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EMBARGOED FOR RELEASE UNTIL 1:00 P.M. (EDT) ON FRIDAY, SEPTEMBER 15, 2006

Research Shows Bisphosphonate Treatment-Induced Skeletal Cracks Do Not Increase In Number Beyond First Year Of Therapy

Contact:    Stephanie West: (202) 367-1219; swest@asbmr.org
 

Sept. 15-19: ASBMR Media Room: 304
Pennsylvania Convention Center, Philadelphia, PA
(215) 418-2028

Philadelphia (Sept. 15, 2006) – Skeletal microdamage resulting from bisphosphonate treatment may be maximal during the first year of treatment, and not continue to accumulate with longer periods of treatment, according to new research being presented today at the 28th Annual Meeting of the American Society for Bone and Mineral Research (ASBMR).

Bisphosphonates are the most common class of drugs used for the treatment of osteoporosis because of their demonstrated effect on fracture reduction, but the incidence of microcracks--small cracks in the skeleton--has been shown to increase with bisphosphonate treatment. This has led to some concerns regarding the potential long-term adverse effects of these agents. This study shows that the continued use of alendronate (a bisphosphonate) is not associated with continued accumulation of microdamage.

Matt Allen, Ph.D., and David Burr, Ph.D., from the Indiana University School of Medicine, Indianapolis, IN, evaluated the effects of alendronate in one-year-old female beagles. The beagles were given oral doses of alendronate at levels comparable to that employed in humans (0.2 mg/kg/day) or at five times the clinical dose (1 mg/kg/day) for either one year or three years.

Researchers found there was no increase in vertebral microcracks after three years of alendronate treatment in comparison to the beagles treated for one year. These results suggest that microcrack accumulation is greatest during the early course of alendronate treatment. This is an encouraging sign for long-term safety of these drugs.

ASBMR President-Elect Steve Goldring, M.D., notes: “These findings have important clinical implications with respect to the long-term safety of bisphosphonates in patients with osteoporosis.”

Disclosures: Dr. Allen and Dr. Burr have received financial support from Eli Lilly, Procter & Gamble (The Alliance for Better Bone Health), Merck, and Amgen. Dr. Burr has been a consultant for Eli Lilly, Procter & Gamble (The Alliance for Better Bone Health), and Amgen, has participated in a speakers bureau for Eli Lilly and Procter & Gamble (The Alliance for Better Bone Health), and holds stock in Pfizer and Amgen.

To obtain a copy of the scientific abstract, contact Stephanie West (contact information above).

The ASBMR Annual Meeting is the pre-eminent scientific meeting on bone and mineral metabolism. More than 5,000 delegates are expected to attend the September 15-19 meeting, where nearly 1,800 scientific abstracts are presented. The ASBMR is the premier professional, scientific and medical society established to promote excellence in bone and mineral research and to facilitate the translation of that research into clinical practice. The ASBMR has a membership of nearly 4,000 physicians, basic research scientists, and clinical investigators. To learn more about the Society and the field of bone and mineral research, visit the ASBMR website at www.asbmr.org.

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The ASBMR is the foremost professional, scientific and medical society for the promotion of bone and mineral research and the translation of that research into clinical practice. To learn more, visit the ASBMR website at www.asbmr.org.

 

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