URBANA, Ill. – Triglycerides, a type of fat in the blood, are important for good health. But having high triglycerides might increase a person’s risk of heart disease, and may be a sign of metabolic syndrome—a combination of high blood pressure, high blood sugar, and too much fat accumulation at the waist. People with metabolic syndrome have increased risk for heart disease, diabetes, and stroke.
A new study from nutrition researchers at the University of Illinois shows that some individuals with variations of a “gene of interest” may be at an even higher risk of developing high triglycerides. Specifically, researchers looked at genetics and risk in a group of young Mexican adults.
Despite genetic predisposition, the study shows that maintaining a healthy body weight or changing diet can help reverse the risk.
Katie Robinson, a former doctoral student in the U of I Division of Nutritional Sciences and fellow of the I-TOPP program, explains that the study, published in the Journal of Nutrigenetics and Nutrigenomics, is a collaboration between the University of Illinois and the Autonomous University of San Luis Potosi in Mexico (UASLP), also known as UP AMIGOS.
“Obesity is a growing problem in the U.S. and Mexico. In the U.S., obesity affects over a third of our population. We’re concerned because obesity is associated with other diseases such as diabetes, heart disease, and high triglycerides,” Robinson explains. Compared to Caucasian groups, Hispanics in the U.S. have higher rates of type 2 diabetes and other obesity-related diseases. Of all Hispanic subgroups, those of Mexican heritage have one of the highest risks for obesity and associated diseases.
The UP AMIGOS project addresses genetic and environmental factors associated with obesity and related conditions among younger adults in Mexico. “A lot of existing data are from Caucasian cohorts, which means we needed to replicate and better understand those findings in groups with different ethnicities. That’s the main goal of the UP AMIGOS project.
“It was a great opportunity that we were able to look at this rich data set from young Mexican adults because we know that this population has a greater likelihood of developing not only obesity but also high triglycerides and diabetes,” Robinson adds.
For the current study, Robinson was interested in a protein made in the liver called fetuin-A (FetA). “It’s an interesting marker connecting inflammation with obesity and its associated diseases,” she says. “FetA is a protein that is released from adipose tissue and also the liver. We know FetA is integral to insulin sensitivity, and that’s where most of the research has been done to look at its function.
“We also know that FetA is elevated in obesity and diabetes. Therefore, we were interested in looking at the genetic implication. If there are alterations or single nucleotide polymorphisms within the gene that codes for FetA, does that change somebody’s risk for obesity or the associated diseases?”
To answer that, the researchers looked at bloodwork from 641 Mexican young adults to analyze biomarkers and genotypes. They also checked body mass index (BMI), took measurements of fasting glucose levels, and had the participants report on their dietary habits.
From the genotyping, they were specifically looking for occurrences of two mutations of the gene, AHSG, a gene that influences the protein FetA. They were interested in the association of those gene mutations with dietary intake, weight, and also biological markers of health.
The AHSG polymorphisms were found to be associated with triglycerides. Robinson explains the most important finding is that one of these polymorphisms, or mutations, was associated with higher circulating triglycerides, but that correlation was very dependent on BMI and dietary intake—the relationship was exaggerated in individuals who were overweight.
“So with an elevated BMI, we saw greater disorder within those carrying the risk genotype. But if these individuals who had the high-risk AHSG genotype had a lower BMI, their triglycerides were lower. It suggests that even if you carry the high-risk genotype, you don’t have a greater risk of high triglycerides if you can maintain a normal BMI or a lower BMI, which I think is a positive finding when we look at genetics.”
Robinson says diet also played a role in higher triglycerides. “Higher carbohydrate intake—specifically sugar or sucrose intake—was associated with elevated triglycerides. This association was mainly in one genotype group. The thought was perhaps these individuals are more sensitive to certain diets than the other genotype groups.”
Regardless of genotype, elevated BMI was associated with higher triglycerides. Due to the relationship between FetA and diabetes, the researchers also wanted to see if there was an association with AHSG mutations and glucose, but surprisingly, they didn’t find any.
While the study looked at relatively healthy young adults in a Mexican population, results were different than what has been observed in previous research from Caucasian groups. Robinson explains that they might have seen different results if they had looked at older Mexican adults with poorer health.
Some good news from the study’s findings is that maintaining a healthy body weight often can overcome the effects of genes related to metabolic disease and type 2 diabetes.
“We know that genes aren’t everything,” Robinson says. “There are a lot of things we can do, behaviorally, to change our individual risk. It’s a silver lining in our research. We can’t modify our genetics, but we can modify our epigenomes and some behaviors. You can still have positive health outcomes.”
The results are also important for the future of developing personalized nutrition as interventions for disease, Robinson says.
“In practical terms, it would be ideal to start by understanding someone’s basic biology, which may influence how they’re metabolizing and utilizing the nutrients they are eating. It would be great to bring people in, find out where their biology is at, and then tailor a diet for them, but we need a lot more research before we get to that point.”
Margarita Teran-Garcia, assistant professor in the Division of Nutritional Sciences and the Department of Human Development and Family Studies at U of I adds, “In order to advance the full potential of precision medical and nutritional sciences, there is a need to invest and create new sustained resources—financial and technological—to build the evidence base needed to guide clinical practice and strategic planning in public health.”
The paper, “Circulating triglycerides and the association of triglycerides with dietary intake are altered by alpha-2-Heremans-Schmid glycoprotein polymorphisms,” is published in the Journal of Nutrigenetics and Nutrigenomics. Co-authors include Katie N. Robinson, Itzel Vazquez-Vidal, Courtney Marques, Flavia Cristina Drumond Andrade, Celia Aradillas-Garcia, Margarita Teran-Garcia, and the UP AMIGOS Team.
This study was funded by University of Illinois at Urbana-Champaign Research Board grant #09070, the Center for Health and Aging, the ACES Office of Research FIRE grant, and the USDA National Institute of Food and Agriculture, Hatch Projects #ILLU-968-312, #ILLU-971-368, and #ILLU-793-327. Funding was also provided by the Universidad Autónoma de San Luis Potosí, Hormones Laboratory at the School of Medicine, the Clinical Biochemistry Laboratory at the Chemical Sciences School, and the Autonomous University of San Luis Potosí University Health Center under agreement support C09-PIFI-030606. Furthermore, K.N. Robinson was supported by the National Institute for Agriculture under the Illinois Transdisciplinary Obesity Prevention Program grant (2010-04886) to the Division of Nutritional Sciences at the University of Illinois.