Restless legs syndrome tied to 140 'hotspots' in the genome

Researchers have uncovered more than 140 sections of the human genome tied to restless legs syndrome (RLS), a neurological condition that affects up to 10% of the U.S. population. 

These stretches of DNA in the genome are known as genetic risk loci, and prior to the new study, only 22 were known to be tied to RLS. The new research, published Wednesday (June 5) in the journal Nature Genetics, increases that number to 164. 

Three of the newfound risk loci are located on the X chromosome, which females typically carry two of in each cell while males carry only one. RLS is more common among women than men, but based on their new results, the researchers don't think this difference is explained by the trio of risk loci on the X chromosome. 

"This study is the largest of its kind into this common — but poorly understood — condition," Steven Bell, co-senior study author and an epidemiologist at the University of Cambridge, said in a statement. "By understanding the genetic basis of restless legs syndrome, we hope to find better ways to manage and treat it, potentially improving the lives of many millions of people affected worldwide."

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This discovery could also be used to help predict a person's risk of developing RLS, the study authors wrote in their paper. 

RLS, also called Willis-Ekbom disease, causes people to experience an unpleasant crawling or creeping sensation in their legs, as well as the irresistible urge to move them. These sensations are often more intense in the evening or at night, while people are resting. The condition is thought to be underdiagnosed, and when it is diagnosed, its exact cause is often unknown. RLS can arise due to another condition, such as iron deficiency, kidney disease or Parkinson's, and it's likely tied to dysfunction in part of the brain that uses dopamine to control movement.