Avicena Group, University of Cincinnati Medical Center, and Cincinnati Children's Hospital Medical Center Begin Research Collaboration on Treatment for Creatine Transporter Deficiency.Business Editors/Health/Medical Writers BIOWIRE2K PALO ALTO, Calif.--(BUSINESS WIRE)--June 12, 2003 The Avicena Group, Inc., based in Palo Alto, CA and Cambridge, MA, has formed a collaboration with The University of Cincinnati The University of Cincinnati is a coeducational public research university in Cincinnati, Ohio. Ranked as one of America’s top 25 public research universities and in the top 50 of all American research universities,[2] Medical Center and the Cincinnati Children's Hospital Medical Center Cincinnati Children's Hospital Medical Center is a hospital in Cincinnati, Ohio. In June of 1883, a meeting of women from parish communities around Cincinnati established a mission to create a Diocesan Hospital for Children. to research the efficacy of creatine creatine /cre·a·tine/ (kre´ah-tin) an amino acid occurring in vertebrate tissues, particularly in muscle; phosphorylated creatine is an important storage form of high-energy phosphate. in the treatment of creatine transporter defect. A joint research effort between the University of Cincinnati (UC) Medical Center and Cincinnati Children's Hospital Medical Center (CCHMC CCHMC Cincinnati Children's Hospital Medical Center ) led to the discovery of a defect on the X-chromosome housing the creatine transporter gene. This defect, named creatine transporter deficiency, is expressed in humans through severe speech and language impairment, short attention span, low IQ, and the inability to follow commands. Research indicates that this disease, resulting in cases of mental retardation mental retardation, below average level of intellectual functioning, usually defined by an IQ of below 70 to 75, combined with limitations in the skills necessary for daily living. , can be diagnosed early and treated. "We need to determine how many people have this disease and detect it early," said Joseph Clark, PhD, associate professor, UC Department of Neurology. "If we successfully develop a good treatment, the earlier the treatment starts the better." Ton DeGrauw, MD, PhD, professor, Pediatrics-Division of Neurology, UC, CCHMC, and Kim M. Cecil, PhD, research assistant professor, Pediatrics-Department of Radiology, UC, CCHMC, first detected the creatine transporter defect in a six-year-old boy three years ago. "The disorder is currently identified using either a proton magnetic resonance Noun 1. proton magnetic resonance - resonance of protons to radiation in a magnetic field NMR, nuclear magnetic resonance magnetic resonance - resonance of electrons or atoms or molecules or nuclei to radiation frequencies as a result of space quantization spectroscopy obtained with a magnetic resonance imaging magnetic resonance imaging (MRI), noninvasive diagnostic technique that uses nuclear magnetic resonance to produce cross-sectional images of organs and other internal body structures. (MRI 1. (application) MRI - Magnetic Resonance Imaging. 2. MRI - Measurement Requirements and Interface. ) examination, or by DNA analysis DNA analysis Any technique used to analyze genes and DNA. See Chromosome walking, DNA fingerprinting, Footprinting, In situ hybridization, Jeffries' probe, Jumping libraries, PCR, RFLP analysis, Southern blot hybridization. ," said Dr. Cecil. While creatine transporter deficiency affects both males and females, the severity of the disease is increased in males because the defect is located on the X-chromosome, of which males have only one. "So far we have recognized five families with this disorder in Cincinnati alone," said Dr. DeGrauw. "The disorder is not well known yet, but I believe that it is quite common. Together with our collaborator, geneticist ge·net·i·cist n. A specialist in genetics. geneticist a specialist in genetics. geneticist Gajja S. Salomons, PhD, in Amsterdam, the Netherlands, we now have diagnosed more than 30 families with creatine transporter deficiency." Creatine (N alpha-methyl-guanidinoacetic acid) plays a central role in energy metabolism and is synthesized in the liver, kidney and pancreas. In healthy patients, it is transported via the blood stream to the muscles, heart and brain with high and fluctuating energy demands by the molecule creatine transporter. Creatine, although naturally synthesized in the human body, can be ingested in the form of supplements and is commonly used by athletes to provide a ready reserve of energy. Research has shown that patients with low levels of creatine in their brain, with no defect on the gene for creatine transporter, may benefit from creatine supplements. This is not the case however, with creatine transporter deficiency patients. Supplements of creatine increase the levels of creatine found in serum and urine, but not in the brain. The defect on the gene for the creatine transporter inhibits creatine from traveling to the brain. "We have been investigating the role of the creatine kinase creatine kinase /cre·a·tine ki·nase/ (ki´nas) an enzyme that catalyzes the phosphorylation of creatine by ATP to form phosphocreatine. system in Central Nervous System Disorders Nervous system disorders A satisfactory classification of diseases of the nervous system should include not only the type of reaction (congenital malformation, infection, trauma, neoplasm, vascular diseases, and degenerative, metabolic, toxic, or deficiency for many years," said Rima Kaddurah-Daouk, Ph.D., co-founder of The Avicena Group, Inc. "We believe that energy impairment compromises neuronal survival and cognitive functions." In February 2003 the UC Medical Center and CCHMC began a clinical study to determine if creatine supplementation can increase brain creatine concentration and improve cognitive function among patients with creatine transporter deficiency. The goal of the treatment is to restore as much as possible of the normal creatine concentration in the central nervous system. Patients with creatine in their brains, determined by proton magnetic resonance spectroscopy, will be treated with high quality, ultra-pure creatine supplements provided by The Avicena Group, Inc. in increasing dosages for several six-week periods. Magnetic resonance magnetic resonance, in physics and chemistry, phenomenon produced by simultaneously applying a steady magnetic field and electromagnetic radiation (usually radio waves) to a sample of atoms and then adjusting the frequency of the radiation and the strength of the spectroscopy will be repeated at the end of each six-week period. If the test shows a significant increase in creatine concentration, the study will be ended and the subjects will be offered to continue the treatment at their current dose of creatine with clinical follow-up in the neurology clinic. "Our clinical research focuses on regulating cellular energy," said Dr. Belinda Tsao-Nivaggioli, Chief Operating Officer Chief Operating Officer (COO) The officer of a firm responsible for day-to-day management, usually the president or an executive vice-president. at The Avicena Group, Inc. "Neurology is a major area of development for us, and we are delighted to be working with UC and CCHMC to identify an effective treatment to overcome this genetic disorder." The Avicena Group's collaboration with UC and CCHMC supports their efforts to translate basic research into commercial products that benefit the public. "Patent protection is currently being sought for the technology, and The Avicena Group, Inc. subsequently licensed the intellectual property under a joint agreement with UC and Children's Hospital Research Foundation (CHRF CHRF Children's Hunger Relief Fund CHRF Canadian Human Rights Foundation CHRF Civil Human Rights Front (Hong Kong) CHRF Collaboration for Healthcare Renewal Foundation CHRF Commonwealth Human Rights Forum )," said Richard Kordal, PhD, director, Intellectual Property Office, UC. "The license agreement is complemented by a collaborative sponsored research agreement program designed to investigate the extent to which this defect is involved in cognitive impairment in males, and to identify diagnostic and treatment methods and therapeutics." Joe Fondacaro, PhD, director of Intellectual Property and Venture Development at CHRF said, "The research project and subsequent license agreement with The Avicena Group, Inc. demonstrates that not only can our two research institutions work together collaboratively, but also cooperate and partner together with industry. We are very pleased to be part of these relationships." About The Avicena Group Avicena is a private biotechnology company based in San Francisco, CA and Cambridge, MA, which is developing products based upon regulating cellular energy and/or mitochondrial mitochondrial pertaining to mitochondria. mitochondrial RNAs a unique set of tRNAs, mRNAs, rRNAs, transcribed from mitochondrial DNA by a mitochondrial-specific RNA polymerase, that account for about 4% of the total cell RNA that energy processes. The company has an extremely rich intellectual property portfolio of 25 US patents and patent applications that also have extensive foreign filings. Avicena is currently involved in thirteen clinical trials in which substrates of creatine kinase are administered to patients with neurodegenerative or neuromuscular diseases or similar conditions. As some studies are taking place at more than one location, there are over 30 institutions involved in these studies. INDUSTRY KEYWORDS: AVICENA GROUP, CREATINE, CREATINE KINASE, PROTEINS, CREATINE TRANSPORTER DEFECT, MENTAL RETARDATION, X-CHROMOSOME LINKED DISEASES |
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