News / Science News

    Researchers identify genetic variations linked to oxygen drops during sleep

    Researchers have identified 57 genetic variations of a gene strongly associated with declines in blood oxygen levels during sleep. Low oxygen levels during sleep are a clinical indicator of the severity of sleep apnea, a disorder that increases the risk of heart disease, dementia, and death.



    Researchers identify genetic variations linked to oxygen drops during sleep. Photo: Zohre Nemati/Unsplash


    “A person’s average blood oxygen levels during sleep are hereditary, and relatively easy to measure,” said study author Susan Redline, M.D., senior physician in the Division of Sleep and Circadian Disorders at Brigham and Women’s Hospital, and professor at Harvard Medical School, Boston. “Studying the genetic basis of this trait can help explain why some people are more susceptible to sleep disordered breathing and its related morbidities.”

    When we sleep, the oxygen level in our blood drops, due to interruptions in breathing. Lung and sleep disorders tend to decrease those levels further, and dangerously so. But the range of those levels during sleep varies widely between individuals and, researchers suspect, is greatly influenced by genetics.

    Despite the key role blood oxygen levels play in health outcomes, the influence of genetics on their variability remains understudied.

    The current findings contribute to a better understanding, particularly because researchers looked at overnight measurements of oxygen levels. Those provide more variability than daytime levels due to the stresses associated with disordered breathing occurring during sleep.

    The newly identified 57 variants of the DLC1 gene were clearly associated with the fluctuation in oxygen levels during sleep. In fact, they explained almost 1% of the variability in the oxygen levels in European Americans, which is relatively high for complex genetic phenotypes, or traits, that are influenced by myriad variants.

    Notably, 51 of the 57 genetic variants influence and regulate human lung fibroblast cells, a type of cell producing scar tissue in the lungs.

    This is important because Mendelian Randomization analysis, a statistical approach for testing causal relationship between an exposure and an outcome, shows a potential causal relationship between how the DLC1 gene modifies fibroblasts cells and the changes in oxygen levels during sleep.

    This relationship suggests that a shared molecular pathway, or a common mechanism, may be influencing a person’s susceptibility to the lack of oxygen caused by sleep disordered breathing and other lung illnesses such as emphysema. (National Institutes of Health)

    OCTOBER 27, 2019



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