Blood mercury levels in autism spectrum disorder: Is there a threshold level?

Mercury (Hg) may significantly impact the pathogenesis of autism spectrum disorders (ASDs). Lab results generated by Vitamin Diagnostics (CLIA-approved) from 2003-2007, were examined among subjects diagnosed with an ASD (n=83) in comparison to neurotypical controls (n=89). Blood Hg levels were determined by analyzing Hg content in red blood cells (RBC) using cold vapor analysis, and consistent Hg measurements were observed between Vitamin Diagnostics and the University of Rochester. Adjusted (age, gender, and date of collection) mean Hg levels were 1.9-fold significantly (P<.0001) increased among subjects diagnosed with an ASD (21.4 microg/L) in comparison to controls (11.4 microg/L). Further, an adjusted significant (P<.0005) threshold effect >15 microg/L) was observed for Hg levels on the risk of a subject being diagnosed with an ASD in comparison to controls (odds ratio=6.4). The weight of scientific evidence supports Hg as a causal factor in subjects diagnosed with an ASD.

[1]  Janet K. Kern,et al.  Biomarkers of environmental toxicity and susceptibility in autism , 2009, Journal of the Neurological Sciences.

[2]  David A Geier,et al.  A Case Series of Children with Apparent Mercury Toxic Encephalopathies Manifesting with Clinical Symptoms of Regressive Autistic Disorders , 2007, Journal of toxicology and environmental health. Part A.

[3]  R. Lathe,et al.  Porphyrinuria in childhood autistic disorder: implications for environmental toxicity. , 2006, Toxicology and applied pharmacology.

[4]  James B. Adams,et al.  Mercury, Lead, and Zinc in Baby Teeth of Children with Autism Versus Controls , 2007, Journal of toxicology and environmental health. Part A.

[5]  M. Berglund,et al.  Environmental Health: a Global Access Science Source Inter-individual Variations of Human Mercury Exposure Biomarkers: a Cross-sectional Assessment , 2022 .

[6]  J. Kern,et al.  A Prospective Blinded Evaluation of Urinary Porphyrins Verses the Clinical Severity of Autism Spectrum Disorders , 2009, Journal of toxicology and environmental health. Part A.

[7]  Note From Editor-in-Chief About Erratum for Ip et al Article , 2007 .

[8]  P. Mierzejewski,et al.  Neonatal administration of a vaccine preservative, thimerosal, produces lasting impairment of nociception and apparent activation of opioid system in rats , 2009, Brain Research.

[9]  J. Prieto,et al.  A Microscopic Study of Language-Related Cortex in Autism , 2008 .

[10]  C. Rice Prevalence of autism spectrum disorders - Autism and Developmental Disabilities Monitoring Network, United States, 2006. , 2009, Morbidity and mortality weekly report. Surveillance summaries.

[11]  Lora D. Delwiche,et al.  Blood Mercury Concentrations in CHARGE Study Children with and without Autism , 2009, Environmental health perspectives.

[12]  Luis E. Maya,et al.  Neurotoxic effects of thimerosal at vaccines doses on the encephalon and development in 7 days-old hamsters , 2008 .

[13]  T. Shors,et al.  Developmental mercury exposure elicits acute hippocampal cell death, reductions in neurogenesis, and severe learning deficits during puberty , 2007, Journal of neurochemistry.

[14]  J. Bizon,et al.  Chronic, low-dose prenatal exposure to methylmercury impairs motor and mnemonic function in adult C57/B6 mice , 2008, Behavioural Brain Research.

[15]  V. Wong,et al.  Attention-Deficit Hyperactivity Disorder and Blood Mercury Level: a Case-Control Study in Chinese Children , 2006, Neuropediatrics.

[16]  Janet K. Kern,et al.  A prospective study of prenatal mercury exposure from maternal dental amalgams and autism severity. , 2009, Acta neurobiologiae experimentalis.

[17]  P. Eriksson,et al.  Neonatal co-exposure to low doses of an ortho-PCB (PCB 153) and methyl mercury exacerbate defective developmental neurobehavior in mice. , 2008, Toxicology.

[18]  David A. Geier,et al.  A prospective assessment of porphyrins in autistic disorders: A potential marker for heavy metal exposure , 2006, Neurotoxicity Research.

[19]  W. J. Walsh,et al.  The Autistic Phenotype Exhibits a Remarkably Localized Modification of Brain Protein by Products of Free Radical-Induced Lipid Oxidation , 2008 .

[20]  D. Paschal,et al.  Determination of total and inorganic mercury in whole blood by on-line digestion with flow injection , 1998 .

[21]  K. Reuhl,et al.  Methylmercury elicits rapid inhibition of cell proliferation in the developing brain and decreases cell cycle regulator, cyclin E. , 2006, Neurotoxicology.

[22]  Zachary Stein,et al.  Environmental mercury release, special education rates, and autism disorder: an ecological study of Texas. , 2006, Health & place.

[23]  Lisa K. Sykes,et al.  A comprehensive review of mercury provoked autism. , 2008, The Indian journal of medical research.

[24]  D. Geier,et al.  A Prospective Study of Mercury Toxicity Biomarkers in Autistic Spectrum Disorders , 2007, Journal of toxicology and environmental health. Part A.

[25]  E. Geis,et al.  The Severity of Autism Is Associated with Toxic Metal Body Burden and Red Blood Cell Glutathione Levels , 2009, Journal of toxicology.

[26]  D. Frank Hsu,et al.  Analysis of Autism Prevalence and Neurotoxins Using Combinatorial Fusion and Association Rule Mining , 2009, 2009 Ninth IEEE International Conference on Bioinformatics and BioEngineering.

[27]  David W. Hosmer,et al.  Applied Logistic Regression , 1991 .

[28]  L. Croen,et al.  Autism Spectrum Disorders in Relation to Distribution of Hazardous Air Pollutants in the San Francisco Bay Area , 2006, Environmental health perspectives.

[29]  S. Al-Saad,et al.  Toxic trace elements in the hair of children with autism , 2005, Autism : the international journal of research and practice.

[30]  M Hornig,et al.  Neurotoxic effects of postnatal thimerosal are mouse strain dependent , 2004, Molecular Psychiatry.

[31]  D. Austin An epidemiological analysis of the 'autism as mercury poisoning' hypothesis , 2008 .

[32]  H. Windom,et al.  Oxidative Stress in Autism: Elevated Cerebellar 3-nitrotyrosine Levels , 2008 .

[33]  M. Desoto,et al.  Blood Levels of Mercury Are Related to Diagnosis of Autism: A Reanalysis of an Important Data Set , 2007, Journal of child neurology.

[34]  R. Rossignol,et al.  Feeding mice with diets containing mercury-contaminated fish flesh from French Guiana: a model for the mercurial intoxication of the Wayana Amerindians , 2008, Environmental health : a global access science source.

[35]  Stanley Lemeshow,et al.  Applied Logistic Regression, Second Edition , 1989 .

[36]  Janet K. Kern,et al.  Evidence of Toxicity, Oxidative Stress, and Neuronal Insult in Autism , 2006, Journal of toxicology and environmental health. Part B, Critical reviews.

[37]  Mark R. Geier,et al.  A Case-Control Study of Mercury Burden in Children with Autistic Spectrum Disorders , 2003 .

[38]  T. Luke,et al.  Nutritional and environmental approaches to preventing and treating autism and attention deficit hyperactivity disorder (ADHD): a review. , 2008 .

[39]  D. Austin,et al.  An Investigation of Porphyrinuria in Australian Children with Autism , 2008, Journal of toxicology and environmental health. Part A.

[40]  J. B. Adams,et al.  Mercury in first-cut baby hair of children with autism versus typically-developing children , 2008 .

[41]  Mark F Blaxill,et al.  Reduced Levels of Mercury in First Baby Haircuts of Autistic Children , 2003, International journal of toxicology.

[42]  Janet K. Kern,et al.  A Prospective Study of Transsulfuration Biomarkers in Autistic Disorders , 2009, Neurochemical Research.

[43]  R. Palmer,et al.  Proximity to point sources of environmental mercury release as a predictor of autism prevalence , 2008 .

[44]  D. A. Geiera,et al.  Mitochondrial dysfunction , impaired oxidative-reduction activity , degeneration , and death in human neuronal and fetal cells induced by low-level exposure to thimerosal and other metal compounds , 2009 .

[45]  R. Lathe,et al.  Porphyrinuria in childhood autistic disorder is not associated with urinary creatinine deficiency , 2008, Pediatrics international : official journal of the Japan Pediatric Society.