Monday, March 31, 2014
Synthon announces successful outcome of the Phase III GATE study with its generic Glatiramer Acetate
Results of world's first cost-effectiveness analysis of flu responses will help governments plan for epidemics
A drug that strengthens the analgesic effect of opioids without increasing constipation has been tested successfully on animals
International study on genome expression
The antidepressant effect of Seroxat enhanced by acupuncture
Chinese herbal treatment for vascular depression
Professionals are divided over best care for hip fracture patients, latest audit results show
Chemotherapy may be assisted by natural plant compounds
Cells measure surface area to know when to divide
Sunday, March 30, 2014
Closure of coal plant in China led to improvements in children's health
Unnecessary lung surgeries halved by preoperative PET
Study reveals less invasive technique for vulvar cancer
Saturday, March 29, 2014
Levels of potentially harmful substances in grilled meats could be reduced by beer marinade
New research explores the impact of stress reduction on migraine attacks
Is it safe to pee in the pool?
Friday, March 28, 2014
CDC: autism rates soar 30% in 2 years
The number of US children with autism spectrum disorder has soared approximately 30% in the past 2 years, according to a new report from the Centers for Disease Control and Prevention.
In the surveillance summary report, published in the Morbidity and Mortality Weekly Report from the Centers for Disease Control and Prevention (CDC), researchers estimate that 1 in 68 children (14.7 per 1,000) now has autism spectrum disorder (ASD), compared with 1 in 88 children (11.3 per 1,000) in 2012.
To reach their findings, CDC investigators analyzed data from the Autism and Developmental Disabilities Monitoring (ADDM) Network - a US surveillance system that estimates ASD prevalence among 8-year-old children whose parents or guardians reside in 11 ADDM sites. The system collects its data from community sources that diagnose, educate, treat and/or provide services for children with developmental disabilities.
The CDC note that the way the data has been collected for this report does not differ from previous reports.
The new estimates vary across ADDM sites, with ASD prevalence standing at 1 in 45 children in New Jersey, while 1 in 175 children in Alabama have the condition.
The data reveals that ASD is almost five times more common among boys than girls, with 1 in 42 boys estimated to have the disorder, compared with 1 in 189 girls. It is also more common among white children than black or Hispanic children.
'Mini heart' may help people with blood flow problems
A researcher at George Washington University in Washington, DC, has made a startling innovation that could improve treatment for people who have impaired blood flow.
Narine Sarvazyan, PhD, has created a tiny heart that can be implanted to encourage blood flow in veins that lack working valves. This "mini heart" is a rhythmically contracting "cuff" of heart muscle cells that surrounds the problem vein and pumps blood through the vein as it palpitates.
Dr. Sarvazyan says that if the cuff is made of the patient's own stem cells, then this will also eliminate the possibility of this miniature organ being rejected.
She says:
"We are suggesting, for the first time, to use stem cells to create, rather than just repair damaged organs. We can make a new heart outside of one's own heart, and by placing it in the lower extremities, significantly improve venous blood flow."
Experts think Dr. Sarvazyan's mini heart could have useful applications in treating chronic venous insufficiency.
What is chronic venous insufficiency?
Chronic venous insufficiency is a long-term condition where the veins have difficulty sending blood from the legs back to the heart. When the condition is chronic, it is because a vein is either partly blocked or because blood is leaking around the valves of the veins.
People with chronic venous insufficiency may have varicose veins and ulcers on their legs and ankles, and the skin around these areas may be become hard and red. Treatments include having surgery to remove varicose veins - if the condition is causing skin sores and leg pain - and using compression stockings to decrease swelling.
This is one of the most widespread diseases in developed countries, where it can affect 20-30% of people over 50 years of age. In the US, chronic venous insufficiency consumes about 2% of health care costs.
Other conditions could also benefit from the mini heart innovation. "Sluggish" blood flow can be an issue for people with diabetes or people who are paralyzed or recovering from surgery.
In the Journal of Cardiovascular Pharmacology and Therapeutics, Dr. Sarvazyan outlines her success in demonstrating the mini heart in a laboratory setting and her plans to test the heart in a living organism.
The video below shows the mini heart in action:
Last month, similar research published in the journal Biomaterials investigated using adult stem cells to create human heart valves. These heart valves could potentially be used in children born with congenital heart defects. Once these valves are implanted, they would grow as the child grows. Currently, only artificial plastic valves are available, which requires the patient to endure multiple surgeries to have these replaced as they grow up.
In 2011, Medical News Today also reported on a study in PLOS One that found similarities between chronic cerebrospinal venous insufficiency and multiple sclerosis. In this variant of chronic venous insufficiency, the blood flow from the central nervous system is decreased, which can interrupt the flow of blood from the brain, causing injury to brain tissue.
Written by David McNamee View all articles written by David, or follow David on:
Heart benefits linked to marathon training, researchers say
It may seem obvious at first: training for a marathon improves risk factors related to cardiovascular disease. But recent years have seen middle-aged male runners dying from cardiac arrest while running a marathon, suggesting older men are at higher risk while running the 26.2-mile race.
Now, research presented at the American College of Cardiology's 63rd Annual Scientific Session suggests training for the big race may be an effective strategy for reducing heart disease risks.
Because little is known about how heart health is affected by the marathon training process - which involves intense long-distance weekly running - researchers decided to study 45 recreational male runners between the ages of 35 and 65.
They were all planning to run the 2013 Boston Marathon as part of the Dana-Farber Marathon Challenge fundraising team.
"We chose charity runners because we wanted to focus on the non-elite type of runner, just the average average Joe who decides to get out there and train for a marathon," says Dr. Jody L. Zilinski, lead investigator from Massachusetts General Hospital.
Around half of the runners had previously run three or more marathons, and all participants were invited to participate in the training program, which lasted 18 weeks.
This involved group runs, endurance training, a detailed training guide, access to cross-training facilities in Boston, nutrition tips, pacing advice, and regular coaching contact. Depending on the training phase, the participants were instructed to run between 12 and 36 miles each week.
The researchers tracked the runners' adherence to the program through running logs the participants kept.
"They turned out to be a healthier population than we expected," says Dr. Zilinski, "with a lot of them already exercising on a pretty regular basis, but they were still nowhere near the levels of elite runners."
Further studies needed to see if reduced risks apply to women
MRI tracking of genes to offer insights into memory and learning
Doctors normally use MRI to look inside the body to examine organs and tissue, for instance to find tumors and other abnormalities. Now, biological engineers in the US want to adapt the scanning technology to work on a much smaller scale.
They want to use magnetic resonance imaging (MRI) as a "molecular imaging" tool to see genes at work in living brains and find out what effect they have on cognitive processes like memory and learning.
The team working on this is at Massachusetts Institute of Technology (MIT). Their leader, Alan Jasanoff, an associate professor of biological engineering, says:
"The dream of molecular imaging is to provide information about the biology of intact organisms, at the molecule level. The goal is to not have to chop up the brain, but instead to actually see things that are happening inside."
MRI uses magnetic fields and radio waves to interact with protons in the body. This interaction produces detailed images of the insides of the body.
Functional MRI allows neuroscientists to see which parts of the brain are active during various tasks by "seeing" where the blood flows. When scanning other organs, doctors sometimes use magnetic "contrast agents" so the tissue they are investigating stands out more clearly.
What the MIT team has done is develop an artificial "reporter gene" that switches on and off to signal certain events in the body - rather like the indicator light that flashes on the dashboard of a car.
New MRI to track reporter gene at the molecular level
The idea is to image the reporter gene with MRI technology at the molecular level.
In a study reported in the journal Chemical Biology, the researchers describe how the reporter gene encodes an enzyme that interacts with a magnetic contrast agent injected into the brain. So when the gene is switched on, it produces the enzyme, which interacts with the contrast agent in such a way that MRI can see it, and thus the researchers can track where and when the gene is switched on in the brain.
In the case of this particular study, the team used a contrast agent called manganese porphyrin. And the reporter gene they developed codes for a genetically engineered enzyme called SEAP that changes the electric charge on the contrast agent.
The MIT team devised the contrast agent so it could be soluble in water and readily eliminated from the body. On its own, it is difficult to track with MRI, but when it encounters SEAP, the enzyme slices phosphate molecules from the manganese porphyrin, which causes it to become insoluble. The agent gradually builds up in brain tissue and becomes visible with MRI.
Researchers plan to investigate 'early immediate genes' in brain plasticity
The purpose of this study was to show that the SEAP gene could be successfully incorporated into brain cells.
In future studies, the team hopes to engineer the SEAP gene so it is only active - and thus making the enzyme - when a particular gene that the researchers want to study is switched on.
The first genes they want to investigate with this method will be what the team calls "early immediate genes," which are important for brain plasticity - the strengthening and weakening of links between neurons, which forms the basis of learning and memory.
Prof. Jasanoff, who is also an associate member of MIT's McGovern Institute for Brain Research, says:
"As people who are interested in brain function, the top questions we want to address are about how brain function changes patterns of gene expression in the brain."
Assaf Gilad, an assistant professor of radiology at Johns Hopkins University who was not involved in the study, says:
"These kinds of genetically engineered reporters have the potential to revolutionize our understanding of many biological processes."
The Raymond and Beverly Sackler Foundation, the National Institutes of Health, and an MIT-Germany Seed Fund grant helped finance the study.
Medical News Today recently learned about new research that suggests a special type of high-resolution MRI may help diagnose Parkinson's earlier. The ultra-high field MRI scans show detailed views of the part of the brain affected by the disease. Parkinson's is hard to distinguish from other brain disorders because there are currently no reliable radiologic techniques.
Written by Catharine Paddock PhD View all articles written by Catharine, or follow Catharine on:
Expert warns of lung disease 'time bomb' in UK
The UK is sitting on a lung disease 'time bomb' says a leading respiratory expert. Referring to the dramatic rise in cases of idiopathic pulmonary fibrosis, Luca Richeldi, professor and consultant in respiratory medicine at Southampton General Hospital in the UK, says there is an urgent need to develop a quick and easy way to diagnose the rare lung disease.
Idiopathic pulmonary fibrosis (IPF) causes 5,000 deaths a year in the UK, and new cases are rising at a rate of 5,000 a year, he warns.
IPF is a rare and poorly understood interstitial lung disease that causes inflammation and scarring of the lungs. Of unknown cause, IPF gets worse over time and is often fatal. There is no known cure, and life expectancy for patients with IPF is between 3 and 5 years.
The disease mostly strikes people between the age of 50 and 70, mainly men and former smokers. In the UK, IPF affects around 15,000 people over 60. In the US, IPF affects about 128,000 people, with about 48,000 new cases diagnosed annually and 40,000 deaths.
IPF often not diagnosed until symptoms appear
IPF is often not diagnosed until symptoms appear, such as shortness of breath and coughing. Consequently, the most that the only available treatment - the anti-fibrotic drug Esbriet - can do, is slow progression of the disease.
Speaking about the UK, Prof. Richeldi, says:
"Nationally, the number of people suffering from IPF and other interstitial lung disease is increasing by thousands every year, but the cause is often unknown. As a result, the majority of patients are diagnosed late when their life expectancy has been cut extremely short."
Of patients currently receiving treatment at Southampton General Hospital's respiratory centre, over a quarter (28%) have some form of interstitial lung disease, and four to six new patients with the condition are arriving every week.
Prof. Richeldi says these numbers show there is an "urgent need" to develop a quick and simple way of diagnosing IPF.
Electronic stethoscopes can detect "ripping Velcro" sounds in patients with IPF
Eye movement when reading could be an early indicator of Alzheimer's disease
Kif15: The acrobatic motor protein that could pave the way for new cancer therapies
Mass participation experiment reveals how to create the perfect dream
Neighboring cells alerted to protect themselves by dying cells in fruit fly
New approach to spine surgery dramatically improves safety
The brain's mechanism knows when to stop drinking water
Too-restricted hours may work for some residents, but not for surgical residents
HIV and hepatitis C vaccines move a step closer with new technique
Intestinal T cell homeostasis disrupted by epigenetic alterations
Thursday, March 27, 2014
Genetic variation linked to heart disease risk through RNA machinery
Stroke patients should receive customized palliative care
Autism begins in the womb, according to a new study
A new study claims to show for the first time that autism begins in the womb, while another examines possible environmental influences on autism development.
The origins of autism have been passionately debated by many scientists and commentators. What is known about autism is that it is a physical condition, which is linked to abnormal biology and brain chemistry.
Genes seem to play an important part in the development of autism - identical twins, for instance, are much more likely to both have autism than non-identical siblings. But there has not been any clear consensus in medical opinion about what other contributing causes there may be.
Some things that have been suspected as being linked to autism - but which have not been proven - include diet, changes in the digestive tract, mercury poisoning, problems with the body processing vitamins and minerals, and vaccines.
A recent, large study in the journal PLoS Computational Biology suggests that environmental pollution could be a contributing factor to autism risk, but the study was unable to name any specific toxins that might be responsible.
That study assessed 100 million US health insurance claims to look at rates of autism on a county-by-county basis. It also used genital malformations in boys - micropenis, undescended testicles and cases where the urethral opening is on the underside of the penis - as indicators of environmental pollution.
The researchers found that for every 1% increase in genital birth defects in a county, the rate of autism there increased by nearly 300%.
"Both genes and environment are important," emphasizes the lead researcher, Andrey Rzhetsky, a professor of genetic medicine at the University of Chicago in Illinois.
Study finding an in-utero basis for autism is the first to do so
The other new study, published in the New England Journal of Medicine, analyzed the brain tissue of children with autism.
The researchers - from the University of California, San Diego School of Medicine and the Allen Institute for Brain Science in Seattle, WA - examined 25 genes in the postmortem brain tissue of children with and without autism. These genes included biomarkers for brain cells in different layers of the cortex, genes that have been linked to autism and several control genes.
Analyzing the brain tissue of deceased children who had autism breaks ground with previous research, which instead has used the brain tissue of adults with autism and attempted to extrapolate back to what might have occurred developmentally.
The team found that key genetic markers across multiple layers of brain cells were missing in the brains of autistic children.
The video below illustrates how the researchers came to their findings:
Genetic defects occurred in 'focal patches' of brain tissue
"Building a baby's brain during pregnancy involves creating a cortex that contains six layers," says researcher Eric Courchesne, PhD. He continues:
"We discovered focal patches of disrupted development of these cortical layers in the majority of children with autism. This defect indicates that the crucial early developmental step of creating six distinct layers with specific types of brain cells - something that begins in prenatal life - had been disrupted."
But equally as important as the evidence of developmental disruption in children with autism, the team believes, is that these defects appeared in "focal patches," particularly around the frontal and temporal cortex. This suggests that this defect does not apply equally to all areas of the brain and may explain why different functional systems are affected in people who have autism.
Alzheimer's puzzle piece found using giant X-ray facilities
Protein fragments that comprise Alzheimer's lesions have been implicated as a hallmark of the disease, but until now, why they accumulate or cause brain cells to die has not been understood.
Now, researchers have used giant X-ray centers - called synchrotrons - to investigate and have found that biological material may contribute to the build-up of toxic iron in the brain.
The researchers, who publish their results in the journal ACS Inorganic Chemistry, say they used the Diamond Light Source synchrotron in the UK, as well as other synchrotrons in Switzerland and the US to arrive at their findings.
The facility in the UK employed beams of light 10 billion times brighter than the sun to study the chemical and magnetic makeup of iron after it had interacted with beta-amyloid peptides, the fragments implicated in Alzheimer's lesions.
Iron is naturally occurring in the human body and brain, and as a part of normal functioning, it converts between two chemical forms.
But when one of these forms - ferrous iron - is overproduced or builds up in tissues, the researchers say it can be highly toxic.
Prosthetic limbs: should they be more advanced by now?
"The psychological challenges for amputees is daunting. More can be done, but in my mind, the key to success resides in enabling the amputee to seamlessly engage in activities of daily living," says David Hankin.
Hankin is CEO of the Alfred Mann Foundation - a medical research foundation based in California that works to create advanced medical technologies for people with debilitating medical conditions with the aim of improving their health and overall quality of life.
One area the foundation focuses on is limb loss - a condition that approximately 1.7 million Americans are living with.
According to the Amputee Coalition, around 185,000 amputations occur in the US every year - of which 97% are lower limb.
The main causes of limb loss are vascular disease - including diabetes and peripheral arterial disease - and trauma. A very small number of amputations are caused by cancer.
Physical and psychological difficulties
Individuals living with limb loss can experience difficulties physically and mentally.
Not only is limb loss a debilitating condition in itself, it can cause other conditions that impact a person's general health. For example, individuals with lower limb loss often have to use much more energy in order to be able to move around on different floor surfaces and terrain, and to travel distances that those with intact limbs would not find an issue.
"The additional energy and the wear and tear on other parts of the body create a host of medical problems for the amputee," says Hankin.
In a psychological sense, Hankin says that many amputees can experience feelings of inadequacy when it comes to engaging in day-to-day tasks. For example, something as simple as taking money out of a wallet may take much longer, which can cause embarrassment when the individual is standing in a grocery line.
When it comes to rehabilitation for amputees, prosthetic limbs are the first port of call. But Hankin says that rejection of artificial limbs - particularly upper limbs - is high. This is because most upper limb prosthetic devices do not have advanced functions that allow the amputee to effectively carry out daily activities.
"As a result, many end up in a closet or a drawer rather than affixed to the amputee," says Hankin, adding:
"There is a feeling among some amputees that not nearly enough has been or is being done to improve the technologies available to them and that there is no hope."
Prosthetic limbs: the road so far
It is believed the world's first prosthetic dates back to more than 3,000 years ago, after a fake toe made of leather and wood was discovered on an Egyptian mummy found near the ancient city of Thebes in 2000.
But of course, prosthetics have changed greatly since then - mainly in function rather than the way they look. In 1912, David Dorrance invented the body-powered arm. This was a device consisting of leather straps and a split hook. Using the power of their remaining arm, the wearer was able to open and close the hooks and pick up items.
Significant polio milestone: 11 countries officially polio-free
Being overweight may benefit older people
A new study from Australia finds that people aged 65 and over with a body mass index in the overweight range live longer and suggests perhaps the World Health Organization guidelines on BMI may not be suitable for older people.
The World Health Organization (WHO) defines overweight as having a body mass index (BMI) greater than or equal to 25, and a BMI of 30 or over as obese. BMI is equal to a person's weight in kilos divided by the square of their height in meters (kg/m2).
Caryl Nowson, professor of nutrition and aging at Deakin University in Melbourne, and colleagues looked at links BMI and risk of death in people aged 65 and over, and found those with the lowest risk of death had a BMI of around 27.5.
They also found those with a BMI between 22 and 23 - considered to be the normal weight range - had a significantly higher risk of death.
They say their findings, which they report in the American Journal of Clinical Nutrition, question whether the WHO guidelines are suitable for older adults. Prof. Nowson suggests it is time to reassess them, and adds:
"Our results showed that those over the age of 65 with a BMI of between 23 and 33 lived longer, indicating that the ideal body weight for older people is significantly higher than the recommended 18.5-25 'normal' healthy weight range."
For their study, the team pooled and re-analyzed results from studies published between 1990 and 2013 that had examined links between BMI and risk of death in people aged 65 and over.
Altogether, the analysis covered over 200,000 older people followed for an average of 12 years, and revealed, with reference to BMI in the range 23.0 to 23.9, that there was no increased risk of death for people in the overweight range, but:
- Risk of death increased by 12% when BMI was between 21 and 22 (near the middle of the healthy weight range)
- Risk of death increased by 19% when BMI was between 20 and 20.9 (still within the healthy weight range)
- Risk of death increased by 8% when BMI was between 33 and 33.9 (in the obese range).
Prof. Nowson says for people aged 65 and over, by the WHO standards, being overweight is not associated with an increased risk of death, and that "it is those sitting at the lower end of the normal range that need to be monitored, as older people with BMIs less than 23 are at increased risk of dying."
Advice on body weight for older people needs to look at more than just BMI
MRI helps diagnose prostate cancer more accurately
In a world first, an Australian clinical trial has shown that biopsy guided by MRI can significantly improve the diagnosis of life-threatening prostate cancer and reduce the over-diagnosis of non-life-threatening cases, thus avoiding the side effects of unnecessary treatment.
At present, to find out if he has prostate cancer - following a test that shows he has raised prostate-specific antigen (PSA) levels - a man has to undergo a painful procedure called transrectal ultrasound guided biopsy (TRUSGB) that involves taking up to 30 random needle biopsies of his prostate through the rectum.
With the new MRI-guided system, doctors first do an MRI scan and get a better idea of where a tumor might be located in the prostate.
Then, if the scan indicates a need for it, they just take two needle samples of that area, sparing the need for multiple biopsies.
The new system uses a method called multi-parametric magnetic resonance imaging (mpMRI).
mpMRI will reduce over-treatment of non-life-threatening prostate cancer
Urologist Dr. Les Thompson, who led the 2-year clinical trial at Brisbane's Wesley Hospital, says:
"This is a significant improvement in terms of accuracy and in reducing discomfort for patients and spares many men the burden of multiple prostate biopsies."
"This latest mpMRI imaging technique will reduce over-treatment of men with non-life-threatening prostate cancer, avoiding the possible side-effects of treatment," he adds.
He and his colleagues report, in the journal European Urology, how the trial showed that use of mpMRI:
- Halved (reduced by 51%) the number of men needing prostate biopsies
- Showed a 92% sensitivity in diagnosing life-threatening disease (compared with the current leading method TRUSGB, which has only a 70% sensitivity in diagnosing life-threatening prostate cancer)
- Cut the problem of over-diagnosis of non-life-threatening prostate cancer by around 90%.
The trial enrolled 223 patients with raised PSA levels. All of the patients underwent both diagnostic procedures: the standard TRUSGB, and the new method where an mpMRI scan is done first, and then only those patients whose MRI image points to high-risk prostate cancer undergo MRI-guided biopsy.
mpMRI uses three parameters to image the prostate
Co-investigator Dr. Rob Parkinson, a specialist radiologist at the hospital, says that mpMRI uses three parameters when scanning the prostate, and that:
"Diffusion-weighted imaging, one of these three parameters, assesses movement of water molecules within tissues. An imaging map is mathematically generated from this information, and prostate cancer is evident as a dark area."
In TRUSGB, which uses ultrasound to guide biopsy sampling, the core samples are random and taken from all areas of the prostate, but, when biopsies are done following a prostate mpMRI, "you know where the tumour is located and thus where to direct the biopsy needle," he explains.
One of the issues that is bound to be raised in deciding how to proceed with the new system as a diagnostic tool is the higher costs associated with MRI.
According to a report in The Australian news channel, Dr. Thompson says he is campaigning to get it listed as a medicare item like mammograms for breast screening.
Campaigners say the cost is small compared with the social and emotional costs of misdiagnoses that occur with the current method.
According to the American Cancer Society, prostate cancer occurs mainly in older men - around 6 in 10 cases are diagnosed in men aged 65 and over. About 1 man in 7 will be diagnosed with prostate cancer during his lifetime.
Prostate cancer is the second leading cause of cancer death in American men, behind only lung cancer. However, although it is a serious disease, most men diagnosed with prostate cancer do not die from it. There are currently 2.5 million men in the US living with prostate cancer.
The study was sponsored by the Wesley Research Institute and the Thorsen Foundation.
Medical News Today recently learned about a study where researchers in the UK found a possible biomarker that could help improve early diagnosis of prostate cancer. They believe their findings, published in the journal Prostate, could lead the way to better tools for the early diagnosis of prostate cancer.
Written by Catharine Paddock PhD View all articles written by Catharine, or follow Catharine on:
Where do you start when developing a new medicine? Novel scientific collaboration to use genomics and big data to drive drug discovery
Diabetes: Good self-management helps to reduce mortality
NICE rejects life-extending bowel cancer drug two weeks after Scottish approval
Stem cell-derived pancreatic cells under the skin replace insulin
Inducing biological tissue damage with plasma tool may destroy cancer cells
New design could reduce threat of infection from millions of urinary catheters
Faster genetic testing method will likely transform care for many patients with breast cancer
Economic growth has little impact on reducing undernutrition in children
Hope for more effective rehabilitation of patients with vestibular or cerebellar dysfunction
Wednesday, March 26, 2014
More effort needed to fight hospital infections, say CDC
At any given time, approximately 1 in 25 patients in the US has at least one infection acquired during their hospital stay, say the Centers for Disease Control and Prevention, who have released two new reports highlighting the need to improve patient safety by eliminating this threat to patients.
The Centers for Disease Control and Prevention (CDC) have updated their previous estimates of health care-associated infections (HAI) through the two reports, one of which is published in the New England Journal of Medicine, NEJM and details 2011 hospital infection estimates from a survey of hospitals in 10 states.
The other is a 2012 annual report on national and state-specific progress toward the HAI prevention goals of the US Health and Human Services.
Combined, the CDC say these reports show that, while some progress has been made, more work is needed to eliminate the threat of hospital infections for patients.
Speaking of this need, CDC Director Dr. Tom Frieden says:
"Although there has been some progress, today and every day, more than 200 Americans with health care-associated infections will die during their hospital stay. The most advanced medical care won't work if clinicians don't prevent infections through basic things such as regular hand hygiene."
He adds that health care workers should follow standard infection control practices all the time to ensure patient safety.
Most common germs from a family of drug-resistant bacteria
Evidence supports it, so why are parents still reluctant to vaccinate their children?
Nearly 16 years after his controversial study was first published, the work of the discredited British doctor Andrew Wakefield - the researcher who linked the measles, mumps and rubella vaccine with autism - is back in the news.
Since 2010, Wakefield has been barred from practicing medicine in the UK. He now lives and works in the US where he retains a cult following.
Twitter comments involving one of Wakefield's most ardent supporters - the TV celebrity Jenny McCarthy, who wrote a foreword to his book Callous Disregard: Autism and Vaccines: The Truth Behind a Tragedy - have reignited the passionate debate over perceived links between vaccines and autism.
In addition, three new studies have found intriguing results on the support among the general public for the theory that vaccines cause adverse effects, particularly autism.
Fear of vaccines is not new and dates back to the invention of this medical procedure in the 17th century. As far back as 1802, vaccine inventor Dr. Edward Jenner was lampooned in the popular media of the time.
"The Cow Pock - or - the Wonderful Effects of the New Innoculation," a satirical painting by James Gillray that displayed commoners sprouting cows from their bodies having received a dose of Jenner's cowpox-derived smallpox vaccine, was emblematic of public fears over the nature of this new medical technology.
In recent times, major outbreaks of diseases previously thought to be under control in the US and UK due to vaccination - measles, mumps, and whooping cough - were assumed to be caused by a renewed fear of vaccination, possibly as a result of the combination measles, mumps and rubella (MMR) vaccine controversy.
Some people are also worried about potentially fatal outbreaks of other vaccine-preventable diseases, such as diphtheria and invasive Haemophilus influenzae, as immunization rates for these diseases have also fallen below federal guidelines.
MMR vaccine - the background
First stem cell model for bipolar disorder could lead to new treatments
It is unclear what causes bipolar disorder - a condition characterized by dramatic changes in mood. But researchers from the University of Michigan Medical School have created the first stem cell model for bipolar disorder, which they say could uncover the origins of the condition and open the door to new treatments.
The research team recently published their study in the journal Translational Psychiatry.
To reach their findings, the investigators obtained skin samples from people with bipolar disorder, alongside skin samples from individuals without the condition.
By exposing small samples of skin cells to carefully controlled conditions, the researchers turned them into induced pluripotent stem cells (iPSCs). These are stem cells that have the potential to be turned into any other type of cell. The team then turned the iPSCs into neurons.
They measured gene expression of the iPSCs and then re-evaluated gene expression once the stem cells became neurons.
From this, the team found significant differences between the stem cells taken from bipolar patients and those taken from individuals without the condition.
Bipolar patients 'express more genes for calcium signaling'
Exercise in youth makes for stronger, bigger bones through life
Our bone is living tissue that responds to the forces that act on it - it gets stronger when we exercise. Now a new study suggests exercising when young helps bones grow big and strong for life, and that this effect persists during aging.
To arrive at this finding, researchers compared the differences between the throwing and non-throwing arms of major league baseball players measured at different points in their careers to differences measured in non-baseball players.
They found that half of the bone size and one-third of the bone strength benefit of exercise performed during youth persisted throughout life.
Lead author Stuart Warden, an associate professor at Indiana University-Purdue University Indianapolis, says:
"This is an impressive level of maintenance, particularly considering that the baseball players had not thrown, or in other words, exercised, in over 50 years and were aged in their mid-80s."
The researchers were not, however, surprised to find that the amount or mass of new bone added as a result of exercising during youth was gradually lost as the players aged.
Prof. Warden says it is "not energy efficient for the skeleton to maintain its mass in excess of its needs."
As we age we lose bone from the inside
But Prof. Warden and his colleagues were still intrigued by the question - how can exercise during youth have a lifelong benefit on bone strength but not bone mass?
You can strengthen any load-bearing structure by adding more mass, especially where it is needed most. And bone is no different, as Prof. Warden explains:
"Exercise during youth adds extra layers to the outer surface of a bone to essentially make the bone bigger. This gives you more 'bang for the buck,' as the addition of a small amount of new material to the outside of a bone results in a disproportionate increase in bone strength relative to the gain in mass."
But as we age, we lose bone mostly from the inside, not the outside. Prof. Warden says this means the bigger and stronger bone that amasses as a result of exercising in younger years endures for a lifetime.
Exercising later in life also benefits bone health
New generation of antibiotics may lie with small peptides
As drug-resistant bacteria - or "superbugs" - get stronger and we run out of current antibiotics to kill them, the pressure to find new types of effective drugs increases. Now, a team in Germany suggests small peptides - which can attack bacteria in several different ways - have the potential to form a new generation of antibiotics.
A new study published in the Proceedings of the National Academy of Sciences, PNAS, and led by researchers from Ruhr University Bochum (RUB), shows how peptides - short chains of amino acids that are smaller than proteins - may be developed to attack bacteria cells without harming human cells, while also making it difficult for the pathogens to develop resistance to them.
Previous studies have already shown that many antimicrobial peptides interact with the cell membrane of bacteria, killing them via this route.
But to authorize new drugs, federal authorities need detailed information about the underlying biology and assurances that the way the new drug attacks pathogen cells does not harm human cells.
The team at RUB has been studying a peptide called MP196, which represents a group of very small, positively charged peptides - cationic peptides - made of between four and 10 amino acids.
They already knew from previous research that MP196 could fight various bacteria, including some that are multi-drug resistant - but it was not clear how it did it.
With their new study, the team showed that MP196 interferes with proteins in the cell membrane of bacteria, and in doing so, disrupts two important cell processes: the biosynthesis of the cell wall and cell respiration.
Peptide disrupts bacterial cell respiration and physical integrity
By disrupting the biosynthesis of the cell wall, the peptide undermines the physical integrity of the bacterial cell, and by interfering with cell respiration, it disrupts production of ATP, the molecule that stores energy used by the cell. Less ATP means the bacterial cell is less able to make the big molecules it needs to grow and flourish.
Because of the nature of these disruptions, the team suggests it will also be difficult for the bacteria to develop resistance to peptides like MP196.
As part of the study, the researchers also discovered ways the bacterial cell responds to attack from the peptide. They write:
"We describe a bacterial survival strategy in which mechanosensitive channels in the bacterial membrane establish osmoprotection against membrane-targeting bacteriolytic peptides."
Peptide does not affect human cells
They are confident that MP196 offers a starting point for developing new drugs that attack certain classes of bacteria without damaging human cells, and their findings go a long way to help such development.
They explain that to attack the membrane of the bacterial cell, MP196 needs the presence of certain fatty acids that only occur in that class of bacteria - they are not present in human cells.
The study forms part of the Innovative Antibiotics from NRW (InA) project that is co-funded by the State of North Rhine-Westphalia and the "Investing in your Future" European Union's European Regional Development Fund.
Meanwhile, Medical News Today recently reported a study where researchers in Belgium discovered antibiotic resistance genes in viruses in 700-year-old human feces. As the feces predate the advent of antibiotics by several centuries, the researchers suggest this shows that the human gut has remained largely unchanged in that time.
Written by Catharine Paddock PhD View all articles written by Catharine, or follow Catharine on:
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Tuesday, March 25, 2014
Scientists find genetic cause of a rare, aggressive ovarian cancer
An international team of scientists has achieved a breakthrough by finding the genetic cause of a very rare and aggressive type of ovarian cancer that most often strikes girls and young women.
The study, led by Translational Genomics Research Institute (TGen) a non-profit organization based in Phoenix, AZ, is published in the journal Nature Genetics.
The researchers say their finding, discovered by groundbreaking work in genomics, reveals many strong links between a mutation in a gene called SMARCA4 and an overwhelming majority of patients with a rare and aggressive form of ovarian cancer known as small cell carcinoma of the ovary, hypercalcemic type (SCCOHT).
The researchers write:
"We identified germline and somatic inactivating mutations in the SWI/SNF chromatin-remodeling gene SMARCA4 in 75% (9/12) of SCCOHT cases in addition to SMARCA4 protein loss in 82% (14/17) of SCCOHT tumors but in only 0.4% (2/485) of other primary ovarian tumors. These data implicate SMARCA4 in SCCOHT oncogenesis."
Dr. Jeffrey Trent, president and research director of TGen and senior author of the study, explains why their findings are so remarkable:
"Many genetic anomalies can be like a one-lane road to cancer; difficult to negotiate. But these findings indicate a genetic superhighway that leads right to this highly aggressive disease. The correlation between mutations in SMARCA4 and the development of SCCOHT is simply unmistakable."
Ovarian cancer is the fifth leading cause of cancer death among American women. Like many other ovarian cancer types, SCCOHT is often not diagnosed until it is already in an advanced stage. Chemotherapy evokes no response and nearly two thirds of patients do not survive more than 2 years after diagnosis.
The average age at which SCCOHT strikes is 24 years, ranging from baby girls as young as 14 months to women aged 58. The youngest patient in this study was 9 years old.
'Landmark study' in field of cancer genomics with wide implications for many cancers
WHO: air pollution responsible for 1 in 8 global deaths
According to a World Health Organization report released today, around 1 in 8 of total global deaths - 7 million deaths annually - are as a result of exposure to air pollution.
The new data challenges previous information on air pollution. The figure of 7 million more than doubles the previous estimate of annual air pollution-caused deaths, making air pollution now the world's largest single environmental health risk.
"The risks from air pollution are now far greater than previously thought or understood, particularly for heart disease and strokes," says Dr. Maria Neira, director of the World Heath Organization's (WHO) Department for Public Health, Environmental and Social Determinants of Health.
"Few risks have a greater impact on global health today than air pollution; the evidence signals the need for concerted action to clean up the air we all breathe," she adds.
Air pollution's contribution to the development of respiratory diseases is well known, but WHO's findings also emphasize a more robust connection than has previously been reported between air pollution and cardiovascular disease and cancer.
New data 'more accurate' than previous estimates
WHO claim that the new figures are more accurate than previous estimates, because not only is more now known about the diseases influenced by air pollution, but also improved technology allows for better measurements of human exposure to air pollution.
This new approach combined satellite data, ground-level monitoring measurements, data on pollution emissions and modeling of how pollution drifts in the air.
Marijuana pills and sprays ease MS symptoms
Multiple sclerosis is characterized by disrupted communication between the brain and the body, resulting in symptoms ranging from blurred vision to muscle weakness and pain. There is no cure for the condition, and therapies have proven difficult, as many have serious side effects. But now, relief may come in the form of a medical marijuana pill.
This is according to a new guideline released from the American Academy of Neurology and published in its journal Neurology.
The guideline investigated complementary or alternative medicine therapies (CAM) for multiple sclerosis (MS). These are unconventional therapies used alongside or instead of doctor-recommended therapies.
Medical News Today recently wrote a spotlight feature focusing on symptoms and treatments for the condition to coincide with National Multiple Sclerosis Awareness Month in March.
In that feature, Arney Rosenblat, associate vice president of the National Multiple Sclerosis Society, told us that though there are currently 10 disease-modifying therapies approved by the Food and Drug Administration (FDA) for MS, "there is deep unmet need for additional therapies, especially to treat progressive forms of disease for which there are few treatment options."
Marijuana treatment eases spasticity and pain
Researchers from the current study, led by Dr. Vijayshree Yadav of Oregon Health & Science University in Portland, focused on what impacts certain CAM therapies have on MS, including oral cannabis, medical marijuana pills, oral medical marijuana spray, ginkgo biloba, magnetic therapy, bee sting therapy, omega-3 fatty acids and reflexology.
Much of bone comprises shock-absorbing 'goo' that stops it shattering
A team of chemists from the UK has made a remarkable discovery about the structure of bone and shown that much of the mineral from which it is made comprises a viscous 'goo-like' fluid that is trapped between the crystals that form bone. They say their findings reveal new insights into bone diseases like osteoporosis.
The goo-like fluid allows movement or slipperiness between the calcium phosphate nano-crystals so they do not shatter under pressure. This newly discovered property is what gives bone its flexibility, say the researchers who write about their findings in the Proceedings of the National Academy of Sciences.
Lead investigator Dr. Melinda Duer of the Department of Chemistry at the University of Cambridge says "it's this layered structure that's been missing from our knowledge, and we can now see that without it you're stuffed."
The study shows that the goo-like viscous fluid is made of the chemical citrate - which is a natural by-product of cell metabolism - mixed with water.
New discovery will shift current thinking about bone diseases
The researchers suggest their discovery may explain how osteoporosis arises and will shift current thinking about the causes of this and other bone diseases.
If the citrate goo leaks out, it fuses with the calcium phosphate crystals, creating big clumps that stick together, causing bone to lose its flexibility and become more brittle.
To arrive at their findings the team used nuclear magnetic resonance spectroscopy, X-ray diffraction, and the latest imaging techniques and high-level molecular modeling to reveal the citrate layers in bone.
Dr. Duer explains what they found:
"Bone mineral was thought to be closely related to this substance called hydroxyapatite. But what we've shown is that a large part of bone mineral - possibly as much as half of it in fact - is made up of this goo, where citrate is binding like a gel between mineral crystals."
The researchers found that the layering of citrate fluid and mineral crystals - which is visible only to the fine instruments they used - means the crystals stay in flat, plate-like shapes that can slip and slide around each other.
Without citrate goo, all crystals in bone mineral would fuse together and shatter
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Monday, March 24, 2014
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Difficulty getting pregnant could be due to stress
Doctors already know stress is tied to increased risk of heart disease and conditions like depression, but now, new research suggests stress may be a reason women trying to conceive experience difficulty getting pregnant.
The researchers, led by Dr. Courtney Denning-Johnson Lynch, director of reproductive epidemiology at Ohio State University Wexner Medical Center in Columbus, report their findings in the journal Human Reproduction.
The new study builds on the team's earlier work - that found a link between high levels of stress and reduced likelihood of pregnancy - by finding it is also tied to increased risk of infertility.
For the new findings, the team examined data on 501 couples trying to conceive who were enrolled in the Longitudinal Investigation of Fertility and the Environment (LIFE) Study between 2005 and 2009 at two research centers in the US, one in Michigan and the other in Texas.
The couples were followed for up to 12 months as they tried to conceive.
As part of the data collection, the female participants, aged between 18 and 40, and free from fertility problems, gave saliva samples the morning after they were enrolled and also the morning after their first period after enrollment. From these samples, the researchers could measure levels of cortisol and alpha-amylase, known biomarkers of stress.
Highest levels of salivary stress marker linked to double the chance of infertility
How can we combat drug-resistant TB?
Coinciding with World TB Day, new consensus statements have been drafted to address the growing problem of multidrug-resistant tuberculosis and extensively drug-resistant tuberculosis.
These statements - published in the European Respiratory Journal - are significant, because this is the first time that doctors treating patients with these new strains of tuberculosis (TB) have reached a consensus on patient management.
The major obstacle to developing guidelines for treatment of these forms of TB has been a lack of clinical evidence. These forms of the disease are so recent, it could be many years before sufficient evidence is available to form the basis of successful treatment.
Although in many parts of the world - the Americas, Europe, western Pacific and southeast Asia - incidence of TB is decreasing, multi-drug resistant TB (MDR-TB) - where the disease is resistant to at least isoniazid and rifampicin - is on the rise.
The first cases of MDR-TB were reported in "resource poor, high burden" areas in the 1980s. The World Health Organization (WHO) now estimate that about 450,000 new cases of MDR-TB occur each year, mostly within Europe.
Lead author Prof. Christoph Lange, head of the Respiratory Infections Assembly at the European Respiratory Society, says:
"These consensus statements provide very valuable support for physicians treating patients with these deadly conditions in all parts of Europe. The current management of patients with multidrug- and extensively drug-resistant TB is complex, very costly for health care systems and burdensome for those who are affected."
He adds:
"We have harmonised individual expert opinions on the management of multidrug- and extensively drug-resistant TB in adults and children to ensure that consensus is available where clinical evidence is still lacking. As clinicians we hope to improve the treatment of multidrug- and extensively drug-resistant TB and the life of our patients who suffer from these difficult-to-treat conditions."
'Totally-drug-resistant tuberculosis'
Uterine cancer risks decrease by 81% with bariatric surgery
Bariatric surgery, or weight-loss surgery, is normally used as a last resort when all other efforts have failed for obese patients who need to lose weight for their health. And now, researchers have found that the weight loss following such surgery significantly reduces the risk of endometrial (uterine) cancer in women.
According to the US Centers for Disease Control and Prevention (CDC), uterine cancer is the fourth most common cancer in women. Though all women are at risk for this cancer, the risk increases with age, and most cases are found in women who have gone through menopause.
Researchers from the study, which is published in the April issue of the journal Gynecologic Oncology, note that obesity is a significant public health problem in the US.
The team, comprised of researchers from the University of California-San Diego (UCSD) and Moores Cancer Center, says around two thirds of adults in the US are overweight or obese. Though obesity is linked to a range of health risks, including heart disease, diabetes and cancer, it is also linked to cancer of the uterus in women.
To investigate these links in detail, the researchers analyzed a retrospective cohort study of over 7 million patients in the University HealthSystem Consortium database, which provides information from academic medical centers and affiliated hospitals in the US.
From this database, the researchers identified 103,797 patients with a history of bariatric surgery, and 44,345 had a diagnosis of uterine malignancy.
Dr. Kristy Ward, first author and senior gynecologic oncology fellow in the Department of Reproductive Medicine at UCSD School of Medicine, explains what they found:
"Estimating from various studies that looked at increasing body mass index (BMI) and endometrial cancer risk, a woman with a BMI of 40 would have approximately eight times greater risk of endometrial cancer than someone with a BMI of 25."
And she says that this risk will likely rise as BMI increases.