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The Future of Dieting Is Personalized Algorithms Based on Your Gut Bacteria

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Your friend has cut out sugar and feels amazing as a result. Another friend, on the other hand, is on what sometimes appears to be a strict all-candy diet and still stays perfectly healthy and trim. And you have tried both of these dietary tactics and have seen no real changes in your own body.

The same could be said for dairy or carbs — whatever the nutrient may be, you likely know from experience that just because some eating habit works for somebody else, that doesn’t necessarily mean that it’ll work for you. Everyone’s body is different, of course, which means everyone’s body responds to food a little differently. And this, some scientists across the globe are now arguing, points to the potential future of healthy eating. The key to fighting the increasing threat posed by diabetes and obesity may be personalized diets — that is, eating plans tailored specifically for each individual — instead of the generalized nutrition guidelines we have now.

The answer is in your gut — more specifically, the trillions of bacteria currently residing there. Two of the scientists currently studying the interaction between the gut microbiome and diet are Eran Segal and Eran Elinav, the biologists behind the Personalized Nutrition Project in Tel Aviv. Preliminary results from their research, presented earlier this summer at the Human Microbiome conference in Germany, suggest that a computer algorithm can predict how individuals’ bodies will respond to certain foods, thus creating a tailored meal plan for each according to his or her own unique bacterial profile.

This project began more than two years ago and has so far included more than 1,000 people. Segal and Elinav first instructed their participants to wear glucose-monitoring devices, which measured and recorded their levels of blood sugar every five minutes for a week; they also used a mobile app to record what and when they ate that week. Altogether, they collected data on more than 50,000 meals and snacks, plus how each person’s blood-glucose levels responded to each food.

Your gut converts the food you eat into sugars, which are subsequently released into the bloodstream; from there, these sugars are either converted to energy or stored away as fat. Certain foods cause too muchsugar to flow into the bloodstream, and this too-high level of glucose in the blood is what can lead to things like diabetes and obesity. But what foods do this? This is part of the point of nutrition guidelines, to recommend the foods least likely to cause this potentially dangerous spike in blood glucose

But from their data, Segal and Elinav could see that the people in their study were responding to similar foods in wildly different ways. “Already, we could see at a very large scale that, indeed, for any food we looked at, we could see a huge variability in the response,” Segal said. “Some people, you give them sugar and they have a very faint response — even to pure sugar. Whereas others, they have a huge response. And this holds for basically every food that we examined.” And there were more surprises. “Some individuals, they eat whole-wheat rice and their blood-sugar levels remain low, and when they eat ice cream they spike,” Segal said. But for others the results showed just the opposite.

Theirs is not the first study to find an individualized response to similar foods. Studies of twins, for instance, have shown that even people with identical DNA sometimes respond differently to the same diet. And so these results, the researchers argue, suggest “that a universal diet, or universal guidelines, they could never work for everybody, because people are different,” Segal said. “General guidelines are going to have limitations, and they might actually be bad for some people.”

But why might this be the case? Segal and Elinav thought that if they could understand the underlying mechanism that might explain these differences in reactions, they could possibly learn to predict them. Their investigation takes a turn here into the gross: They took stool samples from 800 of their participants, sequencing the genes in each person’s DNA, and used this to complete profiles of the bacterial composition of each individual’s gut. (Basically, they knew that a particular gene is present in a particular type of bacteria, so if they found that gene, it means that bacteria is present, too.) They combined this with the records on their glucose responses to certain foods and used the two data sets to create a computer algorithm, which would create a list of foods that would not trigger that spike in blood-glucose levels.

To investigate the algorithm’s accuracy the researchers started the study that would later be presented at the Human Microbiome conference. They used the algorithm to tailor diets for 25 individuals, all of whom had high enough blood-sugar levels to be considered prediabetic. Some of the foods included on the “approved” list were not exactly the foods you might expect. “For some people it included chocolate, ice cream, pizza — things a dietitian would not prescribe,” Segal said. (Plenty of others didn’t, of course, and stuck to things like whole grains or veggies.) For one week they ate according to their personalized food plan; the following week they ate a diet that was similar in total calories consumed and was in line with more typical dietary guidelines for prediabetics. After the week following their personalized diet, fewer individuals experienced those spikes in blood glucose when compared to their week on the standard diet; some of them even saw their blood-sugar levels dip back down to healthy levels.

It’s an intriguing finding, though very much still a preliminary one. More research needs to be done involving many thousands more people, who are followed for a longer period of time, before anything becomes definitive or clear. And it’s also worth noting that other scientists working on the link between the gut microbiome and diet are skeptical of the notion that this research will eventually lead to eating plans tailored for an individual person. Jens Nielsen, a biochemical engineer at Chalmers University of Technology, believes that it’s more likely that this research will eventually lead to groupings of people, categories of individuals who respond to particular foods in similar ways.

Nielsen is co-author of a study published last month in the journal Cell, which found that people with more diverse populations of gut bacteria are healthier even if they are overweight, when compared to people with less diverse bacterial profiles. Within a decade or so, Nielsen expects that his work may be applicable to weight loss. He’s currently working on the inverse of this problem, investigating the microbiomes of children in developing nations who simply cannot put on weight, even when eating foods expressly designed to help them do so.

And Segal and Elinav expect their work, too, will one day be made available to a wider group of people interested in a personalized meal plan, though, again, the practicalities here are undeniably unpleasant. (Musing on future applications of their work, Segal and Elinav could see a world in which it becomes mainstream to mail stool samples into the lab to get diet advice.) We’re still many years away from that, but the more these researchers look into it, the more individual differences they find, each discovery undermining the idea of blanket nutrition guidelines a little further. “The entire nutritional paradigm we all base our decisions on in our study is proven to be at least partially wrong,” Elinav said. “So we are shifting the paradigm to individuals.”

More from Science of Us:

Your Personality Could Be Making You Fat

15 Ways Your Environment Makes You Eat More (or Less)

Watching Cooking Shows Might Lead to Weight Gain

How Many Steps a Day Should You Really Walk?

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Sensitive Blood Test May Help Rule Out Heart Attack

WEDNESDAY, Oct. 7, 2015 (HealthDay News) — A new, highly sensitive blood test may help doctors quickly rule out heart attack for almost two-thirds of people who seek emergency room treatment for chest pain, a new study suggests.

Researchers said their findings could potentially reduce unnecessary hospital admissions and substantially lower health-care costs.

“Until now, there were no quick ways to rule out a heart attack within the emergency department,” said the study’s lead author, Dr. Anoop Shah, from the University of Edinburgh in Scotland.

“Over the last two decades, the number of hospital admissions due to chest pain has tripled. The overwhelming majority of these patients do not have a heart attack,” Shah said.

Assessing a possible heart attack requires lengthy stays in the ER or hospitalization for repeat testing, the study authors pointed out.

The new test is more sensitive than the standard version, Shah’s team said. It can detect far lower blood levels of troponin, a protein released when heart muscle is damaged. The more damage that occurs, the higher blood levels of troponin will be. A slight increase in troponin suggests some damage has occurred, while very high levels indicate a person has had a heart attack, the researchers explained.

Using this new test, doctors could potentially double the number of low-risk patients able to be safely discharged from the emergency room, the researchers reported in the Oct. 8 issue of The Lancet.

“Use of this approach is likely to have major benefits for both patients and health-care providers,” Shah said in a journal news release.

For the study, the researchers measured troponin levels in more than 6,000 patients admitted to the hospital with chest pain, and assessed their risk for heart attack and death from heart attack within 30 days.

The investigators found that 61 percent of the patients with a troponin level below 5 ng/L (nanograms per liter of blood) were at very low risk of heart attack and could have been discharged early, regardless of age, gender, and risk factors for heart disease. One year out, these patients had a three times lower risk of heart attack and cardiac death than those with higher troponin levels, the researchers said.

The authors of an accompanying editorial in the journal said patient follow-up will be needed to validate use of this test in routine practice.

“Trials are needed to assess the safety and effectiveness of clinical pathways that involve no further testing for such patients,” wrote Martin Than from Christchurch Hospital, New Zealand, and colleagues.

More information

The American Heart Association describes the symptoms of heart attack.





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Here’s How to Prevent Runner’s Diarrhea

Illustration: Aad Goudappel

Illustration: Aad Goudappel

I always have to stop at a bathroom on long runs! How can I avoid it?

You’re not alone. Runner’s diarrhea is a real thing. Though doctors aren’t exactly sure why it happens, food does seem to move more quickly through your colon when you run, which can bring on, well, runs of the digestive kind.

Limiting your fiber intake the day before you have an extra-long sweat session can help (that means going easy on normally good-for-you foods like whole grains and beans). So can avoiding caffeine the day you hit the trail or treadmill and refraining from eating two hours prior. Also, be judicious with energy gels, bars and chews; some people find that these products give them digestive problems. Weirdly enough, dehydration can also lead to diarrhea sometimes, so it’s crucial that you load up on water before and after your run.

Try these dietary tweaks before you resort to taking an over-the-counter antidiarrheal medicine—they’re fine in a pinch, but I don’t recommend using them regularly, since they can cause constipation.

Health’s medical editor, Roshini Rajapaksa, MD, is associate professor of medicine at the NYU School of Medicine and co-founder of Tula Skincare.

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Help Your Child Get a Good Night’s Sleep

WEDNESDAY, Oct. 7, 2015 (HealthDay News) — School-age children need adequate sleep for peak performance.

“Children and teens need significantly more sleep than adults to support their rapid mental and physical development,” said Dr. Clay Stallworth, a pediatrician with Georgia Regents University Health System in Augusta.

“A child’s body and brain are busy during slumber preparing for another day of tasks and growth, so it’s essential that children get the proper amount of sleep,” he said in a university news release.

School-age children should get 10 to 11 hours of sleep, according to the American Academy of Pediatrics.

One way to help kids get enough sleep is to set a regular bedtime schedule and stick with it, even on weekends. It’s also important to create a 15- to 30-minute bedtime routine to help children get ready for sleep. This might include taking a bath, dressing for bed, brushing teeth, reading a story and saying good night, Stallworth said.

Don’t let kids have chocolate, sugary foods or caffeinated beverages late in the day, he recommended. It’s also important to halt TV watching, video games and vigorous play 30 minutes or more before bedtime so that children aren’t overstimulated when it’s time to sleep, he added.

Keep a child’s bedroom dark, quiet and at a comfortable temperature, and encourage your child to fall asleep independently. It’s best to train children to do this when they’re infants, Stallworth advised.

“With a solid routine and a little discipline, you can help your children achieve sweet dreams,” he said. “And chances are, if your kids are getting a good night’s sleep, you probably will, too, and that makes for a healthier family all around.”

More information

The U.S. Centers for Disease Control and Prevention has more about sleep.





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New MS Drug Yields Mixed Results in Study

By Maureen Salamon
HealthDay Reporter

WEDNESDAY, Oct. 7, 2015 (HealthDay News) — Multiple sclerosis patients taking a new drug experienced fewer relapse rates but more side effects than patients receiving a standard MS therapy, new research indicates.

In a trial comparing two sets of more than 900 patients with relapsing-remitting multiple sclerosis, scientists found that those taking the drug daclizumab HYP had a 45 percent lower relapse rate than those taking interferon beta-1a.

But patients on the new drug, which has not yet been approved by the U.S. Food and Drug Administration, saw more side effects. Also, they did not experience significantly slower disease progression than those in the interferon beta-1a group over the first several months.

“This is one more drug for multiple sclerosis, which is of course very welcome, but it’s just one in addition to the 11 or 12 drugs we already have,” said Dr. Eugene Lai, a neurologist at Houston Methodist Hospital in Houston, who was not involved in the research.

“It does reduce the relapse rate, but it probably doesn’t get to the real core of the MS disease process, and we still don’t understand exactly how relapse rate and progression are related,” Lai added. “It’s still not the definitive treatment for MS yet that can stop it.”

The study is published Oct. 8 in the New England Journal of Medicine.

More than 2 million people worldwide are affected by multiple sclerosis, a chronic, disabling condition affecting the brain, spinal cord and optic nerves, according to the National MS Society. Symptoms tend to progress over time and include loss of balance, fatigue, vision loss, paralysis, numbness and tingling in the limbs, and bowel and bladder problems.

In the new study, led by scientists at University Hospital Basel in Switzerland, more than 1,800 patients with relapsing-remitting MS — a type in which symptoms wax and wane over time — were randomly assigned to receive either daclizumab HYP or interferon beta-1a over a period averaging about two years.

Daclizumab is a so-called monoclonal antibody drug and is thought to work by binding to receptors on immune system cells linked to multiple sclerosis and other autoimmune disorders. Interferon beta-1a is a synthetic version of a natural substance produced in the body that fights infections and other threats.

While daclizumab recipients experienced much lower relapse rates than those on interferon beta-1a, disability progression 12 weeks after the study’s start was similar in both groups — 16 percent with daclizumab and 20 percent with interferon beta-1a.

But side effects, including serious infections and skin problems such as rash or eczema, were far more common among daclizumab recipients.

Johns Hopkins Hospital in Baltimore was one of the 244 study sites in 28 countries participating in the trial. Dr. Scott Newsome, director of neurology outpatient services at Hopkins, noted that daclizumab might be an easier regimen for MS patients because it’s injected under the skin only once every four weeks. Interferon beta-1a requires a weekly infusion.

Another benefit, Newsome said, is that disease progression seemed to be slightly slower at the six-month mark and beyond in daclizumab patients.

“In my mind, that’s the outcome measure to look at,” he said. “MS is a marathon, not a 50-yard dash. As a group, we need to have better outcome measures in clinical trials that tell us long-term where a patient will be.”

Lai and Newsome agreed that FDA approval for daclizumab seems likely, at which point a more complete idea of side effects will be available once the drug hits the market.

Newsome, also an assistant professor of neurology at Hopkins, said he wasn’t sure how much daclizumab would cost if it becomes widely available, but it’s likely its price would be far higher than for interferon beta-1a, which has been used for many years to treat MS.

“I think it’s fantastic that we have a number of therapies to treat MS patients, because certainly throughout the years we’re noticing an improvement in patients’ overall quality of life and decreased disability over time,” he said. “But it’s becoming more complicated in terms of which medications we choose first or second, and some of what we decide is not driven by the doctor; often it’s driven by the patient and insurer.”

If daclizumab is FDA approved for use, Lai and Newsome said physicians should be vigilant for side effects.

“I myself will probably wait and let it be on the market for a while to make sure it’s safe before I use it,” Lai said. “We’re encouraged to have so many effective medications for MS, but it’s also kind of confusing to weigh the benefits versus the side effects and risks. It’s important for patients to go to a doctor with more expertise in the treatment of MS to get the most benefit and select the right medication for them.”

More information

The National MS Society offers more on MS medications.





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Rihanna Poignantly Explains Why She Went Back to Chris Brown

Photo: Getty Images

Photo: Getty Images

It’s been more than six years since photos of Rihanna’s bruised, bloodied face were leaked to TMZ, after her then-boyfriend, R&B singer Chris Brown, attacked her. But in a new interview for Vanity Fair’s November issue, the 27-year-old superstar tries to answer the question everyone still wonders: Why did she go back to him?

“I was that girl, that girl who felt that as much pain as this relationship is, maybe some people are built stronger than others,” she said as she reflected on her decision to reunite with Brown, for a second time, three years after the assault. “Maybe I’m one of those people built to handle sh-t like this. Maybe I’m the person who’s almost the guardian angel to this person, to be there when they’re not strong enough, when they’re not understanding the world, when they just need someone to encourage them in a positive way and say the right thing.”

RELATED: 1 in 5 American Men Admits to Violence Against Partner

In other words, she thought she could save him from himself. “I was very protective of him,” she went on to say. “I felt that people didn’t understand him.”

But of course, that’s no foundation for a healthy relationship. The on-again, off-again pair broke up for good in 2013.

As Rihanna explained to Vanity Fair, she ultimately recognized she deserved better: “You realize after a while that in that situation you’re the enemy. You want the best for them, but if you remind them of their failures, or if you remind them of bad moments in their life, or even if you say I’m willing to put up with something, they think less of you—because they know you don’t deserve what they’re going to give. And if you put up with it, maybe you are agreeing that you [deserve] this, and that’s when I finally had to say, ‘Uh-oh, I was stupid thinking I was built for this.’ Sometimes you just have to walk away.”

Rihanna’s story is not unusual. Women return to or stay in abusive relationships for many different reasons, including fear, economic dependence, their children, and yes, even because they love the abuser. And the hope that Rihanna described—her faith that her boyfriend’s behavior would change—is also common.

RELATED: Meet Brooke Axtell, the Domestic Violence Survivor Who Performed With Katy Perry at the Grammys

In a Time article published in the aftermath of the Ray Rice video last year, Craig Malkin, PhD, a clinical psychologist at Harvard Medical School, offered a helpful analogy for this mental barrier: He likened the dysfunctional relationship to an addiction. “The person being abused is focused on the positive and waiting for the next positive. There’s a psychological effect like gambling: the moments of tenderness and intimacy are unpredictable, but they are so intense and fulfilling that the victim winds up staying in the hopes that a moment like that will happen again.”

And as months or years pass, the victim becomes accustomed to the cruelty: “Eventually there’s sort of this wearing down for people on the receiving end of the abuse where they continue to tolerate more and over time feel less entitled to safety,” he added.

Fortunately Rihanna is in a much better place these days—and while she believes in the value of raising awareness about relationship violence (“A lot of women, a lot of young girls, are still going through it,” she said) she told Vanity Fair that she’d prefer not to dwell on her own past. “For me, and anyone who’s been a victim of domestic abuse, nobody wants to even remember it. Nobody even wants to admit it.”

Rihanna has her sights set firmly on the future: Her new and long-awaited album, R8, is due to drop soon. And once her life slows down a bit, she expects “a very extraordinary gentleman, with a lot of patience,” to come along when she least expects it.

RELATED: Watch the Chilling New Domestic Violence Ad You’ll See During the Super Bowl




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Are Exercise Recommendations Really Enough to Protect the Heart?

Photo: Getty Images

Photo: Getty Images

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Being inactive is solidly linked to heart problems like heart attack and stroke, and exercise can help lower risk factors—such as high blood pressure and narrowed blood vessels—that are connected to those heart events.

But when it comes to another type of heart condition, heart failure, the effect of physical activity isn’t as clear. If coronary heart disease can be traced to more physical issues, such as blocked arteries or excessive pressure from blood pumping around the body, heart failure is more of a body-wide problem affecting not just the heart but almost every tissue. In heart failure, the heart gradually loses its ability to effectively pump oxygen-rich blood to the rest of the body, and it can’t keep up with supplying muscles and cells with what they need to function properly. 5.1 million people in U.S. have heart failure.

In the latest study, Jarett Berry, associate professor of medicine and clinical sciences at University of Texas Southwestern Medical Center, and his colleagues studied how exercise can affect risk of heart failure. They report in the journal Circulation on how much physical activity is needed to effectively lower risk of the condition.

Berry and his team analyzed responses from 12 large studies involving 370,460 people who were asked about their exercise habits and followed on average for 13 years. Berry found that those who were the most physically active showed a 30% lower risk of having heart failure than those who exercise the least. These people got more activity than what the government currently recommends, which is 150 minutes of moderate physical activity each week. The people who exercise that much also lowered their risk of heart failure, but not by as much: a 15% to 22% drop.

In fact, people who doubled the recommended level of activity lowered their risk of heart failure by 19% while those who quadrupled the amount of exercise reduced their risk by 35%.

“We didn’t start seeing 30% to 40% reduction in risk until the people were out at three times to four times the recommended amount of exercise,” says Berry. “So higher doses of exercise aren’t a waste of time in preventing heart failure.”

Berry stresses that while the people who exercised more clearly derived more benefit from the activity, any amount of exercise is still helpful. Compared to people who were not active at all, those who followed the recommended 150 minutes of activity a week lowered their risk of heart failure by 10%.

The findings do suggest, however, that exercise advice to lower heart failure may be different from recommendations for reducing heart attacks and stroke. That may be because the two categories of heart problems are caused by different factors. “Heart attacks are caused by blocked arteries in the heart that lead to chest pain and damage heart muscle,” says Berry. “Heart failure is more insidious, and the underlying problems it generates are not nearly as specific.”

High blood pressure and obesity are major drivers of both heart attacks and heart failure. But while heart attacks can be traced to specific obstructions in the heart vessels, heart failure can show up in the form of shortness of breath, kidney failure or swelling in the feet.

While previous studies had hinted at the benefit of exercise for preventing heart failure, and even for helping heart failure patients to recover, there was little data about whether the current recommended amount of exercise—the same 150 minutes per week advised for heart attack prevention—was enough. Heart failure patients often have shortness of breath and can’t exercise much, which can make physical activity challenging. “For a long time, the dogma in cardiovascular medicine was that when people were sick with heart failure, they should have bed rest,” says Berry. “But that commonsensical approach turned out not to be true.”

The study alone won’t be enough to change the recommendations for heart failure patients, and Berry notes that it highlights a possible connection between exercise and heart failure. Further studies in which people are randomly assigned to exercise beyond the recommended amount and at the recommended level need to be done. But it should give doctors more confidence in advising their patients to gradually build up to higher amounts of physical activity if they want to protect themselves from the condition. All of the people in the study were healthy and did not yet have any signs of heart trouble, but given the rising prevalence of heart failure as the population ages, having a possible preventive strategy in the form of exercise may be critical in bringing rates down. Understanding that methods for preventing heart attacks may be different from those for preventing heart failure may also be essential to saving more lives.

This article originally appeared on Time.com.




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Bedtime Texting May Be Hazardous to Teens’ Health

WEDNESDAY, Oct. 7, 2015 (HealthDay News) — Many American teens text in bed, leading to lost sleep, daytime drowsiness and poorer school performance, a new study says.

Researchers from New Jersey looked at nearly 3,200 middle and high school students in the state. They found that nearly 62 percent of the kids used their smartphones in some capacity after bedtime; nearly 57 percent texted, tweeted or messaged in bed; and nearly 21 percent awoke to texts.

“Our study confirms that many teenagers are texting late at night when they should be sleeping. This behavior is more common among older teenagers, especially those in high school, and among girls,” said study co-author Vincent DeBari. He is director of research at the Seton Hall University School of Health and Medical Sciences, in South Orange.

“One of the most worrisome aspects of our findings is that in addition to affecting the quality and amount of sleep teenagers are getting, bedtime smartphone use seems to be having a negative impact on their level of alertness during the day and on their grades in school,” DeBari said in a university news release.

His study co-author, Dr. Peter Polos, added that teens whose sleep is disrupted by incoming texts may feel compelled to respond to those texts immediately. These exchanges can go on for hours.

“This leads to excessive stimulation at night. Light from electronic devices can suppress the secretion of melatonin, a hormone that promotes sleep. All of these factors combine to make sleep difficult in the face of excessive smartphone use at night,” said Polos, a member of the sleep medicine division of the JFK Neuroscience Institute in Edison, N.J.

The researchers also found that smartphone use just before or after bedtime may worsen teens’ tendency to go to bed much later and sleep until late morning. This behavior has been linked with depression, anxiety and attention-deficit hyperactivity disorder, the study authors said.

“Repeatedly, studies have shown that today’s adolescent students are seriously sleep-deprived, and that it affects their health, their mood and their safety behind the wheel. Our study shows that the unrestricted use of smartphones at night may be a major contributing factor,” Dr. Sushanth Bhat, an assistant professor of neuroscience at Seton Hall, said in the news release.

“Since getting the proper amount of sleep is very important for brain development and learning in the teenage years, our study should prompt parents and guardians to consider placing reasonable limitations on adolescent smartphone usage at night,” Bhat concluded.

The study findings appear in the October issue of the Journal of Adolescence.

More information

The National Sleep Foundation has more about teens and sleep.





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Sun Exposure in Teen Years May Delay Onset of MS: Study

By Amy Norton
HealthDay Reporter

WEDNESDAY, Oct. 7, 2015 (HealthDay News) — People with multiple sclerosis tend to develop it later if they had regular sun exposure as teenagers, a new study suggests — adding to evidence linking the disease to a lack of sunlight and vitamin D.

The study found that sun exposure during adolescence seemed to influence the age at which people developed MS: The more summer sun they soaked up, the later their symptoms appeared.

Of nearly 1,200 Danish adults with MS, those who’d spent time in the sun every summer day developed symptoms two years later, on average, versus people who’d gotten less sun.

The findings do not mean that basking in the sun will prevent or treat MS, experts stressed.

But the results do support past research suggesting that vitamin D plays some role in the disease, according to Nicholas LaRocca, vice president of health care delivery and policy research for the National Multiple Sclerosis Society, in New York City.

Sunlight triggers the body’s synthesis of vitamin D, and some studies have linked both sun exposure and higher levels of vitamin D in the blood to a lower risk of multiple sclerosis.

No one knows if that’s a cause-effect relationship. But clinical trials are underway to see whether vitamin D supplements can help slow MS progression, said LaRocca, who was not involved in the current study.

Until those trial results are in, it’s too soon to make any specific vitamin D recommendations, according to LaRocca.

But, he added, since adequate vitamin D is important for overall health, people with MS could talk to their doctors about taking a supplement.

“They may be advised to have their vitamin D level tested first,” LaRocca said.

Multiple sclerosis involves an abnormal immune system attack on the protective sheath surrounding nerve fibers in the brain and spine. That leads to symptoms like muscle weakness, numbness, vision problems and difficulty with balance and coordination.

Typically, MS symptoms flare up periodically, followed by periods of remission. Over time, the disease can cause worsening problems with walking and mobility.

The precise cause of MS is unknown, but research suggests it arises from a combination of genetic vulnerability and certain environmental triggers. Inadequate vitamin D — a nutrient needed for normal immune function — is considered one of the suspects.

The new findings support the theory that “avoiding sunlight” could be one of the triggers for MS, said study lead researcher Dr. Julie Laursen, of the Danish Multiple Sclerosis Center, in Copenhagen, Denmark.

Since sun exposure is closely connected to people’s vitamin D levels, it’s possible that the vitamin explains the later MS onset, Laursen said. However, she stressed, the findings do not “directly” support that.

The researchers found no relationship between MS onset and patients’ reported use of multivitamins or vitamin D as teenagers.

According to Laursen, it’s possible that sunlight, like vitamin D, has its own beneficial effects on the immune system.

In the study, adults with multiple sclerosis were asked about their “summer sun” habits and supplement use during their teens. They were also asked to recall their weight at age 20.

It turned out that MS arose later — at the average age of 33 — among people who’d gotten some sun every day as teenagers. Among people who’d gotten less sun, MS developed at age 31, on average.

People’s weight at age 20 also seemed to matter: Those who’d been overweight developed MS almost two years earlier, on average, than those who’d been at normal weight at 20.

Body fat, Laursen explained, also happens to be related to vitamin D: People who are overweight tend to have lower blood levels of the vitamin.

Again, though, it’s not clear that vitamin D explains the connection between weight and multiple sclerosis, Laursen said.

The study does, however, support the theory that adolescence is a critical time in MS development, according to Laursen. She said more research is needed to see whether there are roles for sun exposure, body weight, vitamin D, or all three.

LaRocca agreed. “It’s a complex picture,” he said.

In the meantime, LaRocca said, people can talk to their doctors about whether a vitamin D supplement is a good idea. They can also get the vitamin through certain foods, he added — including fatty fish, and cereals and dairy products fortified with vitamin D.

The study findings were published online Oct. 7 in the journal Neurology.

More information

The National Multiple Sclerosis Society has more on the possible causes of MS.





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Popular Antioxidant Seems to Spread Skin Cancer Cells in Mouse Research

By Dennis Thompson
HealthDay Reporter

WEDNESDAY, Oct. 7, 2015 (HealthDay News) — A man-made antioxidant appears to accelerate the spread of skin cancer in mice, raising questions about its safety in humans, researchers say.

The antioxidant, N-acetylcysteine, is used to relieve mucus production in patients with chronic obstructive pulmonary disease (COPD), said study senior author Martin Bergo, a professor at the University of Gothenburg in Sweden.

It also is used as a supplement by people who believe that the antioxidant can help reduce exercise-related muscle damage, burn fat and prevent fatigue, Bergo added.

But water laced with N-acetylcysteine appeared to speed up the spread of melanoma, the potentially deadly skin cancer, in lab mice, researchers found.

The antioxidant had no effect on the number and size of tumors, but it enhanced the migration and invasion of these tumors to other parts of the body, the research team reported Oct. 7 in the journal Science Translational Medicine.

N-acetylcysteine was linked to a doubling of the number of lymph-node tumors in mice who drank the laced water, compared to untreated animals, according to the findings.

Previously, the same research team reported that certain antioxidants can spur lung tumor growth in mice.

Antioxidants are believed to protect healthy cells from damage caused by unstable molecules called “free radicals,” according to the U.S. National Institutes of Health (NIH).

However, Bergo believes that antioxidants like N-acetylcysteine also protect cancer cells from free radicals that might otherwise slow their growth or keep them from spreading to other parts of the body.

Other studies have linked high doses of beta-carotene to increased risk of lung cancer in smokers. High doses of vitamin E may increase risk of prostate cancer, the NIH says.

“For people with an increased risk of cancer, this means that taking nutritional supplements containing antioxidants may unintentionally speed up the progression of a small tumor or premalignant lesion, neither of which is possible to detect,” Bergo said.

Bergo said his team decided to focus on N-acetylcysteine because it is a potent antioxidant that dissolves quickly in water, which makes it easy to feed to lab mice.

The researchers also performed follow-up lab tests on human melanoma cells, using N-acetylcysteine and vitamin E. Both antioxidants produced similar results in the human skin cancer cells, increasing their ability to migrate and invade other cells.

The boost provided to skin cancer could come from antioxidants’ protective benefits. But the research team also found that the antioxidants activated a protein that regulates cellular processes and is likely involved in promoting the spread of cancer.

Bergo recommends that people with cancer or at high risk for cancer avoid antioxidant supplements.

“For a patient with newly diagnosed lung cancer or melanoma — and potentially other cancer forms — antioxidants could speed up the progression of the disease,” he said. “There is no conclusive evidence that antioxidant supplementation would be beneficial for these patients, and they should be encouraged to avoid this strategy because the risk of worsening the disease is high.”

Dr. Len Lichtenfeld, deputy chief medical officer for the American Cancer Society, said that while the study results are interesting, “it’s difficult to take this information and directly translate it into recommendations for patients.”

The results of animal studies “don’t necessarily translate into what happens for people,” Lichtenfeld said. “One really has to do the clinical trial in people before you can make conclusions about antioxidants or anything else impacting the course of cancer treatment.”

However, Lichtenfeld said cancer patients should make sure their treatment team knows about all supplements they take, so they can get the best advice possible for their particular situation.

“Patients do need to discuss with their doctors and their oncologists not only what traditional medicines they are taking, but alternative medications and vitamins they are consuming,” he said. “It’s important for the care team to know.”

More information

Harvard T.H. Chan School of Public Health has more about antioxidants.





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