Autism
SYNOPSIS
There is, nevertheless, a significant relationship between mercury concentration and autism. Thus, the concentration for mercury can be listed as a pathogenic cause (disease-causing) for autism.
TITLE
The Relationship Between the Level of Copper, Lead, Mercury and Autism Disorders: A Meta-Analysis
CITATION
Jafari Mohammadabadi H, Rahmatian A, Sayehmiri F, Rafiei M. The Relationship Between the Level of Copper, Lead, Mercury and Autism Disorders: A Meta-Analysis. Pediatric Health Med Ther. 2020;11:369-378 https://doi.org/10.2147/PHMT.S210042
SUMMARY
In this study, 18 articles conducted in different countries from 1982 to 2019 were collected to determine the authenticity or lack of relationship between the concentrations of copper, lead, and mercury and autism and to provide a reliable pattern in the field for the researchers and planners. Results: In these 18 studies, 1797 patients (981 cases and 816 controls) aged 2 to 16 years were examined. Concentration of the samples (blood, hair, and nails) for both case and control groups was evaluated. There was no significant relationship between copper concentration and autism; there was a significant relationship between mercury concentration and autism; there was also a significant relationship between lead concentration and autism.
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SYNOPSIS
Higher proportions of parents of color were vaccine hesitant, and all vaccine�?hesitant parents agreed that “toxins in vaccines” were a cause of their child’s ASD.
TITLE
Vaccine Hesitancy and Attributions for Autism among Racially and Ethnically Diverse Groups of Parents of Children with Autism Spectrum Disorder: A Pilot Study
CITATION
Little is known about how racial/ethnic differences may influence attributions for autism spectrum disorder (ASD) and subsequent vaccine hesitancy, the latter of which refers to a continuum of concerns about vaccine safety that may lead to vaccine delays and/or refusals. Two hundred and twenty�?five parents of children with ASD who were enrolled in the SPARK cohort (Simons Foundation Powering Autism Research for Knowledge) completed the Parent Attitudes about Childhood Vaccines survey and the Revised Illness Perception Questionnaire . 28.9% of respondents (n = 65) were vaccine hesitant (PACV score ≥ 50). Significant differences were observed between proportions of vaccine�?hesitant parents (VHP) in the White sample and combined samples of color (Asian, Black, Latinx, Multiracial, and Other): 22.8% of the White sample (n = 39) versus 48.1% of the samples of color (n = 26). White, non�?hesitant parents more often agreed with the child’s brain structure as a cause of their child’s ASD, while White, VHP more often agreed with the deterioration of the child’s immunity as a cause. All VHP (regardless of race) agreed more often with diet , their own decisions , and vaccines as causes. VHP of color more often agreed with accident or injury , environmental pollution , their own general stress , and their own emotional state as causes. Future work should examine this phenomenon in larger, diverse samples to further understand differences across specific racial/ethnic groups.
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SYNOPSIS
Metabolism of metals and toxins may play a role in ADHD and autism development, evidence may be detectable.
TITLE
Dynamical properties of elemental metabolism distinguish attention deficit hyperactivity disorder from autism spectrum disorder
CITATION
Austin et al. Translational Psychiatry (2019) 9:238 https://doi.org/10.1038/s41398-019-0567-6
SUMMARY
Cyclical processes involved in the metabolism of essential and toxic elements during fetal and early postnatal development differ significantly in children with attention deficit-hyperactivity disorder (ADHD) and/or autism spectrum disorder (ASD) and neurotypical children, according to a small study of tooth matrix biomarkers. The study’s findings suggest that metabolic regulation of nutrients and toxins may play a role in the development of ADHD and autism.
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SYNOPSIS
Metabolism-based analysis may enable earlier autism diagnosis and treatment on the basis of an autistic individual’s “unique metabolic signature.”
TITLE
Amino acid dysregulation metabotypes: potential biomarkers for diagnosis and individualized treatment for subtypes of autism spectrum disorder
CITATION
Smith AM, King JJ, West PR, et al. Biological Psychiatry. 2019;85(4):345-354.
SUMMARY
The article describes a large-scale effort to define biomarkers for autism using metabolism-based analysis in young children. Whereas autism is currently diagnosed on the basis of behavioral characteristics, “metabolism-based analysis has the merit of being sensitive to interactions among the genome, gut microbiome, diet, and environmental factors that contribute to the unique metabolic signature” of individuals with autism. Metabolism-based biomarkers may also be able to identify metabolically defined subtypes—“metabotypes”—with the potential for earlier diagnosis and more targeted treatment.
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Children of mothers with asthma are at increased risk of developing autism, highlighting the importance of studying environmental risk factors during pregnancy.
TITLE
Parental asthma and risk of autism spectrum disorder in offspring: a population and family-based case-control study
Citation
Gong T, Lundholm C, Rejno G, et al. Clinical and Experimental Allergy. 2019 Feb 11.
Summary
This large observational study reports that children of mothers with asthma are at increased risk of developing autism spectrum disorder (ASD). The study looked at all children born in Sweden between 1992 and 2007, including almost 23,000 children with ASD. The researchers posit that maternal immune activation during pregnancy may represent a biological mechanism explaining the association. The increased ASD risk could not be explained by socioeconomic, demographic, or genetic factors, underscoring “the importance of investigating other maternal environmental factors.”
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SYNOPSIS
There are statistical increases in the incidence rate of autism, mental retardation , and speech disorders after thimerosal-containing DTaP vaccines in comparison with thimerosal-free DTaP vaccines.
TITLE
Vaccination and autoimmunity-‘vaccinosis’: a dangerous liaison?
CITATION
Shoenfeld Y, Aron-Maor A. Journal of Autoimmunity. 2000 Feb;14(1):1-10.
SUMMARY
An analysis of the Vaccine Adverse Events Reporting System (VAERS) database showed statistical increases in the incidence rate of autism (relative risk [RR] = 6.0), mental retardation (RR = 6.1), and speech disorders (RR = 2.2) after thimerosal-containing diphtheria, tetanus, and acellular pertussis (DTaP) vaccines in comparison with thimerosal-free DTaP vaccines.
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SYNOPSIS
The preponderance of the evidence indicates that mercury exposure is causal and/or contributory to ASD.
TITLE
Current knowledge on endocrine disrupting chemicals (EDCs) from animal biology to humans, from pregnancy to adulthood: Highlights from a national Italian meeting
CITATION
Street ME, et al. International Journal of Molecular Sciences. 2018;19:1647.
SUMMARY
This manuscript reviews the reports of a multidisciplinary national meeting on the effects of endocrine-disrupting chemicals (EDCs). Section 3 specifically discusses EDCs and neurodevelopmental diseases in humans, with a focus on autism. Recent studies point to an equal contribution of environmental factors (particularly environmental toxicants) and genetic susceptibility, but only a few industrial chemicals (e.g., lead [Pb], methylmercury, polychlorinated biphenyls [PCBs], and toluene) are recognized causes of neurodevelopmental disorders and subclinical brain dysfunction. Recent discoveries indicate that heavy metals such as cadmium (Cd), arsenic (As), mercury (Hg), nickel (Ni), and lead (Pb) may exhibit endocrine-disrupting activity in animal models, probably by interfering with zinc-fingers of nuclear estrogen receptors. The authors review research on mercury, PCBs, polycyclic aromatic hydrocarbons, polybrominated diphenyl ethers, phthalates, BPAs and pesticides.
TAGS
SYNOPSIS
Food proteins in vaccines can sensitize the immune system and trigger development of food allergies and other chronic conditions such as autism and type 1 diabetes.
TITLE
Milk containing vaccines cause milk allergies, EoE, autism and type 1 diabetes
CITATION
Arumugham V. BMJ. 2018;361:k2396. [Letter in response to Schulze MB et al., Food based dietary patterns and chronic disease prevention, BMJ 2018;361:k2396.]
SUMMARY
Responding to an article about food and chronic illness, the author criticizes the researchers for overlooking “a major cause of why food has become dangerous,” noting that vaccines contain food proteins that can “program the immune system to recognize food as pathogens.” Injection of vaccines containing cow’s milk proteins can cause sensitization to several bovine proteins (casein, folate receptor and insulin). In addition, studies suggest an association between vaccine-induced sensitization to cow’s milk proteins and the development of eosinophilic esophagitis (EoE), autism and type 1 diabetes.
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SYNOPSIS
Mount Sinai research could result in an early diagnostic system for autism spectrum disorder.
TITLE
Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder
CITATION
Curtin P, et al. Science Advances. 2018;4:eaat1293.
SUMMARY
Using evidence found in baby teeth, researchers from the Institute for Exposomic Research at the Icahn School of Medicine at Mount Sinai report that cycles involved in zinc and copper metabolism are dysregulated in autism spectrum disorder (ASD) and can be used to predict who will later develop the condition. The researchers used the teeth to reconstruct prenatal and early-life exposures to nutrient and toxic elements in healthy and autistic children.
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SYNOPSIS
Autistic children with gastrointestinal symptoms have an imbalance in their immune response that affects behavior and quality of life.
TITLE
Differential immune responses and microbiota profiles in children with autism spectrum disorders and co-morbid gastrointestinal symptoms
CITATION
Rose DR, Yang H, Serena G, Sturgeon C, Ma B, Careaga M, Hughes HK, Angkustsiri K, Rose M, Hertz-Picciotto I, Van de Water J, Hansen RL, Ravel J, Fasano A, Ashwood P. Brain, Behavior, and Immunity. 2018;70:354-368.
SUMMARY
Children with autism spectrum disorder (ASD) and concurrent gastrointestinal (GI) symptoms have a more imbalanced immune response, a more disturbed gut microbiome and worse behavioral outcomes (such as irritability, agitation, social withdrawal, lethargy, hyperactivity and noncompliance) than ASD children without GI symptoms. The study additionally looked at typically developing children with and without GI symptoms and found that ASD+GI children stood out compared to those two groups as well. Children with ASD plus GI symptoms may have a “propensity” toward leaky gut that contributes to their other symptoms and clinical outcomes.
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SYNOPSIS
Fluoride and aluminum, alone or in combination, can produce the condition of “immunoexcitotoxicity” that leads to the pathological changes seen in autism.
TITLE
Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: a possible role of fluoride and aluminum
Citation
Strunecka A, Blaylock RL, Patocka J, Strunecky O. Surgical Neurology International. 2018;9:74.
Summary
Children experience sequential immune stimulation from a growing number of neurotoxic metals and chemicals, vaccines and persistent viral infections. This excessive immune activation is the “initiating and sustaining event” in autism spectrum disorder (ASD), triggering inflammation and a cascade of excitotoxicity (damaged nerve cells). The fluoride added to drinking water and the aluminum in vaccines—singly or synergistically as aluminofluoride—can be potent factors in producing the condition of “immunoexcitotoxicity” that leads to the pathological changes seen in ASD.
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SYNOPSIS
Vaccination can trigger a series of cascading events that disturbs the balance between “protective immunity” and “destructive inflammation.”
TITLE
Vaccines and neuroinflammation
Citation
Giannotta G, Giannotta N. International Journal of Public Health & Safety. 2018;3:3.
Summary
This study explores molecular mechanisms capable of explaining “post-vaccination inflammatory syndrome” and the neuroinflammation observed in children with autism. Focusing especially on vaccines (such as HPV vaccines) that contain biopersistent aluminum adjuvants, the authors describe how “continuously escalating doses of this poorly biodegradable adjuvant…may become insidiously unsafe,” especially in children who are vaccinated repeatedly or who have an immature or altered blood-brain barrier. Vaccination can trigger a series of cascading events (involving overexpression of the signaling molecules that regulate inflammation and activation of brain cells called microglia) that disturbs the balance between “protective immunity” and “destructive inflammation.”
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SYNOPSIS
The offspring of mothers exposed to DDT and its metabolites during pregnancy are at increased risk for autism.
TITLE
Association of maternal insecticide levels with autism in offspring from a national birth cohort
Citation
Brown AS, Cheslack-Postava K, Rantakokko P, et al. American Journal of Psychiatry. 2018;175:1094-1101.
Summary
The study provides the first evidence based on biomarkers of an increased autism risk in the offspring of mothers exposed to certain insecticides during pregnancy. In this large national birth cohort study of Finnish children, the odds of autism plus intellectual disability were increased by greater than twofold in mothers measuring with the highest levels of a DDT metabolite.
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SYNOPSIS
In children under age two, four postnatal risk factors (acetaminophen use, antibiotic use, ear infections and early weaning) were associated with an increased risk of autism.
TITLE
Acetaminophen, antibiotics, ear infection, breastfeeding, vitamin D drops, and autism: an epidemiological study
Citation
Bittker SS, Bell KR. Neuropsychiatric Disease and Treatment. 2018;14:1399-1414.
Summary
This study suggests that increased use of acetaminophen and antibiotics in children under age two, along with an increased incidence of ear infections in the first two years and early weaning, are associated with an increased risk of autism spectrum disorder (ASD). The researchers conducted a large parent Internet survey covering over 1,500 three- to twelve-year-old children who either had or did not have ASD. The findings replicate other studies focused on these postnatal ASD risk factors.
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SYNOPSIS
Two prenatal exposures—stress and maternal immune dysregulation—are associated with autism, probably in combination with other genetic and environmental risk factors.
TITLE
Prenatal stress, maternal immune dysregulation, and their association with autism spectrum disorders
Citation
Beversdorf DQ, Stevens HE, Jones KL. Current Psychiatry Reports. 2018;20:76.
Summary
Prenatal stress and disruption of a pregnant woman’s immune response (“maternal immune activation”) are two environmental factors associated with the increased incidence of autism spectrum disorder (ASD). However, the fact that, in many cases, these prenatal exposures do not result in ASD suggests an “interaction with multiple other risks.” Some evidence points to greater susceptibility to prenatal stress and maternal immune dysregulation in male offspring.
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SYNOPSIS
Preschool children with autism spectrum disorder (ASD) have abnormal connections between certain brain networks that can be visualized using a special MRI technique.
TITLE
Alterations of white matter connectivity in preschool children with autism spectrum disorder
CITATION
Li SJ, Wang Y, Qian L, et al. Radiology 2018; 288:209-217.
SUMMARY
This study is about neural path length (via radiometric imaging). It shows that preschool children with autism spectrum disorder (ASD) have abnormal connections between certain brain networks that can be visualized using an MRI technique called diffusion tensor imaging (DTI). These pathways are generally established as a part of later prenatal and postnatal development and may be associated with dendrite pruning (postnatal), which is altered in ASD children.
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SYNOPSIS
Mercury-associated diagnoses are common among children diagnosed with pervasive developmental disorders.
TITLE
Symptoms observed in pervasive developmental disorders such as autism overlap with symptoms of mercury poisoning.
CITATION
Geier DA, Kern JK, Sykes LK, Geier MR. Metabolic Brain Disease. March 2018. doi: 10.1007/s11011-018-0211-9.
SUMMARY
Research indicates that environmental triggers are contributing to the childhood epidemics of autism and other pervasive developmental disorders (PDDs). The mercury-containing vaccine preservative thimerosal is a biologically plausible candidate to induce PDD. This study reveals that 12 symptom categories associated with mercury poisoning directly overlap with symptoms observed in children who have a PDD.
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SYNOPSIS
Aluminum adjuvants promote brain inflammation, and males appear to be more susceptible to aluminum’s toxic effects.
TITLE
Subcutaneous injections of aluminum at vaccine adjuvant levels activate innate immune genes in mouse brain that are homologous with biomarkers of autism
CITATION
Li D, Tomljenovic L, Li Y, Shaw CA. Journal of Inorganic Biochemistry. 2017;177:39–54.
SUMMARY
Autism manifests in early childhood, during a window of early developmental vulnerability where the normal developmental trajectory is most susceptible to xenobiotic insults. Aluminum (Al) vaccine adjuvants are xenobiotics with immunostimulating and neurotoxic properties to which infants worldwide are routinely exposed. This research found that aluminum triggered innate immune system activation and altered neurotransmitter activity in male mice, observations which are consistent with those in autism. Female mice were less susceptible to aluminum as the frontal cortex was the most affected area in males and the cerebellum in females. These findings suggest that aluminum adjuvants promote brain inflammation and that males appear to be more susceptible to aluminum′s toxic effects. (Note: This study has since been retracted by the Journal of Inorganic Biochemistry, but the importance of the topic prompted our decision to keep it in our science library.)
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SYNOPSIS
Here is a list compiled of the 19 studies from various lists on CDC’s websites to defend the use of thmerosal in vaccines. These are the studies that CDC uses to claim thimerosal’s safety. Each is fatally flawed through the use of incorrect and even fraudulent statistics. Even so, these studies demonstrate that thimerosal has been linked with tics, IQ deficits, speech delay and language delay.
TITLE
Studies that the CDC Claims Exonerate Thimerosal… and Why They Don’t
Here is a list compiled of the 19 studies from various lists on CDC’s websites to defend the use of thimerosal in vaccines. These are the studies that CDC uses to claim thimerosal’s safety. Each is fatally flawed through the use of incorrect and even fraudulent statistics. Even so, these studies demonstrate that thimerosal has been linked with tics, IQ deficits, speech delay and language delay. (Links to studies listed below.)
Poster #1
Name | Authors’ Conflicts of Interest | Type of Study | Journal | Issues Found | Errors and Fraud |
---|---|---|---|---|---|
Madsen et al. 2003 | Plesner and Andersen were affiliated with a for-profit Danish vaccine manufacturer. Thorsen embezzled over $1 million from CDC. | Epidemiology | Pediatrics | Autism rates went down after the removal of thimerosal in Denmark in 1992. | Removed incidence data from 2001. Manipulated inpatient/outpatient data to create an artificial rise in incidence in 1994. |
Stehr-Green et al. 2003 | Stelfeld is an employee of a Danish for-profit vaccine manufacturer. Simpson was Deputy Director of National Immunization Program of CDC. | Epidemiology | American Journal of Preventative Medicine | Autism rates and uptake of thimerosal containing vaccines in California were strongly correlated. | Wrongfully dismissed autism rates in California as inclusion of milder ASD cases to obviate the rise in cases. |
Andrews et al. 2004 | Miller has also actively participated in clinical trials for the approval of human papilloma virus and influenza virus vaccines. Funding by World Health Organization. | Epidemiology | Pediatrics | Thimerosal exposure causes tics. | Numerous statistical errors by correlating thimerosal exposure with year of birth. |
Verstraeten et al. 2003 | Verstraeten worked for vaccine manufacturer GlaxoSmithKline. Other authors worked for insurance companies including Kaiser Permanente. | Epidemiology | Pediatrics | Thimerosal exposure causes tics and language delay. | Effects were diluted through five separate iterations of the study. Numerous exclusion criteria were erroneously applied and data cherry-picking was done to dilute statistically significant effects. |
Hviid et al. 2003 | Stelfeld is an employee of a Danish for-profit vaccine manufacturer. | Epidemiology | Journal of the American Medical Association | Thimerosal exposed children were twice as likely to have an autism diagnosis. | The age of follow-up was as low as 1 year which is too young to receive an autism diagnosis. Records of older children with autism were lost. |
Thompson et al. 2007 | Authors were affiliated with Harvard Pilgrim and Kaiser Permanente insurance companies. | Epidemiology | New England Journal of Medicine | Thimerosal causes tics in boys. Thimerosal lowers IQ in girls. | Overmatching phenomena meant that cases and controls had very little difference in thimerosal exposure. |
Price et al. 2010 | Authors were affiliated with Harvard Pilgrim and Kaiser Permanente insurance compan1es. | Epidemiology | Pediatrics | Prenatal thimerosal exposure causes regressive ASD in boys. | Overmatching phenomena meant that cases and controls had very little difference in thimerosal exposure. Prenatal thimerosal effect was hidden by cherry-picking data. |
Barile et al. 201 2 | CDC employees were told by direct supervisor Dr. Edwin Trevathan to downplay the tic effect. Trevathan was then director of CDC’s National Center for Birth Defects and Developmental Disabilities. | Epidemiology | Journal of Pediatric Psychology | Thimerosal causes tics in boys. | Overmatching phenomena meant that cases and controls had very little difference in thimerosal exposure. |
Poster #2
Name | Authors’ Conflicts of Interest | Type of Study | Journal | Issues Found | Errors and Fraud |
---|---|---|---|---|---|
Tozzi et al. 2009 | Study funded by CDC which has a direct financial stake in vaccine uptake in the United States. | Epidemiology | Pediatrics | Thimerosal showed a higher incidence of tics. | Study was completed using Italian vaccine schedule with much lower thimerosal exposure than U.S. schedule. No zero exposure control was use. |
Ball et al. 2001 | Study was funded by the FDA which has direct links to the pharmaceutical industry and is incentivized by vaccine uptake in the U.S. | Review | Pediatrics | Thimerosal exposure from U.S. vaccine schedule exceeded EPA safe exposure limit. | Study authors ignored prior literature reports of local necrosis, acute hemolysis, disseminated intravascular coagulation, acute renal tubular necrosis and central nervous system damage leading to death in their assessment. |
Burbacher et al. 2005 | Animal Study | None declared. | Environmental Health Perspectives | Vaccine levels of thimerosal exposure resulted in more than double the amount of inorganic mercury deposited in the brain tissue in comparison to equal levels of methyl mercury. | None. |
Hurley et al. 2010 | All authors of the paper were employed by MED Communications, a firm that has multiple pharmaceutical company clients. | Review | Journal of Pediatric Pharmacology and Therapeutics | The toxicokinetics of thimerosal are ill defined and thimerosal exposure can lead to tissue damage. | The authors of the paper dismiss the causal relationship between thimerosal and autism despite a large body of evidence not covered in the paper. The authors rely solely on flawed CDC epidemiology studies. |
McMahon et al. 2008 | lskander is an employee of the CDC which is charged with maximizing vaccine uptake in the U.S. | Epidemiology | Vaccine | Publication did not investigate outcomes beyond local site reactions. | The definition of an adverse event was limited to site reactions and fever. No data were collected regarding any type of neurological outcome. |
Pichichero et al. 2002 | Pichichero has received research grants and/or honoraria from the folowing pharmaceutical companies: Abbott Laboratories, Inc.; Bristol-Myers Squibb Company; Eli Lilly & Company; Merck & Co.; Pasteur Merieux Connaught; Pfizer Labs; Roche Laboratories; Roussel-Uclaf; Schering Corporation; Smith Kline Beecham Pharmaceuticals; Upjohn Company; and Wyeth-Lederle. | Clearance Study | The Lancet | One of the infants in the study showed mercury poisoning (levels as high as 20.55 nmol/L mercury in blood) five days after receipt of 37.5 micrograms of mercury via the DTaP and HepB vaccines. A vaccine expert from the Johns Hopkins Institute for Vaccine Safety estimated that infants receiving 62.5 ug mercury from thimerosal may have experienced peak blood mercury levels of 48.3 nmol/L, well above the EPA limit of 29.0 nmol/L. | Clearance of ethyl and methylmercury from the bloodstream are not indicative of the relative “body burden” of mercury caused by comparable doses of each molecule. Burbacher et al. (2005) saw that despite the rapid clearance of ethylmercury from the bloodstream, it caused a greater quantity and persistence of elemental mercury in the brain. |
Poster #3
Name | Authors’ Conflicts of Interest | Type of Study | Journal | Issues Found | Errors and Fraud |
---|---|---|---|---|---|
Pichichero et al. 2008 | Pichichero has received research grants and/or honoraria from the folowing pharmaceutical companies: Abbott Laboratories, Inc.; Bristol-Myers Squibb Company; Eli Lily & Company; Merck & Co.; Pasteur Merieux Connaught; Pfizer Labs; Roche Laboratories; Rousse-lUclaf; Schering Corporation; Smith Kline Beecham Pha rmaceuticals; Upjohn Company; and Wyeth-Lederle. | Clearance Study | Pediatrics | Exposure guidelines for thimerosal should be different than those for methyl mercury, given than thimerosal clears faster from the blood stream and shows signs of excretion via the gastrointestinal system. | Bloodstream clearance of ethyl and methyl mercury may not be used to predict the accumulation of each of these toxins in tissues. Ethylmercury (from thimerosal) has been shown to persist in brain tissues for a much longer extend than methyl mercury. |
Gadad et al. 201 5 | None declared. | Animal Study | Proc Natl Acad Sci USA | Thimerosal exposed monkeys showed significantly less non-social exploring behavior compared to unexposed control monkeys. This effect was significant for all exposure categories studied. | The sample size of macaque monkeys in each study group was too small to see an effect. The maximum sized group was only 16 macaque monkeys which could never pick up an autism effect if the rate of autism is 1 in 68 children. |
Fombonne et al. 2006 | Fombonne has represented vaccine manufacturers as an expert witness in thimerosal litigation. In addition, Fombonne was brought up on ethics charges by Montreal Children’s Hospital for misuse of patient samples for an unapproved study. Fombonne was demoted from his administrative position at the hospital in the late 2000s. | Epidemiology | Pediatrics | Time trends in autism diagnoses were compared for thimerosal exposure rates per the vaccine schedule which started in 1987 at a maximum of 100 micrograms mercury, with upticks to 125 micrograms mercury and 200 micrograms mercury in 1988 and 1992, respectively. | The school district represented in this study accounts for only 14% of the total school population in Montreal but has the highest rates of POD diagnosis in the five total districts, and in some cases POD rates were three times higher within this district. The claim that the thimerosal exposure in the Canadian vaccine schedule starting in 1996 was “nil” is false. Thimerosal-free HepB formulations were not introduced until 2001 and the thimerosal containing “Penta” vaccine was administered, leading to a cumulative maximum dosage of 137.5 micrograms mercury. This renders any time trend comparison between autism/ASD/PDD prevalence and thimerosal exposure useless. |
Schechter et al. 2008 | Schechter was a part of the Immunization Branch of the California Department of Public Health which is charged with maximizing vaccination uptake in that state. | Epidemiology | Arch Gen Psychiatry | Time trends in autism diagnoses in the State of California continued to increase with the introduction of the thimerosal containing maternal influenza vaccine in 2004. | Study authors claimed that children were no longer exposed to thimerosal in vaccines after 2003, which is false. At that time, thimerosal containing maternal and infant influenza vaccines were introduced as a part of the CDC recommended schedule. |
Destefano 2009 | Destefano is currently Director of the Immunization Safety Office of the CDC, which buys and sells $4.6 billion of vaccines per year. | Editorial | Expert Opinion Drug Safety | Time trends in autism diagnoses in the State of California tracked closely with the uptake of thimerosal containing vaccines through the 1990s. | Destefano relied on flawed epidemiology studies from the U.K. and Denmark which follow different vaccination schedules compared to the U.S. Data from California show clear correlation between thimerosal uptake and autism incidence. |
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SYNOPSIS
Children with ASD have higher urinary levels of mercury and lead.
TITLE
Altered urinary porphyrins and mercury exposure as biomarkers for autism severity in Egyptian children with autism spectrum disorder
CITATION
Khaled EM, Meguid NA, Bjørklund G, et al. Metabolic Brain Disease 2016. DOI 10.1007/s11011-016-9870-6.
SUMMARY
Results of this case-control study showed that children with ASD had higher urinary levels of mercury and lead as well as porphyrins that are characteristic of mercury toxicity as compared to non-ASD control children. Porphyrins are complex molecules that are processed in the body through a series of chemical reactions. Mercury poisons the enzymes that are needed in the process, causing a buildup in the body of excess levels of specific porphyrins. The porphyrins for mercury toxicity also correlated with autism severity in ASD patients.
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SYNOPSIS
Thimerosal reduces people’s ability to make all-important vitamin B12 compounds that help the body detoxify and control inflammation—and B12 deficiencies and severely impaired detoxification are hallmarks of autism.
TITLE
Alternatively spliced methionine synthase in SH-SY5Y neuroblastoma cells: Cobalamin and GSH dependence and inhibitory effects of neurotoxic metals and thimerosal
CITATION
Waly M, Power-Charnitsky V-A, Hodgson N, … Deth R. Oxidative Medicine and Cellular Longevity. 2016, Article ID 6143753.
SUMMARY
Thimerosal inhibited cellular production of cobalamin necessary for detoxification and amelioration of oxidative stress. This caused lower methionine synthase activity and an impaired methylation capacity. Autistic subjects in general show cobalamin deficiencies and severely impaired methylation.
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SYNOPSIS
Mercury exposure is implicated in neuroinflammatory disorders including autism.
TITLE
The levels of blood mercury and inflammatory-related neuropeptides in the serum are correlated in children with autism spectrum disorder
CITATION
Mostafa GA, Bjørklund G, Urbina MA, Al-Ayadhi LY. Metabolic Brain Disease. 2016;31:593–599.
SUMMARY
Blood mercury levels and tachykinins (neuropeptides that cause inflammation) were correlated in children with ASD and statistically significantly higher than neurotypical control children. It has been shown that mercury exposure can elicit tachykinin formation, which has been implicated in neuroinflammatory disorders including autism.
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SYNOPSIS
Autistic children accumulate metals at a much higher level than children who do not have a diagnosis of autism.
TITLE
Assessment of hair aluminum, lead, and mercury in a sample of autistic Egyptian children: Environmental risk factors of heavy metals in autism
CITATION
El Baz Mohamed F, Zaky EA, Bassuoni EI-Sayed A, et al. Behavioural Neurology. 2015, Article ID 545674.
SUMMARY
Researchers found the mean levels of mercury, lead and aluminum in hair of autistic patients were significantly higher than in controls. Mercury, lead and aluminum levels were positively correlated with maternal fish consumption, living near gasoline stations and the usage of aluminum pans, respectively.
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SYNOPSIS
Thimerosal and methylmercury cause cell death in human neurons.
TITLE
Toxicity of organic and inorganic mercury species in differentiated human neurons and human astrocytes
CITATION
Lohren H, Blagojevic L, Fitkau R, et al. Journal of Trace Elements in Medicine and Biology. 2015;32:200–208.
SUMMARY
Thimerosal and methylmercury caused cell death in differentiated human neurons and astrocytes. Differentiated neurons showed a massive uptake of ethylmercury (degradation product of thimerosal). This affirms the type of neural damage seen in patients with autism.
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SYNOPSIS
Thimerosal exposure in humans is associated with neurodevelopmental deficits even at levels currently administered in vaccines.
TITLE
Thimerosal: Clinical, epidemiologic and biochemical studies
CITATION
Geier DA, King PG, Hooker BS, Dórea JG, Kern JK, Sykes LK, Geier MR. Clinica Chimica Acta. 2015;444:212–220.
SUMMARY
This review article includes a section on numerous papers linking thimerosal exposure via infant vaccines to autism. The publication also includes a critique of studies supported or conducted by the U.S. Centers for Disease Control and Prevention (CDC) that deny any associations between exposure to thimerosal in vaccines and the subsequent development of autism. Congress has criticized the CDC for conflicts of interest related to its vaccine development activities and role in vaccine safety oversight.
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SYNOPSIS
Research confirms a link between environmental mercury exposure and an increased risk of autism and shows that some individuals are more susceptible than others.
TITLE
Increased susceptibility to ethylmercury-induced mitochondrial dysfunction in a subset of autism lymphoblastoid cell lines
CITATION
Rose S, Wynne R, Frye RE, Melnyk S, James SJ. Journal of Toxicology. 2015, Article ID 573701.
SUMMARY
The association of autism spectrum disorders with oxidative stress, redox imbalance, and mitochondrial dysfunction has become increasingly recognized. In this study, researchers compared mitochondrial respiration in lymphoblastoid cell lines (LCLs) from individuals with autism and unaffected controls exposed to ethylmercury, an environmental toxin known to deplete glutathione and induce oxidative stress and mitochondrial dysfunction. They also tested whether pretreating the autism LCLs with N-acetyl cysteine (NAC) to increase glutathione concentrations conferred protection from ethylmercury. The findings suggest that the link between environmental mercury exposure and an increased risk of developing autism may be mediated through mitochondrial dysfunction and support the notion that a subset of individuals with autism may be vulnerable to environmental influences with detrimental effects on development through mitochondrial dysfunction.
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SYNOPSIS
Blood levels of mercury and lead are much higher in autistic children as compared to normal controls.
TITLE
Autism: A form of lead and mercury toxicity
CITATION
Yassa HA. Environmental Toxicology and Pharmacology. 2014;38:1016-1024.
SUMMARY
The aim of this study was to find out the relation between exposure to lead and/or mercury as heavy metals and autistic symptoms and assess use of chelating agents for dealing with heavy metals and improving autistic symptoms. The results showed significantly higher levels of mercury and lead among children with autism compared to children without autism, and a significant decline in the blood levels of lead and mercury with the use of DMSA as a chelating agent. In addition, there was a decline in autistic symptoms with the decrease in the lead and mercury levels in blood.
TAGS
SYNOPSIS
Background data (not reported in print) suggest a strong link between thimerosal exposure and autism.
TITLE
Methodological issues and evidence of malfeasance in research purporting to show thimerosal in vaccines is safe
CITATION
Hooker B, Kern J, Geier D, Haley B, Sykes L, King P, Geier M. BioMed Research International. 2014, Article ID 247218.
SUMMARY
This review article shows methodological flaws in six separate CDC studies claiming that thimerosal does not cause autism. In three specific instances (Madsen et al. 2003, Verstraeten et al. 2003 and Price et al. 2010), evidence of malfeasance on the part of CDC scientists is shown. Background data (not reported in print) from these three publications suggest a strong link between thimerosal exposure and autism.
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SYNOPSIS
Chinese scientists find mice injected with thimerosal (vaccine mercury) have behavioral impairments similar to autism.
TITLE
Transcriptomic analyses of neurotoxic effects in mouse brain after intermittent neonatal administration of thimerosal
CITATION
Li X, Qu F, Xie W, et al. Toxicological Sciences. 2014;139:452–465.
SUMMARY
“Thimerosal-treated mice exhibited neural development delay, social interaction deficiency, and inclination of depression. Apparent neuropathological changes were also observed in adult mice neonatally treated with thimerosal. High-throughput RNA sequencing of autistic-behaved mice brains revealed the alternation of a number of canonical pathways involving neuronal development, neuronal synaptic function, and the dysregulation of endocrine system.”
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SYNOPSIS
Mesenchymal stem cells may be promising candidates for addressing autism-related immune dysregulation.
TITLE
Mesenchymal stem cells in treating autism: novel insights
Citation
Siniscalco D, Bradstreet JJ, Sych N, Antonucci N. World Journal of Stem Cells. 2014;6:173-178.
Summary
Mesenchymal stem cells (MSCs) possess unique immunological properties that make them promising candidates in regenerative medicine, with the potential to address the immune dysregulation often observed in autism spectrum disorder (ASD). This study describes a variety of mechanisms through which MSCs could exert a positive effect in ASD.