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Jul 12
Why breast milk is deemed best for baby
Scientists have tried to explain how the age old maxim "breast milk is best for the baby" holds true even now.

Jyllian Kemsley, Chemical and Engineering News senior editor, points out that their findings reveal many intriguing and sometimes counterintuitive ways in which sugars, proteins and fat in milk interact with microbes in infants` intestines to nourish babies and protect their health.

For instance, scientists have discovered that breast milk contains oligosaccharides, complex sugars that babies can`t even digest.

It turns out these oligosaccharides, rather than providing nutritional value directly to infants, actually confers protection.

They feed beneficial intestinal bacteria that seem to crowd out harmful E. coli strains that might otherwise thrive.

The findings are published in the Chemical and Engineering News.

Jul 12
Kids who sleep less tend to have severe behavioural problems
A new study has found that 4-year-olds with shorter than average sleep times have increased rates of "externalizing" behaviour problems.

"Preschool children with shorter night time sleep duration had higher odds of parent-reported overactivity, anger, aggression, impulsivity, tantrums, and annoying behaviours," according to the new research by Dr. Rebecca J. Scharf of University of Virginia, Charlottesville, and colleagues.

They recommend that parents and health care providers discuss steps to improve sleep habits for preschool-age children with behaviour problems.

The researchers analyzed parent responses from a nationally representative study of approximately 9,000 children, followed from birth through kindergarten age.

When the children were four years old, night time sleep duration was estimated by asking the parents what time their child typically went to bed and woke on weekdays.

On a standard child behaviour questionnaire, parents rated their child on six different "externalizing" behaviour problems such as anger and aggression. (Externalizing behaviour problems are outward behaviours, distinguished from "internalizing" problems such as depression and anxiety.)

The relationship between sleep duration and behaviour scores was assessed, with adjustment for other factors that might affect sleep or behaviour.

The average bedtime was 8:39 pm and wake time 7:13 am, giving a mean night time sleep duration of about 10 and a half hours. Eleven percent of children were considered to have "short sleep duration" of less than 9 hours 45 minutes (calculated as one standard deviation below the average).

On the child behaviour questionnaire, 16 percent of children had a high score for externalizing behaviour problems.

Behaviour problems were more common for boys, children who watched more than two hours of television daily, and those whose mothers reported feeling depressed.

After adjustment for other factors, "Children in the shortest sleep groups have significantly worse behaviour than children with longer sleep duration," Dr Scharf and colleagues write.

The effect was greatest for aggressive behaviour problems, which were about 80 percent more likely for children with night time sleep duration of less than 9 hours and 45 minutes.

The study is published in the Journal of Developmental and Behavioral Pediatrics, the official journal of the Society for Developmental and Behavioral Pediatrics.

Jul 11
Brain tumours in children have a common cause
Scientists have found that an overactive signalling pathway is a common cause in cases of pilocytic astrocytoma, the most frequent type of brain cancer in children.

Scientists coordinated by the German Cancer Research Center (as part of the International Cancer Genome Consortium, ICGC) in 96 gemone analyses of pilocytic astrocytomas found defects in genes involved in a particular pathway.

They believe that drugs can be used to help affected children by blocking components of the signalling cascade.

Pilocytic astrocytomas are the most common childhood brain tumours. These tumours usually grow very slowly. However, they are often difficult to access by surgery and cannot be completely removed, which means that they can recur.

In previous work, researchers led by Professor Dr Stefan Pfister and Dr David Jones had already discovered characteristic mutations in a major proportion of pilocytic astrocytomas.

All of the changes involved a key cellular signalling pathway known as the MAPK signalling cascade. MAPK is an abbreviation for `mitogen-activated protein kinase`.

This signalling pathway comprises a cascade of phosphate group additions (phosphorylation) from one protein to the next - a universal method used by cells to transfer messages to the nucleus.

MAPK signalling regulates numerous basic biological processes such as embryonic development and differentiation and the growth and death of cells.

"A couple of years ago, we had already hypothesised that pilocytic astrocytomas generally arise from a defective activation of MAPK signalling," said Jones, first author of the study in journal Nature Genetics.

"However, in about one fifth of the cases we had not initially discovered these mutations. In a whole-genome analysis of 96 tumours we have now discovered activating defects in three other genes involved in the MAPK signalling pathway that have not previously been described in astrocytoma," he said.

"Aside from MAPK mutations, we do not find any other frequent mutations that could promote cancer growth in the tumours. This is a very clear indication that overactive MAPK signals are necessary for a pilocytic astrocytoma to develop," said study director Pfister.

"The most important conclusion from our results is that targeted agents for all pilocytic astrocytomas are potentially available to block an overactive MAPK signalling cascade at various points," said Pfister.

"We might thus in the future be able to also help children whose tumours are difficult to access by surgery," he said.

Jul 11
Nearly six million die from smoking every year: WHO
Despite public health campaigns, smoking remains the leading avoidable cause of death worldwide, killing almost six million people a year, mostly in low- and middle-income countries, the World Health Organization has said.

If current trends hold, the number of deaths blamed on tobacco use will rise to eight million a year in 2030, the WHO said yesterday in a briefing unveiled at a conference in Panama.

About 80 percent of tobacco-related deaths forecast for 2030 are expected in low- and middle-income countries, the report added.

"If we do not close ranks and ban tobacco advertising, promotion and sponsorship, adolescents and young adults will continue to be lured into tobacco consumption by an ever-more aggressive tobacco industry," said WHO Director-General Dr Margaret Chan.

"Every country has the responsibility to protect its population from tobacco-related illness, disability and death."

Among the dead this year, five million were tobacco users or former users, while more than 600,000 died from second-hand smoke, according to the WHO.

Tobacco use is believed to have caused the deaths of 100 million people in the 20th century.

Barring dramatic change, the tally for this century could soar to one billion people, the WHO warned.

"We know that only complete bans on tobacco advertising, promotion and sponsorship are effective," Dr Douglas Bettcher, the Director of the WHO`s Prevention of Noncommunicable Diseases department, told the Panama conference.

"Countries that introduced complete bans together with other tobacco control measures have been able to cut tobacco use significantly within only a few years," he said.

The report noted that 2.3 billion people from 92 countries benefit from some form of smoking restrictions, more than double the number who did five years ago.

However, that figure still represents just a third of the world`s population, it said.

Jul 10
Improving communication in diabetes treatment yields dramatic results: Study
More than a quarter of people over the age of 70s with type 2 diabetes could benefit simply from improving communication and education in the clinic, new research has revealed.

A study led by the University of Exeter Medical School and published in The Lancet found that 27 percent achieved better glycaemic control through individualised care alone.

At the moment, patients over the age of 70 are treated using a blanket method of aggressively reducing blood glucose levels, but that does little to take their complex needs into account.

"People over the age of 70 are more likely to have multiple complications, such as heart disease, as well as type 2 diabetes. Yet perversely, these patients have so far been excluded from clinical trials, precisely because of these complications. It means they are generally treated with a `one-size-fits-all` approach," Dr David Strain, from the University of Exeter Medical School, who led the study, said.

"We found that simply by individualising goals and setting realistic targets, then spending time talking to patients rather than aggressively chasing targets resulted in nearly a quarter of patients achieving better glycaemic control, without the need for medication," he added.


Type 2 diabetes is one of the most common chronic disorders in older adults. The number of people over the age of 65 has grown worldwide, and could now be as high as one in five. Older patients are more susceptible to complications caused by hyperglycaemia, when blood sugar levels are not properly balanced. These complications can increase the risk of falls and dizziness.

The situation has led to calls for treatment to be individualised, but so far evidence to support the case has been lacking.

Jul 10
Working in night shifts up miscarriage risk
Women working in irregular shifts are likely to experience reduced fertility and greater menstrual disruption than those working in regular shifts, according to a new research.

The team of researchers led by Dr Linden Stocker and Dr Ying Cheong, Southampton's Princess Anne Hospital, assessed the impact of non-standard working schedules, which included night and mixed shifts, on the reproductive outcomes of 119,345 women.

The study found that women who worked only nights had 29 percent increased rate of miscarriage.

Women who worked in rotational shifts had an 80 percent higher rate of subfertility - meaning that they were unable to conceive within a year compared with those working regular hours.

Women working out of the typical 9 am to 6 pm schedule also had a 33% higher rate of menstrual disruption, the study found.

"We don't fully understand why shift workers have an increased risk of certain diseases but obviously shift work impacts on your biological functioning, your psychological functioning and your social functioning", Dr Stocker was quoted as saying by an English news website.

The researchers, however, have asked women not to jump to a conclusion and quit jobs as the study is still in the preliminary stage.

Working odd hours is often linked to sleep loss, decreased exercise and poorer diet thereby drastically disrupting a woman's body clock.

In a previous study, researchers had claimed that women who had worked in nights shifts for 30 or more years are twice as likely to suffer from breast cancer.

Jul 09
Half of all cancers caused by a single gene: Study
A new study has found that more than half of all cancerous tumours are associated with defects in a single gene.

The researchers hope that the new findings can lead to new strategies for targeting cancer through genetic manipulation.

A team of cancer scientists - from the University of Cincinnati, Bellvitge Biomedical Research Institute, and Catalan Oncology Institute - said they have determined how the so-called p53 gene acts as a tumour-suppressing gene to protect healthy cells and prevent the development of abnormal cancerous cells.

Researchers believe that the gene produces proteins that can either repair damaged cells or cause tumour cells to die.

But when the gene is not working properly, due to a defect or mutation, the proteins that repair cells or target tumours are not produced, and the cancer grows.

The new study, led by George Thomas, identified the molecular processes that regulate the stability of p53 to keep the gene functioning properly to keep cancer cells in check.

The results suggest genetics play a significant role in cancer development and point the way to potential new treatments based on that the emerging scientific understanding of how tumours grow and spread.

Thomas said understanding how p53 is regulated and function is critical as "more than 50 percent of tumours have mutations in p53."

The findings are published online in the journal Cell Reports.

Jul 09
Irregular bedtimes can affect children`s brains
Irregular bedtimes in early childhood have been linked with low scores in reading, maths in both boys and girls, a study has suggested.

The study authors looked at whether bedtimes in early childhood were related to brain power in more than 11,000 seven year olds, all of whom were part of the UK Millennium Cohort Study (MCS).

The research drew on regular surveys and home visits made when the kids were 3, 5, and 7, to find out about family routines, including bedtimes.

The authors wanted to know whether the time a child went to bed, and the consistency of bed-times, had any impact on intellectual performance, measured by validated test scores for reading, maths, and spatial awareness.

And they wanted to know if the effects were cumulative and/or whether any particular periods during early childhood were more critical than others.

Irregular bedtimes were most common at the age of 3, when around one in five children went to bed at varying times. By the age of 7, more than half the children went to bed regularly between 7.30 and 8.30 pm.

Children whose bedtimes were irregular or who went to bed after 9 pm came from more socially disadvantaged backgrounds, the findings showed.

When they were 7, girls who had irregular bedtimes had lower scores on all three aspects of intellect assessed, after taking account of other potentially influential factors, than children with regular bedtimes. But this was not the case in 7 year old boys.

Irregular bedtimes by the age of 5 were not associated with poorer brain power in girls or boys at the age of 7. But irregular bedtimes at 3 years of age were associated with lower scores in spatial awareness in both boys and girls, suggesting that around the age of 3 could be a sensitive period for cognitive development.

Girls who had never had regular bedtimes at ages 3, 5, and 7 had significantly lower reading, maths and spatial awareness scores than girls who had had consistent bedtimes. The impact was the same in boys, but for any two of the three time points.

The authors point out that irregular bedtimes could disrupt natural body rhythms and cause sleep deprivation, so undermining the plasticity of the brain and the ability to acquire and retain information.

They wrote that sleep is the price that people pay for plasticity on the prior day and the investment needed to allow learning fresh the next day.

They added that early child development has profound influences on health and wellbeing across the life course, therefore, reduced or disrupted sleep, especially if it occurs at key times in development, can have important impacts on health throughout life."

Jul 08
Want to get fit? Chuck your cell phone
Spending too much time with mobile phones can harm your health, a new research has revealed.

The study conducted by Kent State University found that students, who spent lot of time on their phone- up to 14 hours each day- were less fit than those spending about 1 and a half hour a day, New York Daily News reported.

The report also said that people, who spent more time on their mobile devices, were more likely to engage in other sedentary forms of entertainment, like playing video games or watching films.

The authors wrote that the possibility that cell phone use could encourage physical activity among people who use it heavily while disrupting physical activity and encouraging sedentary activity among high-frequency users may help explain the significant negative relationship between cell phone use and cardiorespiratory fitness identified in the study.
The study has been published online in the International Journal of Behavioral Nutrition and Physical Activity.

Jul 08
Why aspirin helps some and not others
Researchers including an Indian origin have shed some light on why aspirin benefits some people and not others.

Researchers at Duke Medicine developed a blood-based test of gene activity that has been shown to accurately identify who will respond to the therapy.

The study showed that the new gene expression profile not only measures the effectiveness of aspirin, but also serves as a strong predictor of patients who are at risk for heart attack.

The Duke researchers enlisted three groups of participants - two of healthy volunteers and one comprised of patients with heart disease seen in outpatient cardiology practices.

The healthy volunteers were given a dosage of 325 mg of aspirin daily for up to a month; the heart disease patients had been prescribed a low dose of aspirin as part of their treatment.

Blood was then analyzed for the impact of aspirin on RNA expression and the function of platelets, which are the blood cells involved in clotting.

The RNA microarray profiling after aspirin administration revealed a set of 60 co-expressed genes that the researchers call the "aspirin response signature," which consistently correlated with an insufficient platelet response to aspirin therapy among the healthy subjects as well as the heart disease patients.

The researchers also examined the aspirin response signature in another group of patients who had undergone cardiac catheterizations. They found the signature was also effective in identifying those patients who eventually suffered a heart attack or died.

Deepak Voora, M.D., assistant professor of medicine at Duke and lead author of the study, said that the aspirin response signature can determine who is at risk for heart attack and death.

He said that there is something about the biology of platelets that determines how well we respond to aspirin and we can now capture that with a genomic signature in blood.

The study has been published in the online edition of the Journal of the American College of Cardiology.

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