Pre-Eclampsia May Be Autoimmune Disease

Posted by poster on August 4th, 2008 under Uncategorized Tags: ,  •  Comments Off

Biochemists at The University of Texas Medical School at Houston say they are the first to provide pre-clinical evidence that pregnancy-induced high blood pressure or pre-eclampsia may be an autoimmune disease. Their research could provide novel diagnostic and therapeutic possibilities for this intractable disease. Findings appear online in Nature Medicine on July 27.
Scientists in the laboratory of Yang Xia, M.D., Ph.D., an assistant professor of biochemistry and molecular biology at the UT Medical School at Houston, provided evidence of the connection by inducing symptoms similar to pre-eclampsia in pregnant mice that had been administered autoantibodies isolated from women with the condition. Buy synthroid pills This proof-of-principle experiment is called adoptive transfer.
Pre-eclampsia typically occurs in the last trimester of pregnancy and is characterized by a sudden increase in blood pressure, excess protein in the urine and swelling of the hands, feet and face. It affects about one in 20 pregnancies and the only cure is delivery of the baby. Pre-eclampsia contributes to 15 percent of premature babies and is associated with a high incidence of mother and infant morbidity and mortality in the United States.
"There is no effective treatment for pre-eclampsia other than delivery, in part because of the lack of complete understanding of the disease," said Susan Ramin, M.D., study co-author, the Emma Sue Hightower Professor and Chair in the Department of Obstetrics, Gynecology and Reproductive Sciences at the UT Medical School at Houston and a member of the medical staff of Memorial Hermann - Texas Medical Center. "This collaborative research is important because of its potential to lead to a possible cure of pre-eclampsia in pregnant women. Using the animal model we were able to prevent pre-eclampsia in pregnant mice. I don’t want to overstate the implications, but this is clearly a very exciting time for all of us involved in the research. We plan to focus our efforts in expanding this research to pregnant women."
Unlike antibodies which attack foreign substances and clear diseases from the body, autoantibodies attack their own cells and cause conditions like lupus in which a person’s immune system attacks the body’s own organs and tissues, said Xia, the senior author. In the case of pre-eclampsia, autoantibodies are believed to bind and activate an angiotensin receptor that results in artery constriction.
Pre-eclampsia like symptoms were prevented when the pregnant mice were given agents designed to block the activation of the angiotensin receptor.
"The antibody injection model of pre-eclampsia described here provides strong experimental support for our working hypothesis that pre-eclampsia is an autoimmune disease in which angiotensin receptor-activating autoantibodies contribute to many features of the disease," Xia and her colleagues wrote in the paper.
If the research is confirmed in human trials, Xia believes this information could be used for both the earlier diagnosis and treatment of pre-eclampsia. By measuring autoantibody levels, clinicians could detect the disease weeks before symptoms appear. In addition, new drugs could be developed to inhibit the activation of the angiotensin receptor.
In the meantime, Xia said further research is needed to determine what triggers the production of the autoantibodies.
"Pre-eclampsia is one of the leading causes of prematurity and Small For Gestational Age (SGA) infants. Many of these babies are born with underdeveloped lungs or poor lung clearance of fluid, necessitating neonatal intensive care admission and various respiratory therapies to support their breathing. We continue to struggle to find a proven prevention or treatment solution for these problems," said Nehal A. Parikh, D.O., an assistant professor of neonatal-perinatal medicine at the UT Medical School at Houston and a member of the medical staff of Children’s Memorial Hermann Hospital.
"If targeting the angiotensin receptor autoantibody is a useful strategy to treat pre-eclampsia, then it will also be a useful way to prevent and treat SGA associated with pre-eclampsia," Xia said.
The risk factors for pre-eclampsia include: having a history of pre-eclampsia; being obese; having twins, triplets or other multiples; and developing gestational diabetes.
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Article adapted by Medical News Today from original press release.
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Xia’s collaborators from the Department of Biochemistry & Molecular Biology at the UT Medical School at Houston include: Cissy Chenyi Zhou, Ph.D., instructor; Yujin Zhang, M.D., Ph.D., research associate; Roxanna Irani, graduate student; Tiejuan Mi; and Rodney Kellems, Ph.D., professor and chairman. Other collaborators included: Ramin; Hong Zhang, M.D., Ph.D., of the Baylor College of Medicine; and Edwina Popek, D.O., and M. John Hicks, M.D., Ph.D., D.D.S., of Texas Children’s Hospital.
The study is titled "Angiotensin receptor agonistic autoantibodies induce pre-eclampsia in pregnant mice." Research was supported by the National Institutes of Health, the March of Dimes, the Texas Higher Education Coordinating Board and Merck.
Source: Robert Cahill
University of Texas Health Science Center at Houston
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Significant Blood Pressure Reductions Seen In Difficult-to-Treat, Black Patients Receiving Exforge(R)-Based Therapy

Posted by poster on August 3rd, 2008 under Uncategorized Tags: , , , , , , ,  •  Comments Off


Generic lasix pills no prescription New multinational data show that black patients treated with Exforge® experienced a significantly higher reduction in systolic blood pressure than those on amlodipine alone (33 mmHg vs. 27 mmHg, PGeneric levitra pills no prescription | Buy clomid pills | Generic zithromax pills no prescription

NexMed Confirms FDA Acceptance Of NDA For Erectle Dysfunction Product

Posted by poster on August 3rd, 2008 under Uncategorized Tags: ,  •  Comments Off

NexMed, Inc. (Nasdaq: NEXM), a developer of innovative transdermal products based on its proprietary NexACT® drug delivery technology, announced that the New Drug Application (NDA) filed by the Company for its erectile dysfunction (ED) product, a topically applied alprostadil cream, was accepted for review by the U.S. Food and Drug Administration (FDA).
"We are pleased to announce the FDA’s acceptance of our submission for our ED product," stated Vivian Liu, President and Chief Executive Officer of NexMed. "We have already begun working with the agency and with our partner, Warner Chilcott, and look forward to gaining regulatory approval for this important new therapy. I am confident in Warner Chilcott’s CEO Roger Boissonneault and his team’s ability to establish a major presence in urology. With their proven success in building new markets, Warner Chilcott is a great partner for launching this product, upon its approval."
The acceptance for review is an indication that the FDA has determined that the filing is sufficient to complete a substantive review of the application, which customarily takes a minimum of eight months, should the FDA not require any additional studies or information.
About NexMed
NexMed, Inc. is leveraging its proprietary NexACT® drug delivery technology to develop innovative topical pharmaceutical products that address unmet medical needs. NexMed’s novel, onychomycosis treatment, licensed to Novartis, is currently in pivotal Phase 3 trials in the U.S. and Europe. NexMed’s pipeline also includes a Phase 2 treatment for female sexual arousal disorder and an early stage treatment for psoriasis. For further information about the Company, go to
Buy levitra without prescription Statements under the Private Securities Litigation Reform Act: with the exception of the historical information contained in this release, the matters described herein contain forward-looking statements that involve risk and uncertainties that may individually or mutually impact the matters herein described, including but not limited to whether and when the FDA will approve the Company’s ED Product.
NexMed
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Auriga Laboratories Announces The Launch Of Extendryl(R) PEM And Extendryl(R) GCP

Posted by poster on August 2nd, 2008 under Uncategorized Tags: ,  •  Comments Off

Auriga Laboratories, Inc. (Generic cialis pills no prescription OTCBB: ARGA), a specialty pharmaceutical company, announced today the launch of Extendryl® PEM and Extendryl® GCP. The two new products will be marketed under the Extendryl brand name which consists of prescription products to treat various cough, cold, and allergy symptoms.
The prescription respiratory market is valued at more than 8 billion dollars in sales and more than 68 million prescriptions are written annually in the US. Extendryl® PEM (phenylephrine HCl 30 mg; methscopolamine nitrate 1.25 mg) Tablets combine two compounds; a decongestant with an anticholinergic/drying agent in an extended release format to provide 8 to 12 hours of relief of symptoms for adults suffering from nasal congestion and mucosal drainage associated with respiratory tract infections and related conditions such as sinusitis, pharyngitis, bronchitis, and asthma. Extendryl® GCP Oral Solution combines three compounds (100 mg/5 mL guaifenesin; 15 mg/5mL carbetapentane citrate; 5 mg/mL hydrochloride), and is indicated for temporary relief of non-productive cough accompanying respiratory tract congestion associated with the common cold, influenza, sinusitis, and bronchitis.
Extendryl® PEM and Extendryl®GCP will be launched in March 2008. "These new products further solidify Auriga’s commitment to enhance the Extendryl product line, and the launch is well timed to coincide with the start of Spring allergy season. These new additions to the Extendryl family will be a highly synergistic addition to Auriga’s current promotional efforts," said Frank Greico, Chief Executive Officer of Auriga.
Extendryl is contraindicated in patients who are sensitive to any of the ingredients or related compounds, and in patients with glaucoma, hypertension, cardiac disease, hyperthyroidism, urinary retention, peptic ulcer, patients on MAO inhibitor therapy and during an asthmatic attack. Extendryl GCP is contraindicated in women who are pregnant and/or nursing. Extendryl PEM is contraindicated in children under 6 years of age. See individual product package inserts for full prescribing information.
About Auriga Laboratories™
Auriga Laboratories is a specialty pharmaceutical company building an extensive product portfolio of prescription brands targeting high growth therapeutic categories in the respiratory, dermatology, and psychiatry markets, which have combined annual revenues of more than fifteen billion dollars in the United States. The company’s high-growth business model combines driving revenues through a primarily variable cost commission-based sales structure, acquisition of proven brand names, introduction of new brands, and a strategic development pipeline, all of which designed to enhance its growing direct relationships with physicians nationwide. Auriga’s exclusive prescription and over-the-counter product portfolio includes Aquoral™ for the treatment of Xerostomia, Akurza™, Xyralid™, Zytopic™, and Coraz™ dermatology products, and the Zinx™ Extendryl ®, and Levall ® Families of products for relief of symptoms associated with a range of acute respiratory diseases. For more information, visit
Forward-Looking Statements
The information contained herein includes forward-looking statements. These statements relate to future events or to the company’s future financial performance, and involve known and unknown risks, uncertainties and other factors that may cause its actual results, levels of activity, performance or achievements to be materially different from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. You should not place undue reliance on forward-looking statements since they involve known and unknown risks, uncertainties and other factors which are, in some cases, beyond the company’s control and which could, and likely will, materially affect actual results, levels of activity, performance or achievements. Any forward-looking statement reflects the company’s current views with respect to future events and is subject to these and other risks, uncertainties and assumptions relating to its operations, results of operations, growth strategy and liquidity.
The company assumes no obligation to publicly update or revise these forward-looking statements for any reason, or to update the reasons actual results could differ materially from those anticipated in these forward-looking statements, even if new information becomes available in the future. Important factors that could cause actual results to differ materially from the company’s expectations include, but are not limited to, those factors that are disclosed under the heading "Risk Factors" and elsewhere in documents filed by the company from time to time with the United States Securities and Exchange Commission and other regulatory authorities. Statements regarding the company’s ability to increase its sales force and the success of such sales force in selling its products in light of competitive and other factors, the regulatory status and/or regulatory compliance of its products, the development of additional products, its ability to sustain market acceptance for its products, its dependence on collaborators, the company’s exposure to product liability claims, and the company’s prices, future revenues and income and cash flows and other statements that are not historical facts contain predictions, estimates and other forward-looking statements. Although the company believes that its expectations are based on reasonable assumptions, it can give no assurance that its goals will be achieved and these statements will prove to be accurate. Important factors could cause actual results to differ materially from those included in the forward-looking statements.
Auriga Laboratories
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NARSAD Researchers Showcase New Treatment Options For Severe Depression; Provide New Clues About Treating Clinical Anxiety And Schizophrenia

Posted by poster on August 2nd, 2008 under Uncategorized Tags: , ,  •  Comments Off

New findings from research supported by NARSAD, the world’s leading charity dedicated to mental health research, and conducted by scientists at Washington University’s School of Medicine (WUSM) now point to new options for treating preschool-aged children with significant clinical depression as well as those severely depressed adults who don’t respond to standard treatments, such as antidepressants and psychotherapy.
Presented at NARSAD’s 5th annual St. Louis Mental Health Research Symposium on May 18th at Washington University, the studies, conducted by four leading St. Louis-based researchers, shed new light on what happens in the brains of children and adults who are affected by clinical depression, anxiety disorders and schizophrenia. Coming at a time when more than 57 million Americans suffer from a diagnosable mental disorder, the new findings have immediate relevance in terms of new treatment options and different strategies for designing more targeted therapies for the future.
Robert Freedman, M.D., chair of the Department of Psychiatry and director of the Schizophrenia Research Center at the University of Colorado Health Sciences Center and Denver VA Medical Center, moderated the discussion.
Electrical Stimulation of the Vagus Nerve: A New Treatment for Depression
Among the most significant new developments in the field is vagus nerve stimulation (VNS), a novel procedure pioneered at St. Louis University and WUSM that acts on the brains of patients with "treatment-refractory depression," a particularly virulent form of depression now affecting between 5-10 percent of those diagnosed with clinical depression.
Originally developed to treat epilepsy and then approved by the Food and Drug Administration (FDA) in 2005 for use in treating depression, VNS is a small electrical impulse generator attached to the large vagus nerve in the neck region that acts as a "pacemaker for the brain."
According to Charles R. Conway, MD, associate professor of psychiatry at WUSM and formerly the medical director at the Vagus Nerve Stimulation Clinic in the St. Louis University Department of Psychiatry, approximately one-third of patients receiving VNS experience significant improvement in mood and better social and cognitive functioning, and for up to 70 percent of these individuals, the reduction in symptoms is long-lasting. An additional one-third of the patients receiving VNS have shown a limited response and the remaining third have not been helped.
VNS acts by stimulating a large nerve in the neck (vagus nerve) which sends thousands of fibers higher up into the brain. Dr. Conway reported that the existing evidence suggests that most patients who respond positively to this treatment do not see immediate results. Although some patients receiving VNS therapy experience improvements within the first few weeks after implantation, there is often a long delay (9-14 months or longer) as the brain adapts to the stimulation and develops an anti-depressive response.
VNS: A Patient’s Perspective
This was the case for St. Louis institutional bond trader, Charles E. Donovan III, who spent years being incapacitated by severe, treatment-resistant depression and was one of the first patients to be implanted with the vagus nerve stimulator in 2001 as part of an investigational trial.
"When I was implanted with VNS, I had been suffering from severe depression for several years and had gotten to the point where I was feeling completely isolated and emotionally paralyzed, " said Donovan who wrote the book, Out of the Black Hole: The Patient’s Guide to Vagus Nerve Stimulation and Depression, to raise awareness about VNS. "It took 14 months for the complete effects of VNS to take place, but now my depression is gone. Not everyone responds to VNS as I did but my story offers hope for those who have long suffered without successful treatment that new options are now possible."
In fact, because VNS works successfully in some depressed patients but not in others, Dr. Conway is now conducting research with neuroimaging techniques to determine which patients are likely to respond to VNS therapy. With research funding from NARSAD, Dr. Conway and his team are recruiting patients in the St. Louis area for a study that will use PET scans to look at how the stimulation of the vagus nerve can lead to short- and long-term changes in the brain’s activity and exactly what regions of the brain undergo change with long-term treatment with VNS.
"We know that the depressed brain looks a specific way on a PET scan. And when we can see what regions of the brain are positively affected by VNS therapy, our hope is to be able to identify the best candidates for this new treatment option," Dr. Conway explained. "Having this new data will not only lead to improved treatment outcomes, but it will support current efforts to get insurance companies to reimburse for VNS implantation." Currently, insurance companies have covered VNS on a case-by-case basis.
Depression in Preschoolers
While Dr. Conway’s research may lead to better treatments for severely depressed adult patients, Joan L. Luby, MD, associate professor of child psychiatry and founder and director of WUSM’s Early Emotional Development Program, is currently investigating the efficacy of a new treatment program for clinically depressed children as young as age 3 — a time of significant neurobiological change when there is the potential to alter the course of depression later in life.
"Clinicians used to think that very young children were not developed enough to experience depression, but studies going back to the 1980s changed this viewpoint," said Dr. Luby. "Now, we know that depression is a major childhood illness with potentially debilitating consequences."
A number of epidemiological studies have reported that up to 2.5 percent of children and up to 8.3 percent of adolescents in the U.S. suffer from depression. But until recently, very little was known about the impact of depression on very young children, which is why Dr. Luby and her colleagues are studying children between the ages of 3 years and 6 years old to identify what clinical depression looks like in preschool children.
Starting with a large-scale study funded by NARSAD and the National Institute of Mental Health, Dr. Luby and her team identified anhedonia — the inability to experience pleasure from activities and play — as a key symptom of depression in very young children. Another common symptom is that depressed children often use play to explore themes about death and sometimes even suicide.
"We learned that depressed children don’t derive pleasure from the same things as a typical 3- to 5-year-old child," said Dr. Luby. "They’re less joyful when they encounter the pleasures of daily life."
Now, Dr. Luby and her colleagues are testing a new treatment program for depressed preschoolers in their laboratory that applies these findings. Using a model similar to speech or other developmental therapies, this new program utilizes the interaction between parents and their children to teach depressed children how to experience positive emotions, manage negative emotions and more generally, how to enhance emotional development on a sustained basis. After pre-testing the new program in eight preschoolers, Dr. Luby’s team is now recruiting 30 more young children from the St. Louis area for the new treatment study.
"The normal developmental curve for any child is very steep at this point in life and being depressed and dysfunctional for a long period of time could actually impair normal development," Dr. Luby explained. "It’s very important that we find a safe way to help them get better and to prevent future episodes."
Understanding and Regulating Anxiety, The Most Prevalent Mental Illness
It is also important to find ways to improve the functioning of the more than 40 million Americans or 18.1 percent of the population that suffer from anxiety disorders — the most common psychiatric illnesses. For this reason, the NARSAD symposium provided the latest thinking on how anxiety disorders affect decision-making, perceptions, learning and concentration.
According to Christina Fales, Ph.D., a postdoctoral fellow in psychology at Washington University, people with general anxiety disorders (GAD) may process information differently than healthy people. They may be more susceptible to attention lapses, making reasoning and problem-solving as well as the avoidance of undesirable thought patterns more difficult.
Compared to people with low anxiety who, on a sustained basis, activate the regions of the brain involved in cognition and problem-solving — called the working memory network — Dr. Fales has found that people with high levels of anxiety access working memory in a transient manner. This doesn’t mean that anxious people are cognitively impaired but rather, they are less efficient in carrying out cognitive tasks, and have to work harder to process information. This extra effort may be necessary because unregulated emotional arousal interferes with normal cognitive processing.
What makes these findings significant is the potential for developing new therapies to improve the cognitive regulation of emotion, explained Dr. Fales. "Many GAD patients report that antidepressants have limited success in dealing with their anxiety, "she said. "The more we know about the interaction between the networks in the brain that process cognition and help regulate emotion, the easier it will be to design more targeted therapies for anxiety disorder."
Living with Schizophrenia: Overcoming Emotional and Motivational Challenges
New research findings may also pave the way for new therapies to regulate the memories and emotions of people with schizophrenia, one of the most debilitating psychiatric disorders. Complementing NARSAD-funded research which showed people with schizophrenia can be assisted in remembering things if they are given proper cues and memory aids, Dr. Deanna M. Barch, Ph.D., director of the Conte Center for the Neuroscience of Mental Illness and chief neuropsychologist at the Washington University Treatment Units Research Network Site, is now focusing on the emotional and motivational problems that affect how people with schizophrenia function on a daily basis.
According to Dr. Buy generic ultram Barch, research has demonstrated that people with schizophrenia are able to experience the same pleasurable responses to stimuli, such as seeing a movie, listening to music, or drinking a beverage, but these reactions were much more intact than what subjects with schizophrenia reported in questionnaires that ask them to imagine how they would feel in very situations.
This inability to either retain pleasurable memories or to anticipate pleasurable experiences in the future may be a major factor contributing to what Dr. Barch calls "the negative symptoms" associated with schizophrenia - including the lack of energy, drive and motivation.
Using functional MRI, structural MRI and cognitive neuroscience methods, Dr. Barch and her research team are trying to identify the neurobiological disturbances in the brain that may cause these negative emotional symptoms. Between 50 and 70 percent of people with schizophrenia have these negative symptoms, especially those who have earlier onset of the disease, according to Dr. Barch.
"This is a very serious public health issue," she said. "Current therapies for schizophrenia have not proven effective in treating negative emotional symptoms, making it harder for those who experience these symptoms to live independently and seek treatment. The goal is to explain what is happening in the brain so we can design better treatments in the future."
About NARSAD
NARSAD’s St. Louis Mental Health Symposium is one of several such programs the organization presents annually around the country to bring the latest development in research to the attention of the public.
NARSAD’s primary mission is to raise funds to advance research on the causes, treatment and prevention of psychiatric disorders. Since it began giving grants in 1987, as the National Alliance for Research on Schizophrenia and Depression, NARSAD has awarded more than $233 million in competitive grants to nearly 2,700 scientists leading universities, medical centers and research institutions around the world who are conducting research on schizophrenia, depression, bipolar disorder, anxiety disorders, childhood mental disorders and other serious mental illnesses.
For additional information on the work of NARSAD, the research it supports, and various psychiatric disorders, visit the organization’s web site at
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