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Key takeaways
- High blood pressure is strongly influenced by genetic variants.
- Lifestyle changes can offset much of the risk, despite the influence of genetic variants.
- Family patterns reflect shared environments, which also can affect blood pressure.
High blood pressure, often called a “silent killer,” can raise the risk of heart attack and premature death. Now large genome-wide studies show that hundreds of small genetic variants can influence lifetime blood pressure risk, especially when combined with aging, lifestyle and environment.
Blood pressure tends to rise as we get older. In fact, three-quarters of Americans ages 65 to 74 have high blood pressure. But aging isn’t the only risk factor; genetics, epigenetics and long-term environmental exposures can also influence blood pressure throughout your life.
A brief genetics glossary
- Genetics: A branch of biology that focuses on genes that carry DNA and pass traits and health risks from parents to children.
- Genome: A complete set of all your DNA, or the genetic instructions inside your body.
- Polygenic: Describes a condition, such as high blood pressure, that is influenced by many genes.
- Epigenetics: The study of factors that can alter your genes without changing your DNA, including aging, diet, stress, smoking and pollution.
“Genetics does play an important role in the development of high blood pressure,” says Dr. Iftikhar Kullo, a cardiologist and professor of medicine at the Medical College of Wisconsin. “We often see it run in families.”
But, he notes, families have a lot more in common than genes, and you can overcome most of your genetic risk for high blood pressure with a healthy lifestyle.
Is high blood pressure hereditary?
Research shows genes may play a bigger role in high blood pressure, or hypertension, than previously believed.
“The field has really exploded, propelled by what you call genome-wide association studies,” Kullo says. This is when researchers analyze the entire genome — all the genes — of very large groups of people to make connections between certain gene variants (permanent changes) and certain health conditions.
Research over the past few years has strengthened this view: Hypertension is now understood to be one of the most strongly polygenic common diseases, which means it is a condition that can be influenced by many different genes.
A May 2024 study in the journal Nature Genetics analyzed the genes of more than 1 million people of European ancestry and identified more than 2,000 independent genetic signals linked to blood pressure, including 113 newly identified regions.
In many cases, geneticists can identify specific regions of DNA that contribute to high blood pressure.
Some people don’t carry any gene variants known to increase the risk of high blood pressure, while others have one or two; some carry many.
“If you have one variant, you might have a half a millimeter or 1 millimeter increase in blood pressure,” Kullo says. “But you can have more than one of these gene variants, and they can add up.”
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