Researchers who studied 100 twin pairs (dizygotic and monozygotic) have identified a gene mutation that may allow the carrier to function normally on less than six hours of sleep per night. The genetic variant also appears to provide greater resistance to the effects of sleep deprivation. Results show that a participant with p.Tyr362His – a variant of the BHLHE41 gene – had an average nightly sleep duration of only five hours, which was more than one hour shorter than the non-carrier twin, who slept for about six hours and five minutes per night. The twin with the gene mutation also had 40 percent fewer average lapses of performance during 38 hours without sleep and required less recovery sleep afterward – sleeping only eight hours after the period of extended sleep deprivation compared with his twin brother, who slept for 9.5 hours. According to the authors, this is only the second study to link a mutation of the BHLHE41 gene – also known as DEC2 - to short sleep duration. The study provides new insights into the genetic basis of short sleep in humans and the molecular mechanisms involved in setting the duration of sleep that individuals need. “This work provides an important second gene variant associated with sleep deprivation and for the first time shows the role of BHLHE41 in resistance to sleep deprivation in humans,” said lead author Renata Pellegrino, Ph.D., senior research associate in the Center for Applied Genomics at The Children’s Hospital of Philadelphia. “The mutation was associated with resistance to the neurobehavioral effects of sleep deprivation.” Study results are published in the August 1, 2014 issue of the journal Sleep. The study group comprised 100 twin pairs – 59 monozygotic pairs and 41 dizygotic pairs – who were recruited at the University of Pennsylvania.
Login Or Register To Read Full Story