Introduction
Exposure of children to lead in their environment continues to be an enormous public health issue, global in scope. As many as 500 000 children ages 1 to 5 years in the United States have blood lead levels (BLL) above the reference value set by the Centers for Disease Control and Prevention (CDC).1 Autism spectrum disorder (ASD) is another major health concern with the prevalence increasing from about 1 in 150 children age 8 years in 2000 to 1 in 68 children age 8 years in 2012.2,3 These 2 childhood conditions together exact an enormous societal toll in terms of suffering and lost productivity. Bellinger4 estimated that 22 947 450 full-scale IQ point losses can be attributed to childhood lead poisoning and 7 109 899 full-scale IQ point losses can be attributed to ASD in children age 0 to 5 years in the United States.
A number of studies have explored the relationship between ASD and lead exposure.5-7 Shannon and Graef6 described a case series of 17 children with both lead poisoning and pervasive developmental disorders (PDDs) or autism. In another study, children with ASD were found to have significantly higher BLL than their siblings without ASD.5 A population-based study of older children with autism living in Alberta, Canada, found elevated BLL in some of these children.8 One twin study using matrix markers from shed baby teeth found differences in the deposition of metals during late pregnancy and early post-natal life between children who later developed ASD and their twin who did not.9 With evidence of such associations, researchers have called for prospective longitudinal studies into the relationship between environmental lead exposure and behaviors typical of autism.10
Published reviews on the management of ASD often advise health care providers to monitor children with ASD and pica behaviors for elevated BLL.11-14 However, there is scant literature providing guidance to health care providers regarding how often to conduct such surveillance or how to medically manage children with both ASD and an elevated BLL. In this review, we offer recommendations to clinicians drawing on recently published guidance as well as our own experience caring for families of children suffering from both conditions.
Neurotoxicity of Lead
Lead is a known neurotoxin, able to produce metabolic and infrastructural perturbations at the molecular and cellular levels of the developing nervous system.15 Children are much more susceptible to the adverse neurodevelopmental effects of lead than are adults, due to the vulnerability of their nervous system, the postnatal continuation of nervous system maturation, and the increased permeability of neuronal structures to lead’s entry.15 Numerous studies have confirmed adverse neurodevelopmental, neurobehavioral, and cognitive effects of prenatal and postnatal lead exposure.16,17 Prospective longitudinal studies have demonstrated the long-lasting sequelae of lead exposure on intellectual and academic achievement later in childhood even after apparently low-level exposures with BLL less than 10 μg/dL.18-20 Neurological outcomes include cognitive damage, hearing loss, visual effects, delayed speech acquisition, learning disabilities, lower reading and arithmetic skills, poor attention, deficits of other aspects of executive function, and other educational, behavioral, and emotional problems, which can persist into adolescence and adulthood.19,21-29
Overlapping Conditions: Lead Poisoning and ASD
Symptoms of ASD share some similar characteristics to the symptoms of lead neurotoxicity noted above.7 For example, DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, 5th edition) criteria for ASD, as detailed by the American Psychiatric Association, includes persistent deficits in social-emotional reciprocity and nonverbal communicative behaviors.30 Significant language delay and coexisting intellectual disability are notable in many children with ASD.31 In addition to neurologic and behavioral symptoms, both childhood lead poisoning and ASD are often associated with poor appetite, restricted food choices, and gastrointestinal symptoms, such as constipation or abdominal discomfort.
These similarities may prompt parents and clinicians to wonder whether lead poisoning in a child can cause ASD, and if there might, therefore, be a treatable cause of their child’s ASD. However, current scientific evidence does not support this hypothesis. Instead, any association of ASD and lead poisoning is more likely secondary to pica habits, the compulsive chewing and eating of nonfood items, seen commonly in children with ASD. This behavior puts them at high risk for exposure to lead-containing dust and other lead-contaminated objects. The association between such pica behaviors and a higher risk of lead poisoning was described as early as 1976 by Cohen et al.5 Another study confirmed that children with ASD are more likely to be re-exposed to sources of lead contamination than children without ASD.6 Unfortunately, the normal hand-mouth behaviors and oral exploratory habits of infancy, which usually extinguish within the preschool years, can persist in children with ASD well into later childhood and beyond such that their risk for lead contamination continues. While these pica behaviors continue, these children also continue to grow taller and stronger, allowing them access to new surfaces and areas of households that may contain lead hazards not previously accessible to them at a younger age. A study that investigated epidemiologic characteristics of severe lead poisoning in New York City found a trend toward severe lead poisoning occurring at older ages in children with ASD compared with the cases without ASD (5.99 years vs 3.69 years, respectively).32
Diagnosis
Misdiagnosis
Despite some overlapping symptoms, there is no convincing evidence that childhood lead poisoning causes ASD; however, rare cases of misdiagnosis can occur. For example, a case was reported in which a child misdiagnosed with severe autism was found, instead, to suffer from chronic lead poisoning. His hearing improved, with accompanying advancement in neurodevelopmental status (receptive and expressive language), after his very severe lead poisoning was treated successfully with chelation.5 The risk of lead poisoning in genetic disorders similar to autism, such as Landau-Kleffner syndrome, has also been reported.33
Lead poisoning may manifest in a number of different ways in a child with ASD. Although potentially asymptomatic, a child may also become more irritable secondary to abdominal colic from lead. While becoming quiet and more withdrawn may seem like an improvement in the behavior of a child with autism and attention-deficit/hyperactivity disorder, this may actually be the unrecognized beginning of lead-induced encephalopathy, a medical emergency.34 Clinicians should maintain a high level of suspicion for lead poisoning in children with ASD when such symptoms arise.
ASD Risk Factors for Exposure to Lead
Pica behaviors predispose children with ASD to unrecognized foreign body ingestion, which poses an additional risk if the foreign body contains lead-leaching materials. Pica also predisposes children to ingestion of other nonfood items that may be contaminated with lead such as dirt, house dust, and paint chips. Because of their restricted diets and related nutritional deficiencies, children with ASD may be iron deficient, a known comorbidity of lead poisoning.35 As evidenced by mouse studies, the presence of iron deficiency may enhance gastrointestinal uptake of lead, predisposing those with lead exposure to elevated blood lead levels.36
Routine Screening and BLL Testing
Providers should be aware of the recommended universal or targeted lead screening guidelines in their locality and, at a minimum, adhere to these guidelines. Most children with ASD will require enhanced and extended monitoring for lead poisoning. Table 1 offers some recommendations to clinicians regarding screening and diagnosis of lead poisoning in children with ASD.
Table 1.
Recommendations: BLL Testing for Children With ASD.
|
Abbreviations: BLL, blood lead level; ASD, autism spectrum disorder.
Some parents take their children to alternative health care providers for assessment of their ASD. These providers may send hair and/or urine for analysis of metals. Hair is a complex medium that is technically difficult to assay with precision. The interpretation of levels of metals found to be elevated in such an analysis has been challenged.37 Hair analyses have been shown to be unreliable when performed in commercial laboratories.38,39 Children with reports of elevated hair lead levels often have very low BLLs, no evidence of exposure to environmental lead, and no need for medical management. In such cases a venous BLL can be obtained to determine the child’s actual lead burden.
Management
Table 2 lists some key features of children suffering from both an elevated BLL and ASD. The complexity of the medical needs of the child with both ASD and an elevated BLL demands a thoughtful, comprehensive, coordinated, and multidisciplinary approach to their care. Social, educational, economic, housing, and occupational challenges confront their parents and guardians. The coordinated team approach often includes involvement of a variety of professionals: physicians and nurse practitioners, developmental specialists, nurses, physical and occupational specialists, pharmacists, social workers, case managers, state and local public health workers, private housing inspectors, certified lead abatement firms and remodeling construction specialists, plumbers, landlords, bankers and/or loan agency staff, teachers and school officials, daycare workers, and other community-level professionals. Primary care providers and developmental medicine specialists often must act as a coordinator of these important resources and advocate on behalf of the family. Below are some special considerations that warrant attention in treating children with ASD and lead poisoning.
Table 2.
Key Features: Children With Both Autism Spectrum Disorder and Lead Poisoning.
|
Outpatient Management
Children with lead poisoning require close medical monitoring with frequent office visits and even occasional emergency department referrals. Table 3 gives recommendations for clinicians in office practice managing children with both ASD and an elevated BLL.
Table 3.
Office Management: Elevated BLL and ASD.
|
Abbreviations: BLL, blood lead level; ASD, autism spectrum disorder; CLPPP, childhood lead poisoning prevention programs.
Hospitalization
Children with ASD and lead poisoning may need to be hospitalized for a number of reasons. If they have a BLL ≥70 μg/dL and/or have evidence of lead encephalopathy, then hospitalization, often triaged to a critical care unit, is the safest course of management. Admittedly, recognizing lead encephalopathy can be difficult in children with ASD who have baseline behavioral problems, though parents are often able to note any changes in their child’s mental status. Children with lower BLLs, such as those with BLL 45 to 69 μg/dL, may also require hospitalization for chelation if compliance with oral medication-taking is questionable and/or a lead-safe home environment cannot be assured.
Hospitalization can be a very difficult time for both the patient and their family, especially in a child with ASD. Table 4 lists some recommendations for clinicians to consider when hospitalizing a patient with ASD for inpatient management of severe lead poisoning.
Table 4.
Hospitalization.
|
Abbreviations: ASD, autism spectrum disorder; BLL, blood lead level.
Chelation
Table 5 addresses chelation in children with ASD whose lead poisoning is severe enough to consider use of these medications to lower the body’s burden of lead. Details of specific chelants have been reviewed elsewhere.41 All of the chelants used to treat lead poisoning can have serious adverse effects, such as bone marrow suppression, nephrotoxicity, chemical hepatitis, allergic rashes, and gastrointestinal disturbances. Administration of iron supplementation or foods with milk, zinc, or iron may decrease the absorption of d-penicillamine.42 The clinician contemplating use of such medications should review these potential adverse effects with the parents/guardians in obtaining their consent for treatment.
Table 5.
Chelation.
|
Abbreviation: ASD, autism spectrum disorder.
Treating a child with ASD with a parenteral medication like CaNa2EDTA requires insertion of an intravenous catheter, which in our experience is likely to be pulled out, interfering with the necessary continuous therapy. Nurses are challenged with protecting the IV’s (intravenous) integrity in a child with ASD so that therapy is not interrupted.
The oral chelant medications used in medical management of moderate-severe lead poisoning are not “kid friendly.” They have sulfur or amines in them causing them to taste bad and smell like rotten eggs. Getting a child with autism to swallow either d-penicillamine or dimercaptosuccinic acid can be a challenge. Disguising the medication by mixing it in a child’s favorite food, such as applesauce or peanut butter, is a strategy successfully employed by many parents. However, children with ASD often have restricted diets. By disguising dimercaptosuccinic acid in their food, there is the risk that they will recognize it and potentially reject one of the few foods contributing to their nutrition. Thus, adherence to the twice or 3-times daily dosing schedule can be particularly difficult.
The use of chelants to treat ASD itself in children who do not have documented lead poisoning is discouraged as a scientifically unfounded practice that may produce untoward consequences or even neurotoxic adverse effects.43-45 Several iatrogenic deaths due to hypocalcaemia have been reported by the mistaken use by alternative practitioners of Na2 EDTA instead of CaNa2 EDTA in the treatment of children with lead poisoning, including children with ASD who had lead poisoning.46-48
Multiple Medications
A child with ASD may be taking a regimen of daily medications, such as anticonvulsants, antipsychotics, or serotonin reuptake inhibitors.49 The clinician must be cognizant of concomitant adverse effects if supplemental iron or chelation medications must be added to his or her regimen. There may be new side-effects or little studied drug-drug interactions to consider in the treatment of these patients
Alternative Therapies
Some parents take their children to alternative health care providers for assessment of their ASD. Complementary and alternative therapies proposed in patients with ASD range in safety from generally safe to dangerous and range in efficacy from ineffective to effective to unknown efficacy.50 When alternative practitioners find the hair or urine lead elevated, such practitioners may recommend chelation or unconventional, scientifically unsupported, costly, and potentially dangerous detoxification regimens.50 These children may have very low BLLs and no evidence of exposure to environmental lead and therefore no need for such management strategies.
Dietary Challenges
Some children with ASD may have nutritional deficiencies, such as iron, calcium, magnesium, or vitamin D. Iron-deficiency anemia is a known comorbidity of childhood lead poisoning.51 Such deficiencies may result in increased lead absorption through the intestinal wall active transport system for metals. Ensuring adequate dietary or supplemental sources of iron, magnesium, calcium, and vitamin D are likely to help protect the child from lead absorption in the gastrointestinal tract.
Developmental Monitoring and Services
Some children with elevated blood lead levels may have previously undiagnosed ASD or other developmental delays. Indeed, there has been a recommendation that all children with an elevated BLL receive Early Intervention Program services.52 Some children with ASD, recognized or unrecognized, may not be getting ABA special educational services for which they are qualified and deserve.
Economics and Social Environment
The lead abatement of a residence often requires days or weeks to accomplish. During the work, for safety, children cannot stay in the house and the family must relocate to a second temporary residence, such as another hazard-free apartment or house, hotel, shelter, or the home of a family member or friend. Such a move interferes with the family’s usual routines and transitions the children to new surroundings, which may have noise-level restrictions and other constraints. Children with autism have difficulty tolerating changes in their routine. They often react negatively with transitions and changes in their caretakers, teachers, or living environments. The abatement of lead hazards in a home can be costly to the parents. This adds an economic burden on a family already laboring under multiple stressors. The necessity of close medical monitoring and/or hospitalization requires that the parent miss considerable days of work and may threaten the parent’s job security, adding to family stress.
Legal Advocacy
Federal policies and lead regulations in many states protect children under the age of 6 years from lead hazards in their environment, requiring hazard abatement if the child is found to have an elevated lead level and lead-contaminated surfaces are discovered at the time of inspection of their residence. These laws were designed with younger children in mind, since they are most vulnerable to the deleterious effects of lead and explore their environment through pica and hand-to-mouth behaviors. However, both pica and oral exploratory habits may not extinguish in preschool years in children with ASD and instead persist throughout childhood and into adolescence. Laws regarding residential lead hazards are not adequately protective for children with ASD and persistent pica behaviors living in a contaminated environment. They may not be afforded the same rights to a lead-free environment as younger children who have been exposed to lead.
Conclusions
We have reviewed the prevalence of both childhood lead poisoning and ASD, the neurologic vulnerability of young children to both conditions, the relationship between lead exposure and ASD, and the diagnosis and management of children with both elevated BLL and ASD. Childhood lead poisoning adds a number of considerable burdens to any family’s ability to function in everyday life: worrisome long-term health concerns regarding their children, economic considerations in bringing their housing into hazard-free compliance, complex medical protocols and therapies to avert lead’s toxic effects, special education needs of the children, transitional housing during residential remediation, insecurity about the safety of secondary homes (eg, uninspected family day care facilities or grandparents’ homes), missed time from work and/or school, and parental feelings of guilt, inadequacy, and loss of control. All of these stressors, and more, are magnified in the families of children with ASD and lead poisoning. The astute clinician will recognize where compromises can be made and where adherence to protocol is necessary in the management of these patients. Health care providers must strive to advocate for these families and mitigate the ill effects of lead exposure on their child’s development, while maximizing their health as well as their social and educational welfare.
Acknowledgments
Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This publication was supported by the cooperative agreement award number 1U61TS000237-05 from the Agency for Toxic Substances and Disease Registry (ATSDR). Its contents are the responsibility of the authors and do not necessarily represent the official views of the Agency for Toxic Substances and Disease Registry (ATSDR). The US Environmental Protection Agency (EPA) supports the PEHSU by providing funds to ATSDR under Inter-Agency Agreement Number DW-75-95877701. Neither EPA nor ATSDR endorse the purchase of any commercial products or services mentioned in PEHSU publications.
Footnotes
Authors’ Note
The content of this review article is meant for education purposes only. Decisions about evaluation and treatment are the responsibility of the treating clinician and should always be tailored to individual clinical circumstances.
Declaration of Conflicting Interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
References
- 1.Centers for Disease Control and Prevention. Lead. https://www.cdc.gov/nceh/lead/. Accessed December 27, 2018.
- 2.Centers for Disease Control and Prevention. Autism spectrum disorder (ASD): data and statistics on autism spectrum disorder. https://www.cdc.gov/ncbddd/autism/data.html. Accessed December 27, 2018.
- 3.Christensen DL, Baio J, Braun KVN, et al. ; Centers for Disease Control and Prevention. Prevalence and characteristics of autism spectrum disorder among children aged 8 years—autism and developmental disabilities monitoring network, 11 sites, United States, 2012. MMWR Surveill Summ. 2016;65(3):1–23. doi: 10.15585/mmwr.ss6503a1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Bellinger DC. A strategy for comparing the contributions of environmental chemicals and other risk factors to neurodevelopment of children. Environ Health Perspect. 2011;120:501–507. doi: 10.1289/ehp.1104170 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Cohen DJ, Johnson WT, Caparulo BK. Pica and elevated blood lead level in autistic and atypical children. Am J Dis Child. 1976;130:47–48. [DOI] [PubMed] [Google Scholar]
- 6.Shannon M, Graef JW. Lead intoxication in children with pervasive developmental disorders. J Toxicol Clin Toxicol. 1996;34:177–181. [DOI] [PubMed] [Google Scholar]
- 7.Lidsky TI, Schneider JS. Autism and autistic symptoms associated with childhood lead poisoning. J Appl Res. 2005;5:80–87. [Google Scholar]
- 8.Clark B, Vandermeer B, Simonetti A, Buka I. Is lead a concern in Canadian autistic children? Paediatr Child Health. 2010;15:17–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Arora M, Reichenberg A, Willfors C, et al. Fetal and postnatal metal dysregulation in autism. Nature Comm. 2017;8:1–10. doi: 10.1038/ncomms154903 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Rauh VA, Margolis AE. Research review: environmental exposures, neurodevelopment, and child mental health—new paradigms for the study of brain and behavioral effects. J Child Psychol Psychiatry. 2016;57:775–793. doi: 10.1111/jcpp.12537 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Myers SM, Johnson CP; American Academy of Pediatrics Council on Children With Disabilities. Management of children with autism spectrum disorders. Pediatrics. 2007;120:1162–1182. doi: 10.1542/peds.2007-2362 [DOI] [PubMed] [Google Scholar]
- 12.Barbaresi WJ, Katusic SK, Voigt RG. Autism: a review of the state of the science for pediatric primary health care clinicians. Arch Pediatr Adolesc Med. 2006;160:1167–1175. doi: 10.1001/archpedi.160.11.1167 [DOI] [PubMed] [Google Scholar]
- 13.Hussain J, Woolf AD, Sandel M, Shannon MW. Environmental evaluation of a child with developmental disability. Pediatr Clin North Am. 2007;54:47–62. doi: 10.1016/j.pcl.2006.11.004 [DOI] [PubMed] [Google Scholar]
- 14.Golnick A, MacCabee-Ryavboy N. Autism: clinical pearls for primary care. Contemp Pediatr. 2010;27: 42–60. [Google Scholar]
- 15.Lidsky TI, Schneider JS. Lead neurotoxicity in children: basic mechanisms and clinical correlates. Brain. 2003;126(pt 1):5–19. doi: 10.1093/brain/awg014 [DOI] [PubMed] [Google Scholar]
- 16.Dietrich KN, Krafft KM, Bornschein RL, et al. Low-level fetal lead exposure effect on neurobehavioral development in early infancy. Pediatrics. 1987;80:721–730. [PubMed] [Google Scholar]
- 17.Bellinger D, Leviton A, Waternaux C, Needleman H, Rabinowitz M. Longitudinal analyses of prenatal and postnatal lead exposure and early cognitive development. N Engl J Med. 1987;316:1037–1043. doi: 10.1056/NEJM198704233161701 [DOI] [PubMed] [Google Scholar]
- 18.Bellinger DC, Stiles KM, Needleman HL. Low-level lead exposure, intelligence and academic achievement: a long-term follow-up study. Pediatrics. 1992;90:855–861. [PubMed] [Google Scholar]
- 19.Lanphear BP, Dietrich K, Auinger P, Cox C. Cognitive deficits associated with blood lead concentrations <10 μg/dL in US children and adolescents. Public Health Rep. 2000;115:521–529. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Canfield RL, Henderson CR Jr, Cory-Slechta DA, Cox C, Jusko TA, Lanphear BP. Intellectual impairment in children with blood lead concentrations below 10 μg per deciliter. NEngl J Med. 2003;348:1517–1526. doi: 10.1056/NEJMoa022848 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.McLaine P, Navas-Acien A, Lee R, Simon P, Diener-West M, Agnew J. Elevated blood lead levels and reading readiness at the start of kindergarten. Pediatrics. 2013;131:1081–1089. doi: 10.1542/peds.2012-2277 [DOI] [PubMed] [Google Scholar]
- 22.Lanphear BP, Hornung R, Khoury J, et al. Low-level environmental lead exposure and children’s intellectual function: an international pooled analysis. Environ Health Perspect. 2005;113:894–899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Nigg JT, Nikolas M, Knottnerus GM, Cavanagh K, Friderici K. Confirmation and extension of association of blood lead with attention-deficit/hyperactivity disorder (ADHD) and ADHD symptom domains at population-typical exposure levels. J Child Psychol Psychiatry. 2010;51:58–65. doi: 10.1111/j.1469-7610.2009.02135.x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Liu J, Liu X, Wang W, et al. Blood lead concentrations and children’s behavioral and emotional problems. JAMA Pediatr. 2014;168:737–745. doi: 10.1001/jamapediatrics.2014.332 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Yuan W, Holland SK, Cecil KM, et al. The impact of early childhood lead exposure on brain organization: a functional magnetic resonance imaging study of language function. Pediatrics. 2006;118:971–977.doi: 10.1542/peds.2006-0467 [DOI] [PubMed] [Google Scholar]
- 26.Sanders T, Liu Y, Buchner V, Tchounwou PB. Neurotoxic effects and biomarkers of lead exposure: a review. Rev Environ Health. 2009;24:15–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Mason LH, Harp JP, Han DY. Pb neurotoxicity: neuropsychological effects of lead toxicity. Biomed Res Int. 2014;2014:840547. doi: 10.1155/2014/840547 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Winter AS, Sampson RJ. From lead exposure in early childhood to adolescent health: a Chicago birth cohort. Am J Public Health. 2017;107:1496–1501. doi: 10.2105/AJPH.2017.303903 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Reuben A, Caspi A, Belsky DW, et al. Association of childhood blood lead levels with cognitive function and socioeconomic status at age 38 years and with IQ change and socioeconomic mobility between childhood and adulthood. JAMA. 2017;317:1244–1251. doi: 10.1001/jama.2017.1712 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Nucklos CC. Autism spectrum disorder In: Diagnostic and Statistical Manual of Mental Disorders. 5th ed. Arlington, VA: American Psychiatric Association Publishing; 2013:24–25. [Google Scholar]
- 31.Johnson CP, Myers SM; American Academy of Pediatrics Council on Children With Disabilities. Identification and evaluation of children with autism spectrum disorders. Pediatrics. 2007;120:1183–1215. doi: 10.1542/peds.2007-2361 [DOI] [PubMed] [Google Scholar]
- 32.Keller B, Faciano A, Tsega A, Ehrlich J. Epidemiologic characteristics of children with blood lead levels ≥45 μg/dL. J Pediatr. 2017;180:229–234. doi: 10.1016/j.jpeds.2016.09.017 [DOI] [PubMed] [Google Scholar]
- 33.Zeager M, Heard T, Woolf AD. Lead poisoning in two children with Landau-Kleffner syndrome. Clin Toxicol (Phila). 2012;50:448. doi: 10.3109/15563650.2012.685523 [DOI] [PubMed] [Google Scholar]
- 34.George M, Heeney MM, Woolf AD. Encephalopathy from lead poisoning masquerading as a flu-like syndrome in an autistic child. Pediatr Emerg Care. 2010;26:370–373. doi: 10.1097/PEC.0b013e3181db2237 [DOI] [PubMed] [Google Scholar]
- 35.Latif A, Heinz P, Cook R. Iron deficiency in autism and Asperger syndrome. Autism. 2002;6:103–114. doi: 10.1177/1362361302006001008 [DOI] [PubMed] [Google Scholar]
- 36.Elsenhans B, Janser H, Windisch W, Schümann K. Does lead use the intestinal absorptive pathways of iron? Impact of iron status on murine 210Pb and 59Fe absorption in duodenum and ileum in vivo. Toxicology. 2011;284:7–11. doi: 10.1016/j.tox.2011.03.005 [DOI] [PubMed] [Google Scholar]
- 37.Harkins DK, Susten AS. Hair analysis: exploring the state of the science. Environ Health Perspect. 2003;111:576–578. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Seidel S, Kreutzer R, Smith D, McNeel S, Gilliss D. Assessment of commercial laboratories performing hair mineral analysis. JAMA. 2001;285:67–72. [DOI] [PubMed] [Google Scholar]
- 39.Steindel SJ, Howanitz PJ. The uncertainty of hair analysis for trace metals. JAMA. 2001;285:83–85. [DOI] [PubMed] [Google Scholar]
- 40.Weitlauf AS, McPheeters ML, Peters B, et al. Comparative Effectiveness Review No. 137: Therapies for Children with Autism Spectrum Disorder: Behavioral Interventions Update. Rockville, MD: Agency for Healthcare Research and Quality; 2014. [PubMed] [Google Scholar]
- 41.Hauptman M, Bruccoleri R, Woolf AD. An update on childhood lead poisoning. Clin Pediatr Emerg Med. 2017;18:181–192. doi: 10.1016/j.cpem.2017.07.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Cuprimine [package insert]. Bridgewater, NJ: Valeant Pharmaceuticals North America LLC; 2018. [Google Scholar]
- 43.Smith D, Strupp BJ. The scientific basis for chelation: animal studies and lead chelation. J Med Toxicol. 2013;9:326–338. doi: 10.1007/s13181-013-0339-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Goldman RH, Woolf A. Chelation therapy—guidance for the general public. https://www.pehsu.net/_Library/facts/chelation_therapy_guidance_general_public_gold-man_woolf_2012.pdf. Published April 2012; Accessed December 28, 2018, 2019. [Google Scholar]
- 45.James S, Stevenson SW, Silove N, Williams K. Chelation for autism spectrum disorder (ASD). Cochrane Database Syst Rev. 2015;(5):CD010766. doi: 10.1002/14651858.CD010766.pub2 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Brown MJ, Willis T, Omalu B, Leiker R. Deaths resulting from hypocalcemia after administration of edetate disodium: 2003-2005. Pediatrics. 2006;118:e534–e536. doi: 10.1542/peds.2006-0858 [DOI] [PubMed] [Google Scholar]
- 47.Baxter AJ, Krenzelok EP. Pediatric fatality secondary to EDTA chelation. Clin Toxicol (Phila). 2008;46:1083–1084. doi: 10.1080/15563650701261488 [DOI] [PubMed] [Google Scholar]
- 48.Atwood KC, Woeckner E. In pediatric fatality, edetate disodium was no accident. Clin Toxicol (Phila). 2009;47:256. doi: 10.1080/15563650802701937 [DOI] [PubMed] [Google Scholar]
- 49.Dove D, Warren Z, McPheeters ML, Taylor JL, Sathe NA, Veenstra-VanderWeele J. Medications for adolescents and young adults with autism spectrum disorders: a systematic review. Pediatrics. 2012;130:717–726. doi: 10.1542/peds.2012-0683 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Akins RS, Angkustsiri K, Hansen RL. Complementary and alternative medicine in autism: an evidence-based approach to negotiating safe and efficacious interventions with families. Neurotherapeutics. 2010;7:307–319. doi: 10.1016/j.nurt.2010.05.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Kwong WT, Friello P, Semba RD. Interactions between iron deficiency and lead poisoning: epidemiology and pathogenesis. Sci Total Environ.2004;330:21–37.doi: 10.1016/j.scitotenv.2004.03.017 [DOI] [PubMed] [Google Scholar]
- 52.Hamp N, Zimmerman A, Hoffen J. Advocating for automatic eligibility for early intervention services for children exposed to lead. Pediatr Ann. 2018;47:e413–e418. doi: 10.3928/19382359-20180924-01 [DOI] [PubMed] [Google Scholar]