New Study = No Link Between Autism and Vaccines

Dafunkdoc_Unlimited

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The Wrong Side of the Tracks
So, as expected, the ONLY objections to the study take the form of 'It was funded by X, therefore, it can't be trusted due to bias.'

The problem with this objection is that peer review takes the "X" out of the process.....

Peer Review in Scientific Publications: Benefits, Critiques, & A Survival Guide
Referees are typically not paid to conduct peer reviews and the process takes considerable effort, so the question is raised as to what incentive referees have to review at all. Some feel an academic duty to perform reviews, and are of the mentality that if their peers are expected to review their papers, then they should review the work of their peers as well. Reviewers may also have personal contacts with editors, and may want to assist as much as possible. Others review to keep up-to-date with the latest developments in their field, and reading new scientific papers is an effective way to do so. Some scientists use peer review as an opportunity to advance their own research as it stimulates new ideas and allows them to read about new experimental techniques. Other reviewers are keen on building associations with prestigious journals and editors and becoming part of their community, as sometimes reviewers who show dedication to the journal are later hired as editors. Some scientists see peer review as a chance to become aware of the latest research before their peers, and thus be first to develop new insights from the material. Finally, in terms of career development, peer reviewing can be desirable as it is often noted on one’s resume or CV. Many institutions consider a researcher’s involvement in peer review when assessing their performance for promotions. Peer reviewing can also be an effective way for a scientist to show their superiors that they are committed to their scientific field.

The key to understanding it is that NO scientist wants his/her name associated with something that is NOT true or valid and it is quite easy to invalidate another scientist's work via the same process of peer review. Now, the objectors state that 'Big Pharma' created the study, but that still leaves the thousands of scientists working independently who are NOT being paid by 'Big Pharma' to make their own critiques and point out problems with the study and it's results

Where they at?

:sas1:

Also, if we take this objection seriously, then that means we cannot trust studies from the Anti-Vaccination Squad as THEY cannot be trusted to give un-biased results.

Too bad they don't submit studies to be peer reviewed.

Wonder why not?

:sas2:
 

Spliff

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Food for thought.

A Scientist’s Rebuttal to the Danish Cohort Study
Headshot-Summer-2016-Hooker-Finished-150x150.png

Brian S. Hooker, PH.D., P.E.

SCIENCE ADVISER, FOCUS FOR HEALTH | BIO

March 13, 2019


The MMR vaccine study recently published by Hviid et al. (2019, Annals of Internal Medicine) entitled, “Measles, Mumps, Rubella Vaccination and Autism: A Nationwide Cohort Study,” leaves many more serious questions than definitive answers.

The authors claim that their work, “strongly supports that MMR vaccination does not increase the risk for autism, does not trigger autism in susceptible children, and is not associated with clustering of autism cases after vaccination.”

This is an extremely broad claim that unfortunately is not supported by the evidence they present. There are eight fundamental flaws in the research study that lead to questions about the accuracy of the conclusions.


1. Children were notably missing from the study sample:

First and foremost is the underascertainment of autism cases within their data sample. The study authors used Denmark population registries of children born in Denmark of Danish-born mothers which should reflect the current reported autism incidence in Denmark at 1.65% (Schendel et al. 2018, JAMA). However, the autism incidence within the sample of the Hviid et al. paper is 0.98%, meaning that approximately 4,400 autistic children are missing from this study. The authors do not discuss the discrepancy in the number of cases.


2. Many of the children in the sample were too young for an autism diagnosis:

The most probable reason for the discrepancy in cases is that the sample in the Hviid et al. paper is too young to completely ascertain autism diagnoses. The average age of sample is 8.64 years with a standard deviation of 3.48 years. Age of autism diagnosis on average is reported as 7.22 years with a standard deviation of 2.86 years. Assuming that the age of diagnosis follows a standard bell curve, this would mean that 31.5% of the sample was too young to get an autism diagnosis. This could account for as many as 3,400 additional cases not included in the analysis, which would bias the outcomes to favor not finding a relationship between the MMR vaccine and autism.


3. Failure to eliminate those with autism related to genetic conditions from the sample:

In addition, individuals who were diagnosed with genetic comorbidities (known to lead to autism) after age 1 were “censored,” meaning that they were followed until the time of diagnosis, but not removed from the study. Thus, they were counted among the sample with many of them most likely autistic due to a genetic condition. These should have appropriately been eliminated from the sample.


4. Use of two (2) different MMR vaccines:

Also, two different MMR vaccines were used in this study. The GlaxoSmithKline Prolix® formulation was used from 2000 to 2007 and Merck’s MMR®II formulation was used from 2008 to 2013. Prolix® contains the Schwarz measles strain and MMR®II contains the Ender’s Edmonston measles strain. Thus, children using the Merck formulation were much too young to receive an autism diagnosis as the oldest they would be at the time of study is 6 years of age or younger. This is important for comparison to the experience in other countries, especially the U.S. where the Merck formulation was used exclusively for the entire study period.


5. Failure to control for the “dosage effect”:

In addition, the age at which Danish children in the sample received their second dose of MMR vaccine was dropped from 12 years to 4 years in 2008. This means that children born after 2004 would get two MMR vaccines prior to the average age of an autism diagnosis, whereas children born prior to 2004 would have received only one MMR vaccine. If indeed there is a “dosage effect” of the MMR (i.e., where both doses were causally related to autism), this could not be elucidated in the sample and again, this would bias the results erroneously to not find a relationship.


6. Statistical method failed to capture those children with a delayed diagnosis of autism:

The authors also used a non-transparent statistical method where “person-years” were considered following the MMR vaccine to an autism diagnosis where children who received a diagnosis soon after receiving their first MMR vaccine would be weighted more heavily than children with a delay in diagnosis. This makes no sense given that the age of autism diagnoses varies widely among populations based on access to services and severity of the autism case, among other factors. This type of method is “borrowed” from infectious disease epidemiology where an exposure directly leads to a disease state rather quickly, for example, chicken pox. However, the method has no place in evaluating chronic sequelae to vaccination which may take a period of years to receive an accurate diagnosis.


7. Vaccinated male siblings of children with autism show more autism diagnoses:

It is interesting to note the increased incidence of autism in boys with autistic siblings in the vaccinated group shown in Figure 2 of the article’s supplement. The increase towards the end of the “survival curve” shows that more boys vaccinated with MMR (with autistic siblings) are diagnosed with autism than unvaccinated boys. The difference is not statistically significant but this may be an artifact of the very small subset of boys considered in this analysis.

The study authors also cite the CDC’s Destefano et al. 2004 study which actually shows a statistically significant relationship between MMR timing and autism incidence. This is discussed further in a reanalysis of CDC’s data in the Journal of American Physicians and Surgeons (Hooker, 2018).


8. Conflict of interest of the study authors:

It should be noted that three of the study authors are currently employed at the Statens Serum Institut which is a for-profit vaccine manufacturer in Denmark. In addition, this work was funded by a grant from the Novo Nordisk foundation. Novo Nordisk is a Danish multinational pharmaceutical manufacturer. These are two serious conflicts of interest.

The lead author, Anders Hviid was the second author on the New England Journal of Medicine MMR autism paper from 2002 (Madsen et al. 2002). This research was completed despite the fact that the study authors had never received proper ethics approval to complete the study. A detailed analysis of this is featured by Children’s Health Defense.


With these issues, this paper cannot be relied upon as evidence that the MMR vaccine does not cause autism.

A Scientist's Rebuttal to the Danish Cohort Study - Focus for Health

Comment, cosigned by aurthor of above:

Vasileios S. March 14th, 2019

The study is flawed by design and mostly from what and how they choose to ‘study.’
I agree with all your remarks and I want to add the following.

1st:
They choose to stop the follow up (08/2013) and that is the reason the autism prevalence at first birth cohort is 1.70% and at the last cohort only 0.2%. One explanation for that choice maybe is because in Denmark they incorporate the PCV7 vaccine (3 doses same as pentavalent) at October 2007. That mean 3 doses of a heavily adjuvanted vaccine before 1st MMR for the last cohort.

2nd:
They choose to ”include and study” only 5 from 8 sub-categories of «F84 Pervasive developmental disorders» – International Statistical Classification of Diseases and Related Health Problem (ICD-10) – Diagnostic criteria - Autism - NCBI Bookshelf

«F84.0 (autistic disorder – 1997 cases)
«F84.1 (atypical autism – 537 cases)
«F84.5 (Asperger syndrome – 1098 cases)
«F84.8 (other pervasive developmental disorder – 576 cases) –
«F84.9 (unspecified pervasive developmental disorder – 2309 cases).

F84.9 PDD unspecified has a description saying that it is a residual category for PDD where there is either inadequate information or contradictory findings regarding diagnosis. F84.8 has no description at all. No description but present!!!!!!!

But they didn’t include at the study from the main ICD-10 category «F84 Pervasive developmental disorders» the 3 following subcategories:

-F84.2. Rett’s syndrome – – so far reported only in girls (they leave out that subcategory and probably that’s why at their flawed analysis it appear that ”Receipt of MMR vaccination reduced the risk for autism in girls” with a statistical significance)

-F84.3. ”Other childhood disintegrative disorder” – «A pervasive developmental disorder (other than Rett’s syndrome) that is defined BY A PERIOD OF NORMAL DEVELOPMENT BEFORE ONSET,AND BY DEFINITE LOSS OVER THE COURSE OF A FEW MONTHS, of previously acquired skills in at least several areas of development, together with the onset of characteristic abnormalities of social, communicative, and behavioural functioning» …. That definition fall exactly under their 3rd objective, … and they CHOOSE to leave all cases under that definition outside of their study
> Objective: ”To evaluate whether the MMR vaccine increases the risk for autism in children, subgroups of children, or time periods after vaccination … We evaluate the risk for autism after MMR vaccination in specific periods in detail.”

-F84.4. ”Overactive disorder associated with mental retardation and stereotyped movements”

So intentionally 1/3 of «F84 Pervasive developmental disorders» subcategories was not included in their BIASED study (and they did’t even explain that decision).

3rd:
MMR vaccination status for all the children that ”appear” no-vaccinated in the registries should had been confirmed by their medical cards since a previous study ’danish mEdical JOURnal- Dan Med J 2017:64(2):A5345 proved that up to 55% of no-vaccinated (as per registries) was actually vaccinated.

4th:
They should analyze the time relation between MMR vaccination and «”the manifest time of autism” or ”time of first symptom appeared” or ”the day of onset”» which could be obtained from children medical cards (which they didn’t review – ” Limitation:No individual medical charts were reviewed”), since they didn’t use the ”time of first symptom appeared” then all the aHR (for time relation between autism and MMR) analysis is complete WRONG.

Conclusion:
The bias and flaws of that study strongly support that health authorities and vaccine promoters don’t want actually to RESEARCH if there is any link between autism and vaccine (or vaccines) thus actually they don’t care for the safety of their products since they are the authority and no one can question them.

My best wishes to you and your family Dr Brian, please correct me if I am wrong at any of my remarks for that study
 
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