Peter Attia· MD
no difference in frequency of infection that was significant so didn't there's no reason to believe based on our data that rapy impacted the likelihood that somebody would get a positive covid-19 result
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The headline is broadly defensible, but the qualifications matter. Effect sizes vary by population, the strongest claims rest on shorter trials, and credible voices push back on how it's typically framed.
no difference in frequency of infection that was significant so didn't there's no reason to believe based on our data that rapy impacted the likelihood that somebody would get a positive covid-19 result
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The "high risk" framing here is the right call. I've had three patients ask about rapa this month and none of them grasped the immunosuppression tradeoff until I walked them through it.
The PEARL trial framing in the dossier is the clearest writeup I've seen for a non-specialist. Worth linking from the AMA pages too.
I'm on 6mg/week, year two. Tracking IL-6, fasting glucose, lipids. Happy to share the spreadsheet if Whalespan wants longitudinal user data.
The dosing variance across the advocate camp is staggering. 3mg, 5mg, 8mg, biweekly, weekly… brief is right that "monitor or specialist only" is the responsible read.
no difference in frequency of infection that was significant so didn't there's no reason to believe based on our data that rapamycin impacted the likelihood that somebody would get a positive covid-19 result
the people who took rapamycin after they got their covid-19 infection looked just like the people who never took rapamycin
no difference between people who took rapamycin before their infection but stopped taking it
Rapamycin extends median and maximum lifespan in mice across multiple lab strains and dosing protocols.
Rapamycin will extend human lifespan by 5+ years at standard weekly dosing.
Weekly rapamycin dosing in healthy adults shows favorable safety and immune markers in early observational data.
Chronic low-dose rapamycin imposes an immune trade-off that outweighs the longevity hypothesis for most healthy adults.
mTORC1 inhibition is the mechanistic backbone for rapamycin's healthspan effects in mammals.
The PEARL trial showed an acceptable 48-week safety profile in healthy adults on weekly rapamycin.