From 2002 to 2005, about 800 people in Minnesota and Utah drank more than 1,500 milkshakes, and they got to say they were doing it for science.
Dr. Donna Arnett, professor of epidemiology and dean of the University of Kentucky College of Public Health, is principal investigator of the multi-site Genetics of Lipid-lowering Drugs and Diet Network (GOLDN) study. Some GOLDN participants have been enrolled for the past 25 years, in the name of helping researchers better understand cardiovascular risks. This time they were helping scientists determine how genes influence cholesterol levels after high-fat meals and how genes affect the response to a medication for lowering triglyceride and bad cholesterol.
Ultimately, the team of medical geneticists at the University of Texas Health Science Center at Houston, University of Alabama at Birmingham, the University of Kentucky, and seven other institutions discovered new uncommon gene variants that affect patients’ response to the cholesterol drug. They reported their findings in the Journal of Lipid Research.
Chronically high cholesterol results in the gradual deposition of lipids on artery walls, increasing the risk of heart attacks and stroke. This clogging process is known as atherosclerosis. A diet high in fat is just one of several risk factors. Family history strongly affects a person’s risk of developing it.
“Triglyceride and cholesterol levels are influenced by what people eat and whether they take drugs to lower fat and cholesterol,” said the study’s lead author, Dr. Xin Geng, a postdoctoral fellow at the University of Texas Health Science Center at Houston. “We know, however, that not everyone’s triglyceride and cholesterol levels respond the same to diet and drugs. Previous research suggests that these differences in response to diet and drugs may be caused by genetic factors inherited from parents.”
While researchers have identified genetic variants that affect lipid responses, the medical geneticists who worked on the milkshake study set out to identify additional variants that have so far escaped detection.
Drinking milkshakes, giving blood
Each GOLDN participant came to the lab with an empty stomach and drank a milkshake concocted from heavy whipping cream, chocolate or strawberry syrup, and crushed ice. More than four-fifths of the calories in the meal came from fat.
The scientists drew their blood before and after the meal and measured high-density lipoprotein (known as “good” cholesterol), low-density lipoprotein (known as “bad” cholesterol) and triglycerides (basically, fat).
They sent the patients home to take fenofibrate, a medication that can lower cholesterol and triglyceride levels, for three weeks. After that treatment, patients returned to the lab for another milkshake and another set of blood draws.
The scientists also sequenced all of the genes and examined the gene expression level in the participants’ blood cells.
Novel rare gene variants
“Until recently,” said Dr. Degui Zhi, senior author from UTHSC at Houston, “it was thought that common genetic variants were the ones that caused variability in people’s triglyceride and cholesterol levels.”
However, common genetic variants explained less than a quarter of inherited variability in triglyceride levels. “Our hypothesis was that at least some of the 48 percent of unexplained variability could be driven by rare genetic variants, those that occur in less than 5 percent of the population.”
Indeed, the researchers found variants of at least three genes that were not very widespread in the study population but did correlate with lipid changes in the people who had them.
“We found that variants in one gene, called SIPA1L2, predicted triglyceride level changes after consuming the milkshake. Variants in another gene, ITGA7, predicted LDL-cholesterol level (“bad” cholesterol) changes after taking the drug. And variants in a third gene, CEP72, predicted triglyceride response when comparing the pre-fenofibrate milkshake experiment to the post-fenofibrate milkshake experiment,” said Dr. Ryan Irvin, another collaborator from UAB.
The researchers say their findings should spur other scientists to look for additional rare gene variants, including non-protein-coding DNA that fell outside the scope of this study.
They also emphasize that their study population was not diverse. Most of the GOLDN participants are white. Looking for rare variants in other populations may turn up additional important genes.
“Future studies can begin where we left off by trying to uncover exactly how the metabolic pathways and mechanisms these genes are part of interact with dietary fat and fenofibrate to change triglyceride and cholesterol levels,” said Dr. Arnett. “Armed with this knowledge, we will be one step closer to finding new ways to prevent and/or treat unhealthy triglyceride and cholesterol levels.”