A 12 month study to compare the effectiveness of alendronate (Fosamax) and risedronate (Actonel) showed Fosamax increased bone mineral density (BMD) by as much as 62% at sites measured in 520 osteoporotic postmenopausal women. The average age of test subjects was 64 years, and 94% were white.
In all, 1,053 individuals participated in the study, the other 533 subjects were given alendrate.
The subjects were given a dose of 35 mg once per week. After a year, alendronate produced BMD increase of as much as 3.4% compared to 2.1% for risedronate.
The results, released at the 26th annual meeting of the American Society for Bone and Mineral Research (ASBMR), verified a two-year study done earlier. Merck & Company, the manufacturer of alendronate , funded the research.
Those taking alendronate showed an overall increase of 2.2% compared to 2.1% for alendrate in the hip, 1.6%, compared to 0.9% at the femoral neck and 3.7% vs 2.6% in the lumbar spine. Positive increases were noticeable after just six months in most cases.
“Overall, 84.5% of women in the alendronate group gained or maintained BMD at hip trochanter vs 67.8% of women in the alendrate group, and 87.3% of the alendronate-treated women gained or maintained BMD at the lumbar spine vs 75.6% of women in the risedronate group.” According to a report on the study.
“The lead investigator of the Fosamax Actonel Comparison Trial (FACT), Clifford Rosen, MD, from the Maine Center of Osteoporosis Research and Education and St. Joseph Hospital in Bangor, Maine, said, "The density of the gains for alendronate were certainly greater than for ris-edronate, but of equal [importance] and perhaps more im- portantly, there was no increase for gastrointestinal side effects with either agent."