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Aug 16
Brushing teeth well can reduce colorectal cancer risk
Two new studies have revealed that gut microbes known as fusobacteria, which are found in the mouth, stimulate bad immune responses and turn on cancer growth genes to generate colorectal tumours.

The findings could lead to more effective strategies for the early diagnosis, prevention, and treatment of colorectal cancer.

"Fusobacteria may provide not only a new way to group or describe colon cancers but also, more importantly, a new perspective on how to target pathways to halt tumour growth and spread," senior study author Wendy Garrett of the Harvard School of Public Health and the Dana-Farber Cancer Institute, said.

Colorectal cancer is the second leading cause of cancer-related death in the United States.

Recent studies have shown that fusobacteria from the mouth are also abundant in tissues from colorectal cancer patients. But until now, it was not known whether these microbes directly contribute to the formation of tumours.

In one of the new studies, Garrett, Matthew Meyerson of the Dana-Farber Cancer Institute, and their collaborators found that fusobacteria are prevalent in human adenomas-benign tumours that can become malignant over time-suggesting that these microbes contribute to early stages of tumour formation.

In a mouse model of colorectal cancer, these bacteria accelerated the formation of tumours by attracting immune cells called myeloid cells, which invade tumours and stimulate inflammatory responses that can cause cancer.

In the second study, Yiping Han of Case Western Reserve University School of Dental Medicine and her collaborators discovered that fusobacteria rely on a molecule called Fusobacterium adhesin A (FadA), which is found on the surface of these bacterial cells, to attach to and invade human colorectal cancer cells.

FadA then turns on cancer growth genes and stimulates inflammatory responses in these cells and promotes tumour formation.

Han and her team also found that FadA levels were much higher in tissues from patients with adenomas and colorectal cancer compared with healthy individuals.

Moreover, they identified a compound that can prevent FadA`s effects on cancer cells.

Aug 16
Drink watermelon juice to ease post-exercise muscle soreness
A new study has found that watermelon juice can help post-exercise muscle soreness.

Encarna Aguayo and colleagues cite past research on watermelon juice`s antioxidant properties and its potential to increase muscle protein and enhance athletic performance.

But scientists had yet to explore the effectiveness of watermelon juice drinks enriched in L-citrulline.

They tested natural watermelon juice, watermelon juice enriched in L-citrulline and a control drink containing no L-citrulline on volunteers an hour before exercise.

Both the natural juice and the enriched juice relieved muscle soreness in the volunteers. L-citrulline in the natural juice (unpasteurized), however, seemed to be more bioavailable - in a form the body could better use, the study found.

The findings have been published in ACS` Journal of Agricultural and Food Chemistry.

Aug 14
Your eyes may be windows to predicting stroke risk
Retinal imaging may someday help assess if you`re more likely to develop a stroke, a new research by an Indian origin author has revealed.

Mohammad Kamran Ikram, M.D., Ph.D., lead author of the study and assistant professor in the Singapore Eye Research Institute, the Department of Ophthalmology and Memory Aging and Cognition Centre, at the National University of Singapore, and his team tracked stroke occurrence for an average 13 years in 2,907 patients with high blood pressure who had not previously experienced a stroke.

At baseline, each had photographs taken of the retina, the light-sensitive layer of cells at the back of the eyeball. Damage to the retinal blood vessels attributed to hypertension evident on the photographs was scored as none, mild or moderate/severe.

During the follow-up, 146 participants experienced a stroke caused by a blood clot and 15 by bleeding in the brain.

Researchers adjusted for several stroke risk factors such as age, sex, race, cholesterol levels, blood sugar, body mass index, smoking and blood pressure readings.

They found the risk of stroke was 35 percent higher in those with mild hypertensive retinopathy and 137 percent higher in those with moderate or severe hypertensive retinopathy.

Even in patients on medication and achieving good blood pressure control, the risk of a blood clot was 96 percent higher in those with mild hypertensive retinopathy and 198 percent higher in those with moderate or severe hypertensive retinopathy.

The study is published in the American Heart Association journal.

Aug 14
Universal dengue vaccine closer to reality
A new strategy has been developed that cripples the ability of the dengue virus to escape the host immune system.

A*STAR`s Singapore Immunology Network (SIgN) made the breakthrough, which has opened the door of hope to what may become the world`s first universal dengue vaccine candidate that can give full protection from all four serotypes of the dreadful virus.

This research done in collaboration with Singapore`s Novartis Institute of Tropical Diseases (NITD) and Beijing Institute of Microbiology and is also supported by Singapore STOP Dengue Translational and Clinical Research (TCR) Programme grant.

Early studies have shown that a sufficiently weakened virus that is still strong enough to generate protective immune response offers the best hope for an effective vaccine.

However, over the years of vaccine development, scientists have learnt that the path to finding a virus of appropriate strength is fraught with challenges. This hurdle is compounded by the complexity of the dengue virus.

Even though there are only four different serotypes, the fairly high rates of mutation means the virus evolve constantly, and this contributes to the great diversity of the dengue viruses circulating globally.

Furthermore, in some cases, the immune response developed following infection by one of the four dengue viruses appears to increase the risk of severe dengue when the same individual is infected with any of the remaining three viruses.

The new strategy uncovered in this study overcomes the prevailing challenges of vaccine development by tackling the virus` ability to `hide` from the host immune system. Dengue virus requires the enzyme called MTase (also known as 2`-O-methyltransferase) to chemically modify its genetic material to escape detection.

In this study, the researchers discovered that by introducing a genetic mutation to deactivate the MTase enzyme of the virus, initial cells infected by the weakened MTase mutant virus is immediately recognised as foreign.

As a result, the desired outcome of a strong protective immune response is triggered yet at the same time the mutant virus hardly has a chance to spread in the host.

Animal models immunised with the weakened MTase mutant virus were fully protected from a challenge with the normal dengue virus. The researchers went on to demonstrate that the MTase mutant dengue virus cannot infect Aedes mosquitoes.

This means that the mutated virus is unable to replicate in the mosquito, and will not be able to spread through mosquitoes into our natural environment. Taken together, the results confirmed that MTase mutant dengue virus is potentially a safe vaccine approach for developing a universal dengue vaccine that protects from all four serotypes.

The team leader, Dr Katja Fink from SIgN said that there is still no clinically approved vaccine or specific treatment available for dengue, so we are very encouraged by the positive results with this novel vaccine strategy.

The findings have been published in the PlosPathogens journal.

Aug 13
Australian scientists discover genes, mutation causing epilepsy
Using advanced gene technology, Australian scientists along with a US team have claimed to have found new genes and genetic mutation that causes severe childhood epilepsies.

Lead researcher Sam Berkovic, Director of the Epilepsy Research Centre at the University of Melbourne and Melbourne`s Austin Hospital, said, as well as providing a pathway to treating epilepsy the research provides answers to patients and families who previously had little or no idea where epilepsy had come from.

"Parents often have a belief that they`ve done something wrong that caused this disease," Berkovic said.

"Not knowing why has been one of the most frustrating things. We`ve never really had the answer. Now we do. This also stops the need for further searching and refines the treatments," he said.

A key aspect of the research has been the ability to sequence the entire human genome, Berkovic said adding "Until now we`ve had these complex patients and we didn`t know what was going on. Now all the genes are known and the jigsaw can be completed," he said.

By using the latest genetic techniques to sequence and analyse DNA of 4,000 epilepsy patients and their relatives, the study known called Epi4Ks shared DNA sequences and patient information among dozens of research institutions.

The researchers compared the exomes, or the complete sets of genes, of 264 children with the sequences of their parents who do not have epilepsy.

Differences in the sequences of parents and children were analysed to identify potential disease-causing mutations.

The study`s other joint leader Dr David Goldstein, the Director of the Human Genome Variation Centre at Duke University Medical Centre in the US, said his team`s work identified an unusually large number of disease-causing mutations and provided a wealth of new information.

"We are now headed toward a future where we can find out why people have this disease and tailor the treatment of it. It establishes a clear path to the genetic explanation of epilepsy," Dr Goldstein said.

Aug 13
Five major psychiatric disorders share common genetic link
Scientists have identified the five psychiatric disorders, bipolar disorder, major depressive disorder, schizophrenia, autism and attention deficit-hyperactivity disorder (ADHD), share a common genetic link.

They showed substantial overlap of genetic risk factors shared between bipolar disorder, major depressive disorder and schizophrenia and less overlap between those conditions and autism and attention deficit-hyperactivity disorder ( ADHD).

They are now moving toward understanding the molecular underpinnings of psychiatric illness.

The findings provide insight into the biological pathways that may predispose an individual to disease and could ultimately lead to the development of new therapeutic avenues to treat the five major psychiatric illnesses.

Study co-senior author Kenneth S. Kendler, M.D., professor of psychiatry, and human and molecular genetics in the Virginia Commonwealth University School of Medicine, and an internationally recognized psychiatric geneticist, said that this is a very large scale study using a new, innovative statistical method.

Kendler asserted that prior to this model, we have not been able to address these questions and their results have given them by far the clearest picture available to date of the degree of genetic similarity between these key psychiatric disorders.

He said that the team is hoping that this will help them both in developing a more scientifically based diagnostic system and understanding the degree of sharing of the biological foundation these illnesses.

The study builds on findings published earlier this year in The Lancet, which reported that specific single nucleotide polymorphisms, or SNPs, are associated with a range of psychiatric disorders that can occur during childhood or adulthood.

The study has been published in Nature Genetics` Advance Online publication.

Aug 12
Genetic birth defects may lead to childhood cancer
Children born with genetic birth defects like Down`s syndrome are at an increased risk of developing childhood cancer, says a study.

Scientists have said that children born with non-chromosomal birth defects have a two-fold higher risk of cancer before age 15, compared to children born without birth defects.
However, cancer risk varies by the specific type of birth defect, and is not significantly increased in many of the more common birth defects, Science Daily reported citing the study published in July in PLOS ONE.

Birth defects are an increasing health concern worldwide, and in 2010 the World Health Organisation identified birth defect prevention and care as a global priority.

"There is a large body of evidence for increased cancer risk in children with Down`s syndrome, a genetic birth defect caused by the presence of an extra copy of chromosome 21," says Lorenzo Botto, professor of paediatrics at the University of Utah School of Medicine and an author of the study.

"However, studies to date have provided inconsistent findings on cancer risk in children with structural birth defects that are not caused by chromosome abnormalities."

Aug 12
Clamping umbilical cord soon after birth could hurt baby`s health
Clamping the umbilical cord too soon after birth could reduce the amount of blood that passes from mother to baby via the placenta, which could affect the baby`s iron stores and birth weight, a new study has found.

The findings of the international review led by La Trobe University are in conflict with the standard practice in many Western countries of clamping and cutting the umbilical cord within a minute of birth.

Published by the Cochrane Collaboration, the new analysis found that newborns that experienced clamping more than a minute after birth had higher haemoglobin levels one to two days later and were also less likely to be iron-deficient three to six months after birth.

Birth weight was also about 90 grams greater with delayed cord clamping, which could provide newborns with an extra 50 to 100 millilitres of blood.

Lead author Susan McDonald from La Trobe University and the Mercy Hospital for Women said that there is much stronger evidence to suggest that delayed cord clamping following a normal-term birth is beneficial.

Aug 10
Gut microbiota fewer in babies born through C-section
Children born through Caesarean section are at greater risk of allergies because they have a less diverse gut microbiota, according to a new study.

Researchers from Sweden and Scotland followed gut microbiota development in 24 children up to the age of two in the Swedish provinces of Ostergotland and Smaland.

Nine were delivered through Caesarean and 15 delivered naturally, through vaginal birth.

The study used a type of molecular biology analysis, which gives a broad overview of the varieties of bacteria present in the intestines.

Children delivered by Caesarean section had a less diverse gut microbiota during their first two years of life than those born vaginally.

Particularly clear was the low diversity among the group Bacteroidetes that, according to earlier observations of the research groups, are particularly linked to protection against allergies.

Thus, these children may run greater risk of developing allergies, but diabetes and irritable bowel syndrome are also more common among children born by Caesarean.

"Sometimes Caesarean sections are necessary. But it is important that both expectant mothers and doctors are aware that such a delivery may affect the child`s health," said Maria Jenmalm, professor of Experimental Allergology at Linkoping University in Sweden and one of the authors of the study.

With natural birth the child is exposed to bacteria in the mother`s birth canal, a good start to the formation of the child`s own gut microbiota.

For those who entered the world through an incision in their mother`s belly, different measures need to be developed, researchers said.

"It might not be so good to have six months of only breast feeding. Earlier exposure to ordinary solid food may stimulate a higher diversity of the gut microbiota," Jenmalm said.

Besides a greater diversity in their intestinal flora, children delivered vaginally in the study also had higher blood plasma levels of substances linked to Th1 cells, a kind of "chief cells" in the immune system, which can inhibit allergic immune responses.

The study was published in the journal Gut.

Aug 10
Junk food craze fuelling diabetes epidemic: Study
A study has blamed the junk food for the diabetes epidemic.

Harmful compounds present in processed red meats like burgers, bacon and sausages could be the cause behind the 132,000 new patients coming up every year, the Daily Express reported.

A review of research by Plymouth University implicated iron in red meat that helped form compounds that attack the immune system and people`s ability to control inflammation that triggers many diseases.

The study has been published in the journal Advances in Nutrition.

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