For the most part, there is only one human chronotype, and it rises with the sun and sleeps relatively shortly after nightfall
People’s minds have been hijacked through marketing to believe that a chronotype is a personality trait. That they’re a “bear” or a “dolphin”
This is New Age pseudoscientific bullshit
A chronotype is simply the timing of when your body naturally wants to sleep and wake, based on how it’s currently synced to light and darkness. It’s the time of day your body clocks are set to under current environmental conditions
The key words to remember are “under current environmental conditions” as we discuss artificial light and circadian disruption
Studies on hunter-gatherer populations with no artificial light show sleep timing clustering within about a 2 hour window across all individuals
2 hours
The 4 to 6 hour spread we see in modern populations is not a matter of genetic expression. A “night owl” doesn’t exist. That is the result of circadian disruption
The genetic variation in chronotype is real but modest, and it lives almost entirely in a handful of clock genes
The core ones are PER1, PER2, PER3, CLOCK, and CRY1. These genes encode the proteins that drive the transcription-translation feedback loop sitting at the heart of every cell’s 24 hour oscillator. Small mutations or polymorphisms in these genes can slightly lengthen or shorten the intrinsic period of that loop, which in turn shifts the phase of the whole system earlier or later
The most studied example is a mutation in CRY1 that extends the intrinsic clock period to around 24.5 hours instead of the normal 24.2. That half hour difference compounds over days and pulls sleep timing progressively later
People carrying this variant have what clinicians call Familial Delayed Sleep Phase Disorder. It’s heritable, it’s real, and it genuinely resists behavioral correction. But, people need to understand that this is a disorder. It sits at the extreme tail of the distribution
PER3 has a well documented length polymorphism, meaning some people carry a longer version of the gene and some carry a shorter one. The longer variant correlates with earlier sleep timing and stronger homeostatic sleep pressure, meaning those people feel the cognitive consequences of sleep deprivation harder and faster. The shorter variant correlates loosely with later sleep timing and slightly more resilience to sleep loss. This is probably the most relevant polymorphism for what people casually call chronotype
The CLOCK gene has a variant associated with evening preference and is also linked to higher rates of mood disorders and metabolic dysfunction, which itself tells you something important, that evening shifted genetics carry health costs, which suggests the ancestral optimal is morning anchored
Now here’s what ties it all together from a circadian standpoint:
These variants do NOT change what your circadian clocks responds to. Light still entrains every genotype. The variants just shift the default period slightly, so a genuinely late running clock needs a stronger morning light signal to land at the same phase as a neutral genotype. Same prescription, but higher dose
Most people claiming a genetic chronotype have never tested that under ancestral circadian aligned light conditions
Hunter-gatherer populations carry the same genetic diversity as industrialized ones, but show dramatically narrower sleep timing variance. The genes are there, but the environment just stops amplifying them
consider this idea:
"if we allow farmers to have tractors, it will eliminate 90% of all farm jobs! the government must take over all agriculture and ensure that productivity does not increase!"
because that's exactly what they are doing again, mistaking labor for the product and not the input, mistaking productivity for a social ill.
it's just wild what grasping, avaricious luddites these people are.
collectivists are always the same: thieves masquerading as benefactors.
Maybe, if ITP results weren't twisted. The first study flubbed the 4000 ppb intended astaxanthin dose to a human equivalent 10 mg (1840 ppb x .081 x 70 kg).
The most recent astaxanthin study halved that to a human equivalent 5 mg, which isn't found anywhere in the commercial marketplace or recent human experiments. Their paper didn't acknowledge the first study's mistake because it's all government funded. And the most recent paper studiously avoided previous and current mistakes, explaining away their Jackson lab female control group age as an anomaly.
All this astaxanthin prevarication showed that the researchers forgot about the primary purpose of rodent studies, to benefit humans.
I don't see anything earth-shaking in the recent past on https://t.co/eWTZ4wKJjo except for "Vitamin C Alleviates Aging in Cynomolgus Monkeys" regarding its human-equivalent dose of ~700 mg/day.
Does the world’s richest person cares about health-company status among mere multi-billionaires? He hasn’t started a health-related venture AFAIK. Maybe one day in the middle of building a million robots and satellites, he’ll have a health emergency that will change everything for everybody else. Or maybe one day he’ll realize that Earth-adapted human physiology can’t survive trips to and life on Mars, and focus back to what can be done on this planet.
TMAO and heavy hydrogen
https://t.co/NpAwL6CuXq
A 2026 review subject was possible involvement of deuterium in TMAO levels, which contrasted with the usual TMAO meme. I’ll curate this paper through an outline of its sections:
@LaurieGreen36 How about getting a better life?
My daughter-in-law is your age, married five+ years. My son and her have two children now. She found out that she is quite the attentive and accomplished mother.
Find out what you can do with bringing life into the world with a suitable man.
@Kevin_McKernan@bryan_johnson Getting shingles isn't all that bad compared to its vaccine. Had it twice, once in my 40s, once in my 50s. Good wakeup calls, first to make efforts to get healthy, second time that I wasn't doing enough to regain a healthy innate immune system.
Add vitamin C to broccoli sprouts?
https://t.co/A1mRdmeR3n
A 2026 paper presented results of a clinical trial that selectively added myrosinase enzyme via mustard powder and vitamin C to measure in vivo effects on glucoraphanin conversion to sulforaphane:
Self-reinforcing feedback loops of aging
https://t.co/iww2vNqAqF
A 2026 rodent study investigated age-associated queuine decline. Queuine is characterized as a “longevity vitamin” in the cited 2018 review Prolonging healthy aging: Longevity vitamins and proteins, along with ergothioneine, astaxanthin, and taurine.
The hops compound xanthohumol
https://t.co/dZMtUeZIYI
Two 2026 papers, with the first an in vitro study of over 2000 compounds to select those that best inhibit BACH1:
Year Six of Changing to a youthful phenotype with sprouts
https://t.co/Xxbo2i1ERj
I’ve continued daily practices from Year Five to experience another year without being sick (if I don’t count getting MSG poisoning from Chinese food.)
2026 diet and supplement changes
https://t.co/hF6rhD3AZX
I switch things around pretty often, but I haven’t said much about diet and supplement changes since this time last year. Here’s what I’ve done in terms of changes that I’ve since abandoned or reduced, followed by additions or increases that I’ve kept.