Silicon Valley is gearing up for a race to create “perfect babies”: An impending ethical dilemma
Currently, gene sequencing technology is advancing at an unprecedented pace, giving rise to a new and controversial field: Preimplantation Genetic Testing for Polygenic Risk (PGT - P). It claims to be able to predict an embryo's future intelligence, appearance, and even personality. This technology is not only rapidly commercializing but also attracting the attention and investment of Silicon Valley elites. The vision of "designer babies" seems to be gradually becoming a reality.
However, the scientific community is questioning the accuracy of these predictions, and ethicists are sounding the alarm, stating that screening for non - disease traits is awakening a long - dormant and disturbing specter - "eugenics." As companies boldly promote "gene optimization" programs, human society has reached a crossroads: Is this the next chapter in the evolutionary history, or a trap that may exacerbate inequality and distort our understanding of human nature?
First, let's focus on the microscope. There, a translucent speck is a human blastocyst. This tiny life form takes shape about five days after the union of sperm and egg. This cell cluster, as small as a grain of sand, carries the blueprint for a unique individual in the future: it contains 46 chromosomes, thousands of genes, and approximately 6 billion DNA base pairs. This is the most primitive and detailed "blueprint" for building a new life.
Today, with the help of advanced gene sequencing technology, doctors can use a laser to create a tiny hole in the zona pellucida of the blastocyst and extract a few cells with a pipette thinner than a human hair. At this moment, we can "read" for the first time the life instructions that will shape someone's entire life.
A new scientific field is trying to decipher this blueprint and predict what kind of person this embryo may become. Some parents turn to this technology to prevent fatal genetic diseases in their families. At the same time, others, driven by the vision of an "Ivy League diploma," "charming appearance," or "gentle temperament," are willing to pay tens of thousands of dollars to "optimize" the intelligence, appearance, and personality of their offspring.
The most enthusiastic early adopters of this technological revolution are the elite from Silicon Valley. Tech billionaires such as Elon Musk, Peter Thiel, and Brian Armstrong, the CEO of Coinbase, are among them.
The question is, can parents who pay for these services really get what they want? Genetic experts have been warning for years that these tests have fundamental flaws. Members of the European Society of Human Genetics clearly stated in a 2021 paper: "No clinical studies have been conducted to evaluate its diagnostic effectiveness in embryos, and patients must be fully informed of the limitations of its application."
Moreover, some core assumptions underlying this technology, namely that a person's development is mainly determined by innate biology rather than post - natal upbringing or environmental factors, have also put it at the center of political and public debate.
Today, this once - niche technology is gradually going mainstream. Scientists and ethicists are urgently addressing the potential huge impact it may bring, which concerns our social contract, our future generations, and our understanding of the fundamental question of "what it means to be human."
"Designer Babies" or a "Gene Store"? The New Reproductive Model Initiated by PGT - P
To understand this storm, we need to start with its technological foundation. In fact, Preimplantation Genetic Testing (PGT) itself is not a brand - new concept. As early as the 1990s, expectant parents undergoing in vitro fertilization (IVF) could already use a series of genetic tests to screen embryos.
The initial technologies, such as Preimplantation Genetic Testing for Monogenic Disorders (PGT - M) and Preimplantation Genetic Testing for Aneuploidy (PGT - A), can be used like probes to identify specific genetic problems, such as single - gene diseases like cystic fibrosis and sickle cell anemia, or chromosomal number abnormalities that may lead to Down syndrome.
However, these tests can only decipher the relatively straightforward "genetic problems" in the book of life. Most of the genetic information contained in an embryo is written in an extremely complex way by hundreds or even thousands of genes, more like a delicate and obscure "combination code."
It is not until recent years that a more powerful decoding tool has emerged - Preimplantation Genetic Testing for Polygenic Risk (PGT - P). Its goal is to decipher this code and predict the complex outcomes determined by the cumulative effects of countless genes and their interaction with the environment. A new market has also emerged accordingly.
Thus, the process of embryo selection has quietly changed. It is no longer like a "medical workshop" aiming to avoid family tragedies, but more like a futuristic "life showroom." Here, parents seem to be browsing models with "attribute cards" and "selecting" their ideal offspring from a limited number of options, with the cards indicating the potential health risks of each embryo in the future.
In 2020, the first baby screened by PGT - P technology was born. Since then, although the exact number remains unknown, it is estimated that hundreds of children have been born using this technology. With the wave of commercialization, this number is almost certain to increase rapidly.
Behind all this are some startups funded with tens of millions of dollars from Silicon Valley. They have developed proprietary algorithms to calculate a "Polygenic Risk Score" (PRS) for each embryo by analyzing a large number of genetic variations, trying to quantify the likelihood of developing various complex traits.
In the past five years, Genomic Prediction and Orchid have dominated this niche market, taking a relatively cautious approach and mainly focusing on disease prevention. However, recently, two more high - profile and radical competitors have entered the arena - Nucleus Genomics and Herasight. They seem unwilling to follow the cautious path of their predecessors and have stepped into the most controversial minefield of genetic intelligence testing, pushing the "perfect baby" competition into a new and more disturbing stage.
The Blind Spots of "Genetic Prediction": When Science Outpaces Evidence
However, behind this seemingly promising technological picture, there are significant scientific limitations and a trust gap.
The limitations of polygenic risk scores are quite obvious. The primary problem lies in the boundaries of scientific knowledge. We still know very little about the complex traits and diseases driven by the subtle interactions of hundreds of genes. A more practical problem is that the large - scale genetic databases supporting these scores mostly come from populations of Western European descent. This serious imbalance in representativeness makes it extremely difficult to provide reliable predictions for patients from other ethnic backgrounds.
These scores also have a fundamental flaw: they completely fail to capture the crucial variables in a person's growth environment - from family upbringing, nutritional status to social resources. All these complex factors that shape an individual disappear in the cold genetic scores. Therefore, although polygenic scores may have some reference value in analyzing macro - group trends, their predictive ability significantly declines when used to evaluate only a few embryos with highly similar genetic backgrounds.
Facing these limitations, the mainstream medical community maintains a cautious attitude. Authoritative institutions such as the American Society of Human Genetics, the American College of Medical Genetics and Genomics, and the American Society for Reproductive Medicine are all cautious about using polygenic scores for embryo selection. The American College of Medical Genetics and Genomics stated bluntly in its 2024 official statement: "The technology is advancing too fast, and the evidence has not kept up."
However, the whirlpool of controversy goes far beyond the scope of scientific validity. The deeper divergence lies in the ideology behind it. More and more critics point out that these companies are intentionally or unintentionally resurrecting a historical specter - eugenics. The dangerous belief that once thought humans could be "improved" through selective breeding is quietly returning in the guise of technology.
A Century - Old Debate: Nature vs. Nurture
The current "perfect baby" competition does not come out of nowhere. In fact, it has added new fuel to an ancient debate that has spanned several centuries - the debate between "nature" (genetics) and "nurture" (environment).
The term "eugenics" was coined by British scholar Sir Francis Galton in 1883, partly inspired by the theory of evolution of his cousin Charles Darwin. Derived from Greek, it means "well - born," and its core idea is that "noble qualities" are genetically endowed.
This debate reached a critical turning point in 2003 - the 13 - year - long and $3 - billion - dollar Human Genome Project was completed, and for the first time, we mapped the basic blueprint of human life. This was a watershed moment. Since then, the cost of gene sequencing has dropped at an astonishing rate and is now as low as a few hundred dollars. This has made it possible to establish ultra - large - scale genetic databases, such as the UK Biobank in the UK and the "All of Us" project in the US, each of which has genetic information from more than 500,000 volunteers.
These large databases allow researchers to conduct "Genome - Wide Association Studies" (GWAS), scanning millions of common genetic variations to find small associations between genes and specific traits. This is the theoretical basis for polygenic risk scores.
Initially, most research focused on diseases. However, in 2011, the trend began to change. The Social Science Genetic Association Consortium (SSGAC) in the US turned its attention to a more sensitive area: they started to explore the genetic basis of complex social and behavioral outcomes (such as years of education).
This shift has pushed scholars like psychologist Kathryn Paige Harden from the University of Texas to the forefront of the storm. Harden challenged her liberal peers, arguing that inherited cognitive ability is an important factor leading to differences in social outcomes. Acknowledging this, rather than avoiding it out of fear of the "eugenics" stigma, can help formulate truly effective progressive policies.
However, this focus on the influence of genes has been caught up in complex forces in today's public opinion. Right - wing individuals and the "neoreactionary" trend on the Internet have exploited this trend to advocate that social inequality has a fixed genetic root and to oppose immigration and racial integration. Since Elon Musk took over Twitter (now X), such remarks have become even more prevalent, and Musk himself often participates, casting a serious political shadow over this ancient "nature - nurture" debate.
From the Laboratory to the Market: The Commercialization of PGT - P Begins
However, these debates have not stopped the commercialization process of PGT - P. In 2019, Genomic Prediction was the first to introduce Preimplantation Genetic Testing for Polygenic Risk (PGT - P) to the market, marking the official entry of this technology into the public eye.
Through Genomic Prediction's "LifeView Embryo Health Score," expectant parents can assess the risk of their embryos developing complex diseases such as cancer, diabetes, and heart disease in the future. This service starts at about $3,500. The company uses SNP chip technology to detect common variations at specific loci in the genome and then cross - compares them with large - scale genetic databases to calculate the risk score.
In 2023, the startup Orchid became a new market player. Its "Whole - Genome Embryo Report" claims to sequence more than 99% of the embryo's genome to detect de novo mutations and promises to diagnose rare diseases more accurately. Parents can pay about $2,500 to get polygenic risk scores for 12 diseases (such as schizophrenia and breast cancer).
Orchid's founder, Noor Siddiqui, is herself a part of the Silicon Valley legend. She received the Thiel Fellowship as a teenager and then studied at Stanford University. Her background has helped her attract tech elites as customers and investors. The company has successfully raised $16.5 million, and the list of investors includes well - known figures in the tech world such as Vitalik Buterin, the founder of Ethereum, and Balaji Srinivasan, the former CTO of Coinbase.
However, the company's aggressive commercial promotion has also sparked controversy. Siddiqui once publicly stated that in the future, parents who choose not to use genetic testing may even be considered "irresponsible," which has put her at the center of public opinion.
The Rift in Public Opinion: The Debate over PGT - P Reflects Social Anxiety
The views of the American public on this emerging technology are significantly divided. A 2024 bioethics survey shows that people's attitudes towards PGT - P vary greatly depending on the testing objectives:
Physical health: Screening for diseases such as cancer, heart disease, and diabetes has received the support of the vast majority of people.
Mental health disorders: The support for screening conditions such as depression, obsessive - compulsive disorder, and attention - deficit/hyperactivity disorder is relatively complex but generally positive.
Appearance characteristics: Public support for testing features such as skin color, baldness, and height is generally low.
Among them, intelligence is undoubtedly the focus of the controversy. Given its historical abuse and the lack of a cultural consensus on its definition, intelligence testing has sparked the most intense ethical debate. In many countries, such operations are strictly regulated, and in the UK, they are completely prohibited.
The survey data clearly reflects this division: 36.9% of respondents support intelligence testing for embryos, 40.5% oppose it, and 22.6% are undecided.
Despite the continuous controversy, the market's exploration of intelligence testing has never stopped. Diego Marin, the global business development and scientific affairs director of Genomic Prediction, revealed that the company has received relevant inquiries from around the world since its establishment.
Genomic Prediction once provided a so - called "intellectual disability" predictor but stopped this service after facing strong opposition regarding its predictive ability and ethics. Marin clarified: "Our company's mission and vision are not to create 'designer babies' but to reduce disease risk. When it comes to traits such as IQ, skin color, height, or other non - disease - related and cosmetic features, we do not invest in this area."
However, Orchid on the other side is still testing genetic markers related to intellectual disability and developmental delay. And according to an anonymous employee of the company, more comprehensive intelligence testing is also provided to a specific group of "high - rollers." Some insiders claim that Elon Musk used Orchid's services during the conception of at least one of his children with tech executive Shivon Zilis.
The Adventurers in Silicon Valley: From "Optimization" to an "Evolutionary Arms Race"
Among the many companies providing PGT - P services, the founders of startups are undoubtedly the most radical flag - bearers in this competition. With the unique "disruptive innovation" logic of Silicon Valley, they are trying to redefine the starting point of human life.
1. Nucleus Genomics: The Ambition of a One - Stop "Genetic Stack"
25 - year - old Kean Sadeghi is a typical Silicon Valley prodigy of his generation. He started modifying beer yeast samples at the age of 16 and dropped out of school a few years later, determined to create "a better 23andMe." He positions Nucleus Genomics as "software - first and consumer - first," targeting the application layer of PGT - P technology.
Similar to its competitors, Nucleus calculates a Polygenic Risk Score (PRS) by comparing an individual's genetic data with trait - related variations identified in large - scale Genome - Wide Association Studies (GWAS), providing predictions based on statistical information.
Nucleus presents the results in two ways: one is the Z - score (ranging from - 4 to 4), which explains the risk of a certain trait compared to people with a similar genetic background. For example, if embryo No. 3 has a Z - score of 2.1 for breast cancer, its risk is higher than the average. The other is the absolute risk score, which combines relevant clinical factors. For instance, given that embryo No. 3 is male, its actual risk of developing breast cancer is extremely low.
Nucleus' real advantage over its competitors lies in the breadth of its service scope. On its platform, expectant parents can screen more than 2,000 possible diseases and traits, from eye color to IQ, from anxiety tendency to alcohol dependence, and even the possibility of being left - handed. Sadeghi said bluntly at a product launch event: "Maybe you want your child to have blue eyes instead of green eyes. It's the parents' freedom." Although he denies that the company is engaged in eugenics, he does not shy away from using the term "gene optimization" and even welcomes the viral spread effect brought about by the controversy.
His ultimate goal is to create a "genetic stack" that integrates all gene sequencing applications, from genealogy to precision medicine to genetic engineering, rather than just being an IVF testing company. Nucleus has raised more than $36 million from investors such as Balaji Srinivasan, the former CTO of Coinbase, the Seven Seven Six venture capital firm, and Thiel's Founders Fund.
2. Herasight: Intelligence Screening and the "Evolutionary Arms Race"
In this already controversial field, political philosopher Jonathan Anomaly and his company Herasight have taken an even more radical stance