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Canadian Paediatric Society

Position statement

ADHD in children and youth: Part 1—Etiology, diagnosis, and comorbidity

Posted: Oct 24 2018


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Principal author(s)

Stacey A. Bélanger, Debbi Andrews, Clare Gray, Daphne Korczak; Canadian Paediatric Society, Mental Health and Developmental Disabilities Committee

Paediatr Child Health 2018, 23(7):447–453.

Abstract

Attention-deficit hyperactivity disorder (ADHD) is a chronic neurodevelopmental disorder. Three position statements have been developed by the Canadian Paediatric Society, following systematic literature reviews. Statement objectives are to:

1) Summarize the current clinical evidence regarding ADHD,

2) Establish a standard for ADHD care, and

3) Assist Canadian clinicians in making well-informed, evidence-based decisions to enhance care of children and youth with this condition.

Specific topics reviewed in Part 1, which focuses on diagnosis, include: prevalence, genetics, pathophysiology, differential diagnosis and comorbid psychiatric disorders and developmental disorders. In addition to database searches, the most recent guidelines of the American Academy of Pediatrics, the American Academy of Child and Adolescent Psychiatry, the National Institute for Health and Clinical Excellence, the Scottish Intercollegiate Guidelines Network, and the Eunethydis European ADHD Guidelines Group, were reviewed. Because ADHD is a heterogeneous disorder, comprehensive medical assessment for ADHD should always include a complete history, a physical examination, and a thorough consideration of differential diagnosis and related comorbidities. Specific recommendations for information gathering, testing, and referral are offered.

Keywords: Attention-deficit hyperactivity disorder; Comorbidity; Diagnosis; Etiology

BACKGROUND

The Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) classifies attention-deficit hyperactivity disorder (ADHD) as a neurodevelopmental disorder and defines it as ‘a persistent pattern of inattention and/or hyperactivity-impulsivity that interferes with functioning or development…. and negatively impacts directly on social and academic/occupational activities’ [1]. Worldwide, ADHD is the third-most-common mental health disorder, after depression and anxiety, affecting an estimated 3.4% of children and youth [2].

ADHD prevalence in the paediatric population has been stable over the past three decades [3] except in the USA [4], where it has increased. Applying the definition of ADHD from the International Classification of Diseases, 10th edition, yields a lower prevalence rate compared with the DSM-5, because the ICD-10 requires criteria be met for both inattention and hyperactivity [5]. ADHD is associated with significant adverse outcomes in childhood and adolescence: educational problems (resulting in low rates of high-school graduation and completion of postsecondary education) [6], difficult peer relationships [7] and increased rates of motor vehicle accidents, accidental injuries, and substance misuse. Risk for substance abuse increases further when ADHD is comorbid with conduct disorder (CD) [8][9]. The presence of these comorbid conditions and ADHD is associated with increased mortality risk [10].

Current estimates show that 50% of children with ADHD continue to have symptoms of ADHD in adolescence and adulthood. Predictors of persistence include combined inattention/hyperactivity, increased symptom severity, comorbid major depressive or other mood disorder, high comorbidity (>3 additional DSM disorders), parental anxiety, and parental antisocial personality disorder [11].

ETIOLOGY

ADHD is a disorder with multiple etiologies. Combinations of genetic, neurological, and environmental factors contribute to pathogenesis and its heterogeneous phenotype [12].

Evidence from family, twin, and adoption studies has suggested strongly that ADHD is a highly hereditary, polygenic disorder [13]. Gene variants predicting risk for ADHD are important for brain development, cell migration, and encoding for catecholamine receptor and transporter genes [13][14]. The identification of gene sets affecting neurotransmitter pathways in the brain [15] has suggested that rare copy number variants or the accumulation of larger deletions and duplications influencing gene transcription are more commonly found in individuals with ADHD [16]. (For more information, see the companion statement on special populations in this issue.) Ongoing pharmacogenetics research aims to identify genes involved in medication response with ADHD [17].

Noninherited neurological factors affecting brain development or resulting in brain injury have been implicated in ADHD pathogenesis. The contribution of pregnancy and birth complications is mixed, but strong evidence supports greater ADHD risk following in utero exposure to alcohol or tobacco [18] and low birth weight (<2,500 g) [19][20]. Hypoxic–anoxic brain injury [21], epilepsy disorders [22], and traumatic brain injury [23][25] also contribute to ADHD risk.

Exposure to environmental toxins (specifically lead, organophosphate pesticides, and polychlorinated biphenyls) has been linked to ADHD symptoms [20][26][27]. Except for children experiencing exceptional early deprivation [28][29], a causal relationship between family environment and psychosocial adversity and ADHD is unclear [20][30][31].

Neuroimaging studies point to ADHD as a disorder of early brain development. Based on volumetric [32] and functional MRI studies [33], differences are found in the structural development and functional activation in the prefrontal cortex, basal ganglia, anterior cingulate cortex, and cerebellum [34]. Activity among these areas depends on catecholaminergic brain circuitry [35]. Despite weak evidence for deficits in these neurotransmitters, their role is substantiated by their distribution in those areas of the brain involved in ADHD and the positive response of ADHD patients to medications that modulate the neurotransmission of catecholamines [36]. A delay in cortical maturation has been documented, with peak cortical thickness attained in the cerebrum at 7 years in typically developing children and at 10 years in those with ADHD [37].

DIAGNOSIS

ADHD remains challenging to diagnose because specific biomarkers and symptom specificity are lacking, the scope for differential diagnosis is large, and comorbidities are often present. Diagnostic improvements in the DSM-5 include criteria that now describe essential behaviours over a broader age range and that natural history is better captured in the lower number of symptoms needed to meet diagnostic threshold in adolescence and adulthood. While some changes occurred between DSM-IV and -5, the same (or similar) questionnaires, rating scales and screening tools (www.cps.ca/en/tools-outils/mental-health-screening-tools-and-rating-scales) can be used to gather diagnostic information from multiple informants. Symptoms must be present across multiple settings and lead to impairment in everyday activities. Key elements of the diagnostic procedure are discussed in several guidelines [38][39] and outlined in Table 1.

Obtaining a diagnosis of ADHD in preschoolers and adolescents can be complicated. Although there is evidence that DSM criteria can be applied to preschool children, it may be difficult to obtain sound observations from nonparent observers [38]. Only the Conner’s Comprehensive Behavior Rating scale and the ADHD Rating Scales IV have been validated in this age group [40]. Before establishing a diagnosis of ADHD and initiating treatment in preschoolers, the American Academy of Pediatrics (AAP) recommends that parents of young children referred for ADHD assessment enrol in a parent training program [38]. Such programs can help parents develop age-appropriate developmental expectations and specific management skills for problem behaviours.

Obtaining diagnostic information from multiple informants for adolescents can also be challenging. There are multiple teachers in high school, primary caregivers may have less opportunity to observe their adolescent’s behaviours than during childhood, adolescents are less likely to exhibit overt behaviours (e.g., hyperactivity), and adolescent self-reporting often minimizes their problematic behaviours. It is important to establish whether manifestations of ADHD were present at a younger age and to strongly consider substance use, depression, and anxiety as alternative or co-occurring diagnoses.

As with many complex presentations, the differential diagnosis for ADHD can be narrowed considerably by a skillful history and physical examination. Both the symptoms and the context in which they occur require exploration (Table 1).

Table 1. Clinical process and ‘pearls’ in the diagnosis of ADHD: Implementation of guidelines and expert consensus
Schedule several office visits to complete the diagnostic evaluation.
Obtain detailed information on prenatal/perinatal events, medical and mental health history.

Obtain developmental/behavioural history (motor, language, social milestones and behaviour, including temperament/emotional regulation and attachment).

(Assessment of developmental milestones is particularly important for diagnosing preschool children because impaired attention and hyperactivity may also be features of a neurodevelopmental disorder.)

Evaluate family medical and mental health, family functioning and coping styles of primary caregivers. Ask about genetic disorders.

Evaluate for comorbid disorder(s) (psychiatric, neurodevelopmental and physical).

(Do comorbid symptoms meet criteria for a separate disorder that is the main diagnosis OR exist in tandem with ADHD as the main diagnosis OR are they secondary symptoms (stemming from the ADHD)?)

Review academic progress (e.g., report cards, sample assignments) and look for symptoms of a learning disorder [69].

(Clinical impressions and use of standardized scales are still the most effective practices for evaluating ADHD symptomatology.)

Obtain standardized behaviour rating scale(s) that evaluate DSM-5 criteria from primary caregivers, teachers and the adolescent being assessed.

For a list of screening tools and rating scales to assess impairment, see: www.cps.ca/en/tools-outils/mental-health-screening-tools-and-rating-scales

(Rating scales are not diagnostic of ADHD but they provide subjective impressions to help quantify the degree to which a behaviour may deviate from the norm and can be used to evaluate the effects of interventions in home or school [70].)

Unless indicated by history and physical examination, do NOT:

  • order laboratory tests, genetic testing, EEG or neuroimaging.
  • order psychological (standardized assessment of intellectual function and academic achievement skills) neuropsychological or speech-language assessments.
  • use psychological tests (e.g., TEACH, Continuous Performance Tests (CPT)) or measures of executive function to diagnose ADHD and/or as a means to monitor symptom or functional improvement in daily activities.

Refer to DSM-5 criteria for core symptoms and characteristics of ADHD:

1. Symptoms are severe, persistent (i.e., present before 12 years of age and continuing >6 months), and inappropriate for the patient’s age and developmental level.

  • Consider the demands and expectations being placed on the child and what the child’s innate capabilities are to meet these expectations. What will this child look like over time?
  • The abilities to self-control attention, activity and impulses emerge in a developmental process [70]. The DSM does not provide for developmental level differences, which may lead to overdiagnosis of ADHD in young preschool-aged children.

2. Symptoms are associated with impairment in academic achievement, peer and family relations and adaptive skills.

  • Impairment' implies greater severity and frequency of symptoms that interfere with ability to function across major life domains.

3. If there is a discrepancy of symptoms across settings, it is important to identify why the discrepancy exists.

4. Specify the type of ADHD presentation as per the DSM-5:

i) Combined presentation (criteria are met for inattention, hyperactivity-impulsivity)

ii) Predominantly inattentive presentation (criteria are met for inattention)

iii) Predominantly hyperactive-impulsive presentation (criteria are met for hyperactivity-impulsivity)

5. Specify current severity (mild, moderate or severe) based on the symptoms and degree of functional impairment.

Medical examinations: Perform thorough physical, neurological and dysmorphology assessments [71].
Adapted from references [38][39][72][75]. ADHD Attention-deficit hyperactivity disorder; DSM Diagnostic and Statistical Manual of Mental Disorders.

DIFFERENTIAL DIAGNOSES

The DSM-5 lists 16 conditions or groups of conditions to be distinguished from ADHD, many of which can also occur as comorbidities. A list of developmental and behavioural conditions that are commonly mistaken for ADHD is presented in Table 2 [41].

Conditions comprising the differential diagnosis may be grouped for ease in history-taking. Beginning with disorders considered to be psychiatric, ADHD is often grouped with externalizing conditions associated with visible, often disruptive and aggressive behaviours, such as oppositional defiant disorder (ODD) and intermittent explosive disorder; a disruptive behaviour can be mistaken for hyperactivity or impulsive reactivity. Unipolar internalizing disorders (e.g., anxiety disorder, depression) may be mistaken for inattentive presentation, while mood disorders with mood swings and poor emotional regulation (e.g., bipolar disorder (BD), disruptive mood dysregulation disorder) can mimic all the symptoms of ADHD (combined presentation).

The DSM-5 groups together trauma- and stressor-related disorders. In reactive attachment disorder, social disinhibition may resemble, initially, the impulsivity and social isolation seen in ADHD. However, exploration of the social history and the child’s relationships over time can help to distinguish among disorders. Many children with ADHD can make initial social overtures but have difficulty maintaining relationships due to emotional dysregulation. Not specifically listed in the DSM-5 differential for ADHD are adjustment disorders, where emotional and/or behavioural symptoms emerge in response to an identified stressor (e.g., the illness or death of a family member or close friend, a separation or divorce), and to post-traumatic stress disorder. Post-traumatic stress disorder should always be considered with a history of identified trauma (e.g., child abuse) [42].

Children who function at extremes of cognitive development, such as those with ID (see the companion statement on special populations in this issue) or superior intellectual functioning, may be disconnected and inattentive in class, the former because material presented in class may be too difficult, and the latter because school work has already been mastered. In either case, children with learning tasks that are poorly matched to their ability may also become disruptive. Similarly, children with a specific learning or language disorder may show inattention and (at times) disruptive symptoms, when their specific area of difficulty is the focus of class or homework assignments (e.g., the student with dyslexia who becomes inattentive during reading period).

The movements associated with autism spectrum disorders (ASDs) (see the companion statement on special populations in this issue) and other neurodevelopmental disorders (e.g., stereotypic movement disorder, Tourette’s syndrome) may be mistaken for hyperactivity. Additional social communication deficits and lack of social overtures can help identify ASD, while movement quality (sudden, rapid, nonrhythmic) and distribution (eyes, face, upper body, vocal) may be useful for distinguishing tic disorders (TD).

The DSM-5 also includes conditions (e.g., personality disorders, psychosis, substance abuse disorders (SUDs)) that are seen less commonly in the paediatric population but should be considered when assessing older children and youth. Although these conditions may present with inattention, impulsivity and academic problems, psychiatry or other appropriate mental health services should be arranged. The child’s medications should be reviewed carefully for potential to induce ADHD symptoms, anxiety, depression or psychosis.

In addition, medical conditions can mimic inattentive ADHD. These include conditions causing fatigue or pain (obstructive sleep apnea, inflammatory bowel disease), sensory impairments (visual or auditory), chronic health conditions affecting school attendance (such that the child no longer understands or follows what is being taught), and neurological conditions that affect attention and arousal (e.g., epilepsy, post-concussion status). All of these conditions may also co-occur with ADHD; treating an identified medical condition may provide insight into possible comorbid ADHD.

Table 2. Conditions commonly misdiagnosed as ADHD (in decreasing order of frequency)
  • Learning disorder
  • Sleep disorder
  • Oppositional defiant disorder
  • Anxiety disorder
  • Intellectual disability
  • Language disorder, mood disorder, tic disorder, conduct disorder
  • Autism spectrum disorder
  • Developmental coordination disorder
Information from reference [41]. ADHD Attention-deficit hyperactivity disorder.

The prevalence of ADHD in children with epilepsy is two to three times higher than in the general population, and is typically inattentive presentation. ADHD symptoms are generally present at or before the first seizure, suggesting comorbidity as opposed to being secondary to epilepsy or antiepileptic medication. Complicated epilepsy, higher seizure frequency, and earlier age of onset are associated with higher ADHD risk, with these patients mostly showing combined presentation. Antiepileptic medications, especially phenobarbital, and to a lesser extent, phenytoin, carbamazepine, and valproic acid, can affect attention and activity. Newer antiepileptics (gabapentin, tiagabine, vigabatrin, and lamotrigine) may have fewer cognitive side effects [43].

Many genetic conditions (fragile X syndrome, Turner syndrome, tuberous sclerosis, neurofibromatosis, 22q11 deletion syndrome), especially those with accompanying developmental symptoms, show a higher prevalence of ADHD than the general population [44][48]. For many, congenital anomalies, significant dysmorphology, seizures or global developmental delay likely will be noted before ADHD symptoms develop. However, in conditions where symptoms and signs are subtle, intermittent or later-developing (e.g., neurofibromatosis, where dermatological findings may increase with age, or syndromes where facial dysmorphology is more apparent over time, or fragile X syndrome), inattention or hyperactivity may be what first brings the child to the physician.

Central auditory processing disorder is a symptom cluster affecting ability to attend to and discriminate among auditory stimuli in the presence of normal hearing and intellect [49]. It has been treated with auditory interventions, including preferential seating, sound field systems, personal FM devices, and headphones, but is questioned as a distinct entity because of high comorbidity with ADHD [50].

COMORBIDITY

ADHD, a neurodevelopmental disorder, is most commonly comorbid with other psychiatric and neurodevelopmental conditions [51]. The presence of a comorbid disorder can affect symptom presentation, increase symptom severity, and lead to greater functional impairment. Clinicians must be aware of common comorbidities to develop an effective, multidimensional treatment approach, first addressing the condition that is causing the greatest impairment, whether it be the ADHD or a comorbid disorder [52].

Disruptive behaviour disorders

ODD and CD comprise the disruptive behaviour disorders, which are characterized by externalizing and aggressive behaviours. Studies report the frequency of ODD/CD comorbidity with ADHD to be as high as 90% [53][54].

Anxiety disorder (AD)/Obsessive compulsive disorder

Anxiety disorders occur in approximately 30% of patients with ADHD [55][56]. Children with comorbid AD/ADHD present with more school fears, inattention, poorer social skills, and greater symptom severity [57] compared with ADHD without AD. Further, ADHD symptoms can interfere with a child’s ability to engage successfully in cognitive behavioural therapy (CBT) for AD and complicate medication choice, because stimulants may increase anxiety symptoms.

Mood disorders, including bipolar disorder (BD)

Children with ADHD may also experience comorbid depressive symptoms, particularly as they approach adolescence and adulthood. There is increasing evidence of heterotypic continuity between these two conditions, suggesting they may represent the same underlying construct for some children [58].

The validity of BD diagnosis, particularly when broadly defined, remains controversial in preadolescent children. Researchers have reported overlapping behavioural symptoms in preadolescent children with ADHD and those with BD that can be challenging to disentangle. The introduction of disruptive mood dysregulation disorder in the DSM-5 may better describe children with extreme mood regulation problems.

Substance use disorders (SUDs)

There is an increase in SUDs as children with ADHD reach adolescence and adulthood [59]. It is possible that substance use occurs as an attempt to self-medicate. The treatment of ADHD comorbid with a SUD is complicated by risks for misuse and diversion of prescription stimulants [59]. A recent meta-analysis [60] found that stimulant treatment neither contributed to nor prevented future SUDs in youth with ADHD.

Tic disorders (TDs)

The co-occurrence of ADHD and TDs can create challenges due to concerns that stimulants may exacerbate tics. Given that tics wax and wane, it has been difficult to establish whether this relationship between stimulants and tics is causal or coincidental [61][62]. Some children with ADHD/TD treated with stimulants are less stressed and experience an improvement in their tics.

Developmental coordination disorder (DCD)

Persistent delays in motor development and coordination are common in individuals with ADHD [63]. Fine motor coordination is one of the most impaired areas of motor performance [64]. A screening questionnaire and a focused neuromotor exam are important when DCD is suspected [63].

Autism spectrum disorders

(See the companion statement on special populations in this issue.)

Specific learning disorder (SLD)

A learning disorder is the most common comorbid condition [51]. Approximately one-third of children with ADHD also have an SLD [65]. However, children with SLD alone can present with symptoms of inattention because they do not understand what is being taught. A careful psychoeducational assessment can help determine whether the child has SLD as a primary diagnosis or whether the two disorders, ADHD and SLD, are comorbid.

Eating disorders

ADHD symptoms, especially in females, increase risk for eating disorders [66]. This comorbidity may underlie difficulties with treatment and remission in some eating disorders [67].

CONCLUSION

ADHD is a heterogeneous disorder. Because paediatricians and family physicians are the first care providers to conduct a medical assessment of children and youth with ADHD, which should always include a complete history, physical examination and consideration of differential diagnosis and possible comorbidities for this disorder, it is essential that their training equips them with the clinical skills needed to assess and manage ADHD and comorbid disorders [68].

RECOMMENDATIONS

  • Given the scope for differential diagnosis and frequent comorbidity in ADHD, physicians must perform a comprehensive but directed history and physical examination.
  • Collateral information about a child’s or adolescent’s behaviour should be obtained whenever possible, because core symptoms diagnostic of ADHD are not always observed in the clinical setting.
  • Current clinical guidelines do not recommend psychological or neuropsychological testing in ADHD. Such testing should never be used alone to diagnose ADHD or without clinical evaluation by an experienced physician.
  • Consider referring to a specialist and subspecialist for diagnosis of complex ADHD, when differential diagnosis and comorbidity are key findings. The limits between what can be handled by a primary care clinician and what should be referred is largely case-based and determined by the expertise and skills of the primary care clinicians involved.
  • Residency training programs for paediatricians and family physicians must include ADHD diagnosis and treatment among their explicit learning objectives and take measures to ensure these objectives are being met.

Acknowledgements

This position statement has been reviewed by the Adolescent Health and Community Paediatrics Committees of the Canadian Paediatric Society. It was also reviewed by representatives of the Canadian Academy of Child and Adolescent Psychiatry (CACAP).


CANADIAN PAEDIATRIC SOCIETY MENTAL HEALTH AND DEVELOPMENTAL DISABILITIES COMMITTEE

Members: Debbi Andrews MD (Chair), Susan Bobbitt MD, Alice Charach MD, Brenda Clark MD (past member), Mark E Feldman MD (past Board Representative), Johanne Harvey MD (former Board Representative), Benjamin Klein MD, Oliva Ortiz-Alvarez MD, Sam Wong MD (Board Representative)

Liaisons: Sophia Hrycko MD, Canadian Academy of Child and Adolescent Psychiatry; Angie Ip MD, CPS Developmental Paediatrics Section; Aven Poynter MD, CPS Mental Health Section

Principal authors: Stacey A. Bélanger MD PhD, Debbi Andrews MD, Clare Gray MD, Daphne Korczak MD


References

  1. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 5th edn (DSM-5). Washington, DC: APA, 2013:59–66.
  2. Polanczyk GV, Salum GA, Sugaya LS, Caye A, Rohde LA. Annual research review: A meta-analysis of the worldwide prevalence of mental disorders in children and adolescents. J Child Psychol Psychiatry 2015;56(3):345–65.
  3. Polanczyk GV, Willcutt EG, Salum GA, Kieling C, Rohde LA. ADHD prevalence estimates across three decades: An updated systematic review and meta-regression analysis. Int J Epidemiol 2014;43(2):434–42.
  4. Visser SN, Danielson ML, Bitsko RH, et al. Trends in the parent-report of health care provider-diagnosed and medicated attention-deficit/hyperactivity disorder: United States, 2003–2011. J Am Acad Child Adolesc Psychiatry 2014;53(1):34–46.e2.
  5. The ICD-10 classification of mental and behavioural disorders. Geneva, Switzerland: WHO, 1993.
  6. Loe IM, Feldman HM. Academic and educational outcomes of children with ADHD. Ambul Pediatr 2007;7(1 Suppl):82–90.
  7. Hoza B. Peer functioning in children with ADHD. J Pediatr Psychol 2007;32(6):655–63.
  8. Whiteford HA, Degenhardt L, Rehm J, et al. Global burden of disease attributable to mental and substance use disorders: Findings from the global burden of disease study 2010. Lancet 2013;382(9904):1575–86.
  9. Erskine HE, Ferrari AJ, Polanczyk GV, et al. The global burden of conduct disorder and attention-deficit/hyperactivity disorder in 2010. J Child Psychol Psychiatry 2014;55(4):328–36.
  10. Dalsgaard S, Østergaard SD, Leckman JF, Mortensen PB, Pedersen MG. Mortality in children, adolescents, and adults with attention deficit hyperactivity disorder: A nationwide cohort study. Lancet 2015;385(9983):2190–6.
  11. Lara C, Fayyad J, de Graaf R, et al. Childhood predictors of adult attention-deficit/hyperactivity disorder: Results from the World Health Organization World Mental Health Survey Initiative. Biol Psychiatry 2009;65(1):46–54.
  12. Akutagava-Martins GC, Rohde LA, Hutz MH. Genetics of attention-deficit/hyperactivity disorder: An update. Expert Rev Neurother 2016;16(2):145–56.
  13. Faraone SV, Mick E. Molecular genetics of attention deficit hyperactivity disorder. Psychiatr Clin North Am 2010;33(1):159–80.
  14. Gizer IR, Ficks C, Waldman ID. Candidate gene studies of ADHD: A meta-analytic review. Hum Genet 2009;126(1):51–90.
  15. Stergiakouli E, Hamshere M, Holmans P, et al.; deCODE Genetics; Psychiatric GWAS Consortium. Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. Am J Psychiatry 2012;169(2):186–94.
  16. Williams NM, Franke B, Mick E, et al. Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: The role of rare variants and duplications at 15q13.3. Am J Psychiatry 2012;169(2):195–204.
  17. Li Z, Chang SH, Zhang LY, Gao L, Wang J. Molecular genetic studies of ADHD and its candidate genes: A review. Psychiatry Res 2014;219(1):10–24.
  18. Linnet KM, Dalsgaard S, Obel C, et al. Maternal lifestyle factors in pregnancy risk of attention deficit hyperactivity disorder and associated behaviors: Review of the current evidence. Am J Psychiatry 2003;160(6):1028–40.
  19. Nigg JT. What Causes ADHD? Understanding What Goes Wrong and Why. New York, NY: Guilford Press, 2006.
  20. Ozlem E. What causes ADHD? AAP Grand Rounds 2012;27(6):72.
  21. Cruikshank BM, Eliason M, Merrifield B. Long-term sequelae of cold water near-drowning. J Pediatr Psychol 1988;13(3):379–88.
  22. Hesdorffer DC, Ludvigsson P, Olafsson E, Gudmundsson G, Kjartansson O, Hauser WA. ADHD as a risk factor for incident unprovoked seizures and epilepsy in children. Arch Gen Psychiatry 2004;61(7):731–6.
  23. Max JE, Schachar RJ, Levin HS, et al. Predictors of attention-deficit/hyperactivity disorder within 6 months after pediatric traumatic brain injury. J Am Acad Child Adolesc Psychiatry 2005;44(10):1032–40.
  24. Max JE, Schachar RJ, Levin HS, et al. Predictors of secondary attention-deficit/hyperactivity disorder in children and adolescents 6 to 24 months after traumatic brain injury. J Am Acad Child Adolesc Psychiatry 2005;44(10):1041–9.
  25. Levin H, Hanten G, Max J, et al. Symptoms of attention-deficit/hyperactivity disorder following traumatic brain injury in children. J Dev Behav Pediatr 2007;28(2):108–18.
  26. Peterson BS, Rauh VA, Bansal R, et al. Effects of prenatal exposure to air pollutants (polycyclic aromatic hydrocarbons) on the development of brain white matter, cognition, and behavior in later childhood. JAMA Psychiatry 2015;72(6):531–40.
  27. Hong SB, Im MH, Kim JW, et al. Environmental lead exposure and attention deficit/hyperactivity disorder symptom domains in a community sample of South Korean school-age children. Environ Health Perspect 2015;123(3):271–6.
  28. Kreppner JM, O’Connor TG, Rutter M; English and Romanian Adoptees Study Team. Can inattention/overactivity be an institutional deprivation syndrome? J Abnorm Child Psychol 2001;29(6):513–28.
  29. Thapar A, Cooper M, Jefferies R, Stergiakouli E. What causes attention deficit hyperactivity disorder? Arch Dis Child 2012;97(3):260–5.
  30. Hjern A, Weitoft GR, Lindblad F. Social adversity predicts ADHD-medication in school children—A national cohort study. Acta Paediatr 2010;99(6):920–4.
  31. Klein B, Damiani-Taraba G, Koster A, Campbell J, Scholz C. Diagnosing attention-deficit hyperactivity disorder (ADHD) in children involved with child protection services: Are current diagnostic guidelines acceptable for vulnerable populations? Child Care Health Dev 2015;41(2):178–85.
  32. Castellanos FX, Lee PP, Sharp W, et al. Developmental trajectories of brain volume abnormalities in children and adolescents with attention-deficit/hyperactivity disorder. JAMA 2002;288(14):1740–8.
  33. Bush G, Valera EM, Seidman LJ. Functional neuroimaging of attention-deficit/hyperactivity disorder: A review and suggested future directions. Biol Psychiatry 2005;57(11):1273–84.
  34. Poelmans G, Pauls DL, Buitelaar JK, Franke B. Integrated genome-wide association study findings: Identification of a neurodevelopmental network for attention deficit hyperactivity disorder. Am J Psychiatry 2011;168(4):365–77.
  35. Arnsten AF, Paspalas CD, Gamo NJ, Yang Y, Wang M. Dynamic network connectivity: A new form of neuroplasticity. Trends Cogn Sci 2010;14(8):365–75.
  36. Barkeley RA. Etiologies of ADHD. In: Barkeley RA, ed. Attention-deficit Hyperactivity Disorder: A Handbook for Diagnosis and Treatment, 4th edn. New York, NY: Guilford Press, 2015.
  37. Shaw P, Eckstrand K, Sharp W, et al. Attention-deficit/hyperactivity disorder is characterized by a delay in cortical maturation. Proc Natl Acad Sci USA 2007;104(49):19649–54.
  38. AAP Subcommittee on ADHD; Steering Committee on Quality Improvement and Management, Wolraich M, et al. ADHD: Clinical practice guideline for the diagnosis, evaluation, and treatment of attention-deficit/hyperactivity disorder in children and adolescents. Pediatrics 2011;128(5):1007–22.
  39. Pliszka S; AACAP Work Group on Quality Issues. Practice parameter for the assessment and treatment of children and adolescents with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2007;46(7):894–921.
  40. McGoey KE, DuPaul GJ, Haley E, Shelton TL. Parent and teacher ratings of attention-deficit/hyperactivity disorder in preschool: The ADHD rating scale-IV preschool version. J Psychopathol Behav Assess 2007;29(4):269–76.
  41. Bonati M, Reale L, Zanetti M, et al. A regional ADHD center-based network project for the diagnosis and treatment of children with ADHD. J Atten Disord 2015;pii:1087054715599573 (Epub ahead of print).
  42. Ouyang L, Fang X, Mercy J, Perou R, Grosse SD. Attention-deficit/hyperactivity disorder symptoms and child maltreatment: A population-based study. J Pediatr 2008;153(6):851–6.
  43. Williams AE, Giust JM, Kronenberger WG, Dunn DW. Epilepsy and attention-deficit hyperactivity disorder: Links, risks, and challenges. Neuropsychiatr Dis Treat 2016;12:287–96.
  44. Lo-Castro A, D’Agati E, Curatolo P. ADHD and genetic syndromes. Brain Dev 2011;33(6):456–61.
  45. Siegel MS, Smith WE. Psychiatric features in children with genetic syndromes: Toward functional phenotypes. Child Adolesc Psychiatr Clin N Am 2010;19(2):229–61, viii.
  46. Templer AK, Titus JB, Gutmann DH. A neuropsychological perspective on attention problems in neurofibromatosis type 1. J Atten Disord 2013;17(6):489–96.
  47. Sullivan K, Hatton D, Hammer J, et al. ADHD symptoms in children with FXS. Am J Med Genet A 2006;140(21):2275–88.
  48. D’Agati E, Moavero R, Cerminara C, Curatolo P. Attention-deficit hyperactivity disorder (ADHD) and tuberous sclerosis complex. J Child Neurol 2009;24(10):1282–7.
  49. Canadian Interorganizational Steering Group for Speech-Language Pathology and Audiology. Canadian Guidelines on Auditory Processing Disorder in Children and Adults: Assessment and Intervention, December 2012: www.cisg-gdci.ca (Accessed January 24, 2018).
  50. Bailey T. Beyond DSM: The role of auditory processing in attention and its disorders. Appl Neuropsychol Child 2012;1(2):112–20.
  51. Larson K, Russ SA, Kahn RS, Halfon N. Patterns of comorbidity, functioning, and service use for US children with ADHD, 2007. Pediatrics 2011;127(3):462–70.
  52. Brown TE, ed. ADHD Comorbidities: Handbook for ADHD Complications in Children and Adults. Arlington, VA: APA, 2009.
  53. Rommelse NN, Altink ME, Fliers EA, et al. Comorbid problems in ADHD: Degree of association, shared endophenotypes, and formation of distinct subtypes. Implications for a future DSM. J Abnorm Child Psychol 2009;37(6):793–804.
  54. Dunn DW, Kronenberger WG. Attention-deficit/hyperactivity disorder in children and adolescents. Neurol Clin 2003;21(4):933–40.
  55. Abramovitch A, Dar R, Mittelman A, Wilhelm S. Comorbidity between attention deficit/hyperactivity disorder and obsessive-compulsive disorder across the lifespan: A systematic and critical review. Harv Rev Psychiatry 2015;23(4):245–62.
  56. Halldorsdottir T, Ollendick TH. Comorbid ADHD: Implications for the treatment of anxiety disorders in children and adolescents. Cogn Behav Practice 2014;21(3):310–22.
  57. Boylan K, Georgiades K, Szatmari P. The longitudinal association between oppositional and depressive symptoms across childhood. J Am Acad Child Adolesc Psychiatry 2010;49(2):152–61.
  58. Biederman J, Wilens T, Mick E, et al. Is ADHD a risk factor for psychoactive substance use disorders? Findings from a four-year prospective follow-up study. J Am Acad Child Adolesc Psychiatry 1997;36(1):21–9.
  59. Mariani JJ, Levin FR. Treatment strategies for co-occurring ADHD and substance use disorders. Am J Addict 2007;16(Suppl 1):45–54; quiz 55–6.
  60. Humphreys KL, Eng T, Lee SS. Stimulant medication and substance use outcomes: A meta-analysis. JAMA Psychiatry 2013;70(7):740–9.
  61. Pidsosny IC, Virani A. Pediatric psychopharmacology update: Psychostimulants and tics—Past, present and future. J Can Acad Child Adolesc Psychiatry 2006;15(2):84–6.
  62. Lin YJ, Lai MC, Gau SS. Youths with ADHD with and without tic disorders: Comorbid psychopathology, executive function and social adjustment. Res Dev Disabil 2012;33(3):951–63.
  63. Harris SR, Mickelson EC, Zwicker JG. Diagnosis and management of developmental coordination disorder. CMAJ 2015;187(9):659–65.
  64. Brossard-Racine M, Shevell M, Snider L, Bélanger SA, Majnemer A. Motor skills of children newly diagnosed with attention deficit hyperactivity disorder prior to and following treatment with stimulant medication. Res Dev Disabil 2012;33(6):2080–7.
  65. DuPaul GJ, Gormley MJ, Laracy SD. Comorbidity of LD and ADHD: Implications of DSM-5 for assessment and treatment. J Learn Disabil 2013;46(1):43–51.
  66. Levin RL, Rawana JS. Attention-deficit/hyperactivity disorder and eating disorders across the lifespan: A systematic review of the literature. Clin Psychol Rev 2016;50:22–36.
  67. Nazar BP, Suwwan R, de Sousa Pinna CM, et al. Influence of attention-deficit/hyperactivity disorder on binge eating behaviors and psychiatric comorbidity profile of obese women. Compr Psychiatry 2014;55(3):572–8.
  68. MacMillan JA, Land M Jr, Leslie LK. Pediatric residency education and the behavioral and mental health crisis: A call to action. Pediatrics 2017;139(1):pii:e20162141.
  69. Andrews A, Mahoney W, eds. Children with School Problems: A Physician’s Manual, 2nd edn. Toronto, Ont.: John Wiley and Sons, 2012.
  70. Rappley MD. Clinical practice. Attention deficit-hyperactivity disorder. N Engl J Med 2005;352(2):165–73.
  71. Jones KL, Jones MC, del Campo M, eds. Smith’s Recognizable Patterns of Human Malformation, 7th edn. New York, NY: Elsevier, 2013.
  72. National Institute for Health and Care Excellence (NICE) Guidelines: www.nice.org.uk; updated February 2016 (Accessed January 24, 2018).
  73. Scottish Intercollegiate Guidelines Network (SIGN). Management of attention deficit and hyperkinetic disorders in children and young people: www.sign.ac.uk, 2009 (Accessed January 24, 2018).
  74. Graham J, Banaschewski T, Buitelaar J, et al.; European Guidelines Group. European guidelines on managing adverse effects of medication for ADHD. Eur Child Adolesc Psychiatry 2011;20(1):17–37.
  75. Taylor E, Dofner M, Sargant J, et al. European clinical guidelines for hyperkinetic disorder—first upgrade. Eur Child Adolesc Psychiatry 2004;13 (Suppl 1):17–30.

Disclaimer: The recommendations in this position statement do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking into account individual circumstances, may be appropriate. Internet addresses are current at time of publication.

Last updated: Oct 26 2018