Navigation Links
Scientists Claim Encouraging Progress On Hereditary Diseases

Scientists have assembled to report encouraging and innovative strategies and probable future therapies for Huntington's disease// and related disorders.

The Hereditary Disease Foundation convened HD 2006: Changes, Advances and Good News (CAG)n in Cambridge, Massachusetts, hosting a group of emeritus scientists world over have assembled for 4 days from 10th to 14th of August for an intense discussion, debate to help create future therapies for Huntington's disease and related disorders.

Almost 400 scientists met together to share their latest discoveries. "The synergy, innovation and enthusiastic collaboration fostered by this gathering of dedicated scientists brings out the best in all of us and will hopefully lead us to a lifesaving cure for Huntington's disease!" stated Nancy S. Wexler, Ph.D., President of the Hereditary Disease Foundation and Higgins Professor of Neuropsychology in the Departments of Neurology and Psychiatry of the College of Physicians and Surgeons at Columbia University, in her opening remarks. "We are gratified that so many excellent scientists from around the world participated and presented their latest, cutting-edge and unpublished data to advance the search for a cure for Huntington's disease," said Carl D. Johnson, Ph.D., and Executive Director for Science of the Hereditary Disease Foundation.

Topics covered:

* Unraveling the cause of Huntington's disease
* Novel therapeutic strategies
* Advances in RNA interference therapy
* Discovering new drugs
* Clinical trials

Participants described the meeting as "the definitive Huntington's disease meeting in the world for this year."

Highlights of the meeting included the following: An extremely promising innovative strategy presented involves tackling the problem at its very source. DNA in the gene causing Huntington's disease expands too much. This abnormal DNA is copied faithfully into R NA. The RNA then makes a protein, which is also abnormal. This abnormal protein wreaks havoc and eventually is the cause of cellular disability and death.

Extraordinary new techniques target the RNA and prevent it from ever making the abnormal protein at all. This strategy is virtually a cure not only for Huntington's disease but also for hereditary forms of Alzheimer's disease, Parkinson's disease, Lou Gehrig's disease, other genetic diseases and even cancer. The meeting presented fabulous advances in the strategies, which are called RNA interference. All of these breakthroughs are currently curing Huntington's disease in mice. They are also being tested for safety in monkeys. Participants grappled with the challenges of rapidly moving these discoveries to people.

Participants also heard the very promising results of cell transplant therapy. People with Huntington's disease in France received cellular transplants into their brains, which then grew and made connections. The initial pilot phases of this research were so encouraging, even after a follow-up of 8 years, which the research has expanded to include 60 or more HD patients in Europe. These clinical trials are being conducted in such a rigorous fashion that they will enable us to learn a great deal about the future of cell replacement therapy.

Participants also learned about significant advances in the development of new stem cell lines. These lines of neurons - or brain cells - could also benefit patients and could potentially be used as a reliable and renewable source of tissue for cell replacement therapy. Interesting and promising pilot research findings were presented using high dose creatine as a therapy for HD patients. At the mouse level, new intriguing findings were reported concerning BDNF, brain-derived neurotrophic factor. BDNF is a kind of support and survival factor without which brain cells can die - like a kind of food for brain cells. When B DNF was administered to mice with Huntington's disease, their lot improved greatly.

Participants were introduced to a new initiative being undertaken by the Hereditary Disease Foundation in collaboration with the European Huntington's Disease Network (EHDN). This initiative involves the development of new guidelines for the care of people with HD, based on the evidence of carefully controlled clinical trials - whenever possible. A follow-up workshop on Monday, August 14, 2006, to develop the guidelines' procedures was hosted by the HDF, EHDN and Sir Michael D. Rawlins, Chair of the United Kingdom's National Institute of Health and Clinical Excellence (NICE).

The Hereditary Disease Foundation's biennial meeting once again brings together an international cadre of junior and senior scientists who comprise the top experts and drivers of the field. It draws both long time HD researchers and investigators just entering the field. The meeting is a magnet for all the key players. Collaborations are formed which catalyse the research of the future.

Researchers from universities and government organizations from around the world attended, including large delegations from Harvard Medical School and Massachusetts General Hospital, Massachusetts Institute of Technology, Johns Hopkins University, the Universities of California at Los Angeles, San Francisco and Irvine and the University of British Columbia as well as smaller groups from nearly 50 other university and research centres around the world. In addition there were participants from biotech and pharmaceutical companies including, Novartis, Merck, Alnylam, Medtronics, Cambridge Laboratories, Trophos, EnVivo, CombinatoRx, Metabolon, Psychogenics, BioFocus, Cambria and Addgene.

The Hereditary Disease Foundation gratefully received support for the meeting from Alnylam Pharmaceuticals, Inc., Cambridge Laboratories Ltd, EnVivo Pharmaceuticals, Inc., Fisher Scientific Internat ional, Inc., Genzyme Corporation, Merck & Co., Inc., Novartis Institutes for BioMedical Research, Inc., Pfizer Inc., Prestwick Pharmaceuticals, Inc., Sirna Therapeutics, Inc. and Vertex Pharmaceuticals, Inc.

Huntington's disease is a fatal neurological illness causing involuntary movements, severe emotional disturbance and cognitive decline. Huntington's disease usually strikes in mid-life, in the thirties or forties, although it can also attack children and the elderly. There is no treatment to halt the inexorable progression, which leads to death after ten to twenty-five years. Each child of a parent with Huntington's disease has a 50% risk of inheriting the illness. It they inherit the abnormal gene and live a normal life span, the disease invariably appears. In the United States, the prevalence of the disease is about 10 people per 100,000 people - about 30,000 symptomatic people in all. There are another 150,000 individuals at risk. This means that approximately 100,000 people may need therapy daily if taking a drug to prevent the disease from ever occurring - a preferred mode of treatment.

Because Huntington's disease destroys so many different capabilities - intellectual, physical and emotional - the insights gained from research on this illness are relevant to the understanding of many other diseases, including schizophrenia, manic depression, Alzheimer's disease, Lou Gehrig's disease, Parkinson's disease and cancer. By focusing on Huntington's disease as a model, the Hereditary Disease Foundation targets neurological and genetic functions relevant to a broad spectrum of disorders.

The Hereditary Disease Foundation (http://www.hdfoundation.org) was founded in 1968 and is dedicated to finding a cure for Huntington's disease and related disorders. The HDF's unique combination of creating and funding innovative, strategic research has sparked an explosion of knowledge in the scientific field. Breakthroughs by the HDF's scientists include the landmark discovery of the Huntington's disease marker in 1983 and the gene itself in 1993. The Hereditary Disease Foundation and its scientists also helped to launch the Human Genome Project. Collectively, they have created a vast, international, collaborative effort that is markedly shortening the journey towards a cure.

The Hereditary Disease Foundation's research programs include grants and John J. Wasmuth postdoctoral fellowships. Special awards, selected by the Scientific Advisory Board of the Hereditary Disease Foundation, include the Milton Wexler Postdoctoral Fellowship Award and the Lieberman Award. A centrepiece of the Foundation is the program of interdisciplinary Mary Jennifer Selznick workshops held several times during the year. These small, informal, dynamic workshops foster dialogue among researchers from a variety of fields, who come without prepared lectures or slides to converse across disciplinary borders.

Source: EurekAlert.
'"/>




Related medicine news :

1. Scientists plan human cloning clinic in the United States
2. Scientists found ancient Human Germ Killer
3. Scientists locate key hormone involved in appetite control
4. Scientists open the book of life
5. Scientists review SARS
6. Scientists crack dengue fever puzzle
7. Scientists push to lower hidden sodium in food
8. Indian Scientists Make Wide-Ranging Analysis And Annotation Of X Chromosome
9. Scientists have found effective brain regions for deep brain stimulation for Parkinson’s
10. Scientists reveal the secrets of sarcasm
11. Scientists Unveil Mechanism Behind Resistance to Severe Malaria
Post Your Comments:
*Name:
*Comment:
*Email:


(Date:2/11/2016)... ... February 11, 2016 , ... Duterte Insurance Group, serving ... introduces a new charity campaign to raise funds for Ronald McDonald House Charities. ... https://donate.rmhc.org/ . , Ronald McDonald House (RMH) is an internationally renowned nonprofit ...
(Date:2/11/2016)... ... February 11, 2016 , ... Pixel Film Studios brings the spirit of ... in the Christmas edition of the ProDrop series. Pick and choose from 30 unique ... the spirit of Christmas using ProDrop's wintry generators. ProDrop Christmas is a Final Cut ...
(Date:2/11/2016)... ... February 11, 2016 , ... Hoggan Scientific, LLC, a company ... physical therapy, occupational therapy and sports medicine clinics, hospitals, universities and ergonomics applications, ... introduces its new microFET Digital Pinch Gauge. , Hoggan Scientific will debut ...
(Date:2/11/2016)... Southborough, MA (PRWEB) , ... February 11, 2016 , ... ... avoid overpaying for IT services, what questions to ask your IT consultant before signing ... them access to your computer network. , “With companies relying heavily on e-mail and ...
(Date:2/10/2016)... ... , ... President Obama’s budget proposal yesterday enables the HHS ... via telehealth, estimated to generate more than $160 million in savings over 10 ... Although there is more to be done, this represents an important victory ...
Breaking Medicine News(10 mins):
(Date:2/11/2016)... North America , ... The global market is expected to reach USD 20,190.1 Million by ... of 10.2%. --> North America , ... MarketsandMarkets, The global market is expected to reach USD 20,190.1 Million ... CAGR of 10.2%. --> According to a new market ...
(Date:2/10/2016)... , Feb. 10, 2016  Fotona, based in the ... will launch its new ST PRO Lightwalker dental laser at ... Dental Society from 25-27 February, 2016 in booth #4815. The ... dental laser with many of the features of the award ... the ST PRO competitive price will be very attractive to ...
(Date:2/10/2016)... Feb. 10, 2016 Mylan N.V. (NASDAQ, TASE: MYL) ... year ended December 31, 2015. --> ... adjusted total revenues of $9.45 billion, up 28% on ... total revenues of $9.43 billion. Excluding the impact of ... and branded generics business (the "EPD Business"), full year ...
Breaking Medicine Technology: