That's an interesting argument, but couldn't you use the same reasoning to argue that telomeres are the main cause of aging-related death? The mental model I'm thinking is: As you run out of telomeres, you get diseases and you can't reproduce - and that’s maladaptive. So there’s evolutionary pressure to slow down the shortening rate, up to the point where you have children (plus grandchildren in the case of humans). When you're living long enough to have one or two generations of offspring, there’s no more pressure to correct the telomere problem.
Wouldn't your argument and mine be equally consistent with the featured article (that shortening rate predicts life span)?
So a truly optimal age system would have no old age at all, you will just die off after your children are self-sustaining.
According to Our World In Data [1] a 20-year-old would expect to live to 60 in 1850 (before penicillin), versus to 80 now.
[1] https://ourworldindata.org/life-expectancy#it-is-not-only-ab...
This means first grandchildren in early 40s (rather than late 50s), and first great grandchildren by mid 60s (rather than mid 80s)
No, at least according to some anthropologists and evolutionary biologists. For example see the Grandmother Hypothesis https://en.m.wikipedia.org/wiki/Grandmother_hypothesis
"Some experiments have raised questions on whether telomerase can be used as an anti-aging therapy, namely, the fact that mice with elevated levels of telomerase have higher cancer incidence and hence do not live longer. Telomerase also favors tumorogenesis, which leads to questions about its potential as an anti-aging therapy.[36] On the other hand, one study showed that activating telomerase in cancer-resistant mice by overexpressing its catalytic subunit extended lifespan.[37]
A study that focused on Ashkenazi Jews found that long-lived subjects inherited a hyperactive version of telomerase.[38] " https://en.wikipedia.org/wiki/Telomerase
Ambiguous.