Skip to Content

Genomics Into Drugs

Kari Stefansson, founder and CEO of deCode Genetics, explains why gene hunting provides tailor-made drug targets.
April 12, 2006

DeCode Genetics, an Icelandic biotech and genomics company, is best known for its unique approach to gene discovery. Scientists use the extensive genealogical records of the Icelandic community to hunt down genetic variations that boost risk for common diseases, such as heart disease, asthma, and diabetes.

In its 10-year history, deCode has developed research programs for 50 diseases and isolated 15 genes linked to common diseases. The company is now translating its genomics success into drug development. Currently, it is testing in clinical trials compounds to treat heart attacks, asthma, and peripheral arterial disease.

Kari Stefansson, deCode’s chief executive officer, tells Technology Review why gene hunting is so well-suited to drug discovery and describes why he thinks big pharma will soon jump on the bandwagon.

Technology Review: DeCode has now isolated many gene variants that have an impact on risk for common diseases. Do they have anything in common?

Kari Stefansson: These gene variants almost always influence where you fall on the disease spectrum – whether you are at risk for a disease or whether you are protected. For example, we found one variant that increases risk for stroke and another that confers protection against stroke. So these two variants influence gene expression in the opposite direction.

This discovery has some interesting implications. You can develop an inhibitor of the enzyme [coded by the gene] – but do you take it to the norm of the general population or to the norm that confers protection? We must be cognizant of the fact that this likely will confer risk of some other problem. Evolution has left that variation for a reason.

TR: So how does that affect the way you study disease genes?

KS: The key to the understanding of common diseases is to study them in the context of evolution and population history. Gene variants involved in common diseases are almost always under selection. That’s important because there is a difference in the variants between, say, Iceland and Africa.

[In a study published last year,] we found a gene variant that boosts risk for heart attacks in African Americans by 250 percent, but increases risk in Caucasians by only 16 percent. This variant is not found in Africa, so it must have [evolved in people after the migration out of Africa.]

[The gene is involved in the leukotriene pathway, which is part of the body’s immune response.] My hypothesis is that when people left Africa 60,000 years ago, they were exposed to different bacteria. So evolution increased the leukotriene pathway, which also increased risk of heart attack. At that time, though, the risk didn’t matter because life expectancy was so low.

But as life expectancy began to increase, Caucasians had many generations to evolve other gene mutations to compensate for the negative effect of the variant. But African Americans, who acquired the gene variant more recently through admixture, have not had the same amount of time to develop compensatory variants.

TR: So genes involved in common diseases are under evolutionary selection. How does that affect drug discovery?

KS: These variants almost always impact [the normal] physiological function of a gene. It’s not like a mutation that makes a dysfunctional [gene product], such as cystic fibrosis or sickle cell anemia. These are examples of accidents in evolution, which are difficult therapeutic challenges. It’s very difficult to replace an abnormal gene product. It’s easier to design a molecule to turn up or down the normal physiological function of a biochemical pathway.

TR: These principles seemed to have worked for deCode’s drug discovery program – the company is set to begin its first round of late-stage clinical trials for a drug to prevent heart attack.

KS: Yes. We isolated a genetic variant that doubles risk of a myocardial infarction [heart attack.] The variant increases production of leukotriene B4, an important inflammatory mediator.

We found that pharma companies had already developed several inhibitors of the protein made by the disease gene, which had been shelved [because they weren’t effective for the application for which they had been developed.] We licensed a compound from Bayer and found that it can down regulate leukotriene B4 to below normal levels in people at risk. We are now starting phase III trials to show that this decreases the risk of heart attack.

We have also found that people who have had a heart attack but do not have the at-risk variants also have up-regulated leukotriene B4. That means we can use the same measure to control genetic and environmental risk.

TR: You also have a substantial benefit when it comes to clinical trials – a built-in way to determine who is most likely to respond to the drug.

KS: You can use genetics as a marker of where people fall on the disease spectrum. Then you can find high-risk people and recruit them into the trial. It’s likely that a clinical trial in that population will be a more sensitive measure of the [effectiveness of the drug.]

We are focusing the clinical trials of [our heart attack drug] largely on African Americans with the gene variation, partly because the need is greatest and partly because it’s the best thing to do in terms of trial design. We are also about to start a phase II trial of a drug for a peripheral artery disease, which will focus on people at risk from the specific pathway [that we identified in genetic studies.]

TR: DeCode has traditionally been known as a genomics company. Has your focus shifted from gene discovery to drug discovery?

KS: The goal of the company is to discover drugs and bring them to market. We are still using genetics – it is a prerequisite for everything we do. It gives us much better drug targets and helps us to go much more swiftly from drug discovery to [late-stage] clinical trials. Traditional drug development companies start with an unproven hypothesis that they don’t know is correct. We start with an observation, so we have proof of concept from the beginning.

TR: When deCode was first starting out, several other genomics companies were also in the game. But they eventually died out or shifted focus. Now you predict more companies will move back into this field?

KS: Back when we started, there were 25 similar companies – but they all changed focus because they could not find disease genes. Genetics is a resource based on people. We were successful because we based our company on a population (see “Translating Iceland’s Genes into Medicine”).

Once genome association technology is refined, it will become easier to find disease genes. Within a relatively short time, there will be many more programs like this.

Companies like GlaxoSmithKline will begin to use genome wide association studies to find targets and to design clinical trials. But my prediction is that many people will have difficulty handling the amount of information [generated by these studies.]

Keep Reading

Most Popular

It’s time to retire the term “user”

The proliferation of AI means we need a new word.

The problem with plug-in hybrids? Their drivers.

Plug-in hybrids are often sold as a transition to EVs, but new data from Europe shows we’re still underestimating the emissions they produce.

Sam Altman says helpful agents are poised to become AI’s killer function

Open AI’s CEO says we won’t need new hardware or lots more training data to get there.

An AI startup made a hyperrealistic deepfake of me that’s so good it’s scary

Synthesia's new technology is impressive but raises big questions about a world where we increasingly can’t tell what’s real.

Stay connected

Illustration by Rose Wong

Get the latest updates from
MIT Technology Review

Discover special offers, top stories, upcoming events, and more.

Thank you for submitting your email!

Explore more newsletters

It looks like something went wrong.

We’re having trouble saving your preferences. Try refreshing this page and updating them one more time. If you continue to get this message, reach out to us at with a list of newsletters you’d like to receive.