Esther Dyson has been an innovator in the high tech fields. She has now turned her attention to health care and how information processing can improve options for health care choices. That led to an interest and career focus on the mapping of the human genome. But it's about good healthcare more than about genomes -- "if you know more about yourself and how things work, on the margin, chances are, you're going to be more healthy."
Esther Dyson: The idea behind the Personal Genome
Project was created by George Church at Harvard Medical School. It
begins with ten people who volunteer to put their entire genome and all
their health records online for anybody to see, with our identities
visible. And the idea there was, in a sense, to demystify it. And then,
ultimately, to [map] hundreds of thousands of people, so that we'd have
a lot more data to [use to] explore the genome and medical care and so
forth and so on. Most medical research, certainly when it's published,
is with unidentified subjects. And the idea here was for us to be role
models, to prove that this information wasn't secret, or scary, or
dangerous.
Dyson is an investor in 23andMe.
23andMe, Inc. is a privately-held company dedicated to helping individuals understand their own
genetic information using recent advances in DNA analysis technologies and web-based interactive tools.
23andMe enables individuals to gain deeper insights into personal ancestry, genealogy and inherited
traits. 23andMe was founded in April 2006 by Linda Avey and Anne Wojcicki.
The name 23andMe refers to the 23 pairs of chromosomes that make up
each individual's genome. 23andMe connects individuals to their unique, paired set of 23 chromosomes.
With a tube of saliva and $399, you can get the latest information about your DNA from 23andMe. Discover how your genes affect your health. Get information on 114 traits and diseases. See your personal history through a new lens with detailed information about your ancient ancestors and comparisons
to global populations today. See what you have in common with other members of 23andMe, and what
makes you unique. Their community discusses new topics every day,
ranging from questions about the latest research discoveries to answers
about the genetics of family resemblances.
Individuals are beginning to assemble their own health records - what the other doctors have done, what drugs you have taken and are taking, what
conditions you might have--your genetic information could be helpful here. Times are changing -- there are companies now that are already using drug-interaction databases. "somebody who's taking 18 or 19 different drugs and you take 10 of them
away, and the patient gets better rather than worse. So, that's the
first part, just the patient having the data aggregated in one place." Dyson points out that people are interested in their own health details -- and that doctors might not have the interest or time to delve into personal histories the same way individuals are. Genomes are part of that "detail".
Genomes themselves give you only--with a few exceptions--percentages. So,
it's not like you put this information up and people are going to stick
pins into it. I actually was expecting more medical spam about, you
know, "We looked at your genome. You should buy such and such
nutri-ceutical." What will be exciting is when you have hundreds of
thousands of these and you say, "Oh, wow. They're these five genes that
seem to interact." Most things are not a gene. It's usually a lot of
different genes--and then, combined with what you eat and whether you
sleep enough and whether you stay warm enough and all these other
things--that actually produce a real outcome in a person of being in
such and such condition.
Health care is changing, and information technology is leveling the playing field some now -- and as Esther predicts, more in the future.
Esther Dyson: I think you'll see a lot of changes in
five to ten years. But not for everybody. Like everything else, this is
going to benefit--let's face it--the rich and the well educated first.
They're the ones right now who, if they have a problem, they probably
have a friend at Mount Sinai [Hospital]. And so, they can get the best
care anyway. You shouldn't need a friend at Mount Sinai to get good
cancer care. That's the real difference. There will still be a leg for
people who live in the wrong place or who are at the bottom of the
pyramid. When you do things with computers and with IT, they actually
scale very well. So, you can't reproduce the friend at Mount Sinai. But
you can reproduce an information system that gives you access to the
same information.