An important scientific evolution puts an end to the mystery around chronic fatigue syndrome, also known as myalgian encephalomyelitis (with). An innovative study, conducted by the University of Edinburgh, managed to reveal the genetic basis of this debilitating disease. As part of the larger research on the disease, the Decodeme program analyzed the DNA of more than 15,000 patients and identified eight specific genetic markers. These differences were found in genes associated with the immune and nervous system. This discovery is the first powerful proof that heredity plays a decisive role in the appearance of the syndrome, giving substantial “validity and credibility” to those who suffer. “These findings are an awakening,” said study leader Chris Ponting. “We now know why an infection can trigger the disease and why pain is such a common symptom. A person’s genes can determine if it is diagnosed with me/cfs. ‘ This statement confirms the testimonies of patients, who […]
Source: News Beast
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