Alzheimers Is Not Normal Aging And We Can Cure It Samuel Cohen TED Talks

In the year 1901,

a woman called Auguste was taken
to a medical asylum in Frankfurt.

Auguste was delusional

and couldn’t remember
even the most basic details of her life.

Her doctor was called Alois.

Alois didn’t know how to help Auguste,

but he watched over her until,
sadly, she passed away in 1906.

After she died, Alois performed an autopsy

and found strange plaques
and tangles in Auguste’s brain –

the likes of which he’d never seen before.

Now here’s the even more striking thing.

If Auguste had instead been alive today,

we could offer her no more help
than Alois was able to 114 years ago.

Alois was Dr. Alois Alzheimer.

And Auguste Deter

was the first patient to be diagnosed with
what we now call Alzheimer’s disease.

Since 1901, medicine has advanced greatly.

We’ve discovered antibiotics and vaccines
to protect us from infections,

many treatments for cancer,
antiretrovirals for HIV,

statins for heart disease and much more.

But we’ve made essentially no progress
at all in treating Alzheimer’s disease.

I’m part of a team of scientists

who has been working to find
a cure for Alzheimer’s for over a decade.

So I think about this all the time.

Alzheimer’s now affects
40 million people worldwide.

But by 2050, it will affect
150 million people –

which, by the way,
will include many of you.

If you’re hoping
to live to be 85 or older,

your chance of getting Alzheimer’s
will be almost one in two.

In other words, odds are
you’ll spend your golden years

either suffering from Alzheimer’s

or helping to look after a friend
or loved one with Alzheimer’s.

Already in the United States alone,

Alzheimer’s care costs
200 billion dollars every year.

One out of every five
Medicare dollars get spent on Alzheimer’s.

It is today the most expensive disease,

and costs are projected
to increase fivefold by 2050,

as the baby boomer generation ages.

It may surprise you that, put simply,

Alzheimer’s is one of the biggest medical
and social challenges of our generation.

But we’ve done relatively
little to address it.

Today, of the top 10
causes of death worldwide,

Alzheimer’s is the only one
we cannot prevent, cure or even slow down.

We understand less about the science
of Alzheimer’s than other diseases

because we’ve invested less time
and money into researching it.

The US government
spends 10 times more every year

on cancer research than on Alzheimer’s

despite the fact
that Alzheimer’s costs us more

and causes a similar number
of deaths each year as cancer.

The lack of resources
stems from a more fundamental cause:

a lack of awareness.

Because here’s what few people know
but everyone should:

Alzheimer’s is a disease,
and we can cure it.

For most of the past 114 years,

everyone, including scientists, mistakenly
confused Alzheimer’s with aging.

We thought that becoming senile

was a normal and inevitable
part of getting old.

But we only have to look at a picture

of a healthy aged brain compared
to the brain of an Alzheimer’s patient

to see the real physical damage
caused by this disease.

As well as triggering severe loss
of memory and mental abilities,

the damage to the brain
caused by Alzheimer’s

significantly reduces life expectancy
and is always fatal.

Remember Dr. Alzheimer
found strange plaques and tangles

in Auguste’s brain a century ago.

For almost a century,
we didn’t know much about these.

Today we know they’re made
from protein molecules.

You can imagine a protein molecule

as a piece of paper that normally folds
into an elaborate piece of origami.

There are spots
on the paper that are sticky.

And when it folds correctly,
these sticky bits end up on the inside.

But sometimes things go wrong,
and some sticky bits are on the outside.

This causes the protein molecules
to stick to each other,

forming clumps that eventually become
large plaques and tangles.

That’s what we see
in the brains of Alzheimer’s patients.

We’ve spent the past 10 years
at the University of Cambridge

trying to understand
how this malfunction works.

There are many steps, and identifying
which step to try to block is complex –

like defusing a bomb.

Cutting one wire might do nothing.

Cutting others might
make the bomb explore.

We have to find the right step to block,

and then create a drug that does it.

Until recently, we for the most part

have been cutting wires
and hoping for the best.

But now we’ve got together
a diverse group of people –

medics, biologists, geneticists, chemists,
physicists, engineers and mathematicians.

And together, we’ve managed
to identify a critical step in the process

and are now testing a new class of drugs
which would specifically block this step

and stop the disease.

Now let me show you
some of our latest results.

No one outside of our lab
has seen these yet.

Let’s look at some videos of what happened
when we tested these new drugs in worms.

So these are healthy worms,

and you can see
they’re moving around normally.

These worms, on the other hand,

have protein molecules
sticking together inside them –

like humans with Alzheimer’s.

And you can see they’re clearly sick.

But if we give our new drugs
to these worms at an early stage,

then we see that they’re healthy,
and they live a normal lifespan.

This is just an initial positive result,
but research like this

shows us that Alzheimer’s is a disease
that we can understand and we can cure.

After 114 years of waiting,

there’s finally real hope
for what can be achieved

in the next 10 or 20 years.

But to grow that hope,
to finally beat Alzheimer’s, we need help.

This isn’t about scientists like me –

it’s about you.

We need you to raise awareness
that Alzheimer’s is a disease

and that if we try, we can beat it.

In the case of other diseases,

patients and their families
have led the charge for more research

and put pressure on governments,
the pharmaceutical industry,

scientists and regulators.

That was essential for advancing treatment
for HIV in the late 1980s.

Today, we see that same drive
to beat cancer.

But Alzheimer’s patients are often
unable to speak up for themselves.

And their families, the hidden victims,
caring for their loved ones night and day,

are often too worn out
to go out and advocate for change.

So, it really is down to you.

Alzheimer’s isn’t,
for the most part, a genetic disease.

Everyone with a brain is at risk.

Today, there are 40 million
patients like Auguste,

who can’t create the change
they need for themselves.

Help speak up for them,

and help demand a cure.

Thank you.

(Applause)

1901 年,

一位名叫奥古斯特的妇女被
送往法兰克福的医疗庇护所。

奥古斯特有妄想症


甚至连她生活中最基本的细节都记不得了。

她的医生叫阿洛伊斯。

阿洛伊斯不知道如何帮助奥古斯特,

但他一直照顾着她,直到
她不幸于 1906

年去世。她死后,阿洛伊斯进行了尸检


在奥古斯特的大脑中发现了奇怪的斑块和

缠结——他就是这样的。 d 从未见过。

现在这是更引人注目的事情。

如果奥古斯特今天还活着,

我们无法为她提供
比 114 年前阿洛伊斯更多的帮助。

阿洛伊斯是阿洛伊斯·阿尔茨海默博士。

奥古斯特·德特

是第一位被诊断出患有
我们现在所说的阿尔茨海默病的患者。

自 1901 年以来,医学有了长足的进步。

我们已经发现了
可以保护我们免受感染的抗生素和疫苗、

许多癌症治疗方法、
艾滋病毒抗逆转录病毒

药物、心脏病他汀类药物等等。

但我们在治疗阿尔茨海默病方面基本上没有取得任何进展

我是一个科学家团队的一员,

他们十多年来一直致力于
寻找治疗阿尔茨海默病的方法。

所以我一直在思考这个问题。

阿尔茨海默氏症现在影响
全球 4000 万人。

但到 2050 年,它将影响
1.5 亿人

——顺便说一下,其中
将包括你们中的许多人。

如果您
希望活到 85 岁或以上,那么

您患老年痴呆症的几率
几乎是二分之一。

换句话说,
你的黄金岁月

很有可能要么患有阿尔茨海默病,

要么帮助照顾
患有阿尔茨海默病的朋友或爱人。

仅在美国,

阿尔茨海默氏症的护理
每年就花费 2000 亿美元。

每 5
美元的医疗保险费用中就有 1 美元用于治疗阿尔茨海默氏症。

它是当今最昂贵的疾病,

随着婴儿潮一代的老龄化,预计到 2050 年成本将增加五倍。

简而言之,

阿尔茨海默病是我们这一代最大的医学
和社会挑战之一,您可能会感到惊讶。

但我们在
解决它方面做得相对较少。

今天,在全球十大
死因中,

阿尔茨海默氏症是唯一一种
我们无法预防、治愈甚至减缓的疾病。

与其他疾病相比,我们对阿尔茨海默病的科学了解更少,

因为我们在研究上投入的时间
和金钱更少。

美国政府
每年

在癌症研究上

的花费是阿尔茨海默氏症的 10 倍,尽管阿尔茨海默氏症每年花费的成本更高,

并且
每年导致的死亡人数与癌症相似。

资源匮乏
源于一个更根本的原因

:缺乏认识。

因为这是很少有人知道
但每个人都应该知道的:

阿尔茨海默氏症是一种疾病
,我们可以治愈它。

在过去 114 年的大部分时间里

,包括科学家在内的每个人都错误地
将阿尔茨海默氏症与衰老混为一谈。

我们认为变老是变

老的正常和不可避免的
一部分。

但我们只需

将健康的老年大脑与
阿尔茨海默病患者的大脑进行比较,

就能看到
这种疾病造成的真正身体损伤。

除了引发严重
的记忆力和智力丧失外,

阿尔茨海默氏症对大脑造成的损害还会

显着降低预期寿命
,并且总是致命的。

请记住,阿尔茨海默博士

在一个世纪前在奥古斯特的大脑中发现了奇怪的斑块和缠结。

近一个世纪以来,
我们对这些知之甚少。

今天我们知道它们是
由蛋白质分子制成的。

您可以将蛋白质分子想象

成一张纸,通常可以折叠
成精美的折纸。

纸上有粘点。

当它正确折叠时,
这些粘性部分最终会在里面。

但有时事情会出错
,一些粘性位在外面。

这导致蛋白质分子
相互粘连,

形成团块,最终变成
大的斑块和缠结。

这就是我们
在阿尔茨海默病患者的大脑中看到的。

过去 10 年来,我们一直
在剑桥大学

试图
了解这种故障是如何工作的。

有很多步骤,确定
要阻止的步骤很复杂——

就像化解炸弹一样。

切断一根电线可能无济于事。

切割其他人可能
会使炸弹探索。

我们必须找到正确的步骤来阻止,

然后创造一种药物来做到这一点。

直到最近,我们大部分时间

都在切断电线
并希望获得最好的结果。

但现在我们聚集
了一群不同的人——

医生、生物学家、遗传学家、化学家、
物理学家、工程师和数学家。

我们一起
设法确定了该过程中的一个关键步骤

,现在正在测试一类新的药物
,该药物将专门阻止这一步骤

并阻止疾病。

现在让我向您展示我们的
一些最新成果。

我们实验室以外的人
还没有看到这些。

让我们看一些视频,了解
我们在蠕虫中测试这些新药时发生了什么。

所以这些是健康的蠕虫

,你可以看到
它们正常移动。

另一方面,这些蠕虫体内的

蛋白质分子
粘在一起——

就像患有阿尔茨海默氏症的人类一样。

你可以看到他们明显生病了。

但是如果我们
在早期阶段给这些蠕虫服用我们的新药,

那么我们就会看到它们是健康的,
而且它们的寿命也很正常。

这只是一个初步的积极结果,
但这样的研究

向我们表明,阿尔茨海默氏症是一种
我们可以理解并且可以治愈的疾病。

经过 114 年的等待,

未来 10 年或 20 年的成就终于有了真正的希望。

但要培养这种希望
,最终战胜老年痴呆症,我们需要帮助。

这不是关于像我

这样的科学家——而是关于你。

我们需要您提高人们
对阿尔茨海默氏症是一种疾病

的认识,如果我们尝试,我们就能战胜它。

在其他疾病的情况下,

患者及其
家属带头进行更多研究,

并向政府
、制药业、

科学家和监管机构施加压力。


对于在 1980 年代后期推进 HIV 治疗至关重要。

今天,我们看到了同样的
战胜癌症的动力。

但阿尔茨海默病患者往往
无法为自己说话。

他们的家人,隐藏的受害者,
夜以继日地照顾他们的亲人,

常常精疲力竭,
无法外出倡导改变。

所以,这真的取决于你。

在大多数情况下,阿尔茨海默氏症不是遗传病。

每个有大脑的人都处于危险之中。

今天,有 4000 万
像奥古斯特这样的患者,

他们无法为自己创造所需的改变

帮助为他们发声,

并帮助要求治愈。

谢谢你。

(掌声)