SNPwatch gives you the latest news about research linking various traits and conditions to individual genetic variations. These studies are exciting because they offer a glimpse into how genetics may affect our bodies and health; but in most cases, more work is needed before this research can provide information of value to individuals. For that reason it is important to remember that like all information we provide, the studies we describe in SNPwatch are for research and educational purposes only. SNPwatch is not intended to be a substitute for professional medical advice; you should always seek the advice of your physician or other appropriate healthcare professional with any questions you may have regarding diagnosis, cure, treatment or prevention of any disease or other medical condition.narcolepsy were traced to the lack of a protein called hypocretin. Further research showed that narcoleptics’ brains are missing the cells that produce this important wakefulness-promoting hormone.Scientists didn’t know exactly why the hypocretin-secreting cells were missing in the brains of narcoleptics, but they did have a hunch. More than 90% of people with narcolepsy carry a particular variation in an immune molecule that helps the body distinguish itself from foreign invaders like bacteria and viruses. This led some researchers to suggest that narcolepsy is an autoimmune disease.But 20% of people without narcolepsy also carry the immune molecule variation, indicating that there must be other genetic and/or environmental factors at work. Now a new report, published online yesterday in the journal Nature Genetics, adds more evidence to the autoimmune theory of narcolepsy by showing that variations in another immune-related gene are also associated with this condition that affects about one out of every 2,000 people.In a sample of approximately 1,800 people (about 800 with narcolepsy and 1,000 without), all with European ancestry and all carrying the immune molecule variation found in most narcoleptics, researchers led by Stanford’s Emmanuel Mignot found that variations in the TRA@ gene, which encodes a receptor found on specialized immune cells called T cells, are associated with narcolepsy.The scientists confirmed their findings in a second group of Caucasians, as well as in Asian (Japanese and Korean) and African American samples, although the size of the African American sample was too small for statistically significant data to be gathered.(23andMe customers can get more information on the identified variations at the end of this post.)In a statement, Mignot said that he thinks it is likely that the T cell receptor variations identified in this study and the immune molecule variation previously found in narcoleptics interact to kill hypocretin-secreting cells, but that more research will be needed to understand exactly how this happens. He went on to say that once these interactions are understood, scientists might be able to identify people at risk for narcolepsy and perhaps stop development of the disease.In addition to shedding light on the biology of narcolepsy, the authors of the study think their findings will help researchers studying other autoimmune diseases such as multiple sclerosis and type 1 diabetes.“I’m sure immunologists are going to be very excited. If we can work out what happens specifically in patients with narcolepsy, we’ll be able to better understand the role of T cells in other autoimmune diseases that are more complicated and difficult to detect,” Mignot said in a statement.
- The strongest link with narcolepsy was found with rs1154155, but 23andMe cannot currently provide data for this SNP. Instead, customers can use the Browse Raw Data feature to look at a closely related SNP also described in the paper: Each copy of the G version of rs12587781 increased the odds of narcolepsy by 1.79 times in Europeans and 1.34 times in Asians. The G version of rs12587781 showed a trend towards increased odds of narcolepsy for African Americans, but the results were not statistically significant.