by Playfuls Staff |
13th April 2007

Scientists have identified the most clear genetic link yet
to obesity in the general population as part of a major study of diseases
funded by the Wellcome Trust, the
UK's largest medical research
charity. People [more] with two copies of a particular gene variant have a 70%
higher risk of being obese than those with no copies.
Obesity is a major cause of disease, associated with an
increased risk of type 2 diabetes, heart disease and cancer. It is typically
measured using body mass index (BMI). As a result of reduced physical activity
and increased food consumption, the prevalence of obesity is increasing
worldwide. According to the 2001 Health Survey for England,
over a fifth of males and a similar proportion of females aged 16 and over in England were
classified as obese. Half of men and a third of women were classified as
overweight.
Scientists from the Peninsula
Medical School,
Exeter, and the University of Oxford
first identified a genetic link to obesity through a genome-wide study of 2,000
people with type 2 diabetes and 3,000 controls. This study was part of the
Wellcome Trust Case Control Consortium, one of the biggest projects ever
undertaken to identify the genetic variations that may predispose people to or
protect them from major diseases. Through this genome-wide study, the
researchers identified a strong association between an increase in BMI and a
variation, or "allele", of the gene FTO. Their findings are published
online today in the journal Science.
The researchers then tested a further 37,000 samples for
this gene from Bristol, Dundee and Exeter as well as a number of other regions in the UK and Finland.
The study found that people carrying one copy of the FTO
allele have a 30% increased risk of being obese compared to a person with no
copies. However, a person carrying two copies of the allele has a 70% increased
risk of being obese, being on average 3kg heavier than a similar person with no
copies. Amongst white Europeans, approximately one in six people carry both
copies of the allele.
"As a nation, we are eating more but doing less
exercise, and so the average weight is increasing, but within the population
some people seem to put on more weight than others," explains Professor
Andrew Hattersley from the Peninsula
Medical School.
"Our findings suggest a possible answer to someone who might ask 'I eat
the same and do as much exercise as my friend next door, so why am I fatter?'
There is clearly a component to obesity that is genetic."
The researchers currently do not know why people with copies
of the FTO allele have an increased BMI and rates of obesity.
"Even though we have yet to fully understand the role
played by the FTO gene in obesity, our findings are a source of great
excitement," says Professor Mark McCarthy from the University of Oxford.
"By identifying this genetic link, it should be possible to improve our
understanding of why some people are more obese, with all the associated
implications such as increased risk of diabetes and heart disease. New
scientific insights will hopefully pave the way for us to explore novel ways of
treating this condition."
The FTO gene was first discovered whilst studying the DNA of
a cohort of patients with type 2 diabetes. The risk of developing type 2
diabetes increases significantly for obese people. Through its effect on BMI,
having one copy of the FTO allele increases the risk of developing type 2
diabetes by 25%, having two by 50%.
"We welcome this result, which holds promise for
tackling rising levels of obesity and the associated risk of developing type 2
diabetes," says Professor Simon Howell, Chair of Diabetes UK, which
funded the original collection of samples from people with diabetes. "The
discovery has been possible not only because of exemplary team work of
scientists from a large number of institutions but also because of the
cooperation of the 5,000 diabetes patients and 37,000 people without diabetes
who gave blood samples for the study."