Researchers have struggled for years to understand how mutations in one gene, called LRRK2, can increase the risk of three very different diseases: Parkinson’s (a brain disease), Crohn’s (a gut disease) and leprosy (a peripheral nervous system disease).
Researchers have struggled for years to understand how mutations in one gene, called LRRK2, can increase the risk of three very different diseases: Parkinson’s (a brain disease), Crohn’s (a gut disease) and leprosy (a peripheral nervous system disease). Now, a Canadian team has found that inflammation is the likely culprit. Their results are published in Science Translational Medicine.
Inflammation, which is associated with swelling, redness, heat and pain, is the body’s first defense against viruses, bacteria and injuries. But when inflammation is too strong or lasts too long, it can cause collateral damage to the body.
“Everyone thought that LRRK2’s primary role was in the brain, because of its association with Parkinson’s disease. But our research shows for the first time that its primary role is probably in the immune system,” said senior author Dr. Michael Schlossmacher, Bhargava Family Research Chair in Neurodegeneration, Director of Neuroscience and a neurologist at The Ottawa Hospital, and professor at the University of Ottawa Brain and Mind Research Institute.
Read more at: The Ottawa Hospital
Increased inflammation may explain the link between Parkinson's, Crohn's and leprosy. Seven research teams from five Canadian institutions contributed to the discovery. Team members from the Schlossmacher Lab include (clockwise from top left) Dr. Michael Schlossmacher, Dr. Bojan Shutinoski, Quinton Hake-Volling, Dr. Julianna Tomlinson and Nathalie Lengacher. (Photo Credit: The Ottawa Hospital)
