Posted on 04/17/2020 11:02:46 AM PDT by a little elbow grease
If SARS-Cov-2 is already endemic in the population, there is nothing we can do to stop it but no great reason to try to stop it, either
Another day, and yet more evidence has appeared that could indicate the number of people who have been infected with SARS-CoV-2, the virus which causes COVID-19, might be vastly higher than official figures suggest. This time a Californian study suggests the figure in one county could be more than 50 times the number who knew they had had the virus.
A team from Stanford University and other colleges recruited volunteers in Santa Clara County via Facebook adverts and produced a sample of 3,000 representatives of the county as a whole. They were then invited for blood tests to detect the presence of antibodies to the virus. The result was positive in 1.5 percent of cases. Adjusting for age, gender and ethnicity the results suggest that 2.8 percent of people in the county had already had the virus. That might not seem many, but at the time of the study on April 4 and 5 only 1,094 people in the county were recorded as having the virus. The study suggests the real figure is between 48,000 and 81,000.
Like many studies which have been pre-published in order to aid understanding of the COVID-19 pandemic, the paper produced by the Stanford-led team has not yet been peer-reviewed. Moreover, it took place in a part of the United States where very few people have so far tested positive with the virus. It would be interesting to see the experiment repeated in New York City, where recorded infections are far higher.
(Excerpt) Read more at spectator.us ...
5000 iu per day. That is one tiny gelcap at WalMart.
“The fact that they didnt test for it at all is an issue. Coronavirus infection is pretty common this time of year.”
Would it not show up as false positive in control blood?
Thanks! Mine are 2000, I take one or 2 so maybe just stick with 2 especially since its been so cloudy and gloomy.
Not necessarily. When were the control blood samples taken? “Pre-Covid sera” suggests to me that the samples date from before cold/flu season hit, so I would expect titers to be fairly low for any respiratory virus at that time. Also, the sample sizes for the controls are problematic, given that prevalence data for the common cold caused by any coronavirus species are unknown.
I also have some issue with the weighting of subject samples. The authors do acknowledge that their test subject selection could have been biased in favor of those who have previously had symptoms. They could have enrolled in the study to seek confirmation (and this would not rule out that they had one of the common coronavirus infections), and that would have heavily weighted the study. The researchers had a raw positive rate of 1.5%, but then used statistical methods to extrapolate a prevalence of 2.49% to 4.16%. How is that kind of extrapolation even valid? Especially given the bias inherent in any study where the subjects are self-selected?
And so on. I’m sure that if I were to take the time to read the study deeply, I could come up with a lot more questions that if I were reviewing it for potential publication, I’d want answered.
Oops, I did not see this until just now.
I am not wrong. Neither of those links show that any Covid-19 antibody test is absolutely 100% specific for Covid-19. And given that coronaviruses have structural similarities, it may not be possible to develop a test that ONLY detects Covid-19 antibodies, and nothing else.
According to one Chinese study, "The specificity of the assays for Ab, IgM and IgG was determined as 99.1% (211/213), 98.6% (210/213) and 99.0% (195/197) by testing of samples collected from healthy individuals before the outbreak of SARS-CoV-2." When there is an error rate of 1-1.4% in an assay, and the measurement of antibody is 1.5% (as in the Stanford study), then I must question the data, since it is right there in the margin of error.
Also, I am posting an image of one of hundreds of immunoassays that I personally conducted, to show graphically the problem with antibody cross-reactivity:
The arrows point to the specific proteins that I was looking for. I knew they were the correct proteins because of their size (I did not show the size ladder on the image). This assay was run on a sample of proteins that had been separated by size. The immunoassays such as they are conducting to detect seropositivity do not separate out anything. Look at my image and imagine that each column was, instead, condensed into a single spot, the way a seropositivity assay would be run. You can see how condensing all of those lines into a spot would create a "positive" result, even if the specific protein wasn't there.
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