How Tweaking Genes May Fix Broken Hearts
Early research reveals some benefit for gene therapy to treat heart failure.
May 31, 2010— -- Replenishing the supply of a gene that controls the way heart muscle cells work appears to slow progression of heart failure, a disease that will be diagnosed in about 670,000 Americans this year.
After six months, patients who received the highest dose of the gene therapy had less worsening of a six-minute walk test, as well as evidence of less rapid enlargement or remodeling of the heart, compared with patients in the placebo group.
Patients who receive the high dose gene therapy were also likely to have shorter hospitalizations -- an average of 0.2 days versus 2.1 days for patients in the placebo group.
But the gene therapy didn't reduce breathlessness, fatigue, or pain associated with advanced heart failure, nor did it make patients feel better or have improved quality of life.
In announcing preliminary results of the first study of gene therapy for treatment of heart disease, Dr. Barry Greenberg of the University of California tried to balance optimism for what has been called a breakthrough treatment against the reality that the results were less than stunning.
Greenberg reported the findings to fellow heart failure researchers gathered in Berlin for the Heart Failure Congress.
Of the 39 patients in the study, just nine received the high-dose gene therapy that Greenberg and his colleagues have identified as demonstrating enough efficacy for it to be investigated in a larger study.
The gene used in the study is called Mydicar, which is a bioengineered or recombinant version of an enzyme called SERCA 2A that is found in heart muscle cells. This enzyme regulates two critical functions: the transport of calcium between cells and the contractility or squeezing power of a heart muscle cell.
Heart failure occurs when the heart loses its ability to efficiently pump blood through the body. As a result the heart enlarges and fluid builds up in the lungs. Earlier studies have suggested that SERCA 2A plays a key roll in this process -- as the cellular supply or level of this enzyme diminishes the heart begins to fail.
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