MAR 23, 2016 7:30 AM PDT

2 genes prevent (and promote) heart attack

To reduce risk of heart attack, the benefits of a healthy lifestyle are clear. But genetics can still stack the deck.
 
Researchers have identified two genes that, when altered in specific ways, either promote or undermine cardiovascular health.

A new study that includes genetic data from more than 190,000 people shows that some people’s genes offer a natural advantage—or disadvantage—in protecting against heart disease, the leading cause of death worldwide.

The research identifies two genes that, when altered in specific ways, either promote or undermine cardiovascular health. The findings may help guide efforts to design new preventive drugs, similar to the way statins now are prescribed to lower “bad” cholesterol to reduce the risk of heart disease.

“We identified genetic variation in several genes that associated with protection from coronary heart disease,” says first author Nathan O. Stitziel, a cardiologist and assistant professor of medicine and genetics at Washington University in St. Louis.

“Our findings support the idea that therapies focused on a major pathway regulating triglycerides should help prevent the buildup of plaque in the heart’s coronary arteries and protect against heart attacks.”

To identify genes that might be relevant for drug discovery, the investigators plumbed DNA data from patients with coronary disease and from healthy controls. They searched across more than 220,000 genetic variants that altered proteins to identify those that appeared to influence heart disease risk. Errors in proteins can have major physiologic consequences.

For the study, published in the New England Journal of Medicine, researchers confirmed past work identifying genes already shown to confer an advantage or a vulnerability in protecting against heart disease risk. Two new ones stood out—ANGPTL4 and SVEP1.

Rare errors in ANGPTL4 were associated with reduced risk of coronary artery disease. The reduction varied from 14 percent for a small error in the gene to cutting risk by about 50 percent when an entire copy of the gene was disabled. The other gene, SVEP1, showed the opposite correlation—a rare error increased risk of coronary artery disease by about 14 percent.
 

Mystery gene


While ANGPTL4 has been the subject of much study, the other gene newly implicated in cardiovascular health is a bit of a mystery. Researchers showed that the error in SVEP1also was linked to higher blood pressure in their study populations, but beyond that there are few clues to what it’s doing.

In contrast, ANGPTL4 has long been known to play a role in processing triglycerides, a type of fat that circulates in the bloodstream. Doctors measure levels of triglycerides as a marker of heart disease risk, though whether these fats play a role in causing plaque to build up in arteries historically has been a matter of debate. ANGPTL4’s role in processing triglycerides is part of a system called the lipoprotein lipase (LPL) pathway. Blocking ANGPTL4 actually opens up this pathway, allowing the body to process triglycerides from the diet and get them out of the bloodstream.

“The gene’s association with lower triglycerides has been known for a while,” Stitziel says. “But for a long time it was not clear that high triglycerides were a cause of coronary disease rather than a marker of it. Now we know that errors in ANGPTL4 associate with both reduced triglycerides and lower risk of coronary disease. This is another piece of the puzzle that points to a causal role for triglycerides in coronary disease.

“If that’s correct, strategies to lower triglycerides should help. Our study indicates that those strategies could include blockingANGPTL4 or manipulating other elements of the LPL pathway.”

In people with a disabled copy of ANGPTL4, triglyceride levels in the blood are reduced by about 35 percent compared with people who have two working copies of the gene. Variations in the gene are not associated with changes in levels of “bad” LDL cholesterol.

So any drug that impacts this pathway would, in theory, work independently of statins as well as PCSK9 inhibitors, a new and potent cholesterol-lowering therapy that was approved in 2015 by the Food and Drug Administration. These recently approved therapeutics that inhibit PCSK9 were developed after similar genetic studies showed an association with LDL cholesterol levels.

“The poster child for human genetic studies leading to new therapies is PCSK9,” Stitziel says. “Rare errors in PCSK9 were first found to cause high LDL cholesterol and different errors were later associated with low LDL cholesterol and protection from coronary disease. And within 12 years of those findings there are now new therapies. The key insight from human genetic studies is the ability to identify biological pathways that are relevant to human disease.”

With future therapeutics in mind, early versions of inhibitors targeting ANGPTL4 and other members of the LPL pathway are in development, Stitziel says.  While none of these are clinically approved therapies, the new study linking these genes to reduced coronary disease and lower triglycerides suggests the line of investigation is worth pursuing.

The National Institutes of Health, the Foundation for Barnes-Jewish Hospital, Massachusetts General Hospital, the Donovan Family Foundation, Fondation Leducq, Merck, the Regione Emilia Romagna Area 1 Grants; the Wellcome Trust, the BHF Centre of Research Excellence, the British Heart Foundation, the UK National Institute for Health Research, the American Heart Association, and the European Research Council funded the work.

Source: Washington University in St. Louis

This article was originally published on futurity.org.
About the Author
  • Futurity features the latest discoveries by scientists at top research universities in the US, UK, Canada, Europe, Asia, and Australia. The nonprofit site, which launched in 2009, is supported solely by its university partners (listed below) in an effort to share research news directly with the public.
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