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A supercomputer analysed data on COVID-19 and helped come up with this new hypothesis
A genetic study of COVID-19 patients, powered by the Summit supercomputer, may
have taken us a step towards understanding how the new corona virus causes
disease. Summit, located at the Oak Ridge National Lab in the US, analysed
40,000 genes from 17,000 samples earlier this summer in an attempt to
understand the virus, AI expert Thomas Smith explained in an article on the
Medium platform. While the machine is the second-fastest computer in the
world, the process required it to analyse 2.5 billion genetic combinations — a
feat that took over two weeks. Its results pointed to the fact that
bradykinin, a natural chemical compound that regulates blood pressure, could
explain many facets of COVID-19 and some of its symptoms. The findings may
shed light on why the virus causes vascular problems in certain patients, from
strokes to inflammation of the skin or toes, as well as indicating new
potential therapies to treat its worst symptoms.
Understanding COVID-19 — a race against time
Faced with a new virus and unknown disease, health authorities and medical
staff have been learning as they go how to treat the new coronavirus. At
first, the virus appeared to manifest as a respiratory syndrome — its full
scientific name is still Severe Acute Respiratory Syndrome 2, SARS-CoV-2 —
with symptoms similar to a bad cold or the flu and treatments reflected this.
But soon, front-line doctors began to report other symptoms that were more
severe: strokes, heart problems, skin conditions and circulatory problems,
mainly in the feet. Hormonal problems were also detected in some cases.
Healthcare workers started to realise that giving critically ill patients
oxygen or intubating them, which is the initial protocol for respiratory
failure, did not always get the desired results. Something else was at work.
Little by little, signs pointed to the most serious cases and deaths being due
to a cytokine storm — an exaggerated response of the patient's immune system,
capable of damaging vital organs. The scientists who interpreted Summit's
data, who published their findings in eLife journal, believe that a bradykinin
storm — a dysfunction of the vascular system that causes blood vessels to leak
—could be to blame. Although, they added that it is possible the two
storms are "intricately linked".
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(Top) Healthy alveolus. (Bottom) Alveolus flooded by a "gelatin", which is favoured by bradykinin.-Life 2020; 9: e59177 DOI: 10.7554/eLife.59177 |
'Bradykinin Hypothesis': COVID-19 like a burglar who throws open your
windows
The Bradykinin Hypothesis suggests that a bradykinin storm is responsible for
many of COVID-19’s deadliest symptoms. The theory is based on the commonly
accepted notion that the infection begins with the virus entering the body
through ACE2 receptors — widely present in the nose, but also in the
intestines, kidneys, and heart. Summit showed the team of researchers that the
effects of COVID-19 were not limited to those caused by the colonisation of
ACE2 receptors: the virus is capable of manipulating them too. Instead, it
actively hijacks the body’s own systems, tricking it into increasing the
response of the receptors.
COVID-19 doesn't just infect cells that already express a lot of ACE2
receptors, instead it actively hijacks the body’s own systems so it is tricked
into upregulating them in places where they’re usually expressed at low or
medium levels, including the lungs, Smith said. "In this sense, COVID-19 is
like a burglar who slips in your unlocked second-floor window and starts to
ransack your house. Once inside, though, they don’t just take your stuff —
they also throw open all your doors and windows so their accomplices can rush
in and help pillage more efficiently," he added. SARS-CoV-2 increases levels
of ACE2, which lowers blood pressure in the human body and works against
another enzyme known as ACE (this has the opposite effect), leaving the door
open for bradykinin, the researchers wrote in the scientific journal.
Uncontrolled bradykinin causes vascular permeability and dilation as well as
hypotension, they added.
When respirators are useless?
Once blood pressure is not controlled and blood vessels increase their
permeability, the body has opened its doors to dysfunctions in almost the
entire body — and the doors stay open. COVID-19 patients affected by a
bradykinin storm "drown" because their lung alveolus are coated with a
jelly-like substance. Many health workers had reported damage to the blood
vessels of the respiratory system and other organs. This would explain why in
some cases administering oxygen or connecting patients to respirators was
futile.
![]() |
(Top) Healthy alveolus. (Bottom) Alveolus flooded by a "gelatin", which is favoured by bradykinin.- Life 2020; 9: e59177 DOI: 10.7554/eLife.59177 |
Could this hypothesis be used to identify at-risk patients?
Another of COVID-19's mysteries is the reason why some patients have suffered
more than others from more serious symptoms, although there are known risk
factors including as age, being overweight and diabetes. Speculation has
pointed to genetic factors, microbiota or even blood group as an explanation
for this. The Bradykinin Hypothesis could help us understand who is most at
risk of being badly affected by the virus. Increasingly, it seems that women
are less likely to die from COVID-19. Researchers believe that the presence of
a protein (thymosin beta-4), which is twice as high in women as in men, could
protect women from some of the novel coronavirus' worst symptoms.
How might this help find a treatment?
The researchers suggested that efforts to find a treatment for symptoms should
be focussed on curbing bradykinin storms. "Further experiments identified
several existing medicinal drugs that have the potential to be re-purposed to
treat the Bradykinin Storm," they wrote. "A possible next step would be to
carry out clinical trials to assess how effective these drugs are in treating
patients with COVID-19. "In addition, understanding how SARS-Cov-2 affects the
body will help researchers and clinicians identify individuals who are most at
risk of developing life-threatening symptoms."
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