A new study published in the online edition of the journal Nature reveals that people who suffer a heart attack are at a greater risk of experiencing a second attack or stroke as the initial heart attack triggers an inflammatory response which worsens atherosclerosis.
"We have known for a long time that heart attack patients are at increased risk for a second heart attack or a stroke, and now we know why," says Matthias Nahrendorf, MD, PhD, of the MGH Center for Systems Biology, senior author of the report from a team of researchers from the USA, Canada, Germany and the Netherlands. "The immune response to the infarct - tissue damaged by lack of oxygen - can accelerate the underlying disease by actually increasing the size and inflammation of the atherosclerotic plaque."
AdvertisementThe study was designed to test the hypothesis that systemic inflammation caused by heart muscle damage would worsen pre-existing atherosclerosis. Using a mouse model genetically programmed to develop atherosclerosis, the researchers conducted a series of experiments showing that experimentally induced heart attacks led to the following:
- increased activity, in atherosclerotic plaques at a distance from the induced heart attack, of enzymes that break down the fibrous plaque cap, possibly leading to future rupture,
- accumulation of monocytes and other inflammatory immune cells in those atherosclerotic plaques,
- increased generation in the spleen of monocyte progenitors, along with changes in the function of those immune cells,
- increased release from the bone marrow of blood stem cells, which traveled to the spleen, triggered by increased activation of the sympathetic nervous system.
Ralph Weissleder, MD, PhD, a corresponding author of this study and director of the MGH Center for Systems Biology where the work was performed, adds that these findings set the stage for a totally novel approach to cardiovascular disease. Therapies directed to the sites of white blood cell production, including the bone marrow or the spleen, may be able to prevent immune-system exacerbation of atherosclerosis. "This gives us potential new therapeutic targets that we had not thought about before. Clinically, we focus on reducing risk factors such as elevated cholesterol and blood pressure, but not inflammation. We hope our work can help change that," he says.
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