{"id":130130,"date":"2014-05-05T01:54:57","date_gmt":"2014-05-05T05:54:57","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/study-unveils-new-approach-to-treating-brittle-bone-disease.php"},"modified":"2014-05-05T01:54:57","modified_gmt":"2014-05-05T05:54:57","slug":"study-unveils-new-approach-to-treating-brittle-bone-disease","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/medicine\/study-unveils-new-approach-to-treating-brittle-bone-disease.php","title":{"rendered":"Study unveils new approach to treating brittle bone disease"},"content":{"rendered":"<p><p>    PUBLIC RELEASE DATE:  <\/p>\n<p>    4-May-2014  <\/p>\n<p>    Contact: Glenna Picton    <a href=\"mailto:picton@bcm.edu\">picton@bcm.edu<\/a>    713-798-4710    Baylor College of    Medicine<\/p>\n<p>    HOUSTON  (May 4, 2014)  Researchers at Baylor College of    Medicine have identified a new approach to treating brittle    bone disease, a congenital disorder that results in fragile    bones that break easily.  <\/p>\n<p>    The study, published in the current issue of the journal    Nature Medicine, showed that excessive activity of an    important signaling protein in the matrix of the bone called    transforming growth factor beta is associated with the cause of    the disease.  <\/p>\n<p>    \"There are many genetic causes of brittle bone disease in    children and adults,\" said Dr. Brendan Lee, professor of    molecular and human genetics at Baylor and a Howard Hughes    Medical Institute investigator. \"We have discovered many of    them but clinicians still cannot easily distinguish the    different forms.\"  <\/p>\n<p>    Lee said the new study suggested that there may be common    mechanisms that cause the decreased quality and quantity of    bone in these different forms.  <\/p>\n<p>    \"This identified an important concept in bone disease that    while many different genetic mutations can affect the proteins    in the bone matrix (like collagen) they act in a common pathway    to cause the bone disease  that is they affect how signaling    proteins called transforming growth factor beta (TGF) are    delivered to cells in the bone,\" said Lee. \"We now have a    deeper understanding for how genetic mutations that affect    collagen and collagen processing enzymes cause weak bones.\"  <\/p>\n<p>    Collagen is the most common protein in the human body, and the    four most common types are found in different types of tissues    including bone, cartilage, blood vessels, and kidney.  <\/p>\n<p>    In animal studies, Lee and his colleagues showed that blockade    of the TGF proteins using an antibody could restore the    quantity of bone in mice with different forms of brittle bone    disease.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read the original:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2014-05\/bcom-sun043014.php\/RK=0\/RS=kHRpXRRnnLiscqbtVGcoOa7gIgM-\" title=\"Study unveils new approach to treating brittle bone disease\">Study unveils new approach to treating brittle bone disease<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> PUBLIC RELEASE DATE: 4-May-2014 Contact: Glenna Picton <a href=\"mailto:picton@bcm.edu\">picton@bcm.edu<\/a> 713-798-4710 Baylor College of Medicine HOUSTON (May 4, 2014) Researchers at Baylor College of Medicine have identified a new approach to treating brittle bone disease, a congenital disorder that results in fragile bones that break easily.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/medicine\/study-unveils-new-approach-to-treating-brittle-bone-disease.php\">Continue reading <span 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