MMR-Autism Link: Who Keeps Getting Rid of the Evidence?

autismrainbowWouldn’t it be nice if researchers were free to do research on important topics like what is causing autism, publish their findings, and have others in the world build on these findings or do research that showed those findings to be in question?  That is what scientific inquiry is supposed to be about.

With autism that was 1 in every 10,000 50 years ago and now is 1 in every 50 in the USA  (a 200X or 20,000% increase),  I would have thought everyone on the planet would embrace anything that might shed light on the causes.

The Hooker article, “Measles-mumps-rubella vaccination timing and autism among young African-American boys: a reanalysis of CDC data,” in Tranlational Neurodegeneration, August 2014, looked at the study published in 2004 Pediatrics and found there was indeed a link between MMR and autism for a subset of boys.

Hooker risked his career in exposing the manipulation of the data in the earlier 2004 study so that it wouldn’t show an increased risk.  Rather than this motivating others to look deeper into this possible link, what has happened is that in less than two months the article is being retracted (no reasons-just going to be gone).  I have previously posted the article knowing something like this might happen.  I now have it again (at the bottom), showing the bright red “retracted” headlines.

Andrew Wakefield published the first study that showed a link.  His findings were impressive and that article published in 1998 resulted in a literal man-hunt against him that a decade later resulted in his loosing his license to practice medicine. His results have been replicated (you can read them here… ) and numerous other articles that support his work are listed at the end of this blog.  But, the damage has been done.  There is basically no ongoing look at the outcomes for families who choose to vaccinate differently. We can only get the real answer to this by doing prospective studies looking at a large enough group of children who don’t do the MMR or don’t do vaccines or choose to selectively vaccinate, and compare them to the business as usual kids.

Please realize, there is not one cause.  There is not one autism.  We are talking about children with no language skills or eye contact, to some genius children who are just socially awkward. There are minor “glitches” in attention, sensitivities to touch or sound, etc, there is anxiety, there are a host of little or big brain or emotional-psychological issues.

I have no doubt that which “glitches” or deficits you see depends on both WHAT (the toxin or insult to the brain) and WHEN it occurred. The most vulnerable time is in the womb and the first few years of life when so much of the brains network is forming.


Who do you suppose has the most information about what might have caused the autism in each child affected?  The parent of that child, right?  They know what happened in pregnancy, what happened after birth, what that child ate or drank, what vaccines were given and when, etc.  As parents, we don’t always know at the time that we have put our children at risk.  When we learn of possible harm we may have caused, many of us go into denial- “no that can’t be”, since we certainly don’t want to believe we may have harmed our children.  I gave my children all the vaccines, on schedule.  I’m not proud of that.  I was an ignorant new pediatrician, doing what I was taught to be the best medicine had to offer.  I hadn’t done my own research yet.

I have hundreds of autism children in my practice ranging from very mild to severe.  For those children with significant or severe issues, I can say about half of the parents saw a decline immediately or within a month or two of the MMR shot and for a few it was after the 18 month vaccines.  Once or twice could be a coincidence, but hundreds of times in just my practice?  The Booker study showed increased autism when the MMR was given before age 3 in African-American boys.  I my practice, parents are mostly choosing to give the MMR at 3 years age or later, and with over 1000 children now over age 3, we have no new cases of autism for those who don’t have a family history of autism. At the going rate of 1 in 50, we should have seen 20 new cases these past 3-6 years.  I have asked two major health systems in the area if they would partner with me to do the prospective study looking at vaccines and autism. I have failed to get any response.

You see, there are some powerful interests that control research funding, and can make or destroy careers based on which side of this debate you choose to take.

My hope is that we stop this suppression of research, embrace the fact that in finding the truth we will have studies on both sides of the controversy.  Encourage good prospective studies.  Our children desperately need us to do this.


Transl Neurodegener. 2014; 3: 16.

Published online Aug 8, 2014. doi:  10.1186/2047-9158-3-16

PMCID: PMC4128611

This article has been retractedRetraction in: Transl Neurodegener. 2014 October 3; 3: 22Transl Neurodegener. 2014 August 29; 3: 18    See also: PMC Retraction Policy

An expression of concern has been published for this articleExpression of Concern in: Transl Neurodegener. 2014 October 3; 3: 22Transl Neurodegener. 2014 August 29; 3: 18

Measles-mumps-rubella vaccination timing and autism among young african american boys: a reanalysis of CDC data

Brian S Hooker1

Author information ► Article notes ► Copyright and License information ►

This article has been retracted. See Transl Neurodegener. 2014 October 3; 3: 22.

The editors have expressed concern about this article. See Transl Neurodegener. 2014 August 29; 3: 18.

This article has been cited by other articles in PMC.



A significant number of children diagnosed with autism spectrum disorder suffer a loss of previously-acquired skills, suggesting neurodegeneration or a type of progressive encephalopathy with an etiological basis occurring after birth. The purpose of this study is to investigate the effectof the age at which children got their first Measles-Mumps-Rubella (MMR) vaccine on autism incidence. This is a reanalysis of the data set, obtained from the U.S. Centers for Disease Control and Protection (CDC), used for the Destefano et al. 2004 publication on the timing of the first MMR vaccine and autism diagnoses.


The author embarked on the present study to evaluate whether a relationship exists between child age when the first MMR vaccine was administered among cases diagnosed with autism and controls born between 1986 through 1993 among school children in metropolitan Atlanta. The Pearson’s chi-squared method was used to assess relative risks of receiving an autism diagnosis within the total cohort as well as among different race and gender categories.


When comparing cases and controls receiving their first MMR vaccine before and after 36 months of age, there was a statistically significant increase in autism cases specifically among African American males who received the first MMR prior to 36 months of age. Relative risks for males in general and African American males were 1.69 (p=0.0138) and 3.36 (p=0.0019), respectively. Additionally, African American males showed an odds ratio of 1.73 (p=0.0200) for autism cases in children receiving their first MMR vaccine prior to 24 months of age versus 24 months of age and thereafter.


The present study provides new epidemiologic evidence showing that African American males receiving the MMR vaccine prior to 24 months of age or 36 months of age are more likely to receive an autism diagnosis.

Keywords: Autism, Measles-mumps-rubella (MMR) vaccine


Autism is defined by persistent deficits in social communication and social interaction across multiple contexts and restricted, repetitive patterns of behavior, interests, or activities [1]. Autism incidence has risen dramatically over the past two decades [2] and it has recently been reported that one in sixty-eight children have this disorder [3]. In addition to these core deficits, autism has also been characterized by many other comorbid conditions including gastrointestinal issues, sleep issues, eating disorders and sensory processing issues [4].

It has been estimated that as many as 62% of children with autism experience a period of regression during early childhood, characterized by loss of previously acquired skills [5]. This period has been reported as ranging between 6 and 36 months of age with the typical age of regression between 18 and 24 months [6]. This period of regression occurs within the same time period that children in the United States typically receive their required vaccinations and thus there have been many studies regarding the incidence of autism and the receipt of specific vaccines. One of the primary concerns has been the timing of the administration of the first measles-mumps-rubella (MMR) vaccine.

The relationship between the MMR vaccine and autism was first hypothesized by Wakefield et al. [7] in 1999 after the observation of a regressive phenotype of autism that appeared in general after the administration of the first MMR vaccine. Although several studies have affirmed such a relationship between the MMR vaccine and neurodevelopmental disorders including autism [8,9], many other studies purport no statistical relationship between the MMR vaccine and autism incidence. The latter studies have been performed using cohorts from Denmark [10], Japan [11] and Poland [12], as well as the MMR vaccine and pervasive developmental disorder in Canada [13]. In addition, in 2004, Destefano et al. [14] published a paper describing a case–control study completed on children, in metropolitan Atlanta, who had been born between 1986 and 1993. Within this study, the age at the first MMR vaccine was assessed as a factor in the incidence of autism. Using conditional logistic regression, with first MMR age as the independent variable and autism incidence as the dependent variable, the study authors assessed relative risk for obtaining an autism diagnosis for those children receiving the first MMR vaccine before and after 18 months, 24 months and 36 months of age. Destefano et al. [14] found a statistically significant relative risk of 1.49 (95% confidence interval [CI]: 1.04 – 2.14) at the 36 month cut-off (i.e., in a comparison of children receiving the MMR before versus after 36 months). Rather than concluding that the first MMR vaccine could be playing a causal role in autism in these children, the study authors instead attributed the increased risk to greater numbers of autistic children receiving timely vaccinations in order to participate in State of Georgia special education services.

In this paper, we present the results of a cohort study using the same data from the Destefano et al. [14] analysis. The focus of the current study is differences in results in specific gender and race groups.


Cohort data

Cohort data were obtained directly as a “restricted access data set” from the Centers for Disease Control and Prevention (CDC) via a Data Use Agreement. Data were deidentified by the CDC in accordance with Family Education Rights and Privacy Act (FERPA) and the Health Insurance Portability and Accountability Act (HIPAA) prior to receipt by the study authors. Use of the CDC specifically for the study described herein was approved by the Simpson University Institutional Review Board, in accordance with U.S. Federal regulations.

Study population

As reported by Destefano et al. [14] (CDC) in the original publication, “Children with autism were identified by the CDC from the Metropolitan Atlanta Developmental Disabilities Surveillance Program (MADDSP), a multiple-source, population-based surveillance program that monitors the occurrence of selected developmental disabilities among children in the 5-county metropolitan Atlanta area”. And further, “Autism cases were identified via screening and abstraction of source files at schools, hospitals, clinics, and specialty providers”. Of the cases identified, vaccination records were located for 660 children. Control children were chosen from “regular” education programs and were within the same age group and schools of attendance or neighboring school as cases. Children missing a vaccination form or with incomplete vaccination forms (where the forms did not list at least 1 diphtheria-tetanus-pertusussis vaccine by 2 years of age or at least 1 MMR vaccine at any age) were excluded from the study. Children with religious or medical exemptions were not excluded from the study. The listed exclusions yielded a cohort size of 624 cases and 1824 controls.

Vaccination histories

Vaccination records were abstracted as described previously [14] from standardized state immunization forms that are required for all children who attend school and early intervention programs in Georgia.

Demographic data

Demographic data including birthdate, gender and race were obtained for both case and control children via birth certificates or registration forms kept as a part of each child’s permanent school record. Georgia state birth certificate information was used to further obtain each child’s birthweight. Although actual birthweight data were not released by the CDC, case and control children were lumped into birthweight categories: under 1500 grams, between 1500 and 2500 grams and over 2500 grams. All individuals less than 3 years of age at the time of testing (1996) were excluded from the analysis.

Statistical analyses

The Pearson’s chi -squared test contained in the SAS® software was utilized for current statistical analyses, and a two-sided p-value<0.05 was considered statistically significant. This is in contrast to the original Destefano et al. [14] (CDC) study, where a case–control study design was used, where 3 control children were matched to each case child, and analyzed using conditional logistic regression dichotomized for the three age cut-offs at 18, 24 and 36 months. Pearson’s chi-squared is, in general, a more conservative analysis and therefore chosen for the present study. However, our results were also confirmed using a conditional logistic regression design similar to the Destefano et al. [14] (CDC) study. In the present study, frequencies of cases were determined for first MMR ages of less than versus greater than 18 months, 24 months and 36 months in each separate analysis. When accounting for cases in the cohort that excluded low birth weight (<2500 g) African American children, it was necessary to report results at 31 months rather than 36 months in order to avoid reporting data from age categories or “cells” that possessed less than 5 individuals.


Table 1 shows the relationship between MMR timing and autism incidence for the entire cohort. As can be observed, there is a statistically significant effect for the cohort at 36 months (RR=1.49, 95% CI: 1.04-2.14, p=0.0289). However, this result appears to be caused by a stronger relationship (RR=1.69, 95% CI: 1.11-2.57, p=0.0138) seen exclusively in boys. Girls did not show any relationship between autism and MMR timing at any age group studied.

Table 1

Fisher’s exact analysis for the entire cohort

When looking specifically at African American children (Table 2), the relationship between MMR timing and autism incidence became more profound (RR=2.30, 95% CI: 1.25-4.22, p=0.0060) at 36 months of age. Again, this result was exclusively found in boys who showed statistically significant effects at both 24 months (RR=1.73, 95% CI: 1.09-2.77, p=0.0200) and 36 months (RR=3.36, 95% CI: 1.50-7.51, p=0.0019) of age. This effect again was not seen in females.

Table 2

Fisher’s exact analysis for African American children only

Table 3 shows results for the entire cohort excluding African American children. As can be observed, there is no statistically significant effect for any of the subclasses in either gender or age cut-off for MMR uptake. This shows that the effect observed overall is due to the very strong “signal” seen exclusively in African American boys. In other words, the strong, statistically significant relationship between younger first MMR age and higher autism incidence in African American males may be skewing the results for larger, more general populations that include African American males (e.g., all boys and all African Americans) to show a “relationship” that is actually only in African American males.

Table 3

Fisher’s exact analysis excluding African American children

Through investigating the cohort demographic data, it was found that there was a higher proportion of low birth weight African Americans compared to the entire cohort, specifically within the portion of the cohort that possessed a Georgia state birth certificate. The number of individuals with a birth weight under 2500 g for African Americans was 11.9% as compared to the total cohort at 8.66%. A final analysis was completed on African American children in the “birth certificate” cohort, excluding low birth weight individuals (Table 4). Results were obtained at 18 months, 24 months and 31 months, rather than 36 months, as there were insufficient cases (less than 5) at the 36 month mark to carry out the analysis. Even at 31 months, there were insufficient cases of African American females. Thus, these results are not included in the analysis. Even excluding low birth weigth individuals, a relationship was seen between first MMR age and autism incidence at 31 months for African American males (RR=2.64, 95% CI: 1.08-6.46, p=0.0280).

Table 4

Fisher’s exact analysis for African American children excluding low birth weight


The results show a strong relationship between child age at the administration of the first MMR and autism incidence exclusively for African American boys which could indicate a role of the vaccine in the etiology of autism within this population group. This particular analysis was not completed in the original Destefano et al. [14] (CDC) study. Although the previous study considered MMR timing and African Americans in general, no statistically significant effect was observed. This is in contrast to our result for African Americans in general, because the CDC study limited the total African American cohort to include only those individuals who possessed a valid State of Georgia birth certificate which decreased the statistical power of their analysis. Although a statistically significant relationship between first MMR age and autism incidence was seen in the general (all races) population within the earlier Destefano et al. [14] study, the coauthors interpreted this result as an artifact of “healthcare seeking behavior” citing that autistic children would receive their vaccines earlier in order to enroll in State of Georgia early intervention programs. However, it is highly unlikely that this type of behavior would be seen exclusively in African American males and thus, alternative hypotheses must be explored, including the possibility that the MMR vaccine may be causally linked to autism in African American males.

It should be noted that a recent publication has shown that the prevalence of autism in African Americans is nearly 25% higher than that of whites [15]. This value was obtained when CDC data were appropriately analyzed based on socioeconomic status. This could be due to issues regarding vitamin D status with African Americans as it has been estimated that vitamin D sufficiency among whites is between 30-60% but is only 5-10% among African Americans [16]. Patrick et al. [17] have very recently proposed a mechanism for the link between vitamin D status and autism via selective production of serotonin in the brain. Disruption of the serotonergic system is a very consistent observation with autism [18] as serotonin promotes prosocial behavior and proper assessment of emotional social cues [19].

Vitamin D has a multitude of other physiological functions in vivo. Vitamin D receptor has been found in many different tissues including the small intestine, colon, osteoblasts, activated T and B lymphocytes, islet cells and most organs in the body [20]. Vitamin D has also been implicated in many important physiological processing including modulation of activated T and B lymphocyte function [21,22] and prevention of inflammatory bowel disease [23]. Lower vitamin D status African American females are more susceptible to lupus [24]. Also, Epstein-Barr Virus antibody titers are significantly higher in African American youth as compared to compared to white youth [25] which may be a consequence of vitamin D insufficiency. Also, childhood adversity, which could be more prevalent in African American boys, can have lasting immune consequences [26].

Gallagher et al. [27] have reported previously regarding the Hepatitis B vaccine and autism in neonates, specifically within the 1997 to 2002 time period when this vaccine series still contained thimerosal. Regarding non-whites they specifically stated in the abstract, “Non-white boys bore greater risk” of receiving an autism diagnosis if they received the Hep B as neonates. The data reported in this paper show a statistically significant risk ratio of 5.53 (p=0.019) for black boys as opposed to white boys who had a risk of 1.87 (p=0.171) which was not statistically significant, when looking at autism in those infants that received their first Hep B vaccine during the first month of life.

A strength of the current study is that the MADDSP data were collected independently of the design used in the analysis. These data were collected as part of the diagnoses individuals received as part of their participation in special education program and as such, the healthcare providers in no way were thinking about the potential association between vaccine exposures and potential health outcomes. Also the current study controlled for a possible association between low birth weight individuals and autism as in the final analysis on the African American cohort, all children of birthweight less than 2500 grams were eliminated from the cohort. Although low birthweight (LBW) has been shown to be associated with an increased risk of autism [28], insufficient information existed within the study population to assess the effect of LBW on autism incidence or any interaction between LBW and MMR timing.

The weaknesses of the current study include the age groups selected for autism cases and controls within the original data set. The average age to receive an autism diagnosis has been reported (using the CDC’s Vaccine Safety Datalink) as between 3.7 [29] and 4.2 years of age [30]. However, the CDC’s dataset included controls as young as 3 years of age who could have been “too young” to receive an autism diagnosis. Accordingly, there is a greater than 50% probability that some of the controls could have later received an autism diagnoses, thus skewing the analysis to the null (“no effect”) hypothesis. However, when the analysis was recompleted using controls that were six years of age or older, very similar results were obtained (data not shown). Also, information on the timing of other infant vaccines was not released by the CDC and thus it was impossible to control this factor in the current analysis. In addition, socioeconomic factors were not assessed in the current analysis. Thus, any differences in “healthcare seeking behavior” among individuals vaccinated ontime versus late could not be assessed.


The present study provides new evidence of a statistically significant relationship between the timing of the first MMR vaccine and autism incidence in African American males. Using a straight-forward, Pearson’s chi-squared analysis on the cohort used in the Destefano et al. [14] (CDC) study, timing of the first MMR vaccine before and after 24 months of age and 36 months of age showed relative risks for autism diagnoses of 1.73 and 3.36, respectively. Future studies should be completed to further evaluate the relationship of first MMR timing and neurodevelopmental maladies, including autism, especially in underserved populations.

Routine childhood vaccination is considered an important public health tool in reducing the morbidity and mortality associated with infectious diseases. However, consideration should be made in the current United States vaccination schedule for genetic subpopulations that may be associated with vaccine adverse events. Additional research is required to better understand the relationship between MMR exposure and autism in African American males.


CDC: Centers for Disease Control and Prevention; CI: Confidence Interval; Hep B: Hepatitis B vaccine; MADDSP: Metropolitan Atlanta Developmental Disabilities Surveillance Program; MMR: measles-mumps-rubella vaccine; RR: Relative Risk.

Competing interests

Dr. Hooker has been involved in vaccine/biologic litigation.

Authors’ contributions

BH was the main manuscript writer and computer programmer.


Funding for this research was provided for by a grant from Focus Autism, Inc. Data for case and control children were provided in a de-identified form by the Centers for Disease Control and Prevention.


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Here is a list of 28 studies from around the world that support Dr. Wakefield’s research:

  1. The Journal of Pediatrics November 1999; 135(5):559-63
  2. The Journal of Pediatrics 2000; 138(3): 366-372
  3. Journal of Clinical Immunology November 2003; 23(6): 504-517
  4. Journal of Neuroimmunology 2005 
  5. Brain, Behavior and Immunity 1993; 7: 97-103
  6. Pediatric Neurology 2003; 28(4): 1-3
  7. Neuropsychobiology 2005; 51:77-85
  8. The Journal of Pediatrics May 2005;146(5):605-10
  9. Autism Insights 2009; 1: 1-11
  10. Canadian Journal of Gastroenterology February 2009; 23(2): 95-98
  11. Annals of Clinical Psychiatry 2009:21(3): 148-161
  12. Journal of Child Neurology June 29, 2009; 000:1-6
  13. Journal of Autism and Developmental Disorders March 2009;39(3):405-13
  14. Medical Hypotheses August 1998;51:133-144.
  15. Journal of Child Neurology July 2000; ;15(7):429-35
  16. 1972;2:883–884.
  17. Journal of Autism and Childhood Schizophrenia January-March 1971;1:48-62
  18. Journal of Pediatrics March 2001;138:366-372.
  19. Molecular Psychiatry 2002;7:375-382.
  20. American Journal of Gastroenterolgy April 2004;598-605.
  21. Journal of Clinical Immunology November 2003;23:504-517.
  22. Neuroimmunology April 2006;173(1-2):126-34.
  23. Neuropsychopharmacol Biol. Psychiatry December 30 2006;30:1472-1477.
  24. Clinical Infectious Diseases September 1 2002;35(Suppl 1):S6-S16
  25. Applied and Environmental Microbiology, 2004;70(11):6459-6465
  26. Journal of Medical Microbiology October 2005;54:987-991
  27. Archivos venezolanos de puericultura y pediatría 2006; Vol 69 (1): 19-25.
  28. 2005:128 (Suppl 2);Abstract-303



Dr. Paul


Stress and Anxiety During Pregnancy Linked to Autism, ADHD, and Anxiety in Children – Hypomethylation Related

200447888-001Anything we can do to reduce the chances our children will suffer from autism, ADD, ADHD, anxiety, etc. would be worth paying attention to right?

I have published a blog (you can see it here… ) showing that maternal folate supplements cut that risk in half.  You will hear over and over that most health issues are “genetic” but they are referring to epigenetic, meaning how our genes respond to the environment (we can often make the environment friendly rather than hostile). 

The study (you can read here… ), “Differential gene body methylation and reduced expression of cell adhesion and neurotransmitter receptor genes in adverse maternal environment”, is an important study, complicated beyond words in the details. I see two very important take home messages:

1.  Avoid maternal stress during pregnancy, it can harm your unborn child when mom is stressed. Treat her like a queen!

2.  Support methylation, and I would recommend in addition to methyl-folate, methyl-B12 and a B-complex.  (Ceralin Forte by Metagenics does it all in one supplement and is available at my office or from Metagenics). Get advice from your provider on whether or not this might be OK for your specific case, but if it were my wife or child I would have them take just one capsule a day (not the 3 recommended on the bottle), along with her prenatal vitamin, extra vitamin D for a total of 4-5,000 IU vitamin D3 a day, omega-3, and make sure the prenatal vitamin has iodine. 

Single nucleotide polymorphisms (SNP’s) are unique codes in our genetic code that respond to the environment.  In this study CRHR1, DRD3, ADORA2A, CHRNA4, GABRG3, and GABBR2 were all methylated differently in the stressed moms and are linked to anxiety. Differential methylation was also detected in GRIN1, the gene for the NMDA NR1 subunit and in GRIK3 and GRIK4 the genes for KA receptor subunits.  Other SNP’s with differential methylation leading to anxiety were the GRIP1, SHANK1, 2, 3 as well as the CACNA1C and KCNJ genes. 

What is exciting, is that with almost all these SNP’s where we each may have hundreds if not thousands of “glitches” (most unknown at this point) representing genetic strengths and weaknesses in enzyme systems and neurotransmitters, rather than thinking you are doomed, you can do something about it.  In most cases, health is just a few supplements, and healthy living life-style changes, away!  Support methylation by taking methyl-B12, methyl-folate, and consider getting your genetic profile tested.  Consider having Spectracell drawn so you will know specifically which nutrients are not getting into your cells.  Spectracell is offered at Integrative Pediatrics for children ( , and at Natura Integrative Medicine ( for adults.



Dr. Paul



Vaccine-Autism Link Center Stage- Let Us See If Our CDC, AAP, and News Media Will Seek the Truth or Once Again Attempt to Suppress This Story

liarThe Vaccine- Autism Link has been there for thimerosal, for MMR, and I suspect for aluminum (just not studied).

Parents of Autistic children are divided.  Many want to believe there is no link between vaccines and autism. After all, they allowed the vaccines to take place.  I gave all the recommended vaccines to my children BEFORE I became informed and did my own digging to get to the truth.  That’s the challenge, “getting to the truth”, when the CDC has systematically engaged in deception that has gone from manipulating data, to designing studies so they won’t show vaccine effects.  They have not done the long-term studies putting head to head a population that is unvaccinated or one that is selectively and intelligently vaccinated, compared to the business as usual vaccine schedule.

Parents of children who may have been vaccine injured, please forgive yourselves and put your efforts into recovering your child’s health and getting the word out.  Educate yourself and then let us join forces to make sure we minimize vaccine risk for others.   I also suggest you not throw the baby out with the bath water, and reject all vaccines, although for those that have one child with severe autism, I would not blame you for not vaccinating subsequent children.  My experience with about 100 families has been that after a child or two became autistic, parents don’t vaccinate the  subsequent children who have been neurotypical (not autistic) with one exception.  I have one other family where the first three children were neuro-typical and their pediatrician convinced them that studies had proven vaccines to be safe (these same manipulated studies) so they gave their 4th child all the vaccines and that child is autistic. 

To minimize vaccine risks, I would:

1.  Not give the Tdap while pregnant (with it’s 170 to 330 micrograms of aluminum).

2.  Not give the Hepatitis B vaccine to newborns or infants (each contains 250 micrograms aluminum).

3.  I would wait until age 3 before giving the MMR.

4.  If you have the MTHFR defect, a strong family history of autism or autoimmune issues, you may need to consider a very slow vaccine schedule, if at all. 

Below is a well written blog from safe minds and links to the studies and documents that have shed light on the CDC manipulation of data and outcomes to dilute out the link that was actually there showing increased autism in vaccinated vs. non-vaccinated children for the particular vaccine or component (thimerosal, for example).

Statement of CDC Dr Thompson regarding the omission of key data that showed a link between MMR and autism can be read here…

The re-analysis study just published August 2014 (retracted in the same month after misters pressure from ?) can be read here…

CDC Thomas Verstraeten initial data that showed 7.6-11.4 times increased autism for those exposed to thimerosal (mercury) can be read here…

Safeminds shows how the CDC manipulated the Verstraeten data to remove the mercury (thimerosal) significance. Read more here…

2007 NEJM article showing increased TICS and language delays in those children receiving thimerosal vaccines. Read here…

For the safe minds blog highlighting all this information so well, read here…



Dr. Paul


AAP Pushes the Tdap for All Pregnancies (NOT A GOOD IDEA)

pregnant-heartAAP (Academy of Pediatrics) News release Feb 1, 2014:  Dr Sarah Long MF FAAP, member of the AAP committee on infectious diseases, (read here…. ) outlines the position of the AAP.  She points out that “recommendations for Dtap use have not changed in more than a decade and include routine administration of the infant series at 2, 4 and 6 months of age, and reinforcing doses at 12 to 18 months and 4 to 6 years.” 

This article is stressing the new changes effective in 2014; “The most recent change, which was included in the 2014 Immunization Schedule, is the recommendation for Tdap administration during each pregnancy, preferably between 27 and 36 weeks of gestation and regardless of time since last Tdap or Td.”

What concerns me and should concern anyone who is thinking clearly about this recommendation is that there have been no studies on the effects of injecting this vaccine during pregnancy. NO STUDIES!   This article mentions: “Why are repeated doses of Tdap not recommended routinely for the general population other than pregnant women? Data do not support a substantial impact of a broader recommendation on pertussis control, and lack of data and licensure are cause for pause.” 

It seems our experts who make vaccine recommendations care about lack of data and licensure when it comes to recommending routine boosters for the general population, but can recommend injecting pregnant women with this vaccine and it’s 330 micrograms of aluminum without any studies or data on the safety of such a recommendation.  Any researcher who wanted to study this would need an IRB (Institutional Review Board) approval to inject half the pregnant women with the Tdap and half with saline then look for 5-10 years at the outcomes (how many cases of brain injury from the toxic aluminum: autism, ADD, ADHD, anxiety, depression, learning challenges etc.).  I cannot find a single study like this in humans or even primates. 

There are plenty of studies raising concerns about aluminum toxicity.  One recent study (you can read it here… ) showed vaccine concentrations of aluminum after birth, triggering autism like symptoms. There is no doubt that injecting aluminum during pregnancy will result in a much higher risk to the developing fetal brain. 


JUST SAY NO to Tdap during pregnancy!

This issue is about balancing risks and benefits.  Does the risk of poisoning an entire generation (every baby born in America whose mother gets the Tdap)  justify the handful of potential saved lives (those rare infant deaths in the first few months of life before the usual vaccine schedule has time to work)?  I think as physicians we should “First Do No Harm”.  This vaccine recommendation clearly causes harm, we just have to wait 5-10 years to see the explosion of the Autism, ADD, ADHD, anxiety, depression, learning disorders, etc.  Make sure your physician is giving you informed consent (telling you about the aluminum in the vaccine, the absence of safety studies on pregnant women, and the known aluminum toxicity), before you agree to take this vaccine while pregnant.


Dr. Paul




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