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A new study found that insomnia is hereditary and may also increase the risk of coronary heart disease.
The study of more than 450,000 people, or 57 genetic sites on our DNA, has identified an increased risk of insomnia.
These genes not only prevent us from sleeping, but also increase our risk of coronary heart disease, which can lead to angina pectoris or even heart failure.
The researchers hope that the discovery of these genes will pave the way for personalized therapies aimed at the "defective" DNA that causes insomnia.
The study was conducted by the Massachusetts General Hospital (MGH) and the University of Exeter. Drs Jacqueline Lane and Recha Saxena participated in the Department of Anesthesiology, Critical Care and Pain.
"Insomnia has a significant impact on millions of people around the world and we have long known that there is a connection between insomnia and chronic diseases.
The genetic sites of the identified DNA included the genes responsible for ubiquitin, an analytic compound found in living cells that play an important role in the analysis of defective and unnecessary proteins.
The genes have been expressed in several regions of the brain, skeletal muscles and the adrenal gland.
The researchers discovered a link between insomnia, leg agitation syndrome and coronary artery disease. This causal link suggests the potential benefits of treating insomnia as a possible treatment for coronary artery disease and depression.
Surprisingly, the identified DNA sites did not include genes known to send signals that interfere with sleep regulation.
Source: Daily Mail.
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