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Number Of Black Organ Donors Increases In Michigan, Many Blacks Still Reluctant To Donate Organs
Although the number of blacks who are registered as organ donors in Michigan has increased in the last 15 years, many are still reluctant to be organ donors, the Detroit News reports. According to Remonia Chapman, director of Gift of Life Michigan"s minority organ tissue transplant education program, many blacks are hesitant to participate with the organ donor registry because they have inadequate access to health care.Chapman said that increased awareness and education about organ donation and the diseases that lead to the need for donated organs, as well as partnerships with minority donors, black ministers and community groups, have encouraged more blacks to be organ donors. In the last 15 years, the percentage of black Michigan residents who are registered organ donors has increased from 10.8% to 21%, with overall minority registration at 24%. Chapman noted that about 41.3% of people on Michigan"s transplant waiting list and about 46% of people in need of a kidney are minorities.According to the News, minority donors are the best matches for minority organ recipients because the genetic profiles of the donor and recipient will have more similarities. Chapman added that the best matches for kidney recipients are donors from the recipient"s family or from the recipient"s ethnic group if a family donor is not available (Stolarz, Detroit News, 5/19).
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Proven Link Between Obesity And Diabetes
A Monash University study has proven a critical link between obesity and the onset of Type 2 diabetes, a discovery which could lead to the design of a drug to prevent the disease.
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Rush University Medical Center Hosts Conference Examining Chicago Breastfeeding Rates And Ways To Reduce The Disparities
Over 100 certified breastfeeding peer counselors, lactation consultants, nurses, physicians, dietitians and community health workers are expected to gather at Rush University Medical Center on Thursday, August 6 from 8 a.m. until 1 p.m. in Room 500 at 1725 W. Harrison Street, Chicago, to attend the Griffin Inaugural Conference on Breastfeeding: The Primary Foundation for Health.
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Skull Fusion Disorder Of Infants: UC Davis Bioengineer Receives Hartwell Grant

With support from a foundation that champions cutting-edge medical research, a biomedical engineer at UC Davis will start work this month on developing a new treatment for infants born with disorders that cause the sutures of their skulls to prematurely fuse together. The new approach is based on creating a synthetic bone matrix that is biodegradable and bio-absorbable. If successful, it could also lead to advances in treating various problematic bone fractures in adults, such as those caused by osteoporosis. Kent Leach, an assistant professor of biomedical engineering, is the first UC Davis faculty member to receive a grant from The Hartwell Foundation, an organization that supports biomedical research projects with the potential for benefiting children. Specifically, the foundation specializes in funding innovative early-stage research that has not yet qualified for support from traditional s. Surgery is the standard treatment for infants diagnosed with craniosynostosis, the generic name for a group of disorders that result in the premature fusing of one or more of the sutures necessary for the skull to expand as the child"s brain grows. If left untreated, the disorder can cause abnormal head shape and increased pressure on the brain resulting in brain damage. In a standard operation, surgeons remove swaths of fused bone, break them into segments then reposition a portion of them along the sutures to protect the exposed brain. The hope is that by removing some bone and rearranging the rest, growth will be slowed long enough to allow the brain to reach full size. But in 6 to 8 percent of cases, a second operation is necessary, and in 25 percent of those cases, even a third operation will be required, with the risk of complications climbing with each ensuing operation. Leach"s hypothesis is that it may not be the bone-forming cells themselves that are growing abnormally, but that the environment surrounding them, known as the extracellular matrix, may be providing improper instructions to the cells. "If we can deliver a different matrix - one that promotes the growth of healthy tissue - our hope is that we can eliminate secondary surgeries," he said. With $300,000 in funding from The Hartwell Foundation, Leach intends to engineer a porous, biodegradable material with the mechanical properties of bone that can be placed along the sutures as a substitute for the fragmented skull bones. His goal for the three-year term of the grant is to demonstrate the feasibility of this approach in laboratory rats. "What we want to do is make a scaffold - a material that the bone-forming cells can enter - that supplies them with the proper directions for how much bone they should be forming and how fast they should be doing it," he said. Leach will be collaborating with two colleagues at the UC Davis School of Medicine: Alice Tarantal, a professor of cell biology and human anatomy who has extensive experience in stem cell research, and Simeon Boyd, an associate professor of pediatrics, who is an internationally recognized expert on congenital anomalies of the head and face. Liese Greensfelder University of California - Davis


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