Scientists have linked 32 genetic variations to Crohn's disease, a bowel disorder, highlighting the complexity of many common diseases and the difficulties facing researchers seeking treatments, according to Reuters. Scientists said on Sunday that new research had tripled the number of genetic regions implicated in Crohn's, the most common form of inflammatory bowel disease, and many more were probably still undiscovered. "These explain only about a fifth of the genetic risk, which implies that there may be hundreds of genes implicated in the disease, each increasing susceptibility by a small amount," said Jeffrey Barrett from the Wellcome Trust Centre for Human Genetics at the University of Oxford, who led the research. Scientists have known for years that genes, along with environmental factors, play a role in increasing the risk that people will develop many common problems like asthma, high blood pressure, rheumatoid arthritis, cancer and heart disease. But they are still trying to work out which parts of the genome -- the 3 billion sub-units of DNA in our cells -- are actually responsible. One way to find out is to conduct genome-wide association studies, in which genetic markers from thousands of volunteers are analysed in order to identify genetic differences between diseased and healthy individuals. The latest picture to emerge for Crohn's, which was reported in the journal Nature Genetics, represents the most complete picture yet assembled of the genetic influences on risk of a common disease. Significantly, three of the individual genes that have been implicated in Crohn's have previously been shown to influence risk of type 1 diabetes and asthma, suggesting a possible common genetic mechanism underlying these disorders. Crohn's disease affects between one in 500 and one in 1000 people in the industrialised world, causing inflammation, pain, ulcers and diarrhoea.
