Johns Hopkins Center Launches Genetic Rights Educational Effort

[August 20, 2008]

By Turna Ray
Editor, Pharmacogenomics Reporter

NEW YORK (GenomeWeb News) - Johns Hopkins University’s Genetics and Public Policy Center has launched an educational effort aimed at informing the public of how their genetic data can and cannot be used under the recently enacted Genetic Information Nondiscrimination Act.

As part of its so-called “Project GINA,” the GPPC plans “to disseminate information” about the legislation to healthcare stakeholders and the general public, GPPC Law and Policy Director Susannah Baruch told GenomeWeb Daily News sister publication Pharmacogenomics Reporter last week.

As part of its plan, the GPPC will launch a web site describing and explaining the federal law that bars health insurers and employers from discriminating based on genetic data. The website, slated to launch in September, will outline what protections are provided under the law, contain a FAQ page, and will provide updates describing how federal and state regulators are implementing the law.

Until the launch of the site, however, GPPC is providing information on GINA under the “What’s Happening” heading on its homepage.

Since GINA became law in May, GPPC Director Kathy Hudson has said that the center intends to spearhead a “major education campaign” to inform “doctors and patients … of these new protections, so that fear of discrimination never again stands in the way of a decision to take a genetic test that could save a life.”

Ahead of the website’s launch, GPPC has made preliminary efforts to educate the public and stakeholders about the law through peer-reviewed publications, webinars, and fact sheets. GPPC recently hosted a series of webinars with the Bureau of National Affairs and has disseminated informational fact sheets describing GINA’s provisions.

Additionally, Hudson co-authored an article in June in the New England Journal of Medicine with Francis Collins, former director of the National Human Genome Research Institute, and M.K. Holohan, an NHGRI senior health-policy analyst, asserting that “it will take much more than sound regulations to ensure that we reap the full benefits” of GINA.

GPPC said it plans to work with Jeremy Gruber of the National Workrights Institute and Karen Pollitz of Georgetown Health Policy Institute to specifically target information to clinicians, health insurers, employers, researchers, ethics boards, and state legislatures. The center will also assist agencies charged with implementing provisions for GINA, Baruch noted.

DNA testing: Doctors search for 100,000 at risk of early heart attack

DNA testing: Doctors search for 100,000 at risk of early heart attack

Sarah Boseley, health editor

The Guardian, Wednesday August 27 2008

Doctors are today told to investigate the family history of every patient with high cholesterol in an attempt to track down tens of thousands of people who carry the gene that makes them a prime candidate for early death from heart attack.

New guidelines from the National Institute for Health and Clinical Excellence (Nice) recommend a major DNA testing programme in an attempt to save the lives of those with inherited high cholesterol - thought to be one in every 500 people. Half of all men with the genetic mutation causing familial hypercholesterolaemia (FH) will die before they are 50 without treatment and a third of all women before they are 60.

FH causes the arteries to clog and narrow, but if it is caught early enough, treatment with statins, together with a healthy diet and lifestyle, particularly no smoking, can give those affected a near-normal life expectancy.

So far, doctors know the identity of 15,000 of the estimated 110,000 people with the gene. Nice today recommends “cascade” testing to find the rest. If doctors suspect a patient has FH, they should ask whether close relatives have died early from heart attacks - and if so, they should advise that other family members should come for cholesterol testing and DNA tests. “This is the first time genetic testing has been recommended for a common disease,” said Steve Humphries, a professor of cardiovascular genetics and member of the Nice guideline development group.

Close family have a 50-50 chance of also having FH, he said. “Using cascade testing, we should be able to move to the point where we have identified the majority [of people with FH]. In the long-term future, we will be able to find them all.”

The children of people with FH should be tested before they reach the age of 10 but not before they are two, said Andrew Neil, professor of clinical epidemiology at Oxford. “Dietary changes are possible from the age of two,” he said. “They can be offered semi-skimmed milk. It is crucially important no children should ever start smoking if they have FH. If they smoke, it multiplies their risk by two-and-a-half-fold. Almost without exception children will require treatment with statins by 18, but very small numbers of children will need treatment earlier.”

Two statins had been licensed for use in children, he said, but there was also very good evidence of their efficacy and safety from widespread adult use and trials. Because of concerns about potential effects on the foetus, women with FH should stop taking statins three months before they try to become pregnant.

Philip Rowlands, who has FH and was a member of the guideline development group, said his father had died of a heart attack at 51, when he was 12. Rowlands has been on statins for 14 years, exercises regularly and has a good diet. “My prognosis is excellent. I was given the chance to control my life, unlike my father,” he said.

guardian.co.uk © Guardian News and Media Limited 2008

Debate regarding euthanasia in France

Un nouveau drame relance le débat sur l’euthanasie

Angélique Négroni, 13/08/2008 | Lefigaro.fr

Lourdement handicapé, Rémy, 23 ans, a mis fin a ses jours après avoir écrit à Nicolas Sarkozy pour lui demander le droit au suicide assisté.

Son suicide a été mûrement réfléchi. Le jeune Rémy s’est installé dans sa chambre, a pris une surdose de médicaments et s’est éteint. Un geste dont il espérait qu’il relance le débat sur l’euthanasie, comme il l’a indiqué dans un court message enregistré laissé à ses parents.

C’est dimanche dernier à Valmondois (Val-d’Oise), dans le logement familial, que ces derniers ont découvert le corps sans vie de leur fils de 23 ans, atteint d’une maladie orpheline dégénérative depuis l’âge de 6 ans. «Rémy nous disait : “Tant que je marcherai je vivrai.” Or depuis quelques mois, il ne pouvait plus se servir de ses jambes et il souffrait terriblement», raconte son père, Jean-Pierre Salvat, qui a toujours soutenu le combat de son fils en faveur de l’euthanasie.

En mai dernier, Rémy avait d’ailleurs écrit à Nicolas Sarkozy pour lui demander de changer la législation existante. «Comme Vincent Humbert, je demande qu’on me permette de mourir pour me libérer de mes souffrances», avait-il indiqué avant de poursuivre : «Je sais qu’en France, il n’y a pas de loi qui permette aux équipes médicales de pratiquer l’euthanasie. Ça m’empêche de vivre en paix… (…) Il faut que la loi change !» La supplique du jeune handicapé s’achevait en ces termes : «Le problème est que vous, monsieur Nicolas Sarkozy, vous ne voulez pas en entendre parler. Moi, Rémy Salvat, je vous demande de laisser de côté votre avis personnel et d’arrêter d’être sourd. Vous le pouvez si vous êtes le président de tous les Français.»

«Ne pas devenir un légume»

Dans un courrier reçu le 6 août dernier et fidèle à la ligne de conduite de la présidence de la République sur le sujet, Nicolas Sarkozy a expliqué au jeune homme : «Pour des raisons philosophiques personnelles, je crois qu’il ne nous appartient pas, que nous n’avons pas le droit, d’interrompre volontairement la vie.» Puis, le chef d’État lui a rappelé quelles étaient, selon lui, les priorités dans ce domaine : «Je voudrais que soit privilégié le dialogue au chevet du malade, entre lui-même, le médecin et la famille, en toute humanité afin que soit trouvée la solution la plus adaptée à chaque situation.» Une phrase qui fait référence au projet de développement des soins palliatifs en France.

En juin dernier, Nicolas Sarkozy a en effet dévoilé un plan consistant à doubler la prise en charge des malades en soins palliatifs d’ici à la fin 2012. 230 millions d’euros devraient être investis afin de créer de nouvelles unités dans les hôpitaux.

Par ailleurs, en mars dernier et peu après le décès de Chantal Sébire qui a relancé le débat sur l’euthanasie, le premier ministre a chargé le député Jean Leonetti de réévaluer sa loi de 2005 sur la fin de vie. Son rapport est attendu d’ici à la fin de cette année.

Selon des proches du jeune handicapé, ce dernier ne souhaitait pas recourir aux soins palliatifs. «Il se savait condamné. Il ne voulait pas finir comme un légume», assure Me Cathy Richard, qui a eu à défendre la mère de Rémy il y a quelques années. Il y a neuf ans, Régine Salvat, dans ce qu’elle qualifie de «moment d’épuisement absolu», avait tenté de mettre fin au calvaire de son fils. Un geste qui lui avait valu une mise en examen pour tentative de meurtre avant d’obtenir un non-lieu. «Rémy a été terriblement courageux. Mais il ne faut plus qu’un enfant soit obligé de se tuer seul dans son coin pour abréger ses souffrances», ajoute l’avocate.

Dans son bref message enregistré, Rémy demande à ses parents de poursuivre «son action pour qu’il y ait un vrai débat public sur le droit à l’euthanasie et au suicide assisté»

Energy concerns - heat pump system and geothermal warmth


With Energy in Focus, Heat Pumps Win Fans
By LIZ GALST, Published: August 13, 2008

The business for ground-source heat pumps is so hot that when some people driving in and around Seattle see Gerard Maloney’s EarthHeat van, with the company’s phone number on the side, they call from their cellphones. “Really, we have people doing this,” Mr. Maloney said.

Like other energy alternatives, ground-source heat pumps have won new admirers as energy costs have skyrocketed.

The pumps, also called geothermal heat pumps, use the relatively constant temperature just below the earth’s surface — six feet below, in many cases — to draw warm air into a building in winter and remove warm air in summer. Advocates say the systems can save building owners 25 percent to 65 percent on energy costs while reducing carbon dioxide emissions.

Around the nation, owners of the small businesses that constitute most of the $2.5 billion ground-source heat pump industry report that demand for their systems and services has surged.

“We started as many jobs by April of 2008 as we had done in all of 2007,” said Bruce Wollaber, president of Comfort Engineered Systems in Nolensville, Tenn., a designer and installer of heat pump systems. Bill Beattie, co-owner of Rockford Geothermal in Rockford, Ill., said, “If we stay on track, we’re probably going to grow by about 40 percent this year.”

All this comes with some growing pains for the industry, which has its sights set on capturing 30 percent of the heating and air-conditioning market by 2030. System manufacturers have a backlog of orders, installers say. Trained workers are increasingly difficult to come by. Still, said Jim Bose, executive director of the International Ground Source Heat Pump Association, an industry and advocacy group, “it’s not a pipe dream. It can be done.”

The systems use a network of water-filled pipes laid either horizontally (6 feet under) or vertically (often 200 to 300 feet down), that attach to a heat exchanger.

The technology can be used almost anywhere, on any type of building. “We’ve got them all the way from Texas to the Arctic Circle,” said Mr. Bose, a professor of engineering technology at Oklahoma State University in Stillwater.

And even without financial incentives from the government or energy utilities, says John Shonder of the Energy Department’s Oak Ridge National Laboratory in Tennessee, “ground-source heat pumps have the lowest life-cycle costs in several cost studies that I’ve done” of heating and air-conditioning systems. (For details on incentives, see www.dsireusa.org.)

The systems pay for themselves in three to eight years, depending on “location and energy prices,” Mr. Shonder said.

In fact, heat pump systems may offer the greatest savings to the owners of commercial buildings, says John W. Lund, director of the Geo-Heat Center at the Oregon Institute of Technology. “For commercial buildings, where you have a fairly large heating and cooling load, the payback period could be two to three years.”

Though no comprehensive survey of the heat pump sector exists, Energy Department statistics on units shipped tell a striking story. In 2003, system manufacturers shipped 36,439 units. In 2006, the last year for which data is available, manufacturers shipped 63,683 units.

Bridgette Oliver, marketing and communications manager for ClimateMaster in Oklahoma City, the nation’s largest manufacturer of ground-source heat pump equipment, confirmed a rapid rise in sales. “Between 2005 and 2007, our revenue increased by 200 percent,” she said. “Our employees increased by 176 percent.”

Similarly, ClimateMaster’s major rival, WaterFurnace of Indiana, reported double-digit growth recently, and company executives said they were running two shifts at their manufacturing plant in Fort Wayne.

“Finding reliable and compliant employees to train” has been one challenge of such rapid growth, Ms. Oliver said. Moreover, system installation is bottlenecked, she says, because “drillers are overwhelmed. Drillers are where we’re really hurting.”

Though equipment manufacturers say they are able to keep pace with demand, many designers and installers have had slowdowns in parts delivery. “All the equipment is customized,” Mr. Maloney of EarthHeat said. “The suppliers are backlogged and a few of the companies are six to eight weeks out from being able to send us everything. Last year, the high-density polyethylene pipe we use was really hard to come by.”

The industry’s expansion is hampered as well by a lack of trained contractors. “Right now, we don’t have enough installers, and we don’t have enough drillers,” said Jack DiEnna, executive director of the Geothermal National and International Initiative, an industry group in Washington. “I’ve got drillers who are booked out for six months.”

Contractors say there is a similar shortage of employees. “We’re bringing in folks who aren’t necessarily career HVAC guys,” Mr. Maloney said, referring to heating, ventilation, and air-conditioning work. “We’re having to train them ourselves.” He says his 10-person company recruits employees using Craigslist in Seattle. “Even folks who have no skills are interested in learning, because it’s such a growth industry,” he said.

Rockford Geothermal is keeping pace by subcontracting “a lot of sheet metal work and plumbing,” Mr. Beattie said. He anticipates hiring three or four employees in the next six to 12 months.

The industry may find sales and workloads booming even further should Congress pass and the president sign the Renewable Energy and Job Creation Act of 2008. The legislation, sponsored by Charles B. Rangel, the New York Democrat who is chairman of the House Ways and Means Committee, would extend tax credits of up to $4,000 through the end of 2014 to homeowners who have ground source heat pumps installed. (The bill offers no aid to businesses.) The House approved the bill in May, and it is awaiting action in the Senate.

To help the industry grow, Mr. DiEnna and others look to models like the work force and contractor training programs now in development at Hudson Valley Community College in New York. The New York State Energy Research and Development Authority, the state’s energy authority, finances the programs.

“What we need to get this industry to its potential of at least 30 percent of the HVAC industry is exactly what’s happening now,” Mr. DiEnna said. “Companies like ClimateMaster are ramping up production. States such as New York are getting involved in work force development and contractor training. And there are increasing incentives from government. With this kind of growth, mom and pop shops can benefit as much as any of the big guys.”

 

“Handle With Care” - Ethical debates about new technologies

By CORNELIA DEAN
Published: August 11, 2008 (nytimes.com)

Last year, a private company proposed “fertilizing” parts of the ocean with iron, in hopes of encouraging carbon-absorbing blooms of plankton. Meanwhile, researchers elsewhere are talking about injecting chemicals into the atmosphere, launching sun-reflecting mirrors into stationary orbit above the earth or taking other steps to reset the thermostat of a warming planet.

This technology might be useful, even life-saving. But it would inevitably produce environmental effects impossible to predict and impossible to undo. So a growing number of experts say it is time for broad discussion of how and by whom it should be used, or if it should be tried at all.

Similar questions are being raised about nanotechnology, robotics and other powerful emerging technologies. There are even those who suggest humanity should collectively decide to turn away from some new technologies as inherently dangerous.

“The complexity of newly engineered systems coupled with their potential impact on lives, the environment, etc., raise a set of ethical issues that engineers had not been thinking about,” said William A. Wulf, a computer scientist who until last year headed the National Academy of Engineering. As one of his official last acts, he established the Center for Engineering, Ethics, and Society there.

Rachelle Hollander, a philosopher who directs the center, said the new technologies were so powerful that “our saving grace, our inability to affect things at a planetary level, is being lost to us,” as human-induced climate change is demonstrating.

Engineers, scientists, philosophers, ethicists and lawyers are taking up the issue in scholarly journals, online discussions and conferences in the United States and abroad. “It’s a hot topic,” said Ronald C. Arkin, a computer scientist at Georgia Tech who advises the Army on robot weapons. “We need at least to think about what we are doing while we are doing it, to be aware of the consequences of our research.”

So far, though, most scholarly conversation about these issues has been “piecemeal,” said Andrew Maynard, chief science adviser for the Project on Emerging Nanotechnologies at the Woodrow Wilson Center in Washington. “It leaves the door open for people to do something that is going to cause long-term problems.”

That’s what some environmentalists said they feared when Planktos, a California-based concern, announced it would embark on a private effort to fertilize part of the South Atlantic with iron, in hopes of producing carbon-absorbing plankton blooms that the company could market as carbon offsets. Countries bound by the London Convention, an international treaty governing dumping at sea, issued a “statement of concern” about the work and a United Nations group called for a moratorium, but it is not clear what would have happened had Planktos not abandoned the effort for lack of money.

“There is no one to say ‘thou shalt not,’ ” said Jane Lubchenco, an environmental scientist at Oregon State University and a former president of the American Association for the Advancement of Science.

When scientists and engineers discuss geoengineering, it is obvious they are talking about technologies with the potential to change the planet. But the issue of engineering ethics applies as well to technologies whose planet-altering potential may not emerge until it is too late.

Dr. Arkin said robotics researchers should consider not just how to make robots more capable, but also who must bear responsibility for their actions and how much human operators should remain “in the loop,” particularly with machines to aid soldiers on the battlefield or the disabled in their homes.

But he added that progress in robotics was so “insidious” that people might not realize they had ventured into ethically challenging territory until too late.

Ethical and philosophical issues have long occupied biotechnology, where institutional review boards commonly rule on proposed experiments and advisory committees must approve the use of gene-splicing and related techniques. When the federal government initiated its effort to decipher the human genome, a percentage of the budget went to consideration of ethics issues like genetic discrimination.

But such questions are relatively new for scientists and engineers in other fields. Some are calling for the same kind of discussion that microbiologists organized in 1975 when the immense power of their emerging knowledge of gene-splicing or recombinant DNA began to dawn on them. The meeting, at the Asilomar conference center in California, gave rise to an ethical framework that still prevails in biotechnology.

“Something like Asilomar might be very important,” said Andrew Light, director of the Center for Global Ethics at George Mason University, one of the organizers of a conference in Charlotte, N.C., in April on the ethics of emerging technologies. “The question now is how best to begin that discussion among the scientists, to encourage them to do something like this, then figure out what would be the right mechanism, who would fund it, what form would recommendations take, all those details.”

But an engineering Asilomar might be hard to bring off. “So many people have their nose to the bench,” Dr. Arkin said, “historically a pitfall of many scientists.” Anyway, said Paul Thompson, a philosopher at Michigan State and former secretary of the International Society for Environmental Ethics, many scientists were trained to limit themselves to questions answerable in the real world, in the belief that “scientists and engineers should not be involved in these kinds of ethical questions.”

And researchers working in geoengineering say they worry that if people realize there are possible technical fixes for global warming, they will feel less urgency about reducing greenhouse gas emissions. “Even beginning the discussion, putting geoengineering on the table and beginning the scientific work could in itself make us less concerned about all the things that we need to start doing now,” Dr. Light said. On the other hand, some climate scientists argue that if people realized such drastic measures were on the horizon, they would be frightened enough to reduce their collective carbon footprint. Still others say that, given the threat global warming poses to the planet, it would be unethical not to embark on the work needed to engineer possible remedies — and to let policy makers know of its potential.

But when to begin this kind of discussion? “It’s a really hard question,” Dr. Thompson said. “I don’t think anyone has an answer to it.”

Many scientists don’t like talking about their research before it has taken shape, for fear of losing control over it, according to David Goldston, former chief of staff at the House Science Committee and a columnist for the journal Nature. This mind-set is “generally healthy,” he wrote in a recent column, but it is “maladapted for situations that call for focused research to resolve societal issues that need to be faced with some urgency.”

And then there is the longstanding scientific fear that if they engage with the public for any reason, their work will be misunderstood or portrayed in inaccurate or sensationalized terms.

Francis S. Collins, who is stepping down as head of the government human genome project, said he had often heard researchers say “it’s better if people don’t know about it.” But he said he was proud that the National Human Genome Research Institute had from the beginning devoted substantial financing to research on privacy, discrimination and other ethical issues raised by progress in genetics. If scientific research has serious potential implications in the real world, “the sooner there is an opportunity for public discussion the better,” he said in a recent interview.

In part, that is because some emerging technologies will require political adjustments. For example, if the planet came to depend on chemicals in space or orbiting mirrors or regular oceanic infusions of iron, system failure could mean catastrophic — and immediate — climate change. But maintaining the systems requires a political establishment with guaranteed indefinite stability.

As Dr. Collins put it, the political process these days is “not well designed to handle issues that are not already in a crisis.” Or as Mr. Goldston put it, “with no grand debate over first principles and no accusations of acting in bad faith, nanotechnology has received only fitful attention.”

Meanwhile, there is growing recognition that climate engineering, nanotechnology and other emerging technologies are full of “unknown unknowns,” factors that will not become obvious until they are put into widespread use at a scale impossible to turn back, as happened, in a sense, with the atomic bomb. At its first test, some of its developers worried — needlessly — that the blast might set the atmosphere on fire. They did not anticipate the bombs would generate electromagnetic pulses intense enough to paralyze electrical systems across a continent.

Bill Joy, a founder of Sun Microsystems, cited the bomb in a famous 2000 article in the magazine Wired on the dangers of robots in which he argued that some technologies were so dangerous they should be “relinquished.” He said it was common for scientists and engineers to fail “to understand the consequences of our inventions while we are in the rapture of discovery” and, as a result, he said, “we have yet to come to terms with the fact that the most compelling 21st-century technologies — robotics, genetic engineering and nanotechnology — pose a different threat than the technologies that have come before. They are so powerful they can spawn whole new classes of accidents and abuses.”

He called it “knowledge-enabled mass destruction.”

But in an essay in the journal Nature last year, Mary Warnock, a philosopher who led a committee formed to advise the British government after the world’s first test-tube baby was born there in 1978, said when people fear “dedicated scientists and doctors may pursue research that some members of society find repugnant” the answer is not to allow ignorance and fear to dictate which technologies are allowed to go forward, but rather to educate people “to have a broad understanding of science and an appreciation of its potential for good.”

In another Nature essay, Sheila Jasanoff, a professor of science and technology studies at the Kennedy School of Government at Harvard, said a first step was for scientists and engineers to realize that in complex issues, “uncertainty, ignorance and indeterminacy are always present.”

In what she described as “a call for humility,” she urged researchers to cultivate and teach “modes of knowing that are often pushed aside in expanding scientific understanding and technological capacity” including history, moral philosophy, political theory and social studies of science — what people value and why they value it.

Dr. Hollander said the new ethics center would take up issues like these. “Do we recognize when we might be putting ourselves on a negative technological treadmill by moving in one direction rather than another?” she said. “There are social questions we should be paying attention to, that we should see as important.

“I mean we as citizens, and that includes people in the academy and engineers. It includes everybody.”

Forever Young: Cell change ‘keeps organs young’

http://news.bbc.co.uk/go/pr/fr/-/2/hi/health/7548874.stm
Published: 2008/08/10 17:05:40 GMT

Researchers may have found a way to halt the biological clock which slows down our bodies over the decades.

A US team thinks it may have found the genetic levers to help boost a system vital to cleaning up faulty proteins within our cells.The journal Nature Medicine reported that the livers of genetically-altered older mice worked as well as those in younger animals.

They suggested it might one day help people with progressive brain diseases.

These results show it’s possible to correct this protein ‘logjam’ that occurs in our cells as we get older, thereby perhaps helping us to enjoy healthier lives well into old age Dr Ana Maria Cuervo, Yeshiva University

The researchers, from Yeshiva University in New York, are focusing on a process which is central to the proper working of cells.

The fundamental chemicals of cells - proteins - often have very short working lives, and need to be cleared away and recycled as soon as possible.

The body has a system for doing just that, but it becomes progressively less efficient as we get older.

This leads to progressive falls in the function of major organs - the heart, liver and brain, some of which contribute to the diseases of old age.

Dr Ana Maria Cuervo, from Yeshiva, created a mouse with two genetic alterations.

The first, when activated, boosted the number of specific cell receptors linked to this protein recycling function, while the second allowed the first to be turned on whenever Dr Cuervo wished simply by modifying the animal’s diet.

She waited until the mice were six months old - the point at which age-related decline in the protein-recycling system begins - then turned on the receptor gene.

When examined at two years old, the liver cells of these mice were far more effective at recycling protein compared with normal mice.

When the overall liver function of the very old genetically-modified mice was tested, they performed at a comparable level to much younger mice.

Dr Cuervo said: “These results show it’s possible to correct this protein ‘logjam’ that occurs in our cells as we get older, thereby perhaps helping us to enjoy healthier lives well into old age.”

She now plans to test animal models of Alzheimer’s and Parkinson’s diseases, believing that the abnormal protein deposits in Alzheimer’s in particular might be dealt with more effectively this way.

Thomas von Zglinicki, Professor of Cellular Gerontology at Newcastle University, said that the results were “very exciting”.

“It’s not often you see studies where they have managed to improve function in this way.

“What they seem to have managed is to maintain the mice at this young stage, and both restore and maintain normal activity.”

He said that it should, in theory, be possible to achieve the same effect across the whole body.

A spokesman for the Alzheimer’s Society said: “As we age we have an increase in protein misfolding and general faults in protein processing, so the ability to maintain an effective system to clear these would be beneficial.

“However, a direct line to the clearance of defective proteins in the brain is not so clear from this research.”

Info found thanks to the Genome Web.

Prescription Data Used To Assess Consumers

Records Aid Insurers but Prompt Privacy Concerns

By Ellen Nakashima
Washington Post Staff Writer
Monday, August 4, 2008; A01

Health and life insurance companies have access to a powerful new tool for evaluating whether to cover individual consumers: a health “credit report” drawn from databases containing prescription drug records on more than 200 million Americans.

Collecting and analyzing personal health information in commercial databases is a fledgling industry, but one poised to take off as the nation enters the age of electronic medical records. While lawmakers debate how best to oversee the shift to computerized records, some insurers have already begun testing systems that tap into not only prescription drug information, but also data about patients held by clinical and pathological laboratories.

Traditionally, insurance companies have judged an applicant’s risk by gathering medical records from physicians’ offices. But the new tools offer the advantage of being “electronic, fast and cheap,” said Mark Franzen, managing director of Milliman IntelliScript, which provides consumers’ personal drug profiles to insurers.

The trend holds promise for improved health care and cost savings, but privacy and consumer advocates fear it is taking place largely outside the scrutiny of federal health regulators and lawmakers.

Ingenix, a Minnesota-based health information services company that had $1.3 billion in sales last year — and Wisconsin-based rival Milliman — say the drug profiles are an accurate, less expensive alternative to seeking physician records, which can take months and hundreds of dollars to obtain. They note that consumers authorize the data release and that the services can save insurance companies millions of dollars and benefit consumers anxious for a decision.

“Some insurers can make a decision in the same day, or right on the spot,” Franzen said. “That’s the real ‘value-add.’ “

But the practice also illustrates how electronic data gathered for one purpose can be used and marketed for another — often without consumers’ knowledge, privacy advocates say. And they argue that although consumers sign consent forms, they effectively have to authorize the data release if they want insurance.

“As health care moves into the digital age, there are more and more companies holding vast amounts of patients’ health information,” said Joy Pritts, research professor at Georgetown University’s Health Policy Institute. “Most people don’t even know these organizations exist. Unfortunately the federal health privacy rule does not cover many of them. . . . The lack of transparency with how all of this works is disturbing.”

Ingenix and Milliman create the profiles by plumbing rich databases of prescription drug histories kept by pharmacy benefit managers (PBMs), which help insurers process drug claims. Ingenix, for instance, has servers in the PBM data centers, updating the drug files as frequently as once a day, said John Stenson, senior vice president of consulting for Ingenix, which is a division of UnitedHealth Group. The corporation also owns UnitedHealthcare, the nation’s second-largest insurer.

When an insurer makes an online query about an applicant, Ingenix or Milliman’s servers scour the data and within minutes or less return reports to a central server at the company. The server aggregates the information going back as far as five years, including the drugs and dosages prescribed, dates filled and refilled, the therapeutic class and the name and address of the prescribing doctor.

Then comes the analysis.

Ingenix’s MedPoint tool provides insurers a “pharmacy risk score,” or a number that represents an “expected risk” for a group of people, such as 30- to 35-year-old women who have taken prescription drugs, Stenson said. Higher scores imply higher medical costs.

Milliman’s IntelliScript codes drugs red, yellow or green, according to the insurer’s instructions, with red signaling the greatest risk, Franzen said. Red codes could include the so-called AIDS cocktail drugs and cancer medications, he said.

The companies receive data only on individuals who are in clients in PBMs’ databases, generally excluding, say, people who pay for drugs in cash. The profiles cost insurers about $15 a search. IntelliScript gets about 1 million queries from insurers a year, largely individual health insurers.

The system can save money for insurers, said Richard Dick, an entrepreneur who built the database system that Ingenix acquired in 2002.

For instance, if MedPoint produces a report that an individual has been on the highest dose of the cholesterol-reducing drug Zocor for 18 monts, the insurer “would be able to know that you have a very high, near-intractable cholesterol problem,” Dick said, and could avoid a costly blood test.

From a business standpoint, it makes no sense for an insurer to sell a plan with a $200 monthly premium if the company knows that the consumer is taking medications that cost $400 every six months, industry experts said. That is why having access to an “objective” source of third-party information is valuable, said Tia Goss Sawhney, a Chicago area health insurance actuary who has used both companies’ tools. “Though most people tell the truth most of the time, there are people out there who don’t, who leave out something that’s incredibly relevant, who may even be able to defraud a company,” she said. “That’s important because ultimately the people who tell the truth have to pay for those who don’t.”

Franzen, whose firm expects revenue of $575 million this year, said his clients tell him that about 10 percent of applicants do not disclose pertinent medical conditions in their applications that are later revealed by prescription drug history.

Some health experts worry that insurance companies can make faulty assumptions by looking at prescription drug records, because many drugs have multiple uses. “I had a patient on Amitriptyline for migraines and they were denied life insurance because it’s also an antidepressant,” said physician Kate Atkinson of Amherst, Mass. “I had to explain it wasn’t being used for depression.” Another patient was on Prozac — not for depression, but for menopausal hot flashes. “I wrote an appeal letter, and they still wouldn’t give it to her,” Atkinson said.

Services such as MedPoint are just “one of many tools” underwriters use to make coverage decisions, said Tyler Mason, a spokesman for UnitedHealthcare, which uses MedPoint. A high-risk score on a profile will often lead to requests for more information from the applicant, he said.

Ingenix and Milliman officials stress that they provide data only with the patient’s consent, as required by the Health Insurance Portability and Accountability Act (HIPAA), a 1996 law that governs personal health records information. But HIPAA does not give the Department of Health and Human Services the ability to directly investigate or hold accountable entities, such as pharmacy benefit managers or companies such as Ingenix and Milliman, who are not covered by HIPAA.

A health privacy proposal pending in Congress would expand federal officials’ ability to regulate such “downstream” organizations, audit their activities and impose civil fines. The bill also includes a prohibition on the sale of electronic medical records.

Tim Sparapani, senior legislative counsel at the American Civil Liberties Union, said that the products that Ingenix and Milliman are marketing represent the “commodification” of electronic medical records by third parties. “We’ve got to stop these practices before the marketplace is fully developed and patients lose all control over their medical information,” he said.

The field is growing rapidly. Realtime Solutions Group, a company in Woodridge, Ill., is testing whether lab data can be aggregated with prescription and other data for underwriting purposes. The firm is working with two major commercial labs and three large insurers, using thousands of real applicants. Initial results are promising enough that the company plans to proceed to the data-analysis stage, company co-founder Tedd Determan said.

“A lot of insurance companies are starting to use this type of data,” said Determan, who co-founded IntelRx, a company that mined prescription databases and was sold to Milliman in 2005. “They said, ‘All right. Prescription data is working, let’s go and look at other types of data, too.’ It’s because of the success of one, that we’re going after others.”

In February, the Federal Trade Commission issued an order saying that MedPoint and IntelliScript are consumer reports under the Fair Credit Reporting Act, so the companies must notify insurers that consumers denied insurance on the basis of these reports have the right to request a copy of the report and that errors be corrected. The FTC’s order followed a settlement of allegations that the companies violated the credit-reporting law by failing to provide such notice to insurers.

Bob Gellman, an independent privacy consultant in Washington, said the FTC’s decision not to fine the companies sends “the message that it is okay to ignore the law.” That, he said, “is absolutely outrageous.”

As more health records become electronic, he said, more parties will compete to sell more comprehensive patient data to insurers, driving down data prices. “It will all likely be lawful,” Gellman said, “but consumers will likely continue to have no real meaningful choices if they want insurance.”

Dick, who conceived the idea of linking the pharmacy databases for underwriting purposes a decade ago, said the pharmacy benefit managers understood the system’s privacy implications. He said their attitude seemed one of, ” ‘Ooh, this is a 60 Minutes’ story in the making.’ Generally, they wanted to make it a super-secret database, restricted to underwriting.”

But now, he said, “there’s a huge case for it being opened up for all legitimate access,” whether for a patient in an emergency room or for federal government purposes. The key, he said, is full transparency.

He said he has created a privacy tool that requires users to consent before specific data, such as prescription histories, can be released. To work, he said, the tool must be independent of all who hold the data.

“Otherwise,” he said, “you have the fox in charge of the henhouse.”

Staff researcher Magda Jean-Louis contributed to this report

Confirmation du lien entre réchauffement et très fortes précipitations (étude)

Confirmation du lien entre réchauffement et très fortes précipitations (étude)

AFP 07.08.08 | 21h10 (lemonde.fr)  

Des climatologues américains et britanniques ont confirmé le lien entre le réchauffement climatique et l’accroissement des très fortes précipitations en comparant modèles informatiques et observations par satellite, selon une étude publiée jeudi.

L’amplification des pluies d’une intensité extrême s’est même révélée nettement plus grande que ce qu’avaient prévu jusqu’à présent les modèles informatiques, soulignent les auteurs de cette étude parue dans la revue américaine Science datée du 8 août.

Pour comprendre comment les précipitations répondaient au réchauffement du climat, ces chercheurs ont étudié les changements naturels liés au courant marin chaud El Niño dans le Pacifique sud qu’ils ont utilisé comme un laboratoire pour vérifier leurs hypothèses.

En se basant sur vingt ans d’observations faites par des satellites, ces scientifiques ont découvert un lien très clair entre l’intensité extrême des pluies tropicales et la température de l’eau, la fréquence de très fortes précipitations augmentant durant les périodes chaudes et diminuant lors des périodes froides.

“Une atmosphère plus chaude contient davantage d’humidité, ce qui accroît l’intensité des trombes d’eau”, explique Brian Soden, professeur de climatologie à l’Université de Miami (sud est), un des co-auteurs de ce rapport.

“La comparaison des observations satellitaires avec les résultats des modèles climatiques informatiques permet de mieux comprendre comment les précipitations répondent au réchauffement du climat”, ajoute Richard Allan, de l’Université de Reading en Grande Bretagne, également co-auteur de cette recherche.

In one year, Decode doubles its revenues

Decode Nearly Doubles Revenues in Q2

[August 7, 2008] By a GenomeWeb staff reporter

NEW YORK (GenomeWeb News) – Decode Genetics reported after the close of the market on Wednesday that its second-quarter revenues nearly doubled to $15 million from $7.6 million year over year.

The Reykjavik, Iceland-based biopharmaceutical and molecular diagnostics firm noted in a statement that it also has $15.1 million in deferred revenue that will be recognized over future reporting periods.

Decode’s net loss increased 13.6 percent to $18.4 million, or $.30 per share, from $16.2 million, or $.27 per share. The quarter includes $1.2 million in non-operating expense tied to a revaluation of the firm’s non-current auction rate security investments. Decode also had taken charges in each of the previous two quarters related to the auction-rate securities.

The company’s R&D spending was cut 44.8 percent to $8 million from $14.5 million year over year, while its SG&A expenses edged up 4.4 percent to $7.1 million from $6.8 million.

Decode finished the quarter with $23.7 million in cash, cash equivalents, and current investments.

“As we ramp up our sales efforts in diagnostics and deCODEme, our discovery engine is providing us with a steady stream of intellectual property and content for new tests that leverage the same product development infrastructure,” Kari Stefansson, CEO of Decode, said in a statement.

Dog Cloning: Business of the Future?

Booger is back: Woman receives 5 cloned puppies

By HYUNG-JIN KIM –SEOUL, South Korea (AP)

Booger is back. An American woman received five puppies Tuesday that were cloned from her beloved late pitbull, becoming the inaugural customer of a South Korean company that says it is the world’s first successful commercial canine cloning service.

Seoul-based RNL Bio said the clones of Bernann McKinney’s dog Booger were born last week after being cloned in cooperation with a team of Seoul National University scientists who created the world’s first cloned dog in 2005.

“It’s a miracle!” McKinney repeatedly shouted Tuesday when she saw the cloned Boogers for which she paid $50,000.

“Yes, I know you! You know me, too!” McKinney said joyfully, hugging the puppies, which were sleeping with one of their two surrogate mothers, both Korean mixed breed dogs.

The team of scientists working for RNL Bio is headed by Lee Byeong-chun, a former colleague of disgraced scientist Hwang Woo-suk, who scandalized the international scientific community when his purported breakthroughs in cloned stem cells were revealed as fake in 2005.

Independent tests confirmed the 2005 dog cloning was genuine, and Lee’s team has since cloned more than 20 canines.

But RNL Bio said that its cloning was the first successful commercial cloning of a canine.

“RNL Bio is commencing its worldwide services with Booger as its first successful clone,” the company said in a statement.

McKinney contacted Lee after Booger died of cancer in April 2006. She had earlier asked U.S.-based Genetics Savings and Clone to clone her dog but the company shut down due to lack of demand in late 2006 after only producing a handful of cloned cats and failing to produce any dog clones.

The Korean scientists brought the dog’s frozen cells to Seoul in March and nurtured them before launching formal cloning work in late May, according to RNL Bio.

Lee’s team have identified the puppies as Booger’s genuine clones, and his university’s forensic medicine team is currently conducting reconfirmation tests.

McKinney said she was especially attached to Booger because he saved her life when she was attacked by another dog three times his size. The incident resulted in her left hand being severely injured, and also damaged her leg nerves and stomach. Doctors later reconstructed her hand and she spent part of her recovery in a wheelchair.

McKinney said Booger acted as more than just a canine companion as she recuperated from the attack.

Her dog pulled her wheelchair when its battery ran out. He opened her house door with his teeth and helped her take off her shoes and socks, even though she never trained him to do so.

“The most unusual thing about Booger was that he has a unique ability to reason,” she said. “He seems to understand I couldn’t use my hands.”

McKinney, a screenwriter who taught drama at U.S. universities, said she will take three of the cloned dogs to her home in California and donate the others to work as service dogs for the handicapped or elderly. She said she lives with five other dogs and three horses.

RNL Bio charges up to $150,000 for dog cloning but will receive just a third of that sum from McKinney because she is the first customer and helped with publicity, said company head Ra Jeong-chan.

Ra said his firm eventually aims to clone about 300 dogs per year and is also interested in duplicating camels for customers in the Middle East.

On the Net: RNL Bio: http://rnl.co.kr/eng/main.asp

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