Zdenek Vrozina Profile picture
Oct 1 13 tweets 3 min read Read on X
This is the strongest evidence yet that ignoring the chronic impacts of COVID in children carries population-level consequences.
A massive Lancet Infect Dis study of >465,000 kids shows:
Reinfections double the risk of long COVID.🧵
After the first infection: about 903 cases of long COVID per million children (within 6 months).
After the second infection: ~1884 cases per million.
That’s more than double the risk (RR = 2.08).
And it’s not just fatigue. Reinfection raised risks across many systems-
myocarditis (RR 3.6),
arrhythmias,
blood clots
kidney injury,
electrolyte issues,
liver enzyme spikes
brain fog, headaches, POTS
anxiety, depression, exhaustion
Key points.
This happened even when the initial infection was mild.
It was seen in both vaccinated and unvaccinated kids.
The biggest increases were in ages 5–11 and 12–20.
Why does this happen?
Each infection brings biological stress - inflammation, immune disruption, vascular strain.
The body may not fully recover before the next hit.
Risks appear to stack up with every reinfection.
This study confirms: long COVID in kids is real.
It’s a multisystem condition - heart, brain, blood vessels, kidneys, liver…
It’s not just in their heads. There’s a clear biological basis
What does it mean?
Reinfections aren’t harmless. Each one adds long-term risk!
Vaccination still matters - it lowers infection risk, which lowers reinfection risk.
Kids need follow-up care after COVID - fatigue, chest pain, cognitive issues may be long COVID.
The bigger picture:
Ignoring long COVID in kids means carrying a huge health burden into the future.
Each wave, each reinfection adds to the risk for an entire generation.
Sum:
Risk of long COVID more than doubles after a second infection.
Effects span multiple organ systems.
Preventing reinfections matters - it protects kids not just in the short term, but for years ahead.
This is the strongest evidence to date that ignoring the chronic impacts of COVID in children has population-level consequences.
Every reinfection adds risk.
Every ignored case adds burden.
What looks mild today may echo across an entire generation tomorrow.
Public health strategy has treated COVID in children as mild and short-lived.
This study shows the opposite - reinfections carry measurable, cumulative risks.
Downplaying this is not just a mistake.
It looks increasingly like gross negligence - with consequences for an entire generation. @szupraha @ZdravkoOnline @strakovka @adamvojtech86 @RobertPlaga
Zhang at al., Long COVID associated with SARS-CoV-2 reinfection among children and adolescents in the omicron era (RECOVER-EHR): a retrospective cohort study. thelancet.com/journals/lanin…
This isn’t just theory anymore - it’s front-page news.
Even The New York Times has started covering this study.
Ignoring the chronic impacts of COVID in children is not just short-sighted. @zdravydenik @SeznamZpravy @hospodarky @novinkycz nytimes.com/2025/09/30/hea…

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More from @ZdenekVrozina

Oct 1
COVID and brain fog.
For millions, it’s the most disabling legacy of the pandemic.
Now, a new brain imaging study reveals a clear biological basis - and the parallels with other diseases are not encouraging.🧵
Researchers used PET scans with a tracer ([11C]K-2) that binds to AMPA receptors - the tiny gates that neurons use to fire signals via glutamate, the brain’s main excitatory messenger.
These receptors are crucial for learning, memory, and attention.
In people with cognitive long COVID, AMPA receptors weren’t just slightly higher in one region.
They were globally increased across the entire brain!
It’s like the brain’s excitatory volume knob was turned way up everywhere.
Read 17 tweets
Sep 30
This preprint shows how SARS-CoV-2 acts like a biological hacker - taking over our protein factories and silencing immune defenses.
It’s not just a respiratory infection. The virus reprograms the fundamental machinery of the cell - and that’s why its impact can linger.🧵
Remember when we learned Nsp1 alone could sabotage ribosomes? Yerlici et al., 2024.
The new preprint reveals SARS-CoV-2 goes even further - broadly reprograms translation to favor viral RNAs + silences immunity.
The main target: translation - the process where ribosomes build proteins from mRNA.
SARS-CoV-2 doesn’t just use it - it reprograms it, so instead of making protective proteins, the cell prioritizes viral ones.
Read 13 tweets
Sep 29
New peer-reviewed study on the chronicity of COVID-19 in Viruses.
One of the authors? Former CDC director Robert Redfield.
The paper warns about persistence of SARS-CoV-2 in Long COVID - and doesn’t shy away from controversy.🧵
LC (PASC) = debilitating chronic disease.
10–20M in the US, >420M globally
200 symptoms, hitting 12 organ systems
No approved treatments
Affects kids, adolescents, healthy adults
Key message.
“Knowledge about chronic LC is still in its embryonic stage.”
Currently, there are more questions than answers.
Read 13 tweets
Sep 27
A study just tested whether an old HIV drug - tenofovir (TDF/TAF) - could work against SARS-CoV-2 and even help with long COVID.
The lab results are striking: it strongly blocked the virus🧵
Tenofovir is a nucleotide analog - a fake building block for viral RNA.
Once inserted, it stops the virus from copying itself.
In experiments, this worked even at high viral loads.
The spotlight is on TAF.
More potent than TDF,
safer for long-term use,
and most importantly - it concentrates in lymphoid tissues (lymph nodes, spleen, immune cells).
Read 12 tweets
Sep 26
A new 3-year follow-up study in Brain Communications tracked patients with post-COVID brain condition for 38 months.
What they found is a story of part compensation, part healing in the brain.🧵
At 6 months, people with post-COVID were still very tired.
Thinking was mostly fine, but attention and alertness were weaker.
Brain scans showed the frontal lobes working overtime - the brain was pushing harder to keep up. That’s early compensation.
At 23 months, there was progress, but not a cure.
Fatigue eased for some, others stayed stuck.
The brain started to spread the workload - brainstem, cerebellum, and temporal areas joined in. More networks pitched in to help - a reorganization phase.
Read 12 tweets
Sep 25
One mystery of Long COVID - why immune cells get stuck in a harmful, inflammatory mode.
A new study shows the switch is metabolic - and a single checkpoint can decide whether Th17 cells protect or drive disease.🧵
In both children and adults with Long COVID, we see immune cells stuck in a harmful mode.
Among them - Th17 cells, which can either protect us or drive chronic inflammation.
A new study in Science Signaling, 2025 uncovers why these cells flip - and what keeps them locked in the pathogenic state.
Th17 cells have two faces -
non-pathogenic (protective, balanced),
pathogenic (autoimmune, chronic inflammation).
The critical switch? Cellular metabolism.
Read 12 tweets

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