Zdenek Vrozina Profile picture
Sep 14 12 tweets 2 min read Read on X
New mega–meta-analysis on #LongCOVID ever prevalence.
Long COVID has affected 36% of people after a COVID-19 infection worldwide.
South America: 51%
Europe: 39%
Asia: 35%
USA: 29%🧵
Important note.
This 36% is “ever prevalence” - the share of people who at any point during follow-up had symptoms lasting ≥2 months after infection.
It does not mean they all still have symptoms today. Current prevalence is lower (eg 9% of US adults).
Why 2 months?
Different studies used different definitions of long COVID (WHO = 3 months, NASEM = 3 months, others = 2 months). To include the widest possible dataset, this meta-analysis defined long COVID as ≥1 new or persistent symptom lasting ≥2 months after infection.
The key point - symptoms often persist for years.
That persistence itself is important - showing long COVID is not just a short-term aftermath, but a condition that can remain a serious health burden well beyond the initial infection.
And the data back this up
35% within 1 year
46% at 1-2 years
43% even beyond 2 years
This doesn’t mean new cases appear later - it shows some people remain sick for a long time, and longer studies often include more severe (hospitalized) cases.
Risk factors.
No vaccination - OR 2.09 >2× higher risk than vaccinated
Pre-Omicron infection (Alpha/Delta) - OR 1.74 - higher risk than Omicron
Female sex: OR 1.56 - higher risk than male
Comorbidities
Cardiovascular disease (OR 1.50)
Hypertension (OR 1.37)
Any comorbidity (OR 1.52)
ICU admission: OR 1.43 - higher risk than non-ICU
Variants matter.
Pre-Omicron (Alpha/Delta) = higher risk.
Omicron = lower risk, especially in vaccinated people.
But many studies classified by calendar date (pre-Omicron vs Omicron), so effects of variants are partly blurred by vaccination rollout.
Most common subtypes:
Respiratory (20%)
Fatigue (20%)
Psychological (18%)
Neurological (16%)
Most common symptoms - memory problems (11%), muscle weakness (11%), breathlessness (8%), joint pain (7%), brain fog (4%).
Neurological impact stands out.
Unlike flu or other respiratory viruses, COVID often leaves memory loss, brain fog, and cognitive dysfunction behind.
Insights.
Definition matters - any fatigue = 20%, severe/constant fatigue = 7% - a lot depends on how symptoms are defined - that’s why numbers vary so much between studies.
Massive heterogeneity between studies (I2 ≈ 100%) - different definitions of long COVID, different health systems, different viral variants, vaccination coverage, testing, and follow-up methods all shape the results.
Underrepresentation - very few studies from Africa & Oceania.
Sum:
Long COVID is a global, long-term health challenge.
Vaccination and variants shape the risk - but millions remain affected.
Hou at al., Global Prevalence of Long COVID, its Subtypes, and Risk factors: An Updated Systematic Review and Meta-Analysis. academic.oup.com/ofid/advance-a…

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More from @ZdenekVrozina

Sep 16
Imagine a school year where 4 out of 5 students and staff get sick with a respiratory infection.
That’s not a dystopia.
That’s what a new study just found in a large US school district.🧵
816 children and staff were followed from November 2022 to May 2023.
They self-collected nasal swabs, reported symptoms, and were tracked week after week.
Result.
85% had at least one virus detected
80% had at least one acute respiratory illness (ARI)
(sic!)
Read 11 tweets
Sep 13
A new Dutch study in BMJ Open 2025 followed people 2 years after COVID-19.
Even among those never hospitalized, 43% still had persistent symptoms.
This is a massive population-level impact.🧵
Hospitalized patients had higher prevalence of post-COVID (65%).
But they are a fraction of all infections.
The real burden comes from the huge group of mild cases!
The CORFU study = Corona Follow Up.
4,200 participants, 7 patient cohorts + controls.
Follow up at 3, 6, 12, 18, and 24 months.
Read 14 tweets
Sep 13
New study in COVID (MDPI) followed 297 people 3 years after a single COVID-19 infection.
Key message: cognitive performance did not return to normal. Even one infection left measurable deficits🧵
Participants.
Mild - 101
Moderate (hospitalized) - 101
Severe (ICU, hypoxia) - 95
These were infections from the era of the original virus & Alpha variant (up to 2021). Omicron was not yet circulating.
Scores after 3 years (higher = better).
Divided attention: 44.5 - 36.1 - 27.3
Working memory: 10.6 - 9.3 - 9.0
Executive control: 9.0 - 7.6 - 7.5
Verbal fluency: 14.6 - 14.3 - 12.2
Recognition memory: 23.9 - 23.2 - 21.6
Trend is clear: more severe illness = greater cognitive loss.
Read 16 tweets
Sep 11
May a new NIH preprint rewrite the COVID textbooks?
Turns out SARS-CoV-2 doesn’t start with ACE2. It latches onto heparan sulfate clusters on the cell surface. ACE2 only acts later, inside endosomes. Robust methods. Still preprint.🧵
Why that matters - NIH labs have the time, tools, and independence to go deep. When they drop a preprint, it’s worth paying attention.
The tech here is next-level.
MINFLUX nanoscopy (1–3 nm precision)
STED super-resolution (60 nm)
electron microscopy
You can literally see individual virions docking.
Read 16 tweets
Sep 11
Behind each number is a child. After COVID, kids had 2× higher risk of self-harm. Now, the same lead author Kim et al. 2025 shows: kids depression & anxiety diagnoses rise by 49% in the year after infection🧵
This was no small study. Researchers tracked 154,000 children aged 6–15 in Utah.
In 2021 -
9.2% of those with COVID developed new depression or anxiety vs 5.3% in children who never had COVID.
That’s almost a doubling of risk.
Severity mattered.
Mild COVID +40% risk.
Severe (hospitalization/ER) +59% risk.
The more severe the illness, the heavier the psychological toll.
Read 9 tweets
Sep 10
A new preprint study shows that the SARS-CoV-2 protein ORF6 directly kills human neurons.
Not by accident, but through necroptosis - a kind of cell death where neurons burst and fuel inflammation.
This may underlie the long-term brain symptoms of Long COVID.🧵
Researchers tested 22 viral proteins. The most toxic? ORF6.
In neurons, it flipped on the necroptosis switch - RIPK3 and MLKL.
Biologically - these molecules punch holes in the cell membrane until the neuron literally ruptures.
In patient brain tissue, especially the hippocampus (memory center), they found the same pattern
dead neurons + necroptosis markers.
That’s a direct biological link between infection and symptoms like brain fog and memory loss.
Read 14 tweets

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