Name: 基因组学有多样性问题（Genomics Has a Diversity Problem）
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Thanks to Skillshare for supporting this episode of SciShow.

There's a lot of buzz surrounding precision medicine,

which is the idea that we can tailor the way we treat disease to every individual person's

And though it's a futuristic idea, it's already helping us to diagnose and treat some

The dream is that someday, the information in our genomes — the sum total of our DNA

could transform healthcare as we know it for everyone.

But there are limitations to overcome before precision medicine can reach its potential.

One major hurdle is the lack of diversity in human genomic databases.

The vast majority of human genetic studies we've carried out since the 1990s were done

It's a massive oversight that's already leading to health disparities,

and it's going to require some ambitious fixes.

It's pretty bad science to base our understanding of the human genome on white-centric data,

considering how many of the humans on this planet aren't white.

But underrepresentation and exploitation of minorities in medical research is nothing

In 1996, the National Institutes of Health introduced a policy to prioritize including

more women and underrepresented minorities in clinical research.

But since then, less than 2% of over 10,000 cancer studies funded by the NIH have included

enough minorities to meet their own guidelines.

There's also the totally justified lack of trust from communities of color when it

comes to research participation because of repeated ethics violations.

The most infamous case is the Tuskegee Syphilis Study that began in nineteen thirty-two,

in which researchers recruited hundreds of African-American subjects with syphilis,

and then… watched, as the deadly disease progressed untreated.

Even /after/ they knew that penicillin could cure syphilis.

President Clinton apologized for the decades-long ethics breach in nineteen ninety-seven, but

that doesn't mean everything is fine now.

For instance, a 2018 analysis revealed that African-Americans

are disproportionately enrolled in clinical trials that don't require patients to give

This exception to consent rules exists for people who are in too life-threatening of

There's also just plain structural inequality throughout society that influences how medical

eading to undeniable healthcare gaps between white people and, well, everyone else.

How does this apply to genetics research and precision medicine?

The Human Genome Project published the first human genome in 2003.

At the time, sequencing a single genome was a landmark accomplishment.

Since then, sequencing technologies have gotten better, faster, and way cheaper,

leading to mountains of genetic data rivaling the amount of data generated by YouTube, Twitter,

And most of that data concerns populations of European ancestry.

Which has led to a sort of snowball effect, as researchers tend to prefer to study the

and go on to do more studies in white people.

One major problem is with the reference genome —

used by researchers worldwide as, well, a reference.

A 2018 study on genetic data from over 900 individuals of African descent found that

over 10 % of their DNA wasn't represented in the reference genome,

most of which is derived from a small number of people.

Now, it's /really/ important to note that none of this is to say that people of different

races or ethnicities have dramatically different DNA.

Other research has found that any given single person differs from the reference genome by

It's just that different individuals have different differences -- and that adds up.

The lack of diversity in genetic databases has already led to disparities in translating

precision medicine research into diagnoses and clinical care.

For example, a 2016 analysis found that African-Americans have been disproportionately misdiagnosed

with a heart condition known as hypertrophic cardiomyopathy.

A gene variant that's more common in black populations had incorrectly been identified

And the researchers suggested that including more African-Americans as controls in genetic

studies could have prevented that mistake.

Researchers have also raised concerns that basing tests for genetic diseases on our current

body of knowledge leaves communities of color by the wayside.

For example, most of what we know about the genetics of asthma comes from studies of European

But studies have found those gene variants are found less often in many African-American

even though their incidence of asthma is higher than in white people.

If you were to design a genetic test based on the presence or absence of those variants,

you'd have something only white people can actually use.

Drug safety and dosage also come into play.

Genetics can affect how well a drug works, the ideal dose, and the likelihood of adverse

For example, warfarin is widely used as a blood thinner.

And variants in three genes can help doctors understand how patients will respond to it

and help them determine the right dose to avoid dangerous side effects.

Except that's only the case in European populations.

It doesn't explain how people of other ethnicities will metabolize the drug.

Which means they're at a greater risk of an adverse reaction.

This lack of diversity isn't going to fix itself, but there are proposed solutions,

The National Institutes of Health launched the All of Us research program in 2015 to

collect genetic and health data from more than a million people living in the U.S.,

with a focus on ensuring a diverse pool of subjects.

Many non-European countries have already launched population-specific genome projects

to produce reference genomes that are more relevant to those populations.

Some experts have also suggested that scientific journals either require researchers to draw

or provide a darn good reason why not, as a requirement to publish.

Researchers will also need to reclassify genomic variants -- like the heart disease genes --

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基因组学有多样性问题（Genomics Has a Diversity Problem）

relevant

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