A new drug lowers levels of a protein related to ‘bad’ cholesterol
The next clinical trial will test if the treatment reduces the risk of heart attack and stroke
Testing for a person’s level of lipoprotein(a), which carries fat and cholesterol, could become widespread if a new drug that can drastically reduce the protein is found to lower the risk of heart attack and stroke.
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Routine blood tests in the not-too-distant future may feature a new line item: lipoprotein(a).
High levels of this fat- and cholesterol-carrying protein increase the risk of cardiovascular disease, research suggests. But there has been little anyone can do about it. How much lipoprotein(a) a person produces is largely locked in by genetics, and the level remains relatively steady throughout life. That’s in contrast to “bad” LDL — low-density lipoprotein — cholesterol, which changes depending on diet and exercise.
Because lipoprotein(a) is genetically determined, “these people who have high levels have had it since birth, and so they can get heart disease earlier,” says Erin Michos, a preventive cardiologist at Johns Hopkins University School of Medicine who was not involved with the clinical trial.
Now, a therapy that specifically targets lipoprotein(a) levels is on the horizon. In a clinical trial, the drug, which blocks the body’s ability to make the protein, reduced people’s levels of lipoprotein(a) by as much as 80 percent, researchers report in the Jan. 16 New England Journal of Medicine. The trial also found the drug to be safe.
Another clinical trial is now under way to determine whether drastically lowering levels of lipoprotein(a) in people who already have cardiovascular disease lessens their risk of heart attack and stroke (SN: 3/15/19).
Lipoprotein(a) is made up of a particle of LDL plus a protein called apolipoprotein(a). The relationship between LDL cholesterol and cardiovascular disease risk is well-established: When there is too much LDL cholesterol in the blood, it can get into the walls of arteries, stoking an inflammatory immune response that leads to thickened walls and narrowed arteries (SN: 5/3/17).
But LDL doesn’t appear to be the whole story, says cardiologist Michelle O’Donoghue of Brigham and Women’s Hospital in Boston, who was not part of the new study. “There are people who have very well-controlled LDL cholesterol levels who do go on to have heart attacks.” As a result, “there’s been a tremendous amount of interest in lipoprotein(a) and its possible role in progression of heart disease,” she says.
The LDL component is part of the reason that cardiovascular disease risk is higher with elevated levels of lipoprotein(a). But the apolipoprotein(a) component adds to the risk, says Sotirios Tsimikas, a cardiologist at the University of California, San Diego School of Medicine in La Jolla. That protein appears to provoke a stronger inflammatory reaction than LDL does, hastening plaque development in artery walls. And apolipoprotein(a) has the potential to prevent blood clots from breaking up — bad news if an artery-blocking clot forms when a plaque ruptures.
“So in a way, it’s kind of a triple hit,” Tsimikas says. “You get all the bad things from LDL, but then you get two other things that are not good for you.”
To directly target the production of lipoprotein(a), Tsimikas and colleagues tested a drug called APO(a)-LRx, developed by Ionis Pharmaceuticals in Carlsbad, Calif., in a phase II clinical trial designed to determine the effectiveness and best dose of the treatment. The drug blocks the messenger RNA that provides genetic instructions to make the protein.
The researchers tested different drug doses in 286 patients with cardiovascular disease whose levels of lipoprotein(a) were at least 60 milligrams per deciliter of blood. Epidemiological data suggest that people with lipoprotein(a) levels between 50 and 100 mg/dL have a modest increase in the risk of cardiovascular problems, Tsimikas says. Those with levels above 100 mg/dL are at high risk. It’s estimated that about 20 percent of the population has lipoprotein(a) levels above 50 mg/dL, he says.
At the highest dose of the drug, trial participants’ lipoprotein(a) levels dropped by an average of 80 percent by the end of the experiment.
To determine if the drug is effective at reducing the risk of heart attack and stroke, a phase III clinical trial, run by Novartis Pharmaceuticals of Basel, Switzerland, has begun recruiting participants. Researchers will test the drug or a placebo over about four years in more than 7,500 people with cardiovascular disease and lipoprotein(a) levels of 70 mg/dL or higher.
If that trial is successful, further research will be needed to see if the drug also helps people with high levels of lipoprotein(a) avoid developing cardiovascular disease in the first place.
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