Obese people who claim they have a “slow metabolism” may have a point after scientists discover a gene that for the first time links being overweight with reduced metabolic activity.

Researchers from Cambridge University found that mutations in a gene known as KSR2 reduce the ability of cells to metabolise glucose and fatty acids, which provide energy.

These gene mutations are also more common in people with severe obesity than in the general, non-obese population, they found.

It has long been suggested that some people may be predisposed to obesity because of a “slow metabolism” but this is the first time that scientists have been able to identify a definite genetic basis for such an idea.
“It was something that most of us didn’t quite believe could happen because there wasn’t much evidence for it until now,” said Professor Sadaf Farooqi of the University of Cambridge. “Up until now, the genes we have identified that
control body weight have largely affected appetite.

This gene also increases appetite but it is also causes a slow metabolic rate,” Professor Farooqi said.

“KSR2 is different in that it also plays a role in regulating how energy is used in the body. In the future, modulation of KSR2 may represent a useful therapeutic strategy for obesity and type-2 diabetes,” she said.

Working with Ines Barroso of the Wellcome Trust Sanger Institute near Cambridge, Professor Farooqi sequenced the DNA from over 2,000 patients with severe, early onset obesity, and found that about 2 per cent of them had multiple mutations in the KSR2 gene – more than twice the rate found in non-obese people.

The study, published in the journal Cell, follows earlier work on mice that established the link between the gene and obesity. Mice that lacked the gene became severely overweight.

The KSR2 gene is responsible for some of the “scaffolding” proteins of the cell which play a crucial role in ensuring that signals from hormones such as
insulin are correctly processed in the body to regulate how cells grow, divide and use energy.

The scientists found that patients with mutations in the KSR2 gene reported that they had an increased drive to eat when they were children but also a
reduced metabolic rate, which meant they were unable to burn off all they energy they consumed.

Low metabolic rate is often linked with an underactive thyroid gland, but in these people their thyroid levels were within normal range, which meant that their metabolic deficit was caused by
something else, such as defected KSR2 genes.
“This work adds to a growing body of evidence that genes play a major role in influencing a person’s weight and may be useful for developing new ways to treat people who are heavy and develop
diabetes,” Professor Farooqi said.

A study published earlier this year by the same scientists found that children with the most severe kinds of obesity are more likely than other children to have one or more of four genetic variations in their DNA which could influence appetite and food
metabolism.

Elliotwiz1: hmmm, interesting, if a gene can cause obesity then It's possible another one can make someone slim: now i know why no matter the quantity of food i take, i never grow fat.... Scientist should look for a way to artificially induce the action of that gene .... I need it

adconline: Another science " amour" to gluttons and chop till I die folks

collins123: I believe in God.

Science rocks too.

I'm trying to find a correllation for both.

mc~evans:



Same things applies to me. I never grow fat no matter the quantity of food I take.

peacettw:

Like I said, environmental factors plays a huge role as well, or how do you explain the likes of struggling artists who go from been frail and thin to huge and obese almost overnight just cos they have hit it big.

Again, I am a big believer that if one can control the environmental factors, the genetic influence will be kept in check cos let us face it, fat is only formed from excess glucose and proteins all gotten from our diet and lack of active lifestyle. Remove that, and the body will have nothing to work with.