Insurance Companies Should Have Access To Genetic Information
Main Category: Health Insurance / Medical InsuranceAlso Included In: Genetics
Article Date: 08 Jun 2007 - 1:00 PDT
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There is no good reason to deny insurers access to genetic information, argues a Professor of Ethics in a debate published in this week's BMJ.
Only if we refuse to give insurers access to all health information can we reasonably stop them seeking genetic test results, says Professor Soren Holm from Cardiff Law School.
If insurers were denied access to any health information they would only be able to differentiate premiums according to very general risk markers, for example, age, gender or occupation. This would mean in effect that the healthy subsidise the unhealthy - but there would be equality.
However, if we allow insurers to have some kinds of health information, such as a person's BMI or cholesterol level we no longer have any principled reason for excluding genetic information:
"Genetic information is not special. It is not inherently more specific, predictive, sensitive or private than other kinds of health information."
Professor Holm concedes there are worries about sharing genetic information - allowing insurers to see genetic information could deter people from getting tested or insurers may use the information inappropriately. This may be the case, he says, but the same is true for other health information - for example whether someone is HIV positive.
He argues a better solution to this problem would be to make challengeable a decision to deny coverage for life or health insurance, thereby forcing insurers to make their reasoning transparent.
On the other side of the argument Professor Richard Ashcroft from the University of London says access to genetic information should not be allowed as it could lead to irrational discrimination. This arises, he says, from false beliefs about genetic information. It can be misunderstood or its significance over-estimated.
He says if insurers had access to complete health information, including genetic test results, it could lead to a situation which was "actuarially fair" but "socially unfair":
"If the point of insurance is to cover the costs of ill luck, the only sort of ill luck you could not insure against would be the misfortune to have a late onset serious genetic disorder. Arguably such people would need insurance more than most yet would be less able than most to get it."
In the face of uncertainty surrounding the interpretation of genetic information, occasional discriminatory practice by individual insurers and a lack of solutions to the problem of social justice, he says, it is preferable to maintain the status quo, at least in the medium term.
Should genetic information be disclosed to insurers?
Head to head BMJ Volume334, pp 1196-97
http://www.bmj.com
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MLA
14 Feb. 2012. <http://www.medicalnewstoday.com/releases/73490.php>
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http://www.medicalnewstoday.com/releases/73490.php.
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Visitor Opinions In Chronological Order (1)
My Genetic Information Is Mine And Mine Only
posted by nsc on 8 Jun 2007 at 8:43 amI disagree with Professor Holm. My genetic information is mine and mine only. Giving it to insurance companies, or anyone else, is a violation of my right to privacy. Knowing what ailments I have or had is understandable, even family history, but giving out genetic code is a slippery slope. It would be too easy for a government agency to utilize something like the Patriot Act to gain access to someone's genetic information.
Not to mention the myriad of problems that would occur once that information slippped out into public domain. Let's face it, it's happened before with every other single type of private information, it will happen here too. Sorry Professor, sound like ethics isn't your thing and your really working for big industry here. And insurance is one of the biggest.
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