Common blood pressure drugs may raise cancer risk

(Reuters) – A widely used class of blood pressure drugs may slightly increase the risk of cancer, U.S. researchers said on Sunday, and they are calling on U.S. regulators to take a closer look.

Health

They said an analysis of available data on drugs in the class known as angiotensin-receptor blockers showed patients were 1.2 percent more likely to be diagnosed with a new cancer over four years than others who did not take the drugs.

Most patients in the trials (86 percent) took German drugmaker Boehringer Ingelheim’s telmisartan, sold as Micardis, which has annual sales of more than $1.5 billion.

“The increased risk of new cancer occurrence is modest but significant,” Dr. Ilke Sipahi and colleagues from Case Western Reserve University in Cleveland and colleagues wrote in the journal Lancet Oncology.

There were not enough data in the studies to say if individual drugs in the class raise the risk or if it is a so-called class effect shared by all such drugs.

Even so, Dr. Steven Nissen, a cardiologist at the Cleveland Clinic, said in a commentary the findings were “disturbing and provocative, raising crucial drug safety questions for practitioners and the regulatory community.”

He said regulators need to look more closely at the risk of cancer with ARB use and that doctors should be more cautious about prescribing ARBs, and especially Micardis.

Privately held Boehringer Ingelheim defended the safety of its drug, saying in a statement its own “internal safety data analysis of primary data contradicts the conclusions” of an increased cancer risk.

Nissen did a similar analysis that raised alarms about heart risks from GlaxoSmithKline diabetes drug Avandia.

Currently, there are no major safety concerns linked with taking angiotensin-receptor blockers or ARBs, which work by blocking receptors for angiotensin II, a hormone that increases blood pressure.

But a 2003 study in patients with heart failure did find that the drug Atacand, or candesartan, made by the Anglo-Swedish firm AstraZeneca, significantly raised the risk of fatal cancers compared with a dummy pill.

PUBLICLY AVAILABLE DATA

Sipahi and colleagues did a so-called meta-analysis, pooling all publicly available data from randomized trials of ARBs published before November 2009.

Other drugs in the class include Merck & Co’s Cozaar, sold generically as losartan; Diovan or valsartan made by Swiss drug firm Novartis; irbesartan, jointly marketed by Sanofi-Aventi and Bristol-Myers Squibb as Avapro; Daiichi Sankyo’s Benicar or olmesartan; and Solvay Pharmaceuticals’ Teveten or eprosartan.

Overall, they found that patients taking the drugs had 7.2 percent risk of having a new cancer diagnosis, compared with 6 percent risk for patients in the control groups.

When they looked at cancer types, only lung cancer stood out, with 0.9 percent of patients taking blood pressure drugs developing a new lung cancer compared with 0.7 percent of patients in the control arm.

The drugs did not appear to increase the risk of death from cancer, but the team said cancers can develop slowly and cancer deaths might not show up in the relatively short studies.

Just three out of seven FDA-approved drugs — telmisartan, losartan, and candesartan — were studied, and it is not clear what affect other drugs in the class might have on cancers.

Nevertheless, they said given how widely the drugs are used, the risk is worth further study.

Boehringer Ingelheim said its own analysis of data from three large trials showed no increased cancer risk associated with Micardis. But in one study, called ONTARGET, there was a slight increased risk in one treatment arm when the drug was taken in combination with common blood pressure drugs known as ACE-inhibitors, such as ramipril.

The company said the product label does not recommend the drug be used in combination with ACE-inhibitors.

Nissen said the study is limited by the fact that the trials were not designed to look at cancer risks.

But he said the drugs are often overprescribed because of aggressive marketing, and patients might fare just as well taking inexpensive ACE inhibitors instead.

Other experts stressed that patients need to keep taking their blood pressure medications.

“At the moment there isn’t enough evidence to draw any firm conclusions about how blood pressure drugs might affect cancer risk and this will need further investigation,” Martin Ledwick, head information nurse at Cancer Research UK, said in a statement.

(Additional reporting by Kate Kelland in London, editing by Philip Barbara)

Common blood pressure drugs may raise cancer risk

CHICAGO, June 13 (Reuters) – A widely used class of blood pressure drugs may slightly increase the risk of cancer, U.S. researchers said on Sunday, and they are calling on U.S. regulators to take a closer look.

They said an analysis of available data on drugs in the class known as angiotensin-receptor blockers showed patients were 1.2 percent more likely to be diagnosed with a new cancer over four years than others who did not take the drugs.

Most patients in the trials (86 percent) took German drugmaker Boehringer Ingelheim’s telmisartan, sold as Micardis, which has annual sales of more than $1.5 billion.

“The increased risk of new cancer occurrence is modest but significant,” Dr. Ilke Sipahi and colleagues from Case Western Reserve University in Cleveland and colleagues wrote in the journal Lancet Oncology.

There were not enough data in the studies to say if individual drugs in the class raise the risk or if it is a so-called class effect shared by all such drugs.

Even so, Dr. Steven Nissen, a cardiologist at the Cleveland Clinic, said in a commentary the findings were “disturbing and provocative, raising crucial drug safety questions for practitioners and the regulatory community.”

He said regulators need to look more closely at the risk of cancer with ARB use and that doctors should be more cautious about prescribing ARBs, and especially Micardis.

Privately held Boehringer Ingelheim defended the safety of its drug, saying in a statement its own “internal safety data analysis of primary data contradicts the conclusions” of an increased cancer risk.

Nissen did a similar analysis that raised alarms about heart risks from GlaxoSmithKline (GSK.L) diabetes drug Avandia.

Currently, there are no major safety concerns linked with taking angiotensin-receptor blockers or ARBs, which work by blocking receptors for angiotensin II, a hormone that increases blood pressure.

But a 2003 study in patients with heart failure did find that the drug Atacand, or candesartan, made by the Anglo-Swedish firm AstraZeneca (AZN.L), significantly raised the risk of fatal cancers compared with a dummy pill.

PUBLICLY AVAILABLE DATA

Sipahi and colleagues did a so-called meta-analysis, pooling all publicly available data from randomized trials of ARBs published before November 2009.

Other drugs in the class include Merck & Co’s (MRK.N) Cozaar, sold generically as losartan; Diovan or valsartan made by Swiss drug firm Novartis (NOVN.VX); irbesartan, jointly marketed by Sanofi-Aventis (SASY.PA) and Bristol-Myers Squibb (BMY.N) as Avapro; Daiichi Sankyo’s (4568.T) Benicar or olmesartan; and Solvay Pharmaceuticals’ (SOLB.BR) Teveten or eprosartan.

Overall, they found that patients taking the drugs had 7.2 percent risk of having a new cancer diagnosis, compared with 6 percent risk for patients in the control groups.

When they looked at cancer types, only lung cancer stood out, with 0.9 percent of patients taking blood pressure drugs developing a new lung cancer compared with 0.7 percent of patients in the control arm.

The drugs did not appear to increase the risk of death from cancer, but the team said cancers can develop slowly and cancer deaths might not show up in the relatively short studies.

Just three out of seven FDA-approved drugs — telmisartan, losartan, and candesartan — were studied, and it is not clear what affect other drugs in the class might have on cancers.

Nevertheless, they said given how widely the drugs are used, the risk is worth further study.

Boehringer Ingelheim said its own analysis of data from three large trials showed no increased cancer risk associated with Micardis. But in one study, called ONTARGET, there was a slight increased risk in one treatment arm when the drug was taken in combination with common blood pressure drugs known as ACE-inhibitors, such as ramipril.

The company said the product label does not recommend the drug be used in combination with ACE-inhibitors.

Nissen said the study is limited by the fact that the trials were not designed to look at cancer risks.

But he said the drugs are often overprescribed because of aggressive marketing, and patients might fare just as well taking inexpensive ACE inhibitors instead.

Other experts stressed that patients need to keep taking their blood pressure medications.

“At the moment there isn’t enough evidence to draw any firm conclusions about how blood pressure drugs might affect cancer risk and this will need further investigation,” Martin Ledwick, head information nurse at Cancer Research UK, said in a statement.

(Additional reporting by Kate Kelland in London, editing by Philip Barbara)

XLRI, Weatherhead B-School to offer global courses for first time

XLRI School of Business & Human Resources is joining hands with the Weatherhead School of Management of the Case Western Reserve University, Cleveland, Ohio, to start for the first time in the country two unique one-year regular programmes in the fields of finance and organization development (OD).

XLRI and Weatherhead had signed an MoU in 2009 to collaborate in different areas which included jointly developing management programmes, exchange of students and faculty, research, etc.

As a first step, the two B-Schools will be focusing on launching two regular international programmes, planned as of now to be of one-year duration, split equally between the two campuses.

While Masters Programme in Organization Development (MPOD) will be for middle/senior level executives with at least five years’ experience, the second one called Master of Science in Finance (MSF) which will be for younger people having exposure in accountancy/finance related studies.

Though nothing has yet been agreed upon, the two programmes intend to target around 40 Asian students each who could be either from India or from the eight Saarc (South Asian Association for Regional Cooperation) countries.

Speaking to FE here, Weatherhead School of Management dean Mohan Reddy, who is here on a two-day visit to XLRI for discussing the programmes to be launched as well as to interact with the B-School’s faculty said, “We haven’t worked out the details as yet; as per the discussions, we are hoping to start at least one of them next year.”

Weatherhead, however, currently offers both the programmes at its US campus. According to Reddy, Organization Development (OD) was very well developed in India as there was a long tradition of organizations in the country.

“The basic agreement has been reached, we have now to work out all the details”, said Prof Jitu Singh, chairperson, international relations, XLRI, adding the two B-Schools have fixed academic year 2011 forlaunching at least one of the programmes “as we need some time to do our homework and market it”.

Talking about the duration of the courses, Reddy said that “market conditions” would decide whether the courses offered would be for one year or two years.

Though the two B-Schools are yet to decide on the fee structure too, candidates joining the courses will be spending half the course’s duration in India while the other half at the Weatherhead School of Management at Cleveland, Ohio in US.

Asked why the two fields of finance and organization development (OD) had been chosen from so many areas, XLRI director Father E Abraham said the two B-Schools happened to be the common strengths for both, with good faculty support.

The Weatherhead dean added the two B-Schools would expand cooperation in future by way of engaging in exchange of faculty as well as by taking up joint research.

Oral bacteria in pregnant mother can cause complications

Washington, May 11 (ANI): Researchers from Case Western Reserve University have warned that even healthy expecting women can be at risk for pregnancy problems caused by oral bacteria.

They have begun to understand how and which bacteria from the 700 species living in the mouth are responsible for the increasing numbers of preterm and stillbirths.

Yiping Han, from the department of periodontics in the School of Dental Medicine, led the study that found several new bacteria originating in the mouth travel through the blood to cause an inflammatory reaction in the placenta and eventually cause a range of health issues from miscarriages to stillbirths.

Researchers have been baffled why oral bacteria have shown up in the placenta or amniotic fluid of pregnant women.

The researchers found that after injecting the blood in the tails of pregnant mice with saliva from healthy people and dental plaque from those with periodontal disease, oral bacteria continued to grow in the placentas after it had left the mice blood 24 hours later.

Prior to Han’s work in connecting oral bacteria to the problems in pregnancy, it was thought that infections were transmitted through the vaginal tract.

Information from Han’s previous studies over the past decade shows that oral bacteria can be transported through the blood when there is a cut in the mouth’s lining or an oral health problem such as gingivitis or periodontitis which breaks down the defenses in the mouth’s lining that block or prevent bacteria from entering the bloodstream.

According to Han, this suggests that even healthy pregnant women should be concerned bacteria that normally lives in the mouth can enter the blood stream and make their way into the placenta’s immune-free environment to ignite an inflammatory reaction that can lead to premature or stillbirths.

The findings were featured in the spotlight section in a recent Infection and Immunity. The study was also reported on the home page of the American Society for Microbiology. (ANI)

Cockroach’s brain fires out walking commands

Washington, May 7 (ANI): Researchers have, for the first time, found that cockroach’s brain fires out commands to walk and run—a feat that has paved way for better rescue robots.

A team led by Roy Ritzmann, Case Western Reserve University biology professor, has shown a direct link between neurons at the center of an insect brain and changes in behaviour.

They recorded neural activity in the central complex of walking cockroaches and found that in the same area of the brain where visual, chemical and tactile information from the world outside is processed, the firing of neurons is correlated to the insect”s stepping rate.

This means that cockroaches walk or run when their brains decide to do so.

“Robots were sent into the World Trade Center after 911. By the time the driver would see an obstacle, they were stuck,” said Ritzmann.

“We see in these animals an ability to adapt to difficult and changing terrain and conditions. What we”d like to see is a robotic brain that can make these kinds of decisions,” he continued.

He believes that the research could help lead to better robots to search collapsed mines and buildings, to pilot drones, and for space exploration, where signals from Earth to a far off planet takes minutes, hours or longer.

Thus, to make a robot that can turn, back up, climb over or burrow under and obstacle without the guidance of a far off rescue worker using computer controls, the best thing would be to mimic an insect”s comparatively simple brain.

However, to get these first recordings of neural activity, Research Assistant Allan Pollack spent more than a year perfecting techniques to perform brain surgery in an area the size of the head of a pin.

After delicately cutting through the brain sheath and exposing the central complex, he inserted a hair-thin braid of four wires that can monitor activity of groups of neurons or stimulate the groups with electricity.

With the braid implanted, cockroaches were tethered over the simplest version of a treadmill—a greased glass plate.

The researchers waited, sometimes for three hours or more, for a cockroach to begin walking, and to change speeds, all without prodding.

“We wanted to study the cockroach when it wants to move,” said Ritzmann.

He found that when he graphed the sums of the insects” step rates and sums of the neural firing, they produce a similar pattern.

The steps come about 450 milliseconds after the neural firing.

“This is a breakthrough on a number of different levels. It was a real accomplishment to record the neural activity of walking. The interesting finding is the cockroach can control speed with the brain,” said Dr. Sasha Zill, a professor of anatomy and pathology at the Joan C. Edwards School of Medicine at Marshal University.

Zill explained research shows animals from humans to – now, cockroaches – walk by sending a signal from the brain down to a part of the spinal cord or the equivalent, which generates a pattern of signals that direct the orderly contraction of muscles needed for each step.

The findings are published online in Current Biology. (ANI)

Three genes linked to Lou Gehrig’s disease identified

Washington, Sep 10 (ANI): Researchers at Michigan Technological University have identified three genes that play a major role in the most common type of amyotrophic lateral sclerosis (ALS), generally known as Lou Gehrig’s disease.

The team of mathematicians, led by Shuanglin Zhang, isolated the genes from the many thousands scattered throughout human DNA.

Zhang noted that the discovery does not mean an end to ALS, but it could provide scientists with valuable clues as they search for a cure.

“I felt very urgent to find the genes for ALS,” Zhang said.

“This is very nice work. It’s very challenging to map genes for complex diseases, and while many statistical methods have been developed, most don’t work well in practice. Zhang’s group has developed a method to detect genes and gene-gene interaction in complex diseases and provided evidence that it works,” said Xiaofeng Zhu, an associate professor of epidemiology at Case Western Reserve University’s School of Medicine.

“Their findings will need to be confirmed by other researchers, but I think this will be very useful for the investigators who are trying to find genes underlying complex diseases such as ALS,” said Zhu.

According to the ALS Association, only about 10 percent of patients have familial ALS, a directly inherited form of the usually fatal neuromuscular disorder, while the remaining 90 percent are diagnosed with the sporadic form of the disease.

While everyone has the three genes in question, but in people with sporadic ALS, they differ from those in people who don’t have ALS.

The mathematicians were not surprised when they tracked down the location of the genes.

“Everybody has 23 chromosomes, and the three genes on chromosomes 2, 4, and 10 interact. If you have this combination of the three genes, you are at high risk of developing the disease. It’s really exciting, especially because my husband has sporadic ALS. Maybe they can find a cure by blocking the genes,” explained Zhang’s wife Qiuying Sha.

ALS destroys the nerves in the brain and spinal cord that control voluntary movement, eventually leading to paralysis.

Zhang’s team used a new statistical method to analyse the genetic codes of 547 individuals, 276 with sporadic ALS and 271 without.

The method, a two-locus interaction analysis approach, allows the researchers to identify multiple genes associated with a complex illness.

The data set they analyzed was provided by National Institute of Neurological Disorders and Stroke (NINDS) Human Genetics Resource Center at the Coriell Institute, a publicly funded “bank” or repository for human cells, DNA samples, clinical data, and other information that aims to accelerate research on the genetics of nervous system disorders.

The study has been published in the open access journal BMC Medical Genetics. (ANI)

Prenatal malaria exposure ‘ups malaria, anaemia risk in some kids’

Washington, July 28 (ANI): A new study led by an Indian origin scientist has unravelled the mystery behind why some children are more susceptible to malaria infection and anaemia.

Lead researcher Indu Malhotra from Case Western Reserve University School of Medicine suggests that children who are exposed to Plasmodium falciparum (P. falciparum) malaria before birth become tolerant to the malaria parasites, or their soluble products.

This tolerance, which persists into childhood, reduces the ability of the immune system to attack and destroy parasites and increases the susceptibility of these children to develop a malaria infection.

It also increases their risk for anaemia.

“This is the first time it has been shown why some children are more susceptible to malaria and anaemia than other children,” said Malhotra.

“This study is timely given President Obama’s Global Health Initiative to assist developing countries to control malaria, one of the ‘big three’ diseases,” she added.

The researchers investigated how prenatal malaria exposure affects anti-malaria immunity in young children and their susceptibility to subsequent malaria infections.

They studied 586 Kenyan newborn babies, the researchers identified those children who had been exposed to P. falciparum malaria in utero.

The babies were classified into three groups: “sensitized” – those babies whose cord blood cells produce activating cytokines in response to the malaria antigens; “exposed, not-sensitized” – babies whose bodies did not produce activating cytokines but made an inhibitory cytokine; and “not-exposed”- babies born to mothers with no P. falciparum malaria infection at delivery.

The study involving Malhotra, Christopher King and colleagues from Case Western Reserve University School of Medicine and Kenya Medical Research Institute and Division of Vector Borne Diseases showed that in first three years of life, the “exposed, not-sensitized” group had a 60 percent greater risk of malaria infection than the “not-exposed” group and a slightly higher risk of malaria infection than the “sensitized” group.

They also had lower hemoglobulin levels, a sign of anaemia, than the other babies. The T cells of “exposed, not-sensitized” children were less likely to make activating cytokines in response to malaria antigens.

The study appears in the open access journal PLoS Medicine. (ANI)

Sleep-related breathing disorders linked to irregular heartbeats

Washington, June 23 (ANI): A new study led by an Indian origin scientist has revealed that sleep-related breathing disorders can lead to serious cardiovascular problems in older adults.

Dr Reena Mehra, of Case Western Reserve University School of Medicine, Cleveland has found a link between apnea (brief pauses in breathing) or hypopnea (shallow breathing) and abnormal heart rhythms (arrhythmias) in older men.

The study involving 2,911 men showed that having more episodes of paused or shallow breathing was associated with increased odds of two types of arrhythmias-one involving the heart’s upper chambers (atria) and one involving the heart’s lower chambers (ventricles).

Obstructive sleep apnea-the most common type, involving a partial or complete blockage of the airways-was associated with irregular heartbeats caused by a problem with the lower chambers or ventricles.

In addition, lower blood oxygen levels also appeared to be associated with this type of arrhythmia.

But central sleep apnea, involving a malfunction in brain signals controlling breathing muscles, was more strongly associated with arrhythmias in the atria or upper chambers.

According to the authors, more severe cases of sleep-disordered breathing were associated with higher odds of arrhythmia; in addition, “there also seems to be a threshold effect such that moderate-to-severe sleep-disordered breathing confers the greatest increased odds of clinically significant arrhythmias independent of self-reported heart failure and cardiovascular disease.”

“The strong associations between central sleep apnea and atrial fibrillation [arrhythmia originating in the heart's upper chambers] suggest that central sleep apnea may be a sensitive marker of underlying abnormalities in autonomic or cardiac dysfunction associated with atrial fibrillation,” they added.

The study appears in Archives of Internal Medicine, one of the JAMA/Archives journals. (ANI)

Healthy teeth can help alleviate rheumatoid arthritis pain

Washington, May 29 (ANI): A new study has shown that people who suffer from gum disease and also have a severe form of rheumatoid arthritis can lower the chronic pain by keeping their teeth healthy.

The research team from Case Western Reserve University School of Dental Medicine and University Hospitals of Cleveland suggest that both inflammatory diseases share similarities in the progression over time.

In both diseases, the soft and hard tissues are destroyed from inflammation caused by toxins from bacterial infection.

“It was exciting to find that if we eliminated the infection and inflammation in the gums, then patients with a severe kind of active rheumatoid arthritis reported improvement on the signs and symptoms of that disease,” said Nabil Bissada, D.D.S., chair of the department of periodontics at the dental school.

“It gives us a new intervention,” Bissada added.

Conventionally teeth were pulled or antibiotics were given for treatment of rheumatoid arthritis, which actually treated the periodontitis, and the patients got better.

Bissada and co-researcher Dr Ali Askari, chair of the department of rheumatology at University Hospitals studied 40 patients with moderate to severe periodontal disease and a severe form of rheumatoid arthritis.

They found that one toxin from the inflamed areas called tumour neurosis factor-alpha (TNF-a) is a marker present in the blood when inflammation is present in the body. TNF-a can initiate new infections or aggravate sites where inflammation already exists.

The study showed that after receiving treatment for the gum disease, improvement in rheumatoid arthritis symptoms was seen in patients who did and did not receive the anti-TNF-a medications which block the production of TNF-a that aggravate or can cause inflammation.

“I’m optimistic that someday the biologic agents that we use successfully in treatment of rheumatoid arthritis will lead to improvement of periodontitis and would be available for use and treatment of this perplexing problem,” said Askari.

The study appears in the Journal of Periodontology. (ANI)

Gene that makes colon cancer resistant to treatment identified

Washington, May 19 (ANI): Researchers have found that low levels of a particular gene make colon cancer patients resistant to celebrex treatment.

Lead researcher Dr Sanford Markowitz, the Markowitz-Ingalls Professor of Cancer Genetics at the Case Western Reserve University School of Medicine and an oncologist at the Ireland Cancer Center of University Hospitals Case Medical Centre said that individuals who have low expression of the gene 15-PGDH also called ‘Celebrex gene’ make individuals resistant to colon cancer treatment.

“These findings have two important practical implications,” said Markowitz, who is also an investigator in the Howard Hughes Medical Institute.

“First, they suggest that measurement of 15-PGDH may identify which individuals are most likely to benefit from treatment with Celecoxib as a colon tumor preventative.

“Second, they suggest that identifying drugs that could increase 15-PGDH expression in the colon could be a potent new strategy for preventing development of tumours in the colon,” Markowitz added.

Previous studies by Markowitz had shown that the gene 15-PGDH is expressed by the normal colon and acts similarly to Celecoxib in preventing colon tumors by inhibiting the COX-2 pathway.

Another study led by Dr Monica Bertagnolli, at the Harvard Brigham and Women’s Hospital showed that with Celecoxib treatment, individuals who had previously developed colon adenomas cut the rate of developing new adenomas by one-third, and cut the rate of developing new large adenomas by two-thirds.

In the new study, the researchers sought to determine whether protection from colon tumors by Celecoxib actually require the joint action of both the drug and the 15-PGDH gene

They found that in mice that genetically lacked the gene 15-PGDH Celecoxib proved unable to prevent the development of colon tumors, suggesting that both the drug and the gene are needed to protect the colon from tumour development.

The study appears in Proceedings of the National Academy of Sciences. (ANI)

Traumatic brain injury victims experience lifelong effects

Washington, Children who suffer traumatic brain injuries can experience either lasting neuro-psychological problems or their onset later in life, according to two new studies.

Researchers at Universities of Ohio State, Case Western Reserve and hospitals in Columbus and Cleveland followed 37 children after severe traumatic brain injury (TBI), 40 after moderate TBI, and 44 children after musculoskeletal injury (a common way to control for trauma and the hospital experience).

All of the children were injured between the ages of six and 12, and assessed six months, 12 months, and three to five years following their injuries.

Predictably, kids with severe TBI showed greater problems than children with other injuries in the areas of mental processing, learning and memory, behaviour, adaptation and academics. Children whose comas were longer and more severe had more, and more serious, problems.

Some children with severe TBI started to fall even further behind their peers than one would normally expect, in a snowball effect that requires further study.

In the second study, the first systematic meta-analysis summarising the collective results of many single studies, the researchers found that problems lasted over time and, in some cases, worsened with more serious injury.

This study, conducted by Talin Babikian and Robert Asarnow, at the University of California-Los Angeles (UCLA), the authors analysed 28 selected articles published between 1988 and 2007.

The children were sorted by TBI severity and time since injury. Severity levels were mild, moderate or severe TBI, and follow-ups were on average 0-five months, six-23 months, or 24+ months, for 14 key aspects of neurocognition.

The worse the injury, the worse the neurocognitive outcome, especially on measures of general intellectual functioning and processing speed.

Most problems stick. Despite modest recovery, weaknesses in many children with moderate TBI persist even two years after the injury, compared to the children in control groups, said a release of the American Psychological Association.

The Centres for Disease Control in 2000 cited traumatic brain injury as the single most common cause of death and disability in children and adolescents.

The results of both studies were published in the May issue of Neuropsychology. (IANS)

How changing light could help people with dementia, other diseases

Washington, May 13 (ANI): Periods of blue-light, like daylight, produced from the blue-white lamp prototypes developed by GE scientists, could help people suffering from dementia and other health problems, according to researchers from Case Western Reserve University.

For the study, the researchers removed some standard fluorescent lighting and installed new blue-white lamp prototypes at the GE’s Nela Park campus, where daylight, which has proven health benefits, is not readily available.

They hypothesized that periods of blue light, like daylight, can help regulate the sleep-wake rhythm, which is a behavioural pattern linked to the 24-hour biochemical circadian cycle of the hormone melatonin. The levels of the hormone determine if people are awake or sleepy.

And by increasing exposure to blue-white light during the day, and yellow-white light in the evening, the researchers hope to help patients regulate their sleep-wake cycles so that they are more awake during the day and more asleep at night.

According to Patricia Higgins, associate professor at the Bolton School of Nursing and one of the lead investigators, the project may prove to be especially beneficial for people suffering from dementia.

In a recent study with five male patients, each person suffering from dementia and living in a long-term care facility, the researchers installed the blue-white lights in an activities room where most residents gathered for meals and daytime activities.

“We wanted to see whether lighting could affect the participants’ sleep-wake rhythms. While the group was small, the results show promise in raising activity levels during daytime hours and increasing sleep at nighttime,” said Higgins.

And they saw one unexpected side effect of the lighting- once adjusted to the blue-white light most employees claimed that they liked the new lighting conditions.

The researchers said that the new lighting used in the test changes the colour without overpowering individuals with brightness.

“Why waste light if you can tune it to the right colour and maximize the amount of useful light,” said Mariana Figueiro, who worked on the study.

“Light is a good stimulus for the circadian system, which regulates your sleep-wake cycles,” says Thomas Hornick, another worker on the study.

He said that it is known that certain drugs do better when given at the appropriate time in the circadian cycle.

Also, the researchers are hoping to apply the study’s findings as a safe, non-pharmacological intervention to change the lighting in hospitals where patients may have a speedier recovery or improved quality of life with a good night’s rest. (ANI)

Imbalance of iron linked to prion disease-related neuronal demise

Washington, March 15 (ANI): An Indian-origin researcher at Case Western Reserve University School of Medicine has found that imbalance of iron homeostasis is a common feature of prion disease-affected human, mouse, and hamster brains.

Dr. Neena Singh, who worked in collaboration with researchers from Creighton University, says that her team’s findings provide new insight into the mechanism of neurotoxicity in prion disorders, and novel avenues for the development of therapeutic strategies.

Unlike other neurodegenerative conditions, prion disorders are sporadic, inherited, and infectious, and affect both humans and animals.

Mad cow disease in cattle, scrapie in sheep, and Creutzfeldt-Jakob disease in humans are some of its examples.

The causative agent is a misfolded protein referred to as PrP-scrapie that replicates itself by changing the conformation of neighbouring copies of the same protein, namely the prion protein. Aggregates of PrP-scrapie are toxic to brain cells and cause a spongy-like appearance in diseased brains.

Neena says that her study suggests that accumulation of PrP-scrapie alters the metabolism of iron in diseased brains.

She adds that the imbalance of brain iron homeostasis worsens with disease progression, and is not an outcome of end-stage disease.

Given that iron is highly toxic when mismanaged, the researchers think that this condition may contribute significantly to prion-disease-associated neurotoxicity.

The likely cause of this condition is loss of normal function of the prion protein in cellular iron metabolism, which has recently been shown by Neena and her colleagues, combined with gain of toxic function by the redox-active PrP-scrapie complex.

Neena says that it was surprising to see that prion disease-affected brains are iron deficient, despite a significant increase in their overall iron content.

She concludes that ferritin, a major iron storage protein, co-aggregates with PrP-scrapie in diseased brains and sequesters bound iron in the complex, creating a state of apparent iron deficiency.

The brain cells respond to this condition by increasing their level of iron uptake, and thereby creates a vicious cycle of increased iron uptake in the presence of increased iron.

The resarchers say that their observations may help understand how the prion agent causes neurotoxicity, and enable the development of novel therapeutic strategies targeted at restoring brain iron homeostasis in prion disorders.

A research article on this study has been published in the journal PLoS Pathogens. (ANI)

Food labels conceal kidney-harming phosphorus content

Washington, Feb 11 (ANI): A large number of processed and fast foods hide information about phosphorus additives, which can be dangerous for kidney patients, according to researchers from MetroHealth Medical Center and Case Western Reserve University School of Medicine in Cleveland.

High blood levels of phosphorus can lead to heart disease, bone disease, and even death among patients with advanced kidney disease.

Thus, patients must avoid foods with naturally high levels of phosphorus – such as certain meats, dairy products, whole grains, and nuts.

However, the researchers found that it has become an increasingly common practice by food manufacturers to include phosphorus additives, such as sodium phosphate or pyrophosphate, to processed foods.

The additives are used to enhance flavour and shelf life -particularly in meats, cheeses, baked goods, and beverages – and thus it gets difficult for consumers to know whether or not these additives are present in products.

“Calories, fat, and sodium content are required to be listed on nutrition labels, but phosphorus is not. This makes it impossible for kidney disease patients to know how much phosphorus they are eating. For example, we discovered that while chicken is often on dialysis patients’ ‘Safe List’ of foods to eat, chicken from fast food and sit down restaurants often contains this phosphorus additive,” said Catherine Sullivan, M.S., R.D., lead researcher from the Center for Reducing Health Disparities.

It was found that the researchers could significantly lower phosphorus levels among advanced kidney disease patients after teaching them how to avoid foods containing phosphorus additives.

Then 279 advanced kidney disease patients receiving dialysis treatment were assigned to a control group that received usual care or to an intervention group that was taught to avoid additive-containing foods when purchasing groceries or eating at fast food restaurants.

After three months, phosphorus levels declined two and a half times more in the intervention group than in the control group.

However, the researchers found that these additives may even affect people with normal kidney function.

Previous research has found that high phosphorus diets appear to lower bone density and increase fracture risk as well.

The study is published in the latest issue of the Journal of the American Medical Association (JAMA). (ANI)

Perception of time pressure impairs performance

Washington, Feb 11 (ANI): If you feel that you don’t have enough time to finish a task in hand, then chances are your finished work won’t be up to the mark, says a new study, which claims that it’s the perception of time pressure that impairs performance.

In a first of its kind study, Michael DeDonno, a doctoral student in psychology at Case Western Reserve University looked at how perceived time pressure affected the performance of 163 subjects in the Iowa Gambling Task (IGT).

IGT is a popular psychological assessment tool that is used to investigate the effect of perceived time pressure on a learning-based task.

“Research has shown that it’s not necessarily the time pressure, but it’s the erception of that time pressure that affects you. If you feel you don’t have enough time to do something, it’s going to affect you,” said DeDonno.

For the study, he divided the participants into two groups: an experimental group that was informed the time allotted to perform the task was insufficient and the control group, which was told they had typically sufficient time to complete the task.

It was found that participants who were advised the time was insufficient performed worse than those who were told they had enough time, regardless of the actual time allotted.

“If I told you that you didn’t have enough time, your performance was low regardless if you had ample time or not. If you were told you had enough time, in both scenarios, they out performed those who were told they didn’t,” said DeDonno.

He said that there are plenty of real-world benefits to understanding the effects of perceived time pressure on decision-making performance.

He cited project team members who perceived a high degree of time pressure had lower job satisfaction.

He also noted standardized tests, like the ACT or LSAT, have a high rate of test anxiety by test takers due mostly to time constraints.

He is planning to further study if a perception of time being insufficient by HMO physicians lead to inappropriate medications or an increase in diagnostic error.

Although it’s still not known why perceived time pressure could impair performance, DeDonno said that it’s possible to combat it.

He said: “Decision-making can be emotion based, keep your emotions in check. Have confidence in the amount of time you do have to do things. Try to focus on the task and not the time. We don’t control time, but we can control our perception. It’s amazing what you can do with a limited amount of time.

“Time is relevant. Just have the confidence with the time you’re given. I tell my students ‘Do the best you can in the time allotted. When it ends, it ends.’”

The study was published in a recent issue of Judgment and Decision Making. (ANI)

Inflammation may be link between extreme sleep durations and poor health

Washington, Feb 02 (ANI): A new study, led by an Indian-origin researcher, has shown that sleep duration is linked to changes in the levels of specific cytokines that are important in regulating inflammation.

The results of the study, conducted by Dr. Sanjay R. Patel, assistant professor of medicine at Case Western Reserve University in Cleveland, Ohio, and his colleagues, suggest that inflammation may be the pathway linking extreme sleep durations to an increased risk for disease.

In the study, the researchers found that each additional hour of self-reported sleep duration was associated with an eight-percent increase in C-reactive protein (CRP) levels and a seven-percent increase in interleukin-6 (IL-6), which are two inflammatory mediators.

On contrary, each hour of reduction in sleep measured objectively by polysomnography was associated with an eight-percent increase in tumour necrosis factor alpha, another pro-inflammatory cytokine.

“The most surprising finding was that we found different relationships based on how sleep was measured,” said Patel.

According to the researchers, their study has linked both short and long sleep durations with an increased risk for mortality, coronary heart disease, diabetes and obesity.

Chronic elevations in cytokines such as CRP and IL-6 also are associated with an increased risk of problems such as diabetes and heart disease.

The study involved 614 individuals from the Cleveland Family Study, a longitudinal family-based epidemiological cohort designed to study the genetics of obstructive sleep apnea (OSA).

Participants completed questionnaires about sleep habits and underwent one night of polysomnography. In the morning a fasting blood sample was collected, and it was analyzed for five inflammatory cytokines.

Mean self-reported habitual sleep duration was 7.6 hours; mean sleep duration measured by polysomnography on the night prior to blood sampling was 6.2 hours.

Those with long sleep durations, assessed by either measure, were significantly younger. Short sleep duration measured by polysomnography was associated with an increased prevalence of diabetes, hypertension and obstructive sleep apnea.

According to the researchers, the differing patterns of association with cytokine levels suggest that self-reported habitual sleep duration may measure chronic sleep exposure, while polysomnography may measure an acute exposure.

They also note that the two methods of measuring sleep duration may be influenced differently by an underlying predictor of sleep habits such as stress or mood, which may have a direct effect on cytokine levels.

The study is published in the February issue of the journal SLEEP. (ANI)