- Research article
- Open Access
- Open Peer Review
Long-term neurocognitive effects of methylphenidate in patients with attention deficit hyperactivity disorder, even at drug-free status
© Huang et al.; licensee BioMed Central Ltd. 2012
- Received: 15 June 2012
- Accepted: 10 October 2012
- Published: 9 November 2012
Methylphenidate (MPH), a psycho-stimulant, is the most widely administered drug for the pharmacological management of patients with attention deficit hyperactivity disorder (ADHD). This study attempts to determine whether sustainable improvements occur in neurocognitive function among ADHD patients following 12-month treatment with MPH, at drug-free status. Whether age groups, gender or ADHD subtypes differ in neurocognitive performance during MPH treatment is also examined.
Study participants consisted of 103 ADHD patients (mean age: 9.1 ± 1.9 years old) who were drug naïve or drug free for at least 6 months. The patients were prescribed oral short-acting MPH at each dose range of 0.3–1.0 mg/kg daily. During 12 months of the study, the patients underwent the test of variables of attention (TOVA) at the baseline, month 6 and month12. Patients were instructed to not intake MPH for one week before the second and the third TOVA.
Seventy five patients completed the study. Results of this study indicated that although commission errors and response sensitivity (d’) significantly improved during MPH treatment for 12 months, omission errors, response time, response time variability and ADHD score did not. While younger ADHD patients (<9 y/o) performed better in response time, response time variability, d’ and ADHD score than older ones (≥9 y/o), the latter more significantly improved in response time than the former during 12 months of treatment. Additionally, boys improved more than girls in omission error and d’. Moreover, although ADHD subtypes significantly differed in ADHD score during the treatment, MPH treatment and ADHD subtypes did not interact with each other for all TOVA indices.
ADHD patients significantly improved in impulsivity and perceptual sensitivity, determined as TOVA, during MPH treatment for 12 months. Age and gender, yet not ADHD subtypes, appear to influence the MPH treatment effects in some indices of TOVA. A future study containing a comparison group is suggested to confirm whether the neurocognitive improvements are attributed to long-term effects of MPH or natural maturation of patients.
- Neuropsychological test
Attention deficit hyperactivity disorder (ADHD) is a common neuropsychiatric disorder among children and adolescents, affecting 3% to 10% of all school-age children . Numerous neuropsychological tests suggest that children inflicted with ADHD have significant cognitive impairments . The current Diagnostic and Statistical Manual, Fourth Edition (DSM-IV)  classifies ADHD into 3 subtypes: inattentive type, hyperactive-impulsive type and combined type, according to the predominant clinical manifestations of inattention, hyperactivity, and impulsivity. Despite the use of neuropsychological methods to identify differentiating endophenotypes among ADHD patients , whether there are distinct neuropsychological deficits between ADHD subtypes is a contentious issue [5–7].
Methylphenidate (MPH), a psycho-stimulant, is the most widely administered drug for the pharmacological management of ADHD patients . The pharmacological profile acts in dual mechanisms by inhibiting the re-uptake of dopamine and norepinephrine . MPH exerts treatment effects for both behavioral and cognitive dimensions in ADHD patients [10, 11]. Numerous studies indicate that various domains of neurocognitive function are enhanced under acute MPH challenge in ADHD patients [12–15]. As is generally assumed, behavioral symptoms or neurocognitive impairment of ADHD patients returns immediately when the drug effect diminishes. However, some studies have investigated the neurocognitive effects over long-term MPH treatment, with a lack of consensus in those findings. The pilot study of Aggarwal and Lillystone indicated that the commission errors (yet not omission errors, response time or variability) significantly ameliorated after stimulant medication therapy at least for 12 months . Konrad et al. demonstrated that children with ADHD did not substantially improve in executive control performance after long-term MPH treatment . However, that study was limited by a small sample size. Moreover, Zhang et al. noted that intelligence quotient of ADHD patients significantly increased after 6 months of MPH treatment . In sum, whether long-term prescription of MPH enhances neurocognitive performance in ADHD patients remains unclear.
The treatment effects are diverse among ADHD patients, with some studies attempting to determine the predictors of treatment outcome [19, 20]. Exactly how MPH affects the neuropsychological profiles between subtypes of ADHD patients still remains a contentious issue. Several studies demonstrated that MPH enhanced cognitive performance equally in patients with ADHD-combined type and ADHD-inattentive type [21–23]. However, other studies demonstrated that patients with ADHD-combined type significantly improved in behavioral symptoms  and executive function performance . Furthermore, although some cross-sectional studies indicated that age and gender were associated with the neurocognitive functions in ADHD patients [26, 27], whether these factors influence the long-term treatment effects of MPH remains unclear.
Therefore, this study attempts to determine whether neurocognitive function among ADHD patients improve in a sustainable manner during 12 months of treatment with MPH, at drug-free status. In addition to the main purpose, we also conduct an explorative analysis to examine whether age groups, gender or ADHD subtypes differ in neurocognitive performance during MPH treatment.
ADHD patients between ages of 6 and 16 years old were recruited from the out-patient Child Psychiatry Department at Chang Gung Children’s Hospital (Linkou, Taiwan). The study received approval from the Institutional Review Board of Chang Gung Memorial Hospital. Written informed consent was obtained from the parents of the patients. ADHD and comorbid disorders were diagnosed by two senior child psychiatrists, based on the DSM-IV criteria  after structured interviews with the Chinese version of the Schedule for Affective Disorder and Schizophrenia for School-Age Children, epidemiologic version (K-SADS-E) . The Chinese version of K-SADS-E was developed by the Child Psychiatry Research Group in Taiwan . ADHD subjects were classified as inattentive, hyperactive-impulsive, or combined type. Patients were excluded from the study if they had a history of co-morbid pervasive developmental disorders or mental retardation, as well as those who had a history of bipolar disorder, psychosis, epilepsy, or brain injury. Included patients were either newly diagnosed with ADHD or had an existing diagnosis, yet had not taken ADHD medication during the previous 6 months or longer.
Neurocognitive function of ADHD patients was assessed using the test of variables of attention (TOVA)-Visual , which is a computerized, continuous performance test comprising a target stimulus and a non-target stimulus. Experienced child psychologists conducted TOVA with individual subjects in a room dedicated to reducing variability in testing conditions.
The TOVA stimuli are coloured squares with a small black square within, which is adjacent to either the top or the bottom edge. The squares with a small inner square near the top edge are designated targets, and the ones with the small squares near the bottom edge are non-targets. The stimuli appear individually and are presented randomly, based on a determined ratio. The tested subject was instructed to immediately press a button after seeing a target and does not respond when a non-target is presented. The test lasted 22.6 minutes and is preceded by a practice session for 2.5 minutes. Two visual stimuli appeared 648 times. The TOVA was reported to achieve satisfactory levels of reliability and concurrent validity in Taiwanese children with ADHD . The indices measured in the TOVA include the following:
Omission errors: this score is evaluated as the failure to respond to the target stimulus. Omission error scores are presented as percentages and are considered to be a measure of inattention.
Commission errors: this score is measured as an inappropriate response to the non-target stimulus. Commission error scores are presented as percentages and are considered to reflect impulsivity or disinhibition.
Response time (in msec): this score is determined as the average of the correct response times. This score denotes response latency in information processing and motor response speed.
Response time variability: this score is evaluated as the standard deviation of the mean of correct response times. It is a measure of the subject’s inconsistency in response times.
Response sensitivity (d’): this score is a response sensitivity score reflecting the ratio of the hit rate to false alarm rate. This score refers to the accuracy of target and non-target discrimination and is interpreted as a measure of perceptual sensitivity.
ADHD score: this score is a composite score generated by the TOVA program. The score is calculated by comparing an individual’s performance on the TOVA to those of an ADHD sample collected by the authors of the TOVA. The score describes how similar an individual’s performance is to the ADHD profile.
Each subject performed the TOVA 3 times. At the first TOVA (month 0), all subjects were drug naïve or had not taken medication for ADHD during the previous 6 months or longer. Subsequently, ADHD patients were prescribed oral short-acting methylphenidate (MPH) twice or three times daily at each dose range of 0.3–1.0 mg/kg, based on the severity of their clinical symptoms as well as their age, height, and body weight. Concomitant medications were prohibited. Patient care was performed based on their usual practice at the out-patient services of the child psychiatry department. There was no additional behavioral therapy or family therapy provided during the period of study. Drug compliance at each visit was confirmed according to the reports of patients’ caregivers.
The second and third TOVA were performed at the 6th and 12th month after treatment with MPH, respectively. Patients were instructed to not intake MPH for one week before the second and the third TOVA. The TOVA tests were compared before treatment, 6 months and 12 months after MPH treatment.
Data were analyzed using the statistical software package SPSS, version 16.0 (SPSS Inc., Chicago, IL, USA). Variables are presented as either the mean (standard deviation) or frequency. Two-tailed p values of <0.05 were considered statistically significant.
The TOVA results were reported as standard deviations, which indicated the extent of deviation from the norm. Variables between ADHD subtypes at baseline were compared using the Fisher’s Exact Test and Kruskal Wallis Test. Missing data at the 6th and 12th months were accounted for by using the method of last observation carried forward (LOCF). The longitudinal data were analyzed using a linear mixed model, with the maximum likelihood estimation method and auto-regression covariance matrix, as the primary analytic strategy. To examine the trends of neuro-cognitive function under MPH treatment within 12 months, the dependent variables were set as the indices in TOVA. The age of patients was divided into a categorical variable based on the median age of 9. This study also investigated the extent of the differences in changes of performance in TOVA between age groups, gender and ADHD subtypes, also by the linear mixed model. The hypothesis that a differential change occurs in dependent measures over 12 months is supported by significant interactions of MPH treatment × age, gender or ADHD subtypes.
Age, gender and performance in TOVA for children with ADHD between subtypes at baseline
Inattentive type (n = 54)
Hyperactive-impulsive type (n = 5)
Combined type (n = 44)
Gender (female/male), n (%)
14 (25.9)/40 (74.1)
0 (0)/5 (100)
7 (15.9)/37 (84.1)
Response time variability
Response sensitivity (d’)
Among the 103 ADHD patients at the initial visit, 75 patients remained in the study at month 6 and month 12. The mean dose of MPH of the 75 patients at the endpoint is 19.8 ± 13.2 mg. Among the 28 drop-out patients, 10 patients withdrawal of consent, and 18 patients lost of follow up. Comparing the remaining patients with the drop-out patients, there were no significant differences in demographic characteristics (age: t = 0.16, p = 0.877; gender: χ 2 = 0.33, p = 0.758; ADHD subtypes: χ 2 = 0.24, p = 0.807) and performances in TOVA (omission errors: t = 0.79, p = 0.434; commission errors: t = −0.37, p = 0.709; response time: t = −0.49, p = 0.624; response time variability: t = −1.95, p = 0.054; response sensitivity (d’) : t = −0.68, p = 0.496; ADHD score: t = −1.25, p = 0.215).
TOVA performance for patients with ADHD at baseline, and at months 6 and month 12 after methylphenidate treatment
Month 0 (N = 103)
Month 6 (N = 75)
Month 12 (N = 75)
Month 12 > Month 0 **
Response time variability
Response sensitivity (d’)
Month 6 > Month 0 **
The effects of age groups, gender, ADHD subtypes and methylphenidate (MPH) treatment on each index of TOVA
Response time variability
Response sensitivity (d’)
Age (<9 years vs. ≥9 years)
Gender (female vs. male)
ADHD subtypes a
Age × MPH treatment
Gender × MPH treatment
ADHD subtypes × MPH treatment
This study demonstrates that commission errors and d’ significantly improved during MPH treatment, while the other indices of TOVA did not. This finding suggests that ADHD patients have an improved ability of impulse control and perceptual sensitivity, but not sustained attention or response speed, under long-term MPH treatment. Our previous study has established that one dose of MPH produced more effects on impulsivity than on inattention in children with ADHD . A previous study involving the long-term effects of MPH on TOVA performance, in which participants were also tested off the drug, also demonstrated a compatible finding . Similarly, a 6-month open-label study showed that children with ADHD receiving MPH improved more in impulsivity dimensions than in attention dimensions of the Conners’ Continuous Performance Test, which were tested while on the medication . Moreover, another study found that neurocognitive effects of MPH were more prominent on tasks without an executive function component than with an executive function component . In summary, the stimulant-related cognitive enhancements may be discrepant in different dimensions of neurocognitive function.
Results of this study also suggest that the effects of MPH on two TOVA indices can be sustained for at least 12 months, even when ADHD patients are tested at drug-free status. These results support the conclusion of a recent review that MPH is continuously effective for an extended period . Some long-term follow-up studies for ADHD patients have found that treatment with medication in childhood may improve some measures of academic achievements [32, 33]. Biederman et al. demonstrated that non-medicated ADHD patients have a more pervasive pattern of cognitive deficits than medicated ADHD ones . In contrast to the studies in self-selected naturalistic settings, the Multimodal Treatment study of children with ADHD (MTA), which conducted with a randomized-controlled design, reported contradictory findings. Although the benefits of stimulant medications persisted for 14 months , the earlier advantage of having continuous intake of medication for 14 months is no longer apparent at the 36-month follow-up . Therefore, the likelihood that selection bias inflated the long-term neurocognitive effects of MPH in previous studies can not be ruled out. Further research is warranted to clarify whether the MPH-related cognitive enhancements exist during long-term treatment, even when the drug effect diminishes.
This study also examines whether differences occur in neurocognitive performance between age, gender and ADHD subtypes during MPH treatment. Analytical results indicate that older patients (≥9 y/o) performed worse in many indices of TOVA than younger ones (<9 y/o), and the older patients more significantly improved in response time during treatment. However, there were differences in some indices of TOVA at baseline between age groups (data not shown). The effect of age in neurocognitive performance is not necessarily implying that older patients gained more from MPH treatment than younger ones, and might be just a regression to the mean. Moreover, male patients more significantly improved in omission error and d’ than female ones during MPH treatment. Despite similar findings found in a previous study on the acute effects of MPH on TOVA performance , a recent study found that gender groups did not differ in neuropsychological performance modulated by MPH . The current studies regarding the interaction of age, gender and MPH treatment effects are still scarce. ADHD symptoms or sample selection may confound differences in neurocognitive effects between age or gender groups. Further study is thus warranted on whether age and gender serve as predictors of MPH-related cognitive improvements.
Results of this study further demonstrate that patients with ADHD-inattentive type had a higher ADHD composite score in TOVA than patients with hyperactive-impulsive or combined type. Meanwhile, MPH treatment and ADHD subtypes did not interact with each other in all TOVA indices. Subjects with hyperactive or combined type of ADHD show more significantly improve in commission errors than those with inattentive ADHD after one dose of MPH . However, several longitudinal studies found that ADHD subtypes do not differ in MPH enhanced cognitive performance [21–23]. We can infer that the diversity of results from studies of MPH effects on the neuropsychological profiles of subtypes of ADHD patients may reflect variations in methodology. This study does not support discriminated effectiveness in terms of neurocognitive performance between ADHD subtypes.
Despite its contributions, this study has certain limitations. First, a comparison group was absent. Exactly how age-related decline in ADHD-symptoms and social and environmental influence affects TOVA performance could thus not be controlled. Longitudinal studies have shown that there is a natural decline of symptoms with age, particularly the symptom of hyperactivity and impulsivity, in children with ADHD . Therefore, the improvements in commission errors and d’ observed in our study might be accounted for an age-related maturation. Second, the subjects performed TOVA 3 times, with 6-month time intervals between each TOVA tests. Practice effects may be minimal, yet could not be completely ruled out. Third, the treatment procedure of MPH was not strictly standardized, and drug adherence was not measured systematically. Furthermore, a high rate of early termination, variation of MPH dosage and possible inadequate drug adherence may influence the estimation for the extent to which MPH affects TOVA performance.
Using TOVA as a neuropsychological assessment scheme revealed that impulsivity and perceptual sensitivity in ADHD patients significantly improved during MPH treatment for 12 months. Age and gender, yet not ADHD subtypes, appear to influence the MPH treatment effects in some indices of TOVA. A future study containing a comparison group is suggested to confirm whether the neurocognitive improvements are attributed to long-term effects of MPH or natural maturation of patients.
This study was funded by the grant (CMRPG260181) from the Chang Gung Memorial Hospital, Taiwan. Ted Knoy is appreciated for his editorial assistance.
- Gau SS, Chong MY, Chen TH, Cheng AT: A 3-year panel study of mental disorders among adolescents in Taiwan. Am J Psychiatry. 2005, 162: 1344-1350. 10.1176/appi.ajp.162.7.1344.View ArticlePubMedGoogle Scholar
- Nigg JT: Neuropsychologic theory and findings in attention-deficit/hyperactivity disorder: the state of the field and salient challenges for the coming decade. Biol Psychiatry. 2005, 57: 1424-1435. 10.1016/j.biopsych.2004.11.011.View ArticlePubMedGoogle Scholar
- American Psychiatric Association: Diagnostic and Statistical Manual of Mental disorders In 4 (ed), DSM-IV-TR (Text Revision). 2000, Washington DC: American Psychiatric AssociationGoogle Scholar
- Solanto MV, Gilbert SN, Raj A, Zhu J, Pope-Boyd S, Stepak B, Vail L, Newcorn JH: Neurocognitive functioning in AD/HD, predominantly inattentive and combined subtypes. J Abnorm Child Psychol. 2007, 35: 729-744. 10.1007/s10802-007-9123-6.View ArticlePubMedPubMed CentralGoogle Scholar
- Chhabildas N, Pennington BF, Willcutt EG: A comparison of the neuropsychological profiles of the DSM-IV subtypes of ADHD. J Abnorm Child Psychol. 2001, 29: 529-540. 10.1023/A:1012281226028.View ArticlePubMedGoogle Scholar
- Nigg JT, Blaskey LG, Huang-Pollock CL, Rappley MD: Neuropsychological executive functions and DSM-IV ADHD subtypes. J Am Acad Child Adolesc Psychiatry. 2002, 41: 59-66. 10.1097/00004583-200201000-00012.View ArticlePubMedGoogle Scholar
- Goth-Owens TL, Martinez-Torteya C, Martel MM, Nigg JT: Processing speed weakness in children and adolescents with non-hyperactive but inattentive ADHD (ADD). Child Neuropsychol. 2010, 16: 577-591. 10.1080/09297049.2010.485126.View ArticlePubMedPubMed CentralGoogle Scholar
- Swanson J, Baler RD, Volkow ND: Understanding the effects of stimulant medications on cognition in individuals with attention-deficit hyperactivity disorder: a decade of progress. Neuropsychopharmacology. 2011, 36: 207-226. 10.1038/npp.2010.160.View ArticlePubMedGoogle Scholar
- Wilens TE: Effects of methylphenidate on the catecholaminergic system in attention-deficit/hyperactivity disorder. J Clin Psychopharmacol. 2008, 28: S46-S53. 10.1097/JCP.0b013e318173312f.View ArticlePubMedGoogle Scholar
- Huang YS, Tsai MH: Long-term outcomes with medications for attention-deficit hyperactivity disorder: current status of knowledge. CNS Drugs. 2011, 25: 539-554. 10.2165/11589380-000000000-00000.View ArticlePubMedGoogle Scholar
- Bidwell LC, McClernon FJ, Kollins SH: Cognitive enhancers for the treatment of ADHD. Pharmacol Biochem Behav. 2011, 99: 262-274. 10.1016/j.pbb.2011.05.002.View ArticlePubMedPubMed CentralGoogle Scholar
- Pietrzak RH, Mollica CM, Maruff P, Snyder PJ: Cognitive effects of immediate-release methylphenidate in children with attention-deficit/hyperactivity disorder. Neurosci Biobehav Rev. 2006, 30: 1225-1245. 10.1016/j.neubiorev.2006.10.002.View ArticlePubMedGoogle Scholar
- Huang YS, Chao CC, Wu YY, Chen YY, Chen CK: Acute effects of methylphenidate on performance during the Test of Variables of Attention in children with attention deficit/hyperactivity disorder. Psychiatry Clin Neurosci. 2007, 61: 219-225. 10.1111/j.1440-1819.2007.01653.x.View ArticlePubMedGoogle Scholar
- Pollak Y, Shomaly HB, Weiss PL, Rizzo AA, Gross-Tsur V: Methylphenidate effect in children with ADHD can be measured by an ecologically valid continuous performance test embedded in virtual reality. CNS Spectr. 2010, 15: 125-130.PubMedGoogle Scholar
- Rubia K, Halari R, Cubillo A, Mohammad AM, Brammer M, Taylor E: Methylphenidate normalises activation and functional connectivity deficits in attention and motivation networks in medication-naive children with ADHD during a rewarded continuous performance task. Neuropharmacology. 2009, 57: 640-652. 10.1016/j.neuropharm.2009.08.013.View ArticlePubMedGoogle Scholar
- Aggarwal A, Lillystone D: A follow-up pilot study of objective measures in children with attention deficit hyperactivity disorder. J Paediatr Child Health. 2000, 36: 134-138. 10.1046/j.1440-1754.2000.00464.x.View ArticlePubMedGoogle Scholar
- Konrad K, Neufang S, Fink GR, Herpertz-Dahlmann B: Long-term effects of methylphenidate on neural networks associated with executive attention in children with ADHD: results from a longitudinal functional MRI study. J Am Acad Child Adolesc Psychiatry. 2007, 46: 1633-1641. 10.1097/chi.0b013e318157cb3b.View ArticlePubMedGoogle Scholar
- Zhang L, Jin X, Zhang Y: Effect of methylphenidate on intelligence quotient scores in Chinese children with attention-deficit/hyperactivity disorder. J Clin Psychopharmacol. 2011, 31: 51-55. 10.1097/JCP.0b013e3182060f3f.View ArticlePubMedGoogle Scholar
- van der Oord S, Prins PJ, Oosterlaan J, Emmelkamp PM: Treatment of attention deficit hyperactivity disorder in children. Predictors of treatment outcome. Eur Child Adolesc Psychiatry. 2008, 17: 73-81. 10.1007/s00787-007-0638-8.View ArticlePubMedGoogle Scholar
- Buitelaar JK, Kooij JJ, Ramos-Quiroga JA, Dejonckheere J, Casas M, van Oene JC, Schauble B, Trott GE: Predictors of treatment outcome in adults with ADHD treated with OROS(R) methylphenidate. Prog Neuropsychopharmacol Biol Psychiatry. 2011, 35: 554-560. 10.1016/j.pnpbp.2010.12.016.View ArticlePubMedGoogle Scholar
- O’Driscoll GA, Depatie L, Holahan AL, Savion-Lemieux T, Barr RG, Jolicoeur C, Douglas VI: Executive functions and methylphenidate response in subtypes of attention-deficit/hyperactivity disorder. Biol Psychiatry. 2005, 57: 1452-1460. 10.1016/j.biopsych.2005.02.029.View ArticlePubMedGoogle Scholar
- Solanto M, Newcorn J, Vail L, Gilbert S, Ivanov I, Lara R: Stimulant drug response in the predominantly inattentive and combined subtypes of attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2009, 19: 663-671. 10.1089/cap.2009.0033.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang LJ, Huang YS, Chiang YL, Hsiao CC, Shang ZY, Chen CK: Clinical symptoms and performance on the continuous performance test in children with attention deficit hyperactivity disorder between subtypes: a natural follow-up study for 6 months. BMC Psychiatry. 2011, 11: 65-10.1186/1471-244X-11-65.View ArticlePubMedPubMed CentralGoogle Scholar
- Gorman EB, Klorman R, Thatcher JE, Borgstedt AD: Effects of methylphenidate on subtypes of attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry. 2006, 45: 808-816. 10.1097/01.chi.0000214191.57993.dd.View ArticlePubMedGoogle Scholar
- Vance AL, Maruff P, Barnett R: Attention deficit hyperactivity disorder, combined type: better executive function performance with longer-term psychostimulant medication. Aust N Z J Psychiatry. 2003, 37: 570-576. 10.1046/j.1440-1614.2003.01238.x.View ArticlePubMedGoogle Scholar
- Barnett R, Maruff P, Vance A, Luk ES, Costin J, Wood C, Pantelis C: Abnormal executive function in attention deficit hyperactivity disorder: the effect of stimulant medication and age on spatial working memory. Psychol Med. 2001, 31: 1107-1115.View ArticlePubMedGoogle Scholar
- Gross-Tsur V, Goldzweig G, Landau YE, Berger I, Shmueli D, Shalev RS: The impact of sex and subtypes on cognitive and psychosocial aspects of ADHD. Dev Med Child Neurol. 2006, 48: 901-905. 10.1017/S0012162206001976.View ArticlePubMedGoogle Scholar
- Kaufman J, Birmaher B, Brent D, Rao U, Flynn C, Moreci P, Williamson D, Ryan N: Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data. J Am Acad Child Adolesc Psychiatry. 1997, 36: 980-988. 10.1097/00004583-199707000-00021.View ArticlePubMedGoogle Scholar
- Gau SF, Soong WT: Psychiatric comorbidity of adolescents with sleep terrors or sleepwalking: a case–control study. Aust N Z J Psychiatry. 1999, 33: 734-739. 10.1080/j.1440-1614.1999.00610.x.View ArticlePubMedGoogle Scholar
- Test of Variables of Attention. Edited by: Greenberg LM. 1996, Los Alamitos: University Attention Disorder IncGoogle Scholar
- Wu YY, Huang YS, Chen YY, Chen CK, Chang TC, Chao CC: Psychometric study of the test of variables of attention: preliminary findings on Taiwanese children with attention-deficit/hyperactivity disorder. Psychiatry Clin Neurosci. 2007, 61: 211-218. 10.1111/j.1440-1819.2007.01658.x.View ArticlePubMedGoogle Scholar
- Hechtman L, Abikoff H, Klein RG, Weiss G, Respitz C, Kouri J, Blum C, Greenfield B, Etcovitch J, Fleiss K, Pollack S: Academic achievement and emotional status of children with ADHD treated with long-term methylphenidate and multimodal psychosocial treatment. J Am Acad Child Adolesc Psychiatry. 2004, 43: 812-819. 10.1097/01.chi.0000128796.84202.eb.View ArticlePubMedGoogle Scholar
- Powers RL, Marks DJ, Miller CJ, Newcorn JH, Halperin JM: Stimulant treatment in children with attention-deficit/hyperactivity disorder moderates adolescent academic outcome. J Child Adolesc Psychopharmacol. 2008, 18: 449-459. 10.1089/cap.2008.021.View ArticlePubMedPubMed CentralGoogle Scholar
- Biederman J, Seidman LJ, Petty CR, Fried R, Doyle AE, Cohen DR, Kenealy DC, Faraone SV: Effects of stimulant medication on neuropsychological functioning in young adults with attention-deficit/hyperactivity disorder. J Clin Psychiatry. 2008, 69: 1150-1156. 10.4088/JCP.v69n0715.View ArticlePubMedGoogle Scholar
- The MTA Cooperative Group: A 14-month randomized clinical trial of treatment strategies for attention-deficit/hyperactivity disorder. The MTA Cooperative Group. Multimodal Treatment Study of Children with ADHD. Arch Gen Psychiatry. 1999, 56: 1073-1086. 10.1001/archpsyc.56.12.1073.View ArticleGoogle Scholar
- Jensen PS, Arnold LE, Swanson JM, Vitiello B, Abikoff HB, Greenhill LL, Hechtman L, Hinshaw SP, Pelham WE, Wells KC, Conners CK, Elliott GR, Epstein JN, Hoza B, March JS, Molina BS, Newcorn JH, Severe JB, Wigal T, Gibbons RD, Hur K: 3-year follow-up of the NIMH MTA study. J Am Acad Child Adolesc Psychiatry. 2007, 46: 989-1002. 10.1097/CHI.0b013e3180686d48.View ArticlePubMedGoogle Scholar
- Gunther T, Herpertz-Dahlmann B, Konrad K: Sex differences in attentional performance and their modulation by methylphenidate in children with attention-deficit/hyperactivity disorder. J Child Adolesc Psychopharmacol. 2010, 20: 179-186. 10.1089/cap.2009.0060.View ArticlePubMedGoogle Scholar
- Polanczyk G, Rohde LA: Epidemiology of attention-deficit/hyperactivity disorder across the lifespan. Curr Opin Psychiatry. 2007, 20: 386-392. 10.1097/YCO.0b013e3281568d7a.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-244X/12/194/prepub
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