A new warning study that deserves attention.
SARS-CoV-2 leaves a long-term endothelial and metabolic footprint in the blood months after infection - even in people without obvious Long COVID symptoms.
And that matters🧵
Researchers followed 262 adults in Germany and measured blood biomarkers about 37 weeks after infection - roughly 9 months later.
People who had previously had COVID showed higher markers of endothelial dysfunction and tissue stress, including soluble thrombomodulin and LDH, compared with never-infected controls.
In simple English.
Their blood still carried signs of vascular and metabolic disturbance long after the acute infection was over.
The most important part?
These changes were not limited to people diagnosed with post-COVID syndrome.
Similar signals were also seen in people recruited from a population cohort after infection - not just in patients who showed up at a Long COVID clinic.
It does show something deeply uncomfortable.
SARS-CoV-2 can leave a measurable biological mark even in people who think they have fully recovered.
The study also found changes in amino-acid pathways linked to nitric oxide metabolism - including L-arginine, citrulline, and taurine.
Nitric oxide is central to vascular tone, microcirculation, and normal endothelial function.
That makes this more than a random lab finding.
In people with more severe fatigue, the signal looked different. Higher levels of specific fatty acids, including linoleic, oleic, and palmitoleic acid.
It may reflect real metabolic and energy-regulation disruption.
This findings also fit into a broader hypothesis emerging across post-COVID research -
that SARS-CoV-2 may push part of the population toward a longer-term shift in lipid and metabolic health - potentially including triglycerides and broader cardiometabolic risk.
So here is the part we should not ignore.
We do not know whether this endothelial and metabolic footprint disappears.
We do not know when it disappears.
And we cannot rule out that, in some people, it persists for years.
That is why the population-level question matters.
Even a modest shift in vascular or metabolic biomarkers across millions of people could translate into a meaningful shift in long-term cardiovascular risk.
This study does not say that everyone after COVID is automatically a cardiovascular patient.
But it does say something serious.
SARS-CoV-2 can leave measurable biological traces even in people who look fine.
And if infections keep repeating, the question is no longer only
Did I get Long COVID?
It is also -
What are repeated infections doing to my blood vessels, my metabolism, and my long-term health?
Participants were recruited in Germany between July 2021 and January 2022 - not just a single wave or variant.
Oestreich at al., Endothelial dysfunction and metabolic biomarkers in post-COVID-19 syndrome. nature.com/articles/s4159…
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This may be one of the more important long COVID papers in a while.
A new study in Frontiers in Immunology suggests that COVID can trigger new-onset insulin resistance - and that this may drive abnormal NETosis in neutrophils months after infection🧵
NETosis is the process where neutrophils release web like structures made of DNA, histones, enzymes.
Normally, this helps trap pathogens.
But when excessive, NETs can -
damage the endothelium
trigger microclots!
amplify inflammation
activate coagulation.
Exactly the kind of pathology seen in COVID.
The study followed 60 COVID patients.
Among 36 people without prior glucose metabolism problems, 24 developed insulin resistance 4 months after infection.
That alone is a striking finding.
Important new study. ME/CFS and Long COVID are not the same thing.
Yes, they can look very similar from the outside - crushing fatigue, PEM, brain fog, dysautonomia.
But when researchers looked deeper into the immune system, the biology looked different🧵
The study compared
103 people with ME/CFS
63 people with Long COVID
41 healthy controls
They used detailed immune profiling of blood cells - especially monocytes, dendritic cells, and T-cell subsets.
Long COVID
The immune system looked chronically activated, but also exhausted.
Almost like a system that has stayed switched on for too long and is no longer working efficiently.
Some children with Long COVID seem to fall into the same trap as adults - and medicine still doesn’t really know how to get them out.🧵
The UK CLoCk study followed young people who had already been living with post-COVID symptoms for two years. Another 1.5 years later, most of those who responded still met the definition of post-COVID condition.
Some describe years of exhaustion, brain fog, sleep problems, breathlessness, pain, and symptoms that come and go without warning.
No slow recovery after a virus.
A new study in Brain, Behavior, & Immunity - Health reports measurable white matter changes in people with neurological long COVID.
Symptoms had persisted for an average of 2.7 years after infection - almost three years. That points to a long-term neurobiological process in the CNS🧵
The study included 80 participants.
54 with neurological PASC and 26 controls.
Using diffusion MRI, the authors found abnormalities mainly in the fornix and forceps minor - pathways involved in memory, limbic circuits, and frontal connectivity.
The imaging pattern was lower FA and higher MD/RD/AD.
In simple terms - the microstructure of white matter looked disrupted. The study cannot prove the exact cause, but the pattern is compatible with neuroinflammation, demyelination, axonal injury, or microvascular damage.
A new population-based study from Japan on Long COVID is out - the Yao COVID-19 Study.
After quite a long gap, we finally have another useful community prevalence study - and importantly, it can distinguish Alpha/Delta from Omicron🧵
The study followed 2,314 adults after COVID-19 and compared them with 1,314 uninfected controls.
Post-COVID condition was defined broadly in line with WHO criteria. Symptoms lasting at least 2 months and present 3 months after infection.
Prevalence of PCC
3 months 14.3%
6 months 12.0%
12 months 6.3%
18 months 5.4%
So even 18 months after infection, about 1 in 20 infected people still reported persistent symptoms.
During the pandemic, physician @leanhealth reported something important.
COVID patients who slept next to bedside air filters often seemed to have milder disease - possibly because they were not re-inhaling virus-laden air for eight hours every night🧵
A new hypothesis paper now points in the same direction using CT data. Cleaner air may not only reduce transmission. It may also reduce how deeply SARS-CoV-2 affects the lungs.
The idea is simple. The virus first replicates in the upper airways. An infected person then exhales tiny virus-containing aerosols. In poorly ventilated indoor spaces, these particles can build up and be inhaled deep into the lungs.