In the case of irritable bowel disease, inflammation may be primed by microbes in the intestine that trigger epigenetics and make people prone to disease.
A new epigenetic signature identified in patient cells appears to predict inflammation risk in a serious type of irritable bowel disease called Crohn's disease. The findings of the study are published in JCI Insights. With an estimated //1.6 million people in the U.S. dealing with inflammatory bowel disease (IBD), physicians can have a hard time telling which newly diagnosed patients have a high risk of severe inflammation or what therapies will be most effective.
‘The microbiome triggers epigenetic change that could make some individuals more prone to intestinal inflammation. ’
Epigenetics is the study of external modifications to DNA and associated proteins that results in genes being switched "on" or "off" in cells. The study was performed in intestinal epithelial cells donated by newly diagnosed IBD patients prior to treatment and in laboratory mouse models. The work provides additional insight about the importance of the body's microbiota--the collection of all the microbes (bacteria, fungi, and viruses) that live in our intestines. Increasing evidence has shown important links between the intestinal microbiota and chronic inflammatory diseases.
"Each person's microbiome is driven by genetics as well as external environmental factors, such as food, where we live, pets, mom's microbiome, etc."
Conducted by a multi-disciplinary research team of scientists and physicians, the basic science and translational data in the study could lead to development of new diagnostics. This includes methods to predict which newly diagnosed patients are at higher risk of severe disease. It also could provide clues to better therapeutic treatments for IBD.
Histone Methylation
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Further analysis of cells showed that changes to histone methylation affected genes involved in immune regulation, metabolism, cell survival and cell signaling. A substantial portion of the genes exhibited levels of histone methylation associated with the severity of inflammation in IBD.
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Alenghat said additional research is needed to understand more about how these pathways work during the onset of IBD. Future research efforts will involve work in mouse models of IBD, patient samples and human intestinal organoids--miniature human tissues generated in a laboratory using stem cells derived from patient cells. These steps should allow researchers to uncover the different biological processes that drive this epigenetic signature.
Source-Eurekalert