But rather than focusing on those who succumbed to illness, they looked at an even smaller sub-group who beat the odds and remained healthy.
These people were born with a genetic predisposition towards developing serious and debilitating conditions such as cystic fibrosis, but something in their genomes caused them to still be resistant to the illnesses.
The researchers found 13 individuals who they believed could hold the answer to beating a range of illnesses.
But they were not able to contact the unnamed people because of consent rules signed by the study participants.
Stephen Friend from the Mount Sinai Hospital’s Icahn School of Medicine launched the project in 2014 with a global crowd-sourcing appeal for access to people’s DNA samples.
Ultimately the project was able to gain access to hundreds of thousands of DNA samples, provided voluntarily to testing laboratories by individuals from around the world who had agreed their samples could be used for research.
“Basically all we need is information, we need a swab of DNA and a willingness to say, ‘what’s inside me?’” Friend said in a 2014 TED Talk.
The research is part of a pilot study for what’s been dubbed “The Resilience Project”.
Friend and his team have now launched a follow-up project in which participants will submit their genetic data with the understanding they will be recontacted.
Bob Williamson from the University of Melbourne, the former director of the Murdoch Children’s Research Institute, is pleased researchers are focusing on the healthy, not just the sick.
“We spend all of our time looking at people who are sick and don’t take into account that many people are very healthy indeed,” he said.
“And this is sometimes in spite of the fact that they have a genetic mutation which in many people will cause the disease.”
Williamson said the work promised to create an extraordinary data bank of material for ongoing medical research.
“Cystic fibrosis is a disease that we assumed would be caused by a mutation and there was just no way around it,” he said. “And yet they found people who had the mutations that cause cystic fibrosis, and because of other genes, because of other mutations, they did not develop the disease.
“Now this is really exciting because of the perspective it puts on human genetics.”
Williamson said the information could be used to design new drugs to treat people who do develop diseases like cystic fibrosis.
Read more at Discovery News
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