April 25, 2008 in Nation/World

Senate passes gene bill 95-0

Jim Abrams Associated Press
 

WASHINGTON – Up to now, people with family histories of breast cancer, Alzheimer’s or some other fearful disease have faced an awful dilemma: Genetic tests that might relieve their anxiety or steer them to preventive therapy might also cost them their jobs or health insurance.

Some of that extra concern about testing could end soon as Congress nears completion of a bill banning discrimination based on genetic information.

A 95-0 vote in the Senate on Thursday sent the Genetic Information Nondiscrimination Act back to the House, which could approve it early next week. President Bush supports the legislation.

The bill, described by Sen. Edward Kennedy as “the first major new civil rights bill of the new century,” would bar health insurance companies from using genetic information to set premiums or determine enrollment eligibility. Similarly, employers could not use the information in hiring, firing or promotion decisions.

“For the first time we act to prevent discrimination before it has taken firm hold, and that’s why this legislation is unique and groundbreaking,” said Sen. Olympia Snowe, R-Maine, who sponsored the Senate bill with Kennedy, D-Mass., and Mike Enzi, R-Wyo.

There are more than 1,100 genetic tests available today, she said, but these are “absolutely useless” if fear of discrimination discourages people from taking tests or participating in clinical trials.

Genetic testing could lead to early therapy for a wide range of diseases with hereditary links such as breast and prostate cancer, diabetes, heart disease and Parkinson’s.

“But right now the ability to realize those goals is somewhat limited” because of patients’ fears that the information will be used against them, said Dr. David Herrington, a professor of cardiology at Wake Forest University and spokesman on genetic issues for the American Heart Association. The legislation “will help them both be more willing to participate in research and avail themselves of the benefits of genetic testing.”

Congressional efforts to set federal standards to protect people from genetic discrimination go back more than a decade, to a time when there were only a small number of genetic tests. But now, with the mapping of the human genome, people have access to far more information about their hereditary disposition to such crippling afflictions as cystic fibrosis, Huntington’s disease or Lou Gehrig’s disease.

Bill sponsors said that has increased the likelihood that a prospective health insurance company or employer will reject a person because of concerns the person will suffer a costly disease in the future.

The Senate passed genetic nondiscrimination bills in 2003 and 2005 but couldn’t get the House to act. A year ago the House approved a White House-backed bill on a 420-3 vote.

Senate action on that legislation has been slowed by Sen. Tom Coburn, R-Okla., who joined some business groups in warning that the bill could encourage a flood of lawsuits.

A compromise worked out this week tightens language to ensure there is a “firewall” between the part dealing with health plans and the section regarding employment, so as to discourage inappropriate claims.

It also makes clear that, while individuals are protected from discrimination based on genetic predisposition, insurance companies still have the right to base coverage and pricing on the actual presence of a disease.

Rep. Louise Slaughter, D-N.Y., chief House sponsor of the bill with Rep. Judy Biggert, R-Ill., said the House would “get it out to the White House as quickly as we can.” Slaughter, who first introduced a genetic discrimination bill 13 years ago, said personalized medicine advanced by genetic research has “the potential to save billions of dollars in health care costs.”

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