One in 25 people from India and other South Asian countries carries a mutated gene that causes heart failure, according to a new study. Studying this gene, and the protein it encodes, could lead to new treatments for heart failure, according to Loyola University Health System (LUHS) researcher Sakthivel Sadayappan, who has
studied the gene and protein for 15 years. Investigating the protein could provide “a better understanding of the mechanics of heart function during health and disease,” Sadayappan and study co-author David Barefield wrote. Barefield is a graduate student and Sadayappan is an assistant professor in the department of cell and molecular physiology at Loyola University Chicago Stritch School of Medicine. Previous studies by Sadayappan and other researchers found that about four per cent of people who live in India, Pakistan, Sri Lanka, Indonesia and Malaysia carry the mutation. Carriers have about a 90 per cent chance of developing heart failure after age 45.
About 60 million people worldwide, including about 40 million Indians, carry the mutation. Sadayappan said the mutation likely arose in a single person roughly 33,000 years ago, and spread throughout South Asia. The gene encodes for a protein, called cardiac myosin binding protein-C (cMyBP-C), that 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. Due to this modification, the protein is not properly incorporated into the functioning unit of cardiac muscle called sarcomere. Consequently, the heart does not contract properly. In younger carriers, the heart can compensate for this defect. But as the person ages, his or her heart is no longer able to compensate. Heart muscle becomes inflamed and does not work well, a condition called cardiomyopathy.
—IANS