From the FDA perspective 23andme has the burden of proof.
It's nice to have the guns.
If you get completely different answer based on the company that you ask about your risk, do you really think that's no issue?
Discrepant diagnoses are hardly a new issue in medicine.
I'd note that the article you referred to is almost 5 years old now. How much more data does 23andMe have to make accurate predictions? A good order of magnitude at least.
How much more will they have next year? Not so much more, as our benevolent protectors have stopped their data collection efforts.
Yes, it would be nice if medicine got a lot better. They'd make predictions, they'd predict the same things, and they'd be right.
It doesn't get better by preventing data collection efforts. It doesn't get better by preventing prediction efforts. Get the FDA out of the way, and we'd have free GoogleCare in a couple of years for most routine doctor visits.
In the article you link, Ventner mentioned
a call to use more markers that provide information on risk factors for taking medication
This is actually the prime use for 23andMe info right now, and was useful 5 years ago. You get info on your particular genotype for some enzymes, which largely determines how well you metabolize different drugs. Turns out I'm a poor metabolizer for the enzyme that metabolizes a drug I was given years ago, and had a bad reaction to. Whaddya know, this crazy science stuff actually works.
A lot of drugs fail in stage 4 trials. Would you really want to have all those drugs on the market?
Yes. And that's even if I don't get the FDA incinerated in the bargain.
Having the drugs on the market doesn't require anyone to use them, it only allows them to use them. Many drugs with failed trials would likely be very useful for a lot of people. And they still have to get permission from a duly deputized agent of the state to get a prescription. Bah! What do doctors know about medicine? About your health? It's not like they're the all knowing, all seeing FDA apparatchiks.
How charming it is that we have to get permission to try to heal ourselves.
By the way, Stage 4 trials? You're talking Phase 4 monitoring?
Get the FDA out of the way, and we'd have free GoogleCare in a couple of years for most routine doctor visits.
I'm not aware that the FDA was responsible for Google ending Google Health.
By the way, Stage 4 trials? You're talking Phase 4 monitoring?
Sorry I was mentally starting to count with 1 and not 0.
Having the drugs on the market doesn't require anyone to use them, it only allows them to use them.
The question would be whether the companies would still run the trials if they weren't legally mandated. Trials are expensive and if the government w...
This is prompted by Scott's excellent article, Meditations on Moloch.
I might caricature (grossly unfairly) his post like this: