No.13002
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Currently, about 2% of babies in the US are conceived via IVF. IVF offers some advantages over traditional fertilization, including polygenic embryo selection (PES). In the near future, gene editing tech might be used to correct multiple undesirable mutations, such as mutations that increase risk of cancer, heart disease, and diabetes.
Do you expect the percent of babies conceived via IVF to rise significantly this century to take advantage of this beneficial technology? I predict that it will be used for a majority of babies within 100 years, assuming we don't get paperclipped by AI or suffer civilizational collapse.
No.13005
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>>13003>It's entirely possible that not only do we hit 100% use within the next century, but also abandon it for something else that takes over before we hit 2124.Oh yeah, there will probably be lots of advances that are hard to even imagine now.
>>13004>I would expect people, given the choice would very much prefer to become pregnant the natural way and give birth the natural way.Ceteris paribus, yes. But if genetic testing reveals that you and your spouse are carriers of an autosomal recessive allele that would greatly increase risk of cancer if homozygous, then it might be worthwhile to use IVF tech to avoid that possibility.
No.13094
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I find any sort of question about the possibility of science to "improve" our genes to be enourmously and often deliberately ignorant of how the adaptability of any gene is contextual and multidimensional. As well as failing to understand the nature of gene expression as contextual and heavily effected by ecosystems and maternal epigenetic systems.
That is to say that a "deliterious" gene can be adaptive in the right ecosystem or even be both adaptive and deleterious. Like sickle cell anemia, it's m9st common in those people of south and east African descent precisely because that's historically the malaria hot zone, and carrying the gene or even expressing the genes for it confer a much greater chance of surviving malaria in childhood while shortening overall adult lifespan.
Likewise I see it as unwise to try and homogenize the human genome to have less "deleterious" genes in the gene pool. What confers an advantage is dependent on ecosystems and we can't confidently say what other genes in other genepools within an ecosystem, like say, new future diseases, will emerge and if other "deleterious" mutations might turn out to be adaptive in those circumstances.
Plus some genetic disorders may be with us forever, particularly a number of major psychiatric disorders (which are the product of complex interactions between genes and ecosystems themselves) because of their connection to genes that have been crucial to our species means of survival (like our intellectual capacities in regard to psychiatric disorders)
No.13095
>the modern world has been quietly fostering the accumulation of deleterious mutations in all of usSo. I wanted to do some research to challenge this claim, but in the process of researching it I found that many of my beliefs were flawed, summarized in this paper that I feel is excellent for addressing any such eugenic nonsense.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276617/For a snippet the abstract offers the conclusion
>estimates are U ≈ 2.2 for the whole diploid genome per generation and ∼0.35 for mutations that change an amino acid of a protein-coding gene. A genome-wide deleterious mutation rate of 2.2 seems higher than humans could tolerate if natural selection is “hard,” but could be tolerated if selection acts on relative fitness differences between individuals or if there is synergistic epistasis. No.13100
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>>13094>That is to say that a "deliterious" gene can be adaptive in the right ecosystem or even be both adaptive and deleterious.In some cases that's true, but other mutations are simply bad. E.g., having
two copies (homozygous) of the allele responsible for Tay-Sachs is definitely bad; it almost certainly results in a painful death during childhood. But having exactly
one copy of the allele (heterozygous) isn't harmful and some speculate that it is actually helpful and might be partially responsible for the higher average IQ of the Ashkenazim. So polygenic embryo selection against
homozygous Tay-Sachs alleles is definitely desirable.
As another example, BRCA mutations are very bad in expectation and are autosomal dominant. Having one mutated allele greatly increase risk of certain cancers, and having two mutated alleles leads to death of the embryo in a majority of cases. Polygenic embryo selection to avoid BRCA mutations are most likely a good thing.
>>13095That paper is from before
Roe v. Wade was overturned. I suspect the dysgenic effects of banning abortion might invalidate the paper's conclusions.