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Researchers have identified a new biochemical pathway that is a major cause of inflammatory bowel disease (IBD) and related disorders that can be addressed with existing medications. An autoimmune disease, such as IBD, which encompasses Crohn’s disease and ulcerative colitis, presently affects approximately 5 per cent of the world’s population and one in every 10 people in the United Kingdom. These diseases are also becoming increasingly widespread, with over half a million individuals in the UK living with IBD by 2022, nearly double the previous prediction of 300,000.

Despite increasing prevalence, current treatments do not work in every patient, and attempts to develop new drugs often fail due to our incomplete understanding of what causes IBD. Researchers done by Francis Crick Institute, in collaboration with UCL and Imperial College London and their findings published in Nature, scientists at the Crick journeyed into a ‘gene desert’ – an area of DNA that doesn’t code for proteins – which has previously been linked to IBD and several other autoimmune diseases. They found that this gene desert contains an ‘enhancer’, a section of DNA that is like a volume dial for nearby genes, able to crank up the amount of proteins they make.



The team discovered that this particular enhancer was only active in macrophages, a type of immune cell known to be important in IBD, and boosted a gene called ETS2, with higher levels correlating with a higher risk of disease. Usin.

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