You are here
Study: Viral Reactivation Likely Link Between Stress and Heart Disease
Looking at blood samples from 299 heart patients, researchers at Ohio State University found that those who had suffered a heart attack were the most likely to have inflammatory proteins circulating in their blood compared with patients with less acute symptoms — and having more of one of these proteins in the blood was linked to the presence of antibodies that signal latent Epstein-Barr virus (EBV) reactivation.
To date, these relationships have been hard to find because scientists have been unable to detect evidence of a virus in diseased areas of the cardiovascular system.
In the new study, however, the researchers looked for antibodies against a protein that can be produced even when only partial or incomplete reactivation of EBV occurs. When this antibody was detected, it was associated with immune-system malfunctions connected with inflammation — a known risk factor for heart disease.
Identifying a solid link between a reactivated virus and heart disease is important because of the prevalence of EBV, a human herpes virus that causes infectious mononucleosis and several different types of tumors. An estimated 95% of Americans are infected with the virus by adulthood, and once a person is infected, the virus remains dormant in the body. It can be reactivated without causing symptoms of illness, but reactivation has the potential to create chaos in the immune system.
Stress is a known predictor of reactivation of EBV, meaning virus reactivation could be a mechanism by which stress leads to chronic inflammation and eventually cardiovascular diseases, according to the authors.
“In the big picture, this may help clarify the role these viruses play in heart disease,” said co-author Dr. Ron Glaser. “And it makes sense, because we know that some viral proteins can induce inflammation, affecting the lining of blood vessels, so that inflammation is in the right place to function as a significant risk factor for heart disease.”
The new research was published in the online journal PLoS One.
Source: Ohio State University; January 22, 2013.