calcif Tissue Int 1997;61:23–27.
15. Agnusdei D, Bufalino L. Efficacy of ipriflavone in established
osteoporosis and long-term safety. Calcif Tissue Int 199:61:S23–7 [includes
review].
16. Rondelli I, Acerbi D, Ventura P. Steady-state pharmacokinetics of
ipriflavone and its metabolites in patients with renal failure. Int J Clin Pharm Res
1991;11:183–92.
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The information presented in Healthnotes is for informational purposes
only. It is based on scientific studies (human, animal, or in vitro), clinical
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making any changes in prescribed medications. Information expires March 2007.