8% of South Asians Carry Mutated Gene MYBPC3 That Causes Heart Failure: Study

Loyola University Chicago Stritch School of Medicine in the US has conducted a study that shows that up to 8 percent of people from India, Pakistan, Bangladesh and other South Asian countries carry a mutated gene called MYBPC3 that causes heart failure and other heart ailments.

The study conducted by Sakthivel Sadayappan of Loyola University demonstrates how this gene mutation impairs the heart’s ability to pump blood, causes hypertrophic cardiomyopathy, the most common form of inherited cardiac disease that leads to sudden cardiac deaths in young people.

Previous studies by Dr. Sadayappan and other researchers have found that between 5 percent and 8 percent of South Asians carry the mutation. Carriers have about an 80 percent chance of developing heart failure after age 45. Dr. Sadayappan first reported the mutation in 2001 at the World Congress of the International Society for Heart Research, and has been studying it ever since. He said that, based on a report from one of his collaborators, the mutation likely arose in a single person roughly 33,000 to 55,000 years ago. The mutation then spread throughout South Asia.

The mutated gene encodes for a protein, called cardiac myosin binding protein-C (cMyBP-C), that controls cardiac muscle contractions and is critical for the normal functioning of the heart. In the mutated gene, 25 base pairs (DNA letters) are missing. As a result, the tail end of the protein is altered.

In his new study, Dr. Sadayappan and colleagues introduced the mutated gene into adult rat cardiomyocytes (heart muscle cells) in a petri dish. These cells were compared with cardiomyocytes that received a normal gene.

In cells with the mutant gene, the cMyBP-C protein was not incorporated into sarcomeres, the basic units of heart muscle. So rather than helping the sarcomeres contract properly, the mutant protein floated around the cell’s cytoplasm, producing a toxic effect. The study showed, for the first time, that expression of the mutant protein is sufficient to cause cardiac dysfunction.

The findings point the way toward future treatments that would remove the mutant protein from cells and introduce normal cMyBP-C protein. Researchers also hope to identify lifestyle and environmental risk factors that aggravate hypertrophic cardiomyopathy in people who carry the gene mutation.

Dr. Sadayappan and colleagues concluded that determining the disease mechanism will help in developing therapies, and is the “first priority to prevent the development of heart failure in millions of carriers worldwide.”

The study is published in the Journal of Biological Chemistry, a publication of the American Society for Biochemistry and Molecular Biology.

Leave a Reply

Your email address will not be published. Required fields are marked *


This site uses Akismet to reduce spam. Learn how your comment data is processed.