Health24.com | Just a small glass of a sugary drink a day – even 100% fruit juice – has been linked to an increased risk of cancer

It’s long been known that sugary drinks help people pack on unwanted kilograms. But new research suggests that sweetened sodas, sports drinks and even 100% fruit juice might raise your risk for some cancers.

The study couldn’t prove cause and effect, but it found that drinking as little as three to four ounces (around 90-120ml) of sugary drinks each day was tied to an 18% rise in overall risk for cancer.

Tied to obesity

Among women, a similar consumption level was tied to a 22% rise in breast cancer risk, the French research team found.

A spokesperson for the American Cancer Society (ACS) said the findings should give consumers pause, because obesity is a known risk factor for cancer.

“A lot of the research on sugar-sweetened drinks and cancer has been tied to obesity,” noted Colleen Doyle, managing director of nutrition and physical activity at the ACS. “Across the board, it’s a good idea to reduce any sugar-sweetened beverage,” she advised.

The new study was led by Mathilde Touvier, research director of nutritional epidemiology at the University of Paris. Her team collected data on more than 100 000 French men and women, average age 42, who took part in a national study.

The participants answered questions about how much of 3 300 different foods and beverages they consumed each day, and were followed for up to nine years (from 2009 to 2018).

The study uncovered links between the consumption of sugary drinks and the risk of cancer in general, and for breast cancer specifically. The investigators found no association between sugary drinks and prostate or colon cancers, but the authors stressed that too few people in the study developed these cancers to make this finding definitive.

Why the connection?

The research uncovered no links between diet sodas and other artificially sweetened beverages and cancer, although more study is needed to confirm that, the authors noted.

The connection between sugary drinks and cancer remained the same even after the team adjusted for age, sex, educational level, family history of cancer, smoking and physical activity, the researchers said.

So, why the connection? According to Touvier’s team, high-calorie drinks may raise cancer risk because sugar helps build body fat, in addition to raising blood sugar levels and inflammation – all of which are risk factors for cancer.

It’s also possible that chemicals found in these drinks might play a part in increasing cancer risk, the researchers theorised.

A group representing the beverage industry said sugary drinks can still be a part of the average diet, however.

In a statement, the American Beverage Association said: “It’s important for people to know that all beverages – either with sugar or without – are safe to consume as part of a balanced diet.

America’s leading beverage companies are working together to support consumers’ efforts to reduce the sugar they consume from our beverages by providing more choices with less sugar or zero sugar, smaller package sizes and clear calorie information right up front.”

We should drink more water

Samantha Heller is a senior clinical nutritionist at NYU Langone Medical Center in New York City. She said she wasn’t surprised by the findings.

“Do we really need more evidence that consuming sugar-sweetened beverages regularly is not healthy?” Heller said. She noted that, for decades, these drinks have been linked with diseases such as obesity, type 2 diabetes and heart disease.

On the other hand, “most of us should be drinking more water than we do,” Heller said. “Being poorly hydrated can affect us in surprising ways. It can impair our driving skills, cognitive abilities, mood, energy levels, kidneys, gastrointestinal function, appearance and more.”

Study author Touvier agreed.

“The only beverage that is recommended is water,” she said. And Touvier supports public efforts to get people away from the soda-and-juices habit.

Water doesn’t have to be boring

Her team’s findings support “existing nutritional recommendations to limit sugary drinks consumption, including 100% fruit juices, as well as policy actions such as taxation and marketing restrictions targeting sugary drinks,” Touvier said.

And water doesn’t have to be boring, Heller added.

“Play around with infusing water with mint, basil, cucumber, or strawberry and lemon slices. Fill a pitcher with water and pop in your favorite herbal teas like berry, vanilla or peppermint, and chill in the refrigerator,” she suggested.

The new report was published online in the BMJ.

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Health24.com | Lungs, hearts infected with hepatitis C can still be transplanted

Patients in dire need of an organ transplant can safely receive a new heart or lung from donors who have hepatitis C, a new clinical trial has shown.

By swiftly administering powerful antiviral drugs, doctors can prevent the organ recipient from contracting hepatitis C following their transplant, said lead researcher Dr Ann Woolley. She’s an infectious disease doctor with Brigham and Women’s Hospital in Boston.

Increase in available organs

None of the first 35 transplant patients enrolled in the trial programme have any detectable levels of hepatitis C virus in their bloodstream after at least six months, Woolley said. Additionally, she said all of their new organs are in fine working order.

The breakthrough strategy could increase the number of potential organs available to patients by 20% to 25%, Woolley said.

“We saw in our centre alone that of all the transplants we’ve done in the past two years, over a third of them have been from hepatitis C-positive donors,” Woolley said.

Although the number of organ transplants in the United States has increased by 20% over the past five years, it’s estimated that about 1 000 people die annually waiting for a new heart or lung, the researchers said in background notes.

Organs typically are washed out as much as possible before transplant, but there’s always a microscopic amount of donor blood within them, Woolley said. Within that blood lies the risk of hepatitis C infection.

“The virus doesn’t come in the organ itself. It’s not in the heart or in the lung. It comes with the blood from the donor within the organ,” Woolley explained.

Blocking viral replication

More than four out of five people who received organs in the past from hepatitis C-positive donors wound up with a chronic infection themselves, researchers said in background notes. This not only threatened the health of their livers, but in some cases damaged their new organ.

The new transplant protocol calls for recipients to receive hepatitis C antivirals starting a few hours after leaving the operating room, Woolley said. Rather than wait for the patient to develop an infection, doctors instead head hep C off at the pass.

“It blocks the viral replication from occurring,” Woolley said. “The virus needs time to get to the liver to set up shop and replicate there. By starting treatment right away, all the recipient is exposed to is a very low level of virus from the donor.”

Since the recipients are exposed to only a tiny amount of virus, they don’t have to undergo a full 12-week regimen of antivirals like people who’ve had chronic hepatitis C for months or years, Woolley said.

Instead, people who get a hep C-positive organ only have to take a four-week course of antivirals costing about $25 000 (R350 000), Woolley said.

The report, published online in the New England Journal of Medicine, said that 44 patients were initially enrolled in the study, including eight people who received new hearts and 36 who received new lungs.

New standard for transplants

But given the study’s success, enrolment has continued and a total of 69 people have received hepatitis C-positive organs to date.

About 42 of the initial 44 patients in the programme had a detectable hepatitis C viral load immediately following transplant, but the amount of virus declined to the point of being undetectable within about two weeks, the report said.

Woolley believes that this could become a new standard for transplants, particularly if the heavy cost of antiviral drugs continues to decrease the longer they are on the market.

Dr Emily Blumberg, director of transplant infectious diseases at Penn Medicine, said the new protocol “has the potential to be a big advance, because currently there is a pretty sizeable number of individuals who have hepatitis C who are potential organ donors.”

The drug regimen was not associated with any toxic effects, but doctors will have to be careful to track potential drug interactions, Blumberg said. For example, the antivirals can have interactions with statins and with certain heart medications.

‘Real’ access to drugs

“Most of the drug interactions are manageable, and we think the sooner you can start the medication, the better the potential for clearing the infection faster,” said Blumberg, who wrote an editorial accompanying the study.

Doctors will need to keep tracking the progress of these patients to show that the safety of the process is long-term, she said.

The next step to making this standard care is to make sure that insurance companies will cover the cost of the antiviral treatment, Blumberg said.

“We need to be able to assure patients they will have real access to the drugs,” Blumberg said. “Some companies are committed to providing the treatment, and some are not.”

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Health24.com | Brain scans spot, track Alzheimer’s

Brain scans can improve diagnosis and management of Alzheimer’s disease, a new study claims.

Researchers assessed the use of PET scans to identify Alzheimer’s-related amyloid plaques in the brain. The study included more than 11 000 Medicare beneficiaries with mild thinking impairment or dementia of uncertain cause.

Better medical management

This scanning technique changed the diagnosis of the cause of mental impairment in more than one-third of the participants in the study.

The brain scan results also changed management – including the use of medications and counselling – in nearly two-thirds of cases, according to the study published in the Journal of the American Medical Association.

“These results present highly credible, large-scale evidence that amyloid PET imaging can be a powerful tool to improve the accuracy of Alzheimer’s diagnosis and lead to better medical management, especially in difficult-to-diagnose cases,” said study co-author Maria Carrillo, chief science officer of the Alzheimer’s Association.

“It is important that amyloid PET imaging be more broadly accessible to those who need it,” she added in an association news release.

Funding for the study came from Avid Radiopharmaceuticals Inc., General Electric Healthcare, and Life Molecular Imaging.

No cure for Alzheimer’s

“We are impressed by the magnitude of these results, which make it clear that amyloid PET imaging can have a major impact on how we diagnose and care for patients with Alzheimer’s disease and other forms of cognitive decline,” said lead author Dr Gil Rabinovici. He’s a professor of neurology at the Memory and Aging Center at the University of California, San Francisco.

There is no cure for Alzheimer’s disease, but early diagnosis means that patients can receive treatment to manage symptoms and be directed to clinical trials for new drugs.

Early diagnosis also means that patients and families can plan for the future, including safety, care, legal and financial issues, and access resources and support programmes, the researchers said.

In this study, the PET scans revealed that about one-third of patients previously diagnosed with Alzheimer’s had no significant amyloid build-up, and their Alzheimer’s diagnosis was reversed.

Accurate diagnoses critical

But in nearly half of patients not previously diagnosed with Alzheimer’s, the PET scans revealed significant amyloid plaque build-up, resulting in a new diagnosis of Alzheimer’s.

One-third of the study participants who had previously been referred to Alzheimer’s clinical trials showed no sign of amyloid build-up based on PET scans. Based on those results, doctors were able to ensure that nearly all (93%) of patients referred to Alzheimer’s trials were amyloid-positive, which is critical to these trials’ success.

“Accurate diagnoses are critical to ensure patients are receiving the most appropriate treatments. In particular, Alzheimer’s medications can worsen cognitive decline in people with other brain diseases,” Rabinovici said.

“But perhaps more fundamentally, people who come into the clinic with concerns about memory problems want answers. An early, definitive diagnosis may allow individuals to be part of planning for the next phase of their lives and to make decisions that otherwise would eventually need to be made by others,” he said.

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East of England 999 software risks missing sepsis

The East of England Ambulance Service says it is working to improve diagnoses by call handlers.

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Babies ‘don’t need tongue-tie surgery to feed’

Babies with tongue-ties rarely need surgery to help them feed, a US study suggests.

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Good gut bacteria ‘helps starving children’

A diet of bananas and peanuts boosted key gut microbes in Bangladeshi children, a study found.

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No evidence of added benefit for most new drugs entering German healthcare system

More than half of new drugs entering the German healthcare system have not been shown to add benefit, argue researchers in The BMJ today.

Beate Wieseler and colleagues at the German health technology assessment agency IQWiG (Institute for Quality and Efficiency in Health Care) say that international drug development processes and policies are responsible and must be reformed.

Between 2011 and 2017, IQWiG assessed 216 drugs entering the German market following regulatory approval, they explain. Almost all of these drugs were approved by the European Medicines Agency for use throughout Europe.

Yet only 54 (25%) were judged to have a considerable or major added benefit. In 35 (16%), the added benefit was either minor or could not be quantified. And for 125 drugs (58%), the available evidence did not prove an added benefit over standard care in the approved patient population.

The situation is particularly shocking in some specialties, they add. For example, in psychiatry/neurology and diabetes, added benefit was shown in just 6% (1/18) and 17% (4/24) of assessments, respectively.

Some people have argued that limited information at the time of regulatory approval (and thus widespread use by patients) is the price to be paid for early access to innovative drugs, explain the authors.

The reality, however, looks quite different. For instance, an evaluation of cancer drugs approved by the EMA between 2009 and 2013 showed that most had been approved with no evidence of clinically meaningful benefit on patient relevant outcomes (survival and quality of life), and several years later little had changed.

What’s more, postmarketing studies often do not happen and globally, regulators do little to sanction non-compliant companies, they write.

Evidence also suggests that many of the investigated drugs add benefit only in subgroups of patients. “For the overall patient population, the current output of drug development may thus be resulting in even less progress than our assessments suggest,” argue the authors.

Clinicians and patients deserve impartial and complete information on what to expect from a certain treatment, including information on the benefit of alternative treatments or no treatment, write the authors. But given the current information gaps this is not possible.

“As a consequence, patients’ ability to make informed treatment decisions consonant with their preferences might be compromised, and any healthcare system hoping to call itself ‘patient centred’ is falling short of its ethical obligations.”

They believe that regulators should become far less tolerant of shortened drug development programmes, and instead should demand robust evidence from longer term and sufficiently large randomised controlled trials to prove efficacy and safety, which in parallel could be used to collect data for health technology assessment.

Information gaps could be closed further by a mandatory requirement to conduct active controlled trials, they add. While reimbursement and pricing decisions “should avoid incentivising marginal outcomes for patients or outcomes based on highly uncertain evidence, but rather reward the achievement of relevant outcomes.”

In the longer term, health policy makers need to take a more proactive approach, they write. “Rather than waiting for drug companies to decide what to develop, they could define the health system’s needs and implement measures to ensure the development of the treatments required.”

They conclude: “Combined action at EU and national levels is required to define public health goals and to revise the legal and regulatory framework, including introducing new drug development models, to meet these goals and focus on what should be the main priority in healthcare: the needs of patients.”

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Strange warping geometry helps to push scientific boundaries

Atomic interactions in everyday solids and liquids are so complex that some of these materials’ properties continue to elude physicists’ understanding. Solving the problems mathematically is beyond the capabilities of modern computers, so scientists at Princeton University have turned to an unusual branch of geometry instead.

Researchers led by Andrew Houck, a professor of electrical engineering, have built an electronic array on a microchip that simulates particle interactions in a hyperbolic plane, a geometric surface in which space curves away from itself at every point. A hyperbolic plane is difficult to envision — the artist M.C. Escher used hyperbolic geometry in many of his mind-bending pieces — but is perfect for answering questions about particle interactions and other challenging mathematical questions.

The research team used superconducting circuits to create a lattice that functions as a hyperbolic space. When the researchers introduce photons into the lattice, they can answer a wide range of difficult questions by observing the photons’ interactions in simulated hyperbolic space.

“You can throw particles together, turn on a very controlled amount of interaction between them, and see the complexity emerge,” said Houck, who was the senior author of the paper published July 4 in the journal Nature.

Alicia Kollár, a postdoctoral research associate at the Princeton Center for Complex Materials and the study’s lead author, said the goal is to allow researchers to address complex questions about quantum interactions, which govern the behavior of atomic and subatomic particles.

“The problem is that if you want to study a very complicated quantum mechanical material, then that computer modeling is very difficult. We’re trying to implement a model at the hardware level so that nature does the hard part of the computation for you,” said Kollár.

The centimeter-sized chip is etched with a circuit of superconducting resonators that provide paths for microwave photons to move and interact. The resonators on the chip are arranged in a lattice pattern of heptagons, or seven-sided polygons. The structure exists on a flat plane, but simulates the unusual geometry of a hyperbolic plane.

“In normal 3-D space, a hyperbolic surface doesn’t exist,” said Houck. “This material allows us to start to think about mixing quantum mechanics and curved space in a lab setting.”

Trying to force a three-dimensional sphere onto a two-dimensional plane reveals that space on a spherical plane is smaller than on a flat plane. This is why the shapes of countries appear stretched out when drawn on a flat map of the spherical Earth. In contrast, a hyperbolic plane would need to be compressed in order to fit onto a flat plane.

“It’s a space that you can mathematically write down, but it’s very difficult to visualize because it’s too big to fit in our space,” explained Kollár.

To simulate the effect of compressing hyperbolic space onto a flat surface, the researchers used a special type of resonator called a coplanar waveguide resonator. When microwave photons pass through this resonator, they behave in the same way whether their path is straight or meandering. The meandering structure of the resonators offers flexibility to “squish and scrunch” the sides of the heptagons to create a flat tiling pattern, said Kollár.

Looking at the chip’s central heptagon is akin to looking through a fisheye camera lens, in which objects at the edge of the field of view appear smaller than in the center — the heptagons look smaller the farther they are from the center. This arrangement allows microwave photons that move through the resonator circuit to behave like particles in a hyperbolic space.

The chip’s ability to simulate curved space could enable new investigations in quantum mechanics, including properties of energy and matter in the warped space-time around black holes. The material could also be useful for understanding complex webs of relationships in mathematical graph theory and communication networks. Kollár noted that this research could eventually aid the design of new materials.

But first, Kollár and her colleagues will need to further develop the photonic material, both by continuing to examine its mathematical basis and by introducing elements that enable photons in the circuit to interact.

“By themselves, microwave photons don’t interact with each other — they pass right through,” said Kollár. Most applications of the material would require “doing something to make it so that they can tell there’s another photon there.”

This research was supported by the National Science Foundation, including the Division of Materials Research and the Multidisciplinary University Research Initiatives program.

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New alternate cell growth pathway could lead to better treatments for metastatic cancers

While researchers have a basic understanding of how primary cancer cells grow, less is known about metastasis, the deadly process by which cancers spread. A team led by Dr. Paul Krebsbach, dean of UCLA’s School of Dentistry and professor of periodontics, has found that mEAK-7, a gene they discovered last year, may play a significant role in cancer metastasis, at least in lung cancers.

Building on that earlier gene discovery in human cells, the team compared mEAK-7 expression levels in normal and cancer cells using tumor cell genetic information from several databases as well as tissue samples from cancer patients.

“By focusing on non-small cell lung cancer, we found that mEAK-7, which is important for cell proliferation and migration, was highly expressed in metastatic non-small cell lung cancer,” said Dr. Joe Nguyen, first author and postdoctoral scholar at the National Cancer Institute. “We also discovered that mEAK-7 was expressed in primary cancer cells but not expressed in non-cancerous cells, which shows that the protein could be a key culprit in cancer metastasis.”

The research was published in the journal iScience.

The researchers also found that mEAK-7, when combined with a large molecule called DNA-PKcs (which helps regulate DNA repair and controls or enhances cancer growth), created an alternative mTOR signaling pathway used by cancer cells for their growth and proliferation. In normal cells, two well-studied pathways are controlled by a gene called mTOR, which regulates normal cell growth, proliferation and survival.

“This third complex or pathway is very important for cancer stem cells, which begin the process of colony formation and cell proliferation, and lead to metastasis that is the leading cause of death in most cancers,” Krebsbach said. “We determined that there are high mEAK-7 protein levels in the tumors and lymph nodes of metastatic cancer patients. Development of mEAK-7 inhibitors may benefit patients with metastatic cancers that demonstrate aberrant mTOR signaling associated with high levels of mEAK-7.”

The researchers, who also looked at these signaling molecules in cancer stem cells, determined that the novel, “third” mTOR complex in cancer cells was made up of mTOR, mEAK-7 and DNA-PKcs.

“Understanding the molecular interactions of metastatic cancer is crucial to determining treatments for cancer at these later stages,” said Jin Koo Kim, co-author and a UCLA Dentistry project scientist. “Currently, treatments for solid tumors include surgery and radiation therapies. However, many patients relapse, as the target tumors develop resistance to radiation and other treatments. This study found that this resistance is correlated to higher mEAK-7 expression in cancer cells.”

Additional study authors are Fatima Haidar, Alexandra Fox, Connor Ray and Daniela Mendonça, all from the University of Michigan.

The study was supported in part by the National Institute of Dental and Craniofacial Research, and the Stuart and Barbara Padnos Research Award from the Rogel Cancer Center at the University of Michigan. The authors have no competing interests to declare.

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