MILLIONS of people are taking anti-ageing drugs
every day – they just don't know it. Drugs to slow ageing sound
futuristic but they already exist in the form of relatively cheap
medicines that have been used for other purposes for decades.
Now that their promise is emerging, some
scientists have started using them off-label in the hope of extending
lifespan – and healthspan. "We are already treating ageing," said
gerontologist Brian Kennedy at the International Symposium on Geroprotectors
in Basel, Switzerland, last week, where the latest results were
presented. "We have been doing ageing research all along but we didn't
know it."
Last year Google took its first steps into longevity research with the launch of Calico, an R&D firm that aims to use technology to understand lifespan. Geneticist Craig Venter announced he is pursuing a similar goal via genome sequencing.
Now pharmaceutical companies look set to join in. At the conference,
the head of Swiss drug firm Novartis said research into "geroprotectors"
or longevity drugs was a priority.
Google and Venter's plans may have
injected an over-hyped field with a measure of credibility but they are
unlikely to bear fruit for some time. Yet evidence is emerging that some
existing drugs have modest effects on lifespan, giving an extra 10
years or so of life. "We can develop effective combinations for life
extension right now using available drugs," says Mikhail Blagosklonny of the Roswell Park Cancer Institute in New York.
One of the most promising groups of drugs
is based on a compound called rapamycin. It was first used to suppress
the immune system in organ transplant recipients, then later found to
extend lifespan in yeast and worms. In 2009, mice were added to the list
when the drug was found to lengthen the animals' lives by up to 14 per cent, even though they were started on the drug at 600 days old, the human equivalent of being about 60.
This led to an explosion of research into whether
other structurally similar compounds – called rapalogs – might be more
potent. Now the first evidence has emerged of one such drug having an
apparent anti-ageing effect in humans. A drug called everolimus, used to
treat certain cancers, partially reversed the immune deterioration that
normally occurs with age in a pilot trial in people over 65 years old.
Immune system ageing is a major cause of
disease and death. It is why older people are more susceptible to
infections, and why they normally have a weaker response to vaccines.
That weak response, however, has proved
useful for studying ageing, as it provides an easy read-out of immune
system health. "In humans you can't do decades-long clinical trials,"
says Novartis researcher Joan Mannick. Instead, the company looked at a
proxy that would quickly show results.
They gave 218 people a six-week course of
everolimus, followed by a regular flu vaccine after a two-week gap.
Compared with those given a placebo, everolimus improved participants'
immune response – as measured by the levels of antibodies in their blood
– by more than 20 per cent, to two out of the three vaccine strains
tested.
Of
the three everolimus doses tested, the highest caused fatigue and mouth
ulcers, while two lower doses had no apparent ill effects. Previous
experiments in mice with rapamycin suggest this class of drug acts by inhibiting a protein called mTOR. mTOR also seems to be affected by calorie restriction – the strategy of trying to live longer by eating less.
mTOR is involved in sensing the level of
nutrients available within cells, so one idea is that when times are
scarce, cells shift into energy-conserving mode, which has knock-on
anti-ageing effects, including on the immune system.
Mannick stresses that the study needs
repeating, and the big question, of whether the drug keeps the
participants healthier, can only be settled by long-term follow-up.
There's also the issue of side effects beyond those seen in the trial.
High doses of rapamycin used in organ transplants seem to nudge the
recipient's metabolism into a prediabetic state – a harm that might outweigh its anti-ageing effect.
For now, it is an encouraging sign that
rapalogs have similar effects in people as in mice, at least on the
immune system, says Alex Zhavoronkov, CEO of biotech firm InSilico Medicine in Baltimore, Maryland.
Everyday remedies
And rapalogs are not the only game in town.
The most commonly used medicine for type 2 diabetes, metformin, also
seems to extend the lifespan of many small animals, including mice, by
around 5 per cent.
There have been no trials of metformin as a longevity drug in people, but a recent study
hinted that it might have a similar effect. The study was designed to
compare metformin with another diabetes medicine, using records of
180,000 UK patients. To tease out the differences between the drugs,
people who started taking them were compared with people without
diabetes who had been closely matched for age and other health factors,
and tracked over five years.
Surprisingly, diabetics taking metformin were not only
less likely to die in that time than those on the other medicine but
they were also about 15 per cent less likely to die than people without
diabetes who took neither drug. "This shows we already have a drug that
we can potentially use in humans," says Nir Barzilai, who heads the Institute for Aging Research at the Albert Einstein College of Medicine in New York.
Other familiar drugs might also fit the
bill. Low-dose aspirin and statins are widely taken by healthy people to
reduce their risk of heart disease. Both extend lifespan in animals and
seem to have anti-inflammatory effects.
Inflammation is one of the proposed
mechanisms behind ageing, so aspirin and statins could be effective
heart drugs in part because they slow ageing, says Kennedy, who heads
the Buck Institute for Research on Aging in Novato, California.
The fact that common mechanisms seem to be
behind the major diseases of ageing, like heart disease, stroke and
dementia, is good news, as it suggests we should be able to extend our
lifespan while also extending healthspan, according to many conference
speakers. Indeed, it would be difficult to imagine an effective
longevity agent that worked without alleviating or delaying such
conditions. Rapamycin, for instance, has been found to reduce the
cognitive decline that accompanies ageing in animals.
Some researchers are already convinced and
have started taking various combinations of drugs – including low-dose
rapamycin. Blagosklonny is one such convert, and he's not alone: "I know
many people at this meeting who are taking it," he said. No doctor
would advise such a move, though, as rapamycin's potential for causing
diabetes could well outweigh its anti-ageing effects.
Nevertheless, the fact that anti-ageing
prescription drugs are being developed at all is a measure of how far
the longevity field has come, says Zhavoronkov. "It's the first time
pharma has embraced ageing."
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