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  #1   ^
Old Wed, Jan-02-13, 08:08
Demi's Avatar
Demi Demi is offline
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Default Revealed: fructose 'may spur overeating'

Quote:
From The Independent
London, UK
2 January, 2012

Revealed: fructose 'may spur overeating'

Scientists have used imaging tests to show for the first time that fructose, a sugar that saturates the American diet, can trigger brain changes that may lead to overeating.

After drinking a fructose beverage, the brain does not register the feeling of being full as it does when simple glucose is consumed, researchers found.

The small study does not prove that fructose or its relative, high-fructose corn syrup, can cause obesity, but experts say it adds evidence that they may play a role.

These sugars are often added to processed foods and beverages and consumption has risen dramatically since the 1970s along with obesity. A third of US children and teens and more than two-thirds of adults are obese or overweight.

All sugars are not equal - even though they contain the same amount of calories - because they are metabolised differently in the body.

Table sugar is sucrose, which is half fructose, half glucose. High-fructose corn syrup is 55% fructose and 45% glucose. Some nutrition experts say this sweetener may pose special risks, but others and the industry reject that claim. And doctors say we eat too much sugar in all forms.

For the study, scientists used magnetic resonance imaging, or MRI, scans to track blood flow in the brain in 20 young, normal-weight people before and after they had drinks containing glucose or fructose in two sessions several weeks apart.

Scans showed that drinking glucose "turns off or suppresses the activity of areas of the brain that are critical for reward and desire for food", said one study leader, Yale University endocrinologist Dr Robert Sherwin. With fructose, "we don't see those changes", he said. "As a result, the desire to eat continues - it isn't turned off."

What is convincing, said Dr Jonathan Purnell, an endocrinologist at Oregon Health & Science University, is that the imaging results mirrored how hungry the people said they felt, as well as what earlier studies found in animals.

"It implies that fructose, at least with regards to promoting food intake and weight gain, is a bad actor compared to glucose," he said. He wrote a commentary that appears with the federally funded study in today's Journal of the American Medical Association.

Researchers now are testing obese people to see if they react the same way to fructose and glucose as the normal-weight people in this study did.

The solution is to cook more at home and limit processed foods containing fructose and high-fructose corn syrup, Dr Purnell said. "Try to avoid the sugar-sweetened beverages. It doesn't mean you can't ever have them," but control their size and how often they are consumed, he said.

A second study in the journal suggests that only severe obesity carries a high death risk - and that a few extra pounds might even provide a survival advantage.

However, independent experts say the methods are too flawed to make those claims.

The study comes from a federal researcher who drew controversy in 2005 with a report that found thin and normal-weight people had a slightly higher risk of death than those who were overweight.

Many experts criticised that work, saying the researcher - Katherine Flegal of the Centres for Disease Control and Prevention - painted a misleading picture by including smokers and people with health problems ranging from cancer to heart disease. Those people tend to weigh less and therefore make pudgy people look healthy by comparison.

Ms Flegal's new analysis bolsters her original one, by assessing nearly 100 other studies covering almost 2.9 million people around the world. She again concludes that very obese people had the highest risk of death but that overweight people had a 6% lower mortality rate than thinner people. She also concludes that mildly obese people had a death risk similar to that of normal-weight people.

Critics again have focused on her methods. This time, she included people too thin to fit what some consider to be normal weight, which could have taken in people emaciated by cancer or other diseases, as well as smokers with elevated risks of heart disease and cancer.

"Some portion of those thin people are actually sick, and sick people tend to die sooner," said Donald Berry, a biostatistician at the University of Texas MD Anderson Cancer Centre in Houston.

The problems created by the study's inclusion of smokers and people with pre-existing illness "cannot be ignored", said Susan Gapstur, vice president of epidemiology for the American Cancer Society.

A third critic, Dr Walter Willett of the Harvard School of Public Health, was blunter: "This is an even greater pile of rubbish" than the 2005 study, he said. Dr Willett and others have done research since the 2005 study that found higher death risks from being overweight or obese.

But Ms Flegal said she used standard categories for weight classes and said statistical adjustments were made for smokers, who were included to give a more real-world sample. She also said study participants were not in hospitals or hospices, making it unlikely that large numbers of sick people skewed the results.
http://www.independent.co.uk/life-s...ng-8434959.html



Quote:
Effects of Fructose vs Glucose on Regional Cerebral Blood Flow in Brain Regions Involved With Appetite and Reward Pathways

Importance Increases in fructose consumption have paralleled the increasing prevalence of obesity, and high-fructose diets are thought to promote weight gain and insulin resistance. Fructose ingestion produces smaller increases in circulating satiety hormones compared with glucose ingestion, and central administration of fructose provokes feeding in rodents, whereas centrally administered glucose promotes satiety.

Objective To study neurophysiological factors that might underlie associations between fructose consumption and weight gain.

Design, Setting, and Participants Twenty healthy adult volunteers underwent 2 magnetic resonance imaging sessions at Yale University in conjunction with fructose or glucose drink ingestion in a blinded, random-order, crossover design.

Main Outcome Measures Relative changes in hypothalamic regional cerebral blood flow (CBF) after glucose or fructose ingestion. Secondary outcomes included whole-brain analyses to explore regional CBF changes, functional connectivity analysis to investigate correlations between the hypothalamus and other brain region responses, and hormone responses to fructose and glucose ingestion.

Results There was a significantly greater reduction in hypothalamic CBF after glucose vs fructose ingestion (−5.45 vs 2.84 mL/g per minute, respectively; mean difference, 8.3 mL/g per minute [95% CI of mean difference, 1.87-14.70]; P = .01). Glucose ingestion (compared with baseline) increased functional connectivity between the hypothalamus and the thalamus and striatum. Fructose increased connectivity between the hypothalamus and thalamus but not the striatum. Regional CBF within the hypothalamus, thalamus, insula, anterior cingulate, and striatum (appetite and reward regions) was reduced after glucose ingestion compared with baseline (P < .05 significance threshold, family-wise error [FWE] whole-brain corrected). In contrast, fructose reduced regional CBF in the thalamus, hippocampus, posterior cingulate cortex, fusiform, and visual cortex (P < .05 significance threshold, FWE whole-brain corrected). In whole-brain voxel-level analyses, there were no significant differences between direct comparisons of fructose vs glucose sessions following correction for multiple comparisons. Fructose vs glucose ingestion resulted in lower peak levels of serum glucose (mean difference, 41.0 mg/dL [95% CI, 27.7-54.5]; P < .001), insulin (mean difference, 49.6 μU/mL [95% CI, 38.2-61.1]; P < .001), and glucagon-like polypeptide 1 (mean difference, 2.1 pmol/L [95% CI, 0.9-3.2]; P = .01).

Conclusion and Relevance In a series of exploratory analyses, consumption of fructose compared with glucose resulted in a distinct pattern of regional CBF and a smaller increase in systemic glucose, insulin, and glucagon-like polypeptide 1 levels.

http://jama.jamanetwork.com/article...ticleid=1555133



Quote:
Fructose Ingestion and Cerebral, Metabolic, and Satiety Responses

Fructose found in sucrose and high-fructose corn syrup, both of which contain roughly equal amounts of glucose, has been the subject of intense debate. Products containing fructose are preferred by consumers and cooks over those containing only glucose, owing to the intrinsically greater sweetness of fructose and its ability to improve the appearance and texture of baked goods. As a result, sucrose and high-fructose corn syrup are added not just to sodas, energy drinks, and sports drinks favored by adolescents and adults but also to juice drinks consumed by infants and toddlers and to snacks, processed meats, sauces, and many other foods consumed by people of all ages.

http://jama.jamanetwork.com/article...ticleid=1555104
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  #2   ^
Old Wed, Jan-02-13, 09:34
Nancy LC's Avatar
Nancy LC Nancy LC is offline
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Default

So...

Case A: Non-caloric sweeteners cause mice to eat more.

Case B: Fructose (i.e. 50% of sugar) causes people to eat more.

I think I'll stick with Case A.
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  #3   ^
Old Thu, Jan-03-13, 00:57
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aj_cohn aj_cohn is offline
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In other news, scientists conclude that rain may get you wet.
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