Transverse section of the bone. Source: Wikimedia Commons and BDB

A new study from the Mount Sinai School of Medicine in New York suggests that a polyclonal antibody that blocks follicle-stimulating hormone (FSH) in mice without ovaries might offer a more effective way to prevent or arrest osteoporosis than currently available treatments.

The study, published online August 20 in the Proceedings of the National Academy of Sciences, used a mouse model of menopause to show that an injection of a polyclonal antipeptide antibody enhances bone regeneration by simultaneously slowing bone destruction and building bone. In addition, the monoclonal antibody is likely to be safer because it is cleared from the blood and is not retained in bone.

“Bone loss in women begins very early, at least two to three years before a woman’s last period and within eight to ten years, a woman will lose 50% of her lifetime bone loss, ” says the study’s senior investigator, Mone Zaidi, M.D., in the August 20, 2012 news release. Dr. Zaidi is professor of Medicine and of Structural and Chemical Biology, at Mount Sinai School of Medicine in New York. “It occurs painlessly, without notice up to a point where women fracture.”

Dr. Zaidi, who is director of the Mount Sinai Bone Program at Mount Sinai School of Medicine, New York, is the senior investigator of the research that developed the polyclonal antipeptide antibody to FSH and tested it in mice whose ovaries were removed. Peptides are short chains of amino acids, and the FSH antibody is a highly specific antibody.

“A few years ago, we showed that FSH directly regulates bone by bypassing the estrogen axis, ” says Dr. Zaidi. FSH rises early in menopause, stimulates bone removal and negatively regulates bone formation. “By blocking FSH with the FSH-specific polyclonal antibody, we were able to block bone resorption by osteoclasts and stimulate bone formation through osteoblasts cells.”

Dr. Zaidi added, “Our aim is to find a way to prevent osteoporosis rather than simply treat established disease using medicines that are well tolerated. We believe that a future humanized monoclonal antibody to FSH is likely to be safer than existing treatments because it will not reside in the bone.”

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