A major breakthrough concerning the genes involved in brittle bone disease could help millions of us around the world, say experts in the field. Scientists have been studying the human genome in order to discover which genes lead to the development of a common bone wellness problem, with encouraging results.
Why genes matter
Finding out the specific genes that result in disorders is the first step to treating and possibly eradicating the disease concerned. Researchers joined together to concentrate on identifying the genetic code that means we have a very high likelihood of developing osteoporosis. The condition already has a strong genetic link, and when doctors are diagnosing the syndrome they take into account whether close family members have fractures linked to brittle bones. Researchers have already discovered several genes responsible for osteoporosis, but this new study has identified a further 13 genes that are linked to the disease. Researchers explain that as they understand more about what makes bones weak they can develop treatments that intervene in this process, so bones stay stronger.
Who will benefit?
The International Osteoporosis Foundation says a third of women and a fifth of men over 50 will suffer from some kind of fracture, with half of people getting breakages dying within two years. These figures highlight the vast number of us around the world whose bone density is so light that we could suffer breakages that eventually may have a fatal impact on our lives. This can be due to complications from fractures, including disability and changes to our independence and mobility. Currently there are several ways we can promote our wellbeing even if we have been diagnosed with brittle bones. Experts explain that the disease is treatable and more importantly preventable if we eat well and exercise regularly, combined with knowledge about genetic risk factors we may eventually beat the condition altogether.
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