A research team has successfully helped children with Prader-Willi Syndrome, a kind of hereditary obesity, lose weight by improving the bacterial flora in their gastrointestinal tract.

 

Prader-Willi Syndrome is a complex genetic disease that is caused by the absence of some genes that function in a particular part of chromosome 15.

 

Children with PWS are called "angels who never get the sense of being full", because they develop an insatiable appetite when entering into childhood, which leads to chronic overeating and obesity, then on to bulimia. The disease is rare, but deadly.

 

How to help children with PWS control their weight has long been a problem worldwide. At present, the major clinical treatment methods for PWS include the use of drugs to suppress appetite, gastrointestinal surgery or a long-term low calorie diet.

 

"Appetite suppressants usually don't produce much significant effect, while gastrointestinal surgery often comes with higher risk," said Professor Zhao Liping from Shanghai Jiao Tong University, who led the research.

 

In Zhao's clinical trials, the foods best suited to help the children were primarily carbohydrates, such as whole grains, and other foods with probiotics.

 

After 12 weeks' nutritional intervention, without extra exercise, hunger in the children with PWS had been alleviated and their bulimia was well controlled.

 

Among these volunteers, one child's weight had dropped to 73 kg from 140 kg after 430 days' treatment. The child's weight has since stabilized, no longer steadily increasing as it did before the treatment. 

Name

Email

Title

Comment

smaller | bigger

Subscribe via email (Registered users only)

I have read and agree to the Terms of Usage.

Write the displayed characters

Add Comment