Psychiatry Investig Search

CLOSE


Psychiatry Investig > Volume 23(5); 2026 > Article
Kim, Ahn, Park, Kim, Kim, and Kim: Comparison of the K-WPPSI-IV Profiles Between Children With Attention-Deficit/Hyperactivity Disorder and Children With Autism Spectrum Disorder: A Retrospective Study

Abstract

Objective

This study aimed to: 1) compare the cognitive profiles of children with autism spectrum disorder (ASD), attention-deficit/hyperactivity disorder (ADHD), and comorbid ADHD+ASD with typically developing (TD) children; and 2) examine the associations between indices of the Korean Wechsler Preschool and Primary Scale of Intelligence-Fourth Edition (K-WPPSI-IV) and other clinical assessments.

Methods

A retrospective chart review was conducted for 233 children aged 4-6 years who visited Asan Medical Center between April 2017 and September 2024. The study population included 74 children with ADHD+ASD, 46 with ASD, 84 with ADHD, and 29 TD children. The full-scale intellectual quotient, 5 indices, and 12 subtest scores of the K-WPPSI-IV were compared using analysis of covariance, adjusting for age. Correlations were analyzed between the K-WPPSI-IV indices and the symptom severity measures: Childhood Autism Rating Scale (CARS), ADHD Rating Scale (ARS), and Advanced Test of Attention (ATA) across the full population.

Results

Children with ADHD+ASD, ASD, and ADHD scored significantly lower than TD peers on the Working Memory Index (WMI; p<0.001) and Processing Speed Index (PSI; p<0.001). The ASD group showed significantly lower scores than the ADHD group in Vocabulary (p=0.001) and Comprehension (p<0.001). CARS scores negatively correlated with the WMI, while ATA negatively correlated with the PSI.

Conclusion

Both ADHD and ASD are associated with relative weakness in processing speed and working memory. Furthermore, ASD is characterized by additional difficulties in verbal abilities. These findings highlight distinct and overlapping cognitive features across these disorders.

INTRODUCTION

Attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) are two of the most common neurodevelopmental disorders typically emerging in early childhood, with global prevalence rates estimated at 5% to 8% and 1% to 4%, respectively [1,2]. In the South Korean population, these rates have been reported to be 8.5% and 2.6%, respectively [3,4]. ADHD and ASD are significant public health concerns, as they are lifelong conditions that often persist into adulthood. These disorders exert long-term impacts not only on the individuals’ functional outcomes but also on the quality of life and well-being of their families, requiring continuous support and comprehensive management across the lifespan [5,6]. ADHD is primarily characterized by inattention, hyperactivity, and impulsivity [7], symptoms that frequently contribute to academic underachievement, difficulty in school adjustment, and life-long economic and social problems [8-10]. In contrast, ASD is characterized by persistent difficulties in social communication and interaction, along with restricted and repetitive behaviors [7], often resulting in social withdrawal, loneliness, and limited participation in group activities [11]. Consequently, children with ADHD and/or ASD are at a heightened risk for bullying and emotional difficulties, including anxiety, depression, and low self-esteem [8,11,12].
Although ADHD and ASD are classified as distinct diagnostic entities, they frequently co-occur. Studies have shown that 50%-70% of children with ASD also meet the diagnostic criteria for ADHD [13], and 21%-30% of children with ADHD exhibit significant autistic traits [14]. Children with comorbid ADHD and ASD often demonstrate additive difficulties across behavioral, cognitive, and social domains, leading to more complex clinical presentations and more affected functional outcomes than those with either condition alone [14,15].
Both disorders are associated with cognitive dysfunction, although their profiles differ. ADHD is strongly linked to relatively weaker executive functions, with differences in attention regulation, working memory, cognitive flexibility, and planning [16]. In contrast, ASD is more commonly associated with cognitive rigidity, difficulty in set-shifting, and a detail-focused rather than holistic cognitive style [17,18]. Nonetheless, overlapping difficulties—particularly in processing speed, working memory, and response inhibition—have been observed in both groups [19,20].
Intelligence quotient (IQ) tests are widely used to assess general intellectual functioning and to delineate cognitive strengths and weaknesses [21]. In individuals with ASD, IQ has consistently emerged as one of the strongest predictors of long-term functional outcomes, often surpassing core symptom severity in its association with adaptive behavior [22]. For children with ADHD, a detailed IQ profile is valuable as it helps identify specific weaknesses and strengths that require targeted educational support [23,24]. The IQ profile can thus serve as a diagnostic aid for ASD and a guide for individualized ADHD interventions.
Several studies have examined the cognitive profiles of children with ADHD and ASD using various intelligence test batteries. A common finding is that children with ASD and ADHD exhibit lower functioning on the Working Memory Index (WMI) and Processing Speed Index (PSI) of intelligence tests [25,26]. However, further distinctions emerge between the two disorders in their IQ profiles. Children with ASD often present with a “spiky” profile on the Wechsler scales, typically showing relative strengths in the Block design subtest alongside weaknesses in the Comprehension subtest [17,27]. In contrast, children with ADHD generally demonstrate weaknesses more specifically in subtests related to working memory and processing speed [23,25,28].
Given these shared and divergent cognitive profiles associated with ASD and ADHD, it is helpful to understand how the distinct symptom patterns of ASD and ADHD are associated with performance across IQ profiles. Previous research has established specific links between ASD or ADHD symptomatology and cognitive abilities. Previous studies on ASD suggested that lower verbal abilities relative to nonverbal abilities are associated with greater communication and social difficulties [29,30]. Similarly, studies conducted on children with ADHD also demonstrated an association between ADHD symptoms and weaknesses in both working memory and processing speed [29,30]. However, those studies did not consider the impact of comorbid ADHD and ASD. Therefore, research is needed to examine the relationship between ASD or ADHD symptoms and IQ profiles while accounting for the effects of comorbid ADHD and ASD.
Most existing research regarding ADHD and ASD has focused on school-aged children or adults, with limited data available on preschool-aged children, a population for whom early identification of cognitive weaknesses is especially important to improving cognitive and academic outcomes [31]. This critical period is characterized by high neuroplasticity, meaning early identification allows for immediate, targeted intervention, potentially maximizing long-term outcomes [32]. Despite the critical need for early and accurate assessment in this population, little is known about the cognitive profiles of children with comorbid ADHD and ASD. One contributing factor to this disparity is the challenge of accurately assessing cognitive function in young children, where factors like test-taking cooperation, short attention spans, and the inherent instability of cognitive scores may complicate data collection and interpretation [33].
This study therefore aims to: 1) compare the IQ profiles of preschool children diagnosed with ADHD, ASD, comorbid ADHD and ASD, and TD peers, using the Korean Wechsler Preschool and Primary Scale of Intelligence-Fourth Edition (K-WPPSI-IV)—a widely used tool for assessing cognitive abilities in preschool-aged children in Korea [34]; and 2) examine the associations between IQ profiles and clinical measures commonly used to assess ADHD and ASD symptoms.
Based on previous research, it is hypothesized that children with ADHD and those with ASD will share weaknesses in the PSI. Additionally, it is hypothesized that children with ASD will show further weakness in the Comprehension subtest, while those with ADHD will show specific weaknesses in the working memory subtests. Furthermore, it is hypothesized that ASD symptoms will correlate negatively with the Verbal Comprehension Index (VCI), and that ADHD symptoms will relate negatively with the WMI and PSI.

METHODS

Study design and population

This retrospective chart review included 233 children who were administered the K-WPPSI-IV between April 2017 and September 2024. The participants comprised 204 children with ADHD and/or ASD who visited the Department of Child and Adolescent Psychiatry at Asan Medical Center and 29 children of the control group were recruited through an internet bulletin board at the Asan Medical Center. The children were categorized into four diagnostic groups based on Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) criteria: 1) ADHD+ASD (comprising children with both disorders), 2) ASD, 3) ADHD, and 4) typically developing (TD) (children without a diagnosis of either condition).
The inclusion criteria were: 1) aged between 4 and 6 years and 2) completion of the K-WPPSI-IV.
Exclusion criteria were: 1) presence of physical or neurological conditions that could affect cognitive function (e.g., epilepsy); 2) full-scale IQ (FSIQ) below 70; 3) current use of ADHD medications (e.g., methylphenidate) at the time of assessment; 4) comorbid mood, anxiety, or tic disorders requiring pharmacological treatment; 5) diagnosis of a psychotic disorder; and 6) known genetic syndromes.
This study was approved by the Institutional Review Board (IRB) of Asan Medical Center (IRB No. 2024-1436), and the requirement for informed consent was waived due to the retrospective nature of the study.

Measures

The IQ profile is evaluated using the K-WPPSI-IV. Autism symptoms are assessed via the Childhood Autism Rating Scale (CARS), and ADHD symptoms are comprehensively evaluated using the parent-rated ADHD Rating Scale (ARS) and the child-administered neuropsychological test, Advanced Test of Attention (ATA). Including both the parent-rated scale (ARS) and the objective test (ATA) for attention is crucial for assessing attention problems more comprehensively. Parent ratings capture the pervasiveness and clinical significance of symptoms in natural settings. Conversely, the neuropsychological test provides objective quantification of underlying cognitive weakness, free from rater bias. While acknowledging that using two overlapping constructs presents a potential for collinearity, this specific analytical approach was not utilized in the current study.

K-WPPSI-IV

IQ functioning was assessed using the K-WPPSI-IV, administered by licensed clinical psychologists trained in its administration and interpretation. The K-WPPSI-IV is standardized for children aged 2 years 6 months to 7 years 7 months, and provides an FSIQ along with five primary index scores. These indices are calculated from specific subtests: the VCI utilizes core subtests (Information, Similarities) and supplementary subtests (Comprehension, Vocabulary); the Visual Spatial Index (VSI) comprises the Block design and Object assembly subtests; the Fluid Reasoning Index (FRI) is derived from the Matrix reasoning and Picture concepts subtests; the WMI is based on the Picture memory and Zoo locations subtests; and the PSI is determined by the Bug search and Cancellation subtests. Each index yields age- and gender-standardized scores (mean=100, standard deviation [SD]=15), and higher scores indicate better cognitive abilities. The K-WPPSI-IV is widely used in both clinical and research settings, and demonstrates high inter-rater reliability (0.96-1.00) as well as robust discriminant validity across its subtests and indices among the Korean preschool children [21,34].

CARS

The CARS was completed by parents or caregivers to help differentiate ASD from other developmental disorders. It includes 15 items rated on a 4-point scale across three domains: social interaction, imitation, and body use. Higher scores reflect greater symptom severity of ASD. Specifically, a total score of 30 is typically used as the threshold for ASD [35]. The CARS has demonstrated strong inter-rater reliability (0.71), high internal consistency (0.94), and acceptable validity in the Korean population aged 2 to 36 years [36-39].

ARS

ADHD symptom severity was assessed using the ARS, which was completed by parents or caregivers. This 18-item scale includes two subscales—Inattentive and Hyperactive-Impulsive—each rated on a 4-point scale. Higher scores reflect greater symptom severity of ADHD. Specifically, 90th percentile (typically corresponding to a total score of 17-19) serves as the threshold for clinical significance in preschool-aged children [40,41]. The ARS has demonstrated acceptable internal consistency (coefficient=0.77) and age-related validity in both the Korean population and preschool aged children [40,42].

ATA

Attention and impulsivity were assessed using the ATA, a computerized continuous performance test administered by clinical psychologists. The ATA incorporates both visual and auditory tasks and generates Z-scores for four key variables: Omission errors (reflecting inattention), Commission errors (reflecting impulsivity), Response time (reflecting processing speed), and Response time variability (reflecting attention consistency). Scoring at or above 1.5 SDs (Z-scores of 1.5) from the mean of the control group is considered impaired. The test is standardized for the Korean population and has demonstrated validated psychometric properties in children aged 5 years and older [43]. While formal validation of the ATA in the preschool population remains limited by the narrow age range studied, the test is nonetheless frequently employed in clinical settings for assessing attention in this age group [44].

Statistical analysis

All statistical analyses were performed using SPSS version 26.0 for Windows (IBM Corp.). A two-tailed p-value was used for significance testing. To account for multiple comparisons, a Bonferroni-corrected significance threshold was applied: p<0.002 for analyses reported in Table 1 and p<0.003 for analyses in Table 2. Following the Mukaka’s guide [45], correlation coefficients with an absolute value of |r|>0.3 were interpreted as potentially meaningful.
Group comparisons for categorical variables were conducted using the chi-square test or Fisher’s exact test, as appropriate. Continuous variables were analyzed using one-way analysis of variance (ANOVA) or the Kruskal-Wallis test, depending on the normality and homogeneity of variance. Post hoc comparisons were performed using Scheffé’s test after ANOVA and Bonferroni correction following Kruskal-Wallis tests.
Intelligence measures were compared across groups using analysis of covariance, adjusting for age. Partial Pearson correlation analyses were used to examine associations between K-WPPSI-IV subtest scores and clinical variables, with age included as a covariate.

RESULTS

Demographics and clinical characteristics

Table 1 summarizes the demographics and clinical characteristics of the 233 study participants. Significant age differences were observed among the four groups (p<0.001), with the ASD group (n=46, median age [interquartile range, IQR]: 56 months [51-61], age range: 48-71 months) being younger than the other groups, and the ADHD group (n=84, median age [IQR]: 66 months [62.5-69.5], age range: 48-71 months) older than the ADHD+ASD group (n=74, median age [IQR] 60 months [54.5-65.5], age range: 48-71 months). TD group (n=29, median age [IQR] 62 months [57-67], age range: 48-71 months) showed no significant difference. Age was therefore controlled for in subsequent analyses. No significant differences were found in sex distribution across groups.
In terms of ADHD presentation, the ADHD+ASD group (n=74) had a higher proportion of inattentive (n=16) and combined (n=53) types, whereas the ADHD group (n=84) had more cases of hyperactive-impulsive type (n=15) and other specified ADHD (n=16) (p<0.001). No significant group differences were found for psychiatric comorbidities, except for tic disorders (p=0.005). However, the observed significance for tic disorders was lost after multiple comparison correction.

Comparison of K-WPPSI-IV profiles

Table 2 presents the results of group comparisons for the K-WPPSI-IV indices and subtests. Overall, FSIQ did not differ significantly across the four groups (p=0.084). The WMI and PSI scores were significantly lower in the ADHD+ASD (n=74), ASD (n=46), and ADHD (n=84) groups compared with the TD group (n=29), after adjusting for age (WMI, p<0.001; PSI, p<0.001).
Among the VCI subtests, two of four showed significant group differences. Particularly, the Vocabulary and Comprehension subtests were conducted for 74 children with ADHD and ASD, 46 children with ASD, 80 children with ADHD, and 23 and 22 TD children, respectively. In Vocabulary subtest, the ADHD group showed higher scores than the ASD group (p=0.001). Comprehension scores were significantly higher in ADHD group compared with the ADHD+ASD and ASD groups (p<0.001).
For WMI subtests, the TD group had significantly higher Zoo locations scores compared with all other groups (p<0.001), while Picture memory scores did not differ significantly among groups.
Among PSI subtests, Bug search scores were significantly higher in the TD group than in the ADHD+ASD and ADHD groups (p<0.001).

Correlation between K-WPPSI-IV profiles and clinical assessments

Partial Pearson correlation analyses, controlling for age, were conducted to examine the associations between K-WPPSI-IV profiles and clinical assessment measures (Table 3). The CARS scores (n=144) demonstrated significant inverse correlations with aspects of cognitive functioning. Specifically, higher severity of CARS scores was significantly associated with lower performance on the WMI (r=-0.325, p<0.001) and its subtest, Picture memory (r=-0.337, p<0.001). No meaningful correlations were observed between ARS scores and any of the K-WPPSI- IV indices or subtests. In contrast to the ARS findings, several significant associations emerged between ATA scores and cognitive performance. Weaknesses in visual attention were consistently associated with lower scores in working memory and processing speed. Specifically, visual Omission errors (n=118) were negatively correlated with the WMI (r=-0.302, p<0.001), particularly the Zoo locations subtest (r=-0.376, p<0.001), and the Bug search subtest of the PSI (r=-0.313, p<0.001). Visual Commission errors (n=118) were negatively correlated with the overall PSI (r=-0.308, p<0.001) and its Cancellation subtest (r=-0.308, p<0.001), and the Picture memory subtest of the WMI (r=-0.302, p<0.001). Visual Response time variability scores (n=118) were negatively correlated with the Cancellation subtest of the PSI (r=-0.338, p<0.001).

DISCUSSION

Our findings revealed that children with ADHD and ASD exhibited shared difficulties in working memory and processing speed, yet they differed in verbal abilities, as expected. Specifically, differences were noted on the Vocabulary and Comprehension subtests of the K-WPPSI-IV, with children with ASD scoring significantly lower than those with ADHD alone on the Comprehension subtest. Furthermore, CARS scores showed a negative correlation with WMI, while ATA scores were negatively correlated with PSI. Crucially, while these patterns are consistent with those documented in previous studies examining school-aged children [26,27,46], the novelty of our work is the demonstration of these specific profile differences within the understudied preschool-aged population. This finding provides critical new data for early differential diagnosis.
Working memory is a foundational cognitive mechanism that supports the ability to process stimuli, retrieve relevant information based on past experiences, and maintain attentional focus on ongoing tasks [47]. It also underlies core executive functions, including attention regulation, inhibition, planning, and temporal sequencing [48]. In ADHD, reduced working memory is a well-documented core neuropsychological weakness, strongly associated with behavioral challenges [23,49-51], and typically assessed using the WMI on Wechsler intelligence tests. Numerous studies have confirmed lower WMI scores in ADHD, often attributed to diminished attention [25,28]. Children with ASD also present with a distinctive profile of executive dysfunction, including difficulties with cognitive flexibility, working memory, and selective attention [52,53], which contributes to lower WMI scores [18,26]. While some research reports overlapping working memory weaknesses associated with attentional difficulties in both ADHD and ASD [54,55], other evidence suggests more pronounced spatial working memory difficulties in ADHD, potentially stemming from greater weaknesses in inhibitory control [56]. In contrast, our study found that both the ADHD and ASD groups exhibited weaknesses in working memory, while the WMI scores did not significantly differ between the ADHD, ASD, and ADHD+ASD groups. This finding was further corroborated by the significant correlations observed between the WMI and its subtests and the ATA and CARS scores, suggesting a direct link between working memory weaknesses and core symptom severity. While working memory differences are commonly observed across various neurodevelopmental disorders, they are most consistently reported as a core cognitive characteristic of ADHD [57]. Therefore, low performance in working memory may represent a shared cognitive vulnerability among preschool-aged children with ADHD and ASD. The common weaknesses in working memory across both conditions highlight that interventions focusing on executive function, including working memory, should be integrated into treatment plans for both ASD and ADHD.
As hypothesized, processing speed also emerged as a shared area of weakness in children with ADHD and ASD. Processing speed reflects the efficiency with which individuals perceive, process, and respond to stimuli [58] and is a key determinant of performance across a range of cognitive tasks [59]. Previous research has shown that children with ADHD often display reduced processing speed, particularly when cognitively underaroused, leading to slower responses and impaired output generation [60,61]. Similarly, ASD has been conceptualized as a disorder of general information processing, with relative weaknesses observed in both simple and complex cognitive tasks [62-65]. The PSI in the Wechsler scales assesses visual scanning, sustained attention, and interference control—cognitive functions that are frequently influenced in both ADHD and ASD.66 Consistent with prior studies [18,28,46,67], our results demonstrated uniformly low PSI scores across the ADHD, ASD, and ADHD+ASD groups. Furthermore, PSI scores and their subtests showed negative correlations with visual indices on the ATA, suggesting that reduced processing speed is associated with diminished visual attention capabilities. However, interpreting these shared weaknesses requires accounting for the measurement bias inherent in the K-WPPSI-IV. The substantial verbal demands of this standardized tool can confound performance in the working memory and processing speed domains for children with ASD, often resulting in lower scores that may not fully reflect their innate capacity [68,69]. Additionally, it is important to consider that reduced PSI scores have been observed in various other neurodevelopmental conditions [70], mood disorders [71], and even in states of fatigue [72]. Therefore, while reduced processing speed is common in both ADHD and ASD, they should be interpreted as a non-specific neuropsychological marker rather than a condition-specific weakness.
In terms of verbal cognitive profiles, our results showed significantly lower scores on the Vocabulary and Comprehension subtests in children with ASD compared with those with ADHD, despite no significant group differences in overall VCI scores. The Comprehension subtest demands complex verbal reasoning and social understanding, while Vocabulary assesses verbal expression [26]. These tasks vary in the degree of linguistic and social-cognitive processing required, which may explain the particular difficulty children with ASD experience with Comprehension [17,73]. Language delays are well-documented in ASD, with approximately 75% of preschool-aged children showing mild-to-severe variations [74]. Although relative language difficulties in ASD are heterogeneous, there is a broad consensus that many children struggle with linking language with real-world referents—a process requiring both semantic understanding (word meaning) and pragmatic skills (contextual language use and discourse), which are closely tied to social reasoning [73]. Prior research has also identified profound weaknesses in speech comprehension and pragmatic-semantic language use in young children with ASD [75,76]. In contrast, children with ADHD did not exhibit similar difficulties on these subtests. These findings of differential subtest performance highlight a distinctive verbal cognitive profile associated with ASD. This finding offers clinical insight for differential diagnosis within the preschool context and underscores the necessity of early intervention programs targeting social-cognitive skills and verbal reasoning, particularly in real-world situation.
Several limitations should be considered when interpreting our findings. First, this study utilized a retrospective chart review design, which inherently limits the consistency and depth of data collection. Given the young age of our sample, this design also precludes the ability to track diagnostic trajectories over time. Some children currently classified with a single diagnosis may later meet the criteria for co-occurring ASD and ADHD, as one condition often precedes the other during development [77]. Second, sample sizes varied across clinical assessments within each group because different assessments were selectively administered based on presenting symptoms. Consequently, caution is warranted when interpreting the correlational analyses. This variability, however, does not compromise the interpretation of the K-WPPSI-IV profiles, which was the primary focus of this study. Third, clinical diagnoses were based on DSM-5 criteria rather than standardized structured diagnostic tools such as the autism diagnostic interview-revised, autism diagnostic observation schedule, or Korean version of the kiddie-schedule for affective disorders and schizophrenia for school-age children-present and lifetime version, which may limit the diagnostic reliability of the sample. However, we sought to mitigate this limitation by utilizing supplementary rating scales, such as the CARS and the ARS, to support diagnostic validity. Fourth, the exclusion of children with FSIQ below 70, as well as children requiring psychotropic medication, resulted in participants primarily composed of high-functioning individuals with relatively less severe symptoms. Thus, our findings may not fully represent the cognitive profiles of children with comorbid intellectual disabilities or those with greater clinical severity. Fifth, the TD group’s unusually low Vocabulary score relative to their average FSIQ suggests a potential sampling bias in verbal ability. This bias may compromise the validity of our verbal comparisons. Last, the relatively small sample size, especially for the TD group (n=29), constitutes a significant limitation. This restricts the statistical power to reliably detect medium- or small-sized effects. Future research should prioritize prospective designs and recruiting a larger, more representative TD cohort to enhance power and strengthen the validity of the findings.
Despite these limitations, our study has several notable strengths. First, we focused exclusively on preschool-aged children (4-6 years), ensuring that children were at similar stages of cognitive and neurodevelopmental maturity. Second, all children were drug-naive and not taking psychotropic medications at the time of assessment. Since stimulant medications are known to influence FSIQ and other cognitive measures on the K-WPPSI-IV, limiting the sample to unmedicated children allowed for more accurate assessment of their baseline cognitive profiles. Third, our sample comprised Asian children—a population underrepresented in previous comparative studies of cognitive functioning in ADHD and ASD. The replication of cognitive profile distinctions largely consistent with Western findings suggests that the fundamental cognitive manifestations of ASD and ADHD may be robust across cultural boundaries, adding to the generalizability of the findings. Fourth, we included four distinct groups: children with ADHD only, children with ASD only, those with comorbid ADHD and ASD, and TD controls. This comprehensive design allowed for a nuanced examination of the unique and overlapping cognitive features associated with each diagnostic category.
Overall, our findings suggest that preschool-aged children with ADHD and those with ASD share common weaknesses in working memory and processing speed. However, children with ASD showed greater difficulties in verbal expression and complex reasoning, indicating meaningful differences in cognitive profiles between the two conditions. These results provide preliminary insights into early cognitive characteristics of ADHD and ASD. Notably, children with comorbid ADHD and ASD demonstrated more variable patterns, underscoring the need for further research to better characterize the cognitive abilities associated with comorbidity in this young population.

Notes

Availability of Data and Material

The datasets generated or analyzed during the study are available from the corresponding author on reasonable request.

Conflicts of Interest

The authors have no potential conflicts of interest to disclose.

Author Contributions

Conceptualization: Hyo-Won Kim, Gaeun Kim. Data curation: Sungik Kim, Haejin Kim, Gaeun Kim, Soojin Ahn. Formal analysis: Gaeun Kim, Hyo-Won Kim. Funding acquisition: Hyo-Won Kim. Investigation: Donghui Park, Soojin Ahn, Gaeun Kim, Hyo-Won Kim. Methodology: Gaeun Kim, Hyo-Won Kim. Project administration: Hyo-Won Kim. Resource: Soojin Ahn, Dong-hui Park, Sungik Kim, Haejin Kim, Hyo-Won Kim. Supervision: Hyo-Won Kim. Validation: Hyo-Won Kim. Visualization: Gaeun Kim, Hyo-Won Kim. Writing—original draft: Gaeun Kim, Hyo-Won Kim. Writing—review & editing: Gaeun Kim, Hyo-Won Kim.

Funding Statement

This work was supported by the National Research Foundation of Korea (NRF) Grant funded by the South Korean government (Ministry of Science and ICT) (NRF-RS-2020-NR049567).

Acknowledgments

None

Table 1.
Demographic and clinical characteristics of the study population
ADHD+ASD (N=74) ASD (N=46) ADHD (N=84) TD (N=29) t or χ² p Post hoc
Age (mon) 60 (54.5-65.5) 56 (51-61) 66 (62.5-69.5) 62 (57-67) 37.35* <0.001 ADHD>ADHD+ASD=TD>ASD
Male 61 (82.4) 36 (78.3) 61 (72.6) 21 (72.4) 2.51 0.473
ADHD presentation 22.31 <0.001
 Inattentive 16 (21.6) 7 (8.3)
 Hyperactive-impulsive 2 (2.7) 15 (17.9)
 Combined 53 (71.6) 46 (54.8)
 Other specified 3 (4.1) 16 (19.0)
Comorbid diagnoses
 ODD 0 (0) 0 (0) 1 (1.2) 0 (0) 2.41 >0.999
 Anxiety disorder 2 (2.7) 0 (0) 1 (1.2) 1 (3.4) 2.05 0.544
 OCD 0 (0) 0 (0) 1 (1.2) 1 (3.4) 3.12 0.272
 Enuresis 1 (1.4) 0 (0) 1 (1.2) 0 (0) 1.25 >0.999
 Encopresis 3 (4.1) 0 (0) 1 (1.2) 1 (3.4) 2.69 0.397
 Tic disorder 2 (2.7) 1 (2.2) 14 (16.7) 2 (8.2) 11.87 0.005
 PTSD 0 (0) 1 (2.2) 1 (1.2) 0 (0) 2.20 0.770
Clinical assessment
 CARS (N) 69 44 21 10
29.2±3.4 29.2±2.9 22.7±2.4 21.5±3.0 41.86 <0.001 ADHD+ASD=ASD>ADHD=TD
 ARS (N) 61 12 83 27
  Inattentive 12.2±4.6 7.1±2.7 11.9±5.9 5.6±3.4 40.08* <0.001 ADHD+ASD=ADHD>ASD=TD
  Hyperactive-impulsive 11.2±5.4 4.8±3.1 11.9±6.4 4.2±3.7 46.78* <0.001 ADHD+ASD=ADHD>ASD=TD
 ATA visual (N) 32 1 73 12
  Omission errors 4.6±3.8 NA 2.6±3.3 0.8±1.9 16.26* <0.001 ADHD+ASD>ADHD=TD
  Commission errors 2.3±3.1 NA 2.4±2.9 0.8±1.9 3.18* 0.156
  Response time 0.9±2.7 NA 0.5±2.1 0.4±1.5 2.56* 0.278
  Response time variability 2.3±2.2 NA 1.2±2.0 0.2±1.3 5.51 0.005
 ATA auditory (N) 32 1 73 12
  Omission errors 0.7±1.6 NA 0.4±1.5 0.6±1.7 0.62* 0.735
  Commission errors 0.5±1.9 NA 0.5±1.6 -0.3±1.3 2.16* 0.339
  Response time -1.6±1.8 NA -1.6±1.6 -0.6±1.6 2.04 0.135
  Response time variability -0.5±1.2 NA -0.5±1.1 -0.8±1.1 1.06* 0.588

Participants with non-medicated comorbid diagnoses were included. Multiple comparison corrected significance level p<0.002. N (%) presents percentage within each group. Values are presented as median (interquartile range), N (%), number only, or mean±standard deviation.

* using Kruskal-Wallis test.

ADHD, attention-deficit/hyperactivity disorder; ASD, autism spectrum disorder; TD, typically developing; ODD, oppositional defiant disorder; OCD, obsessive-compulsive disorder; PTSD, posttraumatic stress disorder; CARS, Childhood Autism Rating Scale; ARS, ADHD Rating Scale; ATA, Advanced Test of Attention; IQR, interquartile range; NA, no answer.

Table 2.
K-WPPSI-IV profile comparison between the four groups, adjusted for age
Assessment, mean±SD ADHD+ASD (N=74) ASD (N=46) ADHD (N=84) TD (N=29) Adjusted p Partial eta² Post hoc
FSIQ 94.0±15.3 90.5±13.9 99.0±17.0 99.1±14.6 0.084 0.029
VCI 99.5±20.3 93.6±20.5 104.0±18.2 97.1±19.4 0.048 0.034
 Information 9.5±4.2 8.5±3.9 11.2±3.2 10.2±3.8 0.006 0.053
 Similarities 10.2±3.7 9.2±3.7 10.0±3.7 8.8±3.5 0.159 0.022
 Vocabulary 8.6±3.0 7.9±3.0 9.5±3.4* 7.6±3.8** 0.001 0.068 ADHD>ASD
 Comprehension 6.4±2.8 6.4±2.3 8.9±2.9* 7.3±3.9*** <0.001 0.152 ADHD>ADHD+ASD=ASD
VSI 97.2±18.1 93.7±12.8 100.2±15.5 102.6±14.6 0.186 0.021
 Block design 10.1±3.6 9.3±2.7 10.6±3.4 10.7±3.1 0.316 0.015
 Object assembly 9.2±3.7 8.9±2.8 9.8±3.0 10.4±3.2 0.339 0.015
FRI 93.0±18.1 92.4±12.3 99.0±16.4 99.7±12.1 0.100 0.027
 Matrix reasoning 9.5±3.5 8.3±3.1 10.2±3.5 9.1±2.7 0.227 0.019
 Picture concepts 7.7±3.9 8.6±2.8 9.0±3.5 10.3±2.5 0.003 0.059
WMI 95.6±14.1 96.0±13.9 99.9±15.9 110.3±12.4 <0.001 0.082 TD>ADHD+ASD=ASD=ADHD
 Picture memory 9.5±2.8 9.8±2.5 10.1±3.6 11.2±2.7 0.116 0.025
 Zoo locations 8.8±3.4 8.7±2.9 9.6±2.9 11.8±2.5 <0.001 0.084 TD>ADHD+ASD=ASD=ADHD
PSI 85.6±14.9 88.5±12.8 90.5±15.0 100.3±16.1 <0.001 0.079 TD>ADHD+ASD=ASD=ADHD
 Bug search 7.4±2.9 8.2±3.2 7.9±3.0 10.2±3.3 <0.001 0.074 TD>ADHD+ASD=ADHD
 Cancellation 7.3±3.1 7.5±2.3 8.5±3.4 9.8±3.3 0.011 0.048

Multiple comparison corrected significance level p<0.003. Sample sizes for each test conditions. Values are presented as mean±standard deviation.

* N=80;

** N=23;

*** N=22.

ADHD, attention-deficit/hyperactivity disorder; ASD, autism spectrum disorder; TD, typically developing; FSIQ, full-scale intelligence quotient; VCI, Verbal Comprehension Index; VSI, Visual Spatial Index; FRI, Fluid Reasoning Index; WMI, Working Memory Index; PSI, Processing Speed Index.

Table 3.
Partial Pearson correlation analyses among indices and subtests of the K-WPPSI-IV and clinical assessments, adjusted for age
FSIQ VCI VSI FRI WMI PSI IN SI VC CO BD OA MR PC PM ZL BS CA
CARS (N) 144 144 144 144 144 144 144 144 144 144 144 144 144 144 144 144 144 144
-0.282** -0.170* -0.168* -0.313** -0.325** -0.137 -0.217** -0.082 -0.266** -0.229** -0.090 -0.188* -0.200* -0.302** -0.337** -0.178* -0.120 -0.125
ARS (N) 183 183 183 183 183 183 183 183 173 172 183 183 183 183 183 183 183 183
 Inattentive -0.055 -0.020 -0.023 -0.044 -0.190* -0.154* -0.056 0.017 0.089 -0.005 -0.004 -0.036 0.061 -0.120 -0.100 -0.190** -0.149* -0.115
 Hyperactive-impulsive 0.023 0.017 0.009 0.039 -0.084 -0.031 -0.023 0.048 0.105 0.072 0.060 -0.047 0.107 -0.041 -0.009 -0.116 -0.124 0.067
ATA visual (N) 118 118 118 118 118 118 118 118 108 107 118 118 118 118 118 118 118 118
 Omission errors -0.318** -0.257* -0.247** -0.226* -0.302** -0.250** -0.270** -0.186* -0.253** -0.304** -0.125 -0.303** -0.174 -0.196* -0.123 -0.376** -0.313** -0.124
 Commission errors -0.298** -0.236* -0.153 -0.103 -0.284** -0.308** -0.138 -0.278** -0.136 -0.150 -0.163 -0.079 -0.009 -0.162 -0.302** -0.142 -0.216* -0.308**
 Response time 0.120 0.066 0.014 -0.033 0.157 0.095 0.069 0.050 0.110 0.054 0.086 -0.072 -0.066 0.006 0.179 0.061 0.133 0.033
 Response time variability -0.307** -0.257** -0.214* -0.245 -0.210* -0.288** -0.191* -0.251** -0.146 -0.223* -0.175 -0.176 -0.165 -0.243** -0.195* -0.138 -0.144 -0.338**
ATA auditory (N) 118 118 118 118 118 118 118 118 108 107 118 118 118 118 118 118 118 118
 Omission errors -0.210* -0.123 -0.117 -0.204* -0.153 -0.166 -0.108 -0.118 -0.180 -0.142 -0.142 -0.047 -0.184* -0.150 -0.028 -0.231* -0.214* -0.078
 Commission errors -0.229* -0.274** -0.122 -0.217* -0.118 -0.142 -0.195* -0.283** -0.085 -0.038 -0.033 -0.174 -0.128 -0.226* -0.120 -0.072 -0.081 -0.162
 Response time 0.416** 0.404** 0.182* 0.261** 0.269** 0.242** 0.357** 0.362** 0.238* 0.235* 0.203* 0.090 0.172 0.256** 0.166 0.281** 0.273** 0.149
 Response time variability 0.065 0.076 0.026 0.021 0.049 0.014 0.084 0.066 0.003 0.058 0.059 -0.019 -0.008 0.041 -0.036 0.126 0.050 -0.026

* p<0.05;

** p<0.001.

K-WPPSI-IV, Korean Wechsler Preschool and Primary Scale of Intelligence-Fourth Edition; FSIQ, full-scale intelligence quotient; VCI, Verbal Comprehension Index; VSI, Visual Spatial Index; FRI, Fluid Reasoning Index; WMI, Working Memory Index; PSI, Processing Speed Index; IN, Information; SI, Similarities; VC, Vocabulary; CO, Comprehension; BD, Block design; OA, Object assembly; MR, Matrix reasoning; PC, Picture concepts; PM, Picture memory; ZL, Zoo locations; BS, Bug search; CA, Cancellation; CARS, Childhood Autism Rating Scale; ARS, ADHD Rating Scale; ATA, Advanced Test of Attention.

REFERENCES

1. Moffitt TE, Houts R, Asherson P, Belsky DW, Corcoran DL, Hammerle M, et al. Is adult ADHD a childhood-onset neurodevelopmental disorder? Evidence from a four-decade longitudinal cohort study. Am J Psychiatry 2015;172:967-977.
crossref pmid pmc
2. Zeidan J, Fombonne E, Scorah J, Ibrahim A, Durkin MS, Saxena S, et al. Global prevalence of autism: a systematic review update. Autism Res 2022;15:778-790.
crossref pmid pmc pdf
3. Kim MJ, Park I, Lim MH, Paik KC, Cho S, Kwon HJ, et al. Prevalence of attention-deficit/hyperactivity disorder and its comorbidity among Korean children in a community population. J Korean Med Sci 2017;32:401-406.
crossref pmid pmc pdf
4. Kim YS, Leventhal BL, Koh YJ, Fombonne E, Laska E, Lim EC, et al. Prevalence of autism spectrum disorders in a total population sample. Am J Psychiatry 2011;168:904-912.
crossref pmid
5. French B, Nalbant G, Wright H, Sayal K, Daley D, Groom MJ, et al. The impacts associated with having ADHD: an umbrella review. Front Psychiatry 2024;15:1343314
crossref pmid pmc
6. Lebeña A, Faresjö Å, Faresjö T, Ludvigsson J. Clinical implications of ADHD, ASD, and their co-occurrence in early adulthood-the prospective ABIS-study. BMC Psychiatry 2023;23:851
pmid pmc
7. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders. 5th ed. Arlington: American Psychiatric Publishing; 2013.

8. Yeh YC, Huang MF, Wu YY, Hu HF, Yen CF. Pain, bullying involvement, and mental health problems among children and adolescents with ADHD in Taiwan. J Atten Disord 2019;23:809-816.
crossref pmid pdf
9. Seo JY, Park WJ. [The meta analysis of trends and the effects of nonpharmacological intervention for school aged ADHD children]. J Korean Acad Psychiatr Ment Health Nurs 2010;19:117-132. Korean.
crossref
10. Schein J, Adler LA, Childress A, Cloutier M, Gagnon-Sanschagrin P, Davidson M, et al. Economic burden of attention-deficit/hyperactivity disorder among children and adolescents in the United States: a societal perspective. J Med Econ 2022;25:193-205.
crossref pmid
11. Lee K, Jung S. [School violence experience and coping of students with high functioning autism spectrum disorders in inclusive education environment]. Journal of The Korean Society of Integrative Medicine 2016;4:69-79. Korean.
crossref
12. Oerlemans AM, van der Meer JM, van Steijn DJ, de Ruiter SW, de Bruijn YG, de Sonneville LM, et al. Recognition of facial emotion and affective prosody in children with ASD (+ADHD) and their unaffected siblings. Eur Child Adolesc Psychiatry 2014;23:257-271.
crossref pmid pdf
13. Hours C, Recasens C, Baleyte JM. ASD and ADHD comorbidity: what are we talking about? Front Psychiatry 2022;13:837424
crossref pmid pmc
14. Avni E, Ben-Itzchak E, Zachor DA. The presence of comorbid ADHD and anxiety symptoms in autism spectrum disorder: clinical presentation and predictors. Front Psychiatry 2018;9:717
crossref pmid pmc
15. Factor RS, Ryan SM, Farley JP, Ollendick TH, Scarpa A. Does the presence of anxiety and ADHD symptoms add to social impairment in children with autism spectrum disorder? J Autism Dev Disord 2017;47:1122-1134.
crossref pmid pdf
16. Ahn JG, Sin MS. [The comparison of the neuropsychological functions in subtypes of children with ADHD]. Kor J Psychol: Gen 2010;29:959-973. Korean.

17. Zayat M, Kalb L, Wodka EL. Brief report: performance pattern differences between children with autism spectrum disorders and attention deficit-hyperactivity disorder on measures of verbal intelligence. J Autism Dev Disord 2011;41:1743-1747.
crossref pmid pdf
18. Wilson AC. Cognitive profile in autism and ADHD: a meta-analysis of performance on the WAIS-IV and WISC-V. Arch Clin Neuropsychol 2024;39:498-515.
crossref pmid pmc pdf
19. Karalunas SL, Hawkey E, Gustafsson H, Miller M, Langhorst M, Cordova M, et al. Overlapping and distinct cognitive impairments in attention-deficit/hyperactivity and autism spectrum disorder without intellectual disability. J Abnorm Child Psychol 2018;46:1705-1716.
crossref pmid pmc pdf
20. Lee S. Executive function variability in autism spectrum disorder: subdomains, developmental trajectories, and clinical implications. Int J Dev Disabil 2025;Nov 8 [Epub]. https://doi.org/10.1080/20473869.2025.2581644.
crossref
21. Wechsler D. Wechsler preschool and primary scale of intelligence—fourth edition. San Antonio: The Psychological Corporation; 2012.

22. Kanne SM, Gerber AJ, Quirmbach LM, Sparrow SS, Cicchetti DV, Saulnier CA. The role of adaptive behavior in autism spectrum disorders: implications for functional outcome. J Autism Dev Disord 2011;41:1007-1018.
crossref pmid pdf
23. Kim Y, Koh MK, Park KJ, Lee HJ, Yu GE, Kim HW. WISC-IV intellectual profiles in Korean children and adolescents with attention deficit/hyperactivity disorder. Psychiatry Investig 2020;17:444-451.
crossref pmid pmc pdf
24. Theiling J, Petermann F. Neuropsychological profiles on the WAIS-IV of adults with ADHD. J Atten Disord 2016;20:913-924.
crossref pmid pdf
25. Mayes SD, Calhoun SL. WISC-IV and WISC-III profiles in children with ADHD. J Atten Disord 2006;9:486-493.
crossref pmid pdf
26. Mayes SD, Calhoun SL. WISC-IV and WIAT-II profiles in children with high-functioning autism. J Autism Dev Disord 2008;38:428-439.
crossref pmid pdf
27. Happé FG. Wechsler IQ profile and theory of mind in autism: a research note. J Child Psychol Psychiatry 1994;35:1461-1471.
crossref pmid
28. Snow JB, Sapp GL. WISC-III subtest patterns of ADHD and normal samples. Psychol Rep 2000;87:759-765.
crossref pmid pdf
29. Joseph RM, Tager-Flusberg H, Lord C. Cognitive profiles and social-communicative functioning in children with autism spectrum disorder. J Child Psychol Psychiatry 2002;43:807-821.
crossref pmid pmc
30. Oliveras-Rentas RE, Kenworthy L, Roberson RB 3rd, Martin A, Wallace GL. WISC-IV profile in high-functioning autism spectrum disorders: impaired processing speed is associated with increased autism communication symptoms and decreased adaptive communication abilities. J Autism Dev Disord 2012;42:655-664.
crossref pmid pmc pdf
31. Hennessy A, Nichols ES, Al-Saoud S, Brossard-Racine M, Duerden EG. Identifying cognitive profiles in children with neurodevelopmental disorders using online cognitive testing. Clin Child Psychol Psychiatry 2024;29:591-607.
crossref pmid pmc pdf
32. Sullivan K, Stone WL, Dawson G. Potential neural mechanisms underlying the effectiveness of early intervention for children with autism spectrum disorder. Res Dev Disabil 2014;35:2921-2932.
crossref pmid pmc
33. Dietz C, Swinkels SH, Buitelaar JK, van Daalen E, van Engeland H. Stability and change of IQ scores in preschool children diagnosed with autistic spectrum disorder. Eur Child Adolesc Psychiatry 2007;16:405-410.
crossref pmid pdf
34. Park H, Lee K, Lee SH, Park M. [A study on standardization of K-WPPSI-IV: analyses of reliability and validity]. Korean Journal of Childcare and Education 2016;12(4):111-130. Korean.
crossref
35. Moon SJ, Hwang JS, Shin AL, Kim JY, Bae SM, Sheehy-Knight J, et al. Accuracy of the Childhood Autism Rating Scale: a systematic review and meta-analysis. Dev Med Child Neurol 2019;61:1030-1038.
crossref pmid pdf
36. Schopler E, Reichler RJ, DeVellis RF, Daly K. Toward objective classification of childhood autism: Childhood Autism Rating Scale (CARS). J Autism Dev Disord 1980;10:91-103.
crossref pmid pdf
37. Shin MS, Kim YH. [Standardization study for the Korean version of the Childhood Autism Rating Scale: reliability, validity and cut-off score]. Korean Journal of Clinical Psychology 1998;17(1):1-15. Korean.

38. Perry A, Condillac RA, Freeman NL, Dunn-Geier J, Belair J. Multi-site study of the Childhood Autism Rating Scale (CARS) in five clinical groups of young children. J Autism Dev Disord 2005;35:625-634.
crossref pmid pdf
39. Lee S, Yoon SA, Shin MS. Validation of the Korean Childhood Autism Rating Scale-2. Research in Autism Spectrum Disorders 2023;103:102128
crossref
40. So YK, Noh JS, Kim YS, Ko SG, Koh YJ. [The reliability and validity of Korean parent and teacher ADHD rating scale]. J Korean Neuropsychiatr Assoc 2002;41:283-289. Korean.

41. Jang SJ, Suh DS, Byun HJ. [Normative study of the K-ARS (Korean ADHD Rating Scale) for parents]. J Korean Acad Child Adolesc Psychiatry 2007;18:38-48. Korean.

42. Alexandre JL, Lange AM, Bilenberg N, Gorrissen AM, Søbye N, Lambek R. The ADHD rating scale-IV preschool version: factor structure, reliability, validity, and standardisation in a Danish community sample. Res Dev Disabil 2018;78:125-135.
crossref pmid
43. Shin MS, Cho S, Chun SY, Hong KEM. [A study of the development and standardization of ADHD diagnostic system]. J Korean Acad Child Adolesc Psychiatry 2000;11:91-99. Korean.

44. Fujioka T, Takiguchi S, Yatsuga C, Hiratani M, Hong KE, Shin MS, et al. Advanced test of attention in children with attention-deficit/hyperactivity disorder in Japan for evaluation of methylphenidate and atomoxetine effects. Clin Psychopharmacol Neurosci 2016;14:79-87.
crossref pmid pmc
45. Mukaka MM. Statistics corner: a guide to appropriate use of correlation coefficient in medical research. Malawi Med J 2012;24:69-71.
pmid pmc
46. Li G, Jiang W, Du Y, Rossbach K. Intelligence profiles of Chinese school-aged boys with high-functioning ASD and ADHD. Neuropsychiatr Dis Treat 2017;13:1541-1549.
crossref pmid pmc pdf
47. Baddeley A. Working memory: looking back and looking forward. Nat Rev Neurosci 2003;4:829-839.
crossref pmid pdf
48. Rubia K. “Cool” inferior frontostriatal dysfunction in attention-deficit/hyperactivity disorder versus “hot” ventromedial orbitofrontal-limbic dysfunction in conduct disorder: a review. Biol Psychiatry 2011;69:e69-e87.
crossref pmid
49. Barkley RA. Behavioral inhibition, sustained attention, and executive functions: constructing a unifying theory of ADHD. Psychol Bull 1997;121:65-94.
crossref pmid
50. Diamond A, Barnett WS, Thomas J, Munro S. Preschool program improves cognitive control. Science 2007;318:1387-1388.
crossref pmid pmc
51. Zang YF, He Y, Zhu CZ, Cao QJ, Sui MQ, Liang M, et al. Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. Brain Dev 2007;29:83-91.
crossref pmid
52. Craig F, Margari F, Legrottaglie AR, Palumbi R, de Giambattista C, Margari L. A review of executive function deficits in autism spectrum disorder and attention-deficit/hyperactivity disorder. Neuropsychiatr Dis Treat 2016;12:1191-1202.
pmid pmc
53. O’Hearn K, Asato M, Ordaz S, Luna B. Neurodevelopment and executive function in autism. Dev Psychopathol 2008;20:1103-1132.
crossref pmid
54. Hovik KT, Egeland J, Isquith PK, Gioia G, Skogli EW, Andersen PN, et al. Distinct patterns of everyday executive function problems distinguish children with Tourette syndrome from children with ADHD or autism spectrum disorders. J Atten Disord 2017;21:811-823.
crossref pmid pdf
55. Semrud-Clikeman M, Walkowiak J, Wilkinson A, Butcher B. Executive functioning in children with Asperger syndrome, ADHD-combined type, ADHD-predominately inattentive type, and controls. J Autism Dev Disord 2010;40:1017-1027.
crossref pmid pdf
56. Takeuchi A, Ogino T, Hanafusa K, Morooka T, Oka M, Yorifuji T, et al. Inhibitory function and working memory in attention deficit/hyperactivity disorder and pervasive developmental disorders: does a continuous cognitive gradient explain ADHD and PDD traits? Acta Med Okayama 2013;67:293-303.
pmid
57. Rapport MD, Chung KM, Shore G, Isaacs P. A conceptual model of child psychopathology: implications for understanding attention deficit hyperactivity disorder and treatment efficacy. J Clin Child Psychol 2001;30:48-58.
crossref pmid
58. Shanahan MA, Pennington BF, Yerys BE, Scott A, Boada R, Willcutt EG, et al. Processing speed deficits in attention deficit/hyperactivity disorder and reading disability. J Abnorm Child Psychol 2006;34:585-601.
crossref pmid pdf
59. Cepeda NJ, Blackwell KA, Munakata Y. Speed isn’t everything: complex processing speed measures mask individual differences and developmental changes in executive control. Dev Sci 2013;16:269-286.
crossref pmid pmc pdf
60. Sergeant JA. Modeling attention-deficit/hyperactivity disorder: a critical appraisal of the cognitive-energetic model. Biol Psychiatry 2005;57:1248-1255.
crossref pmid
61. van der Meere J, Stemerdink N, Gunning B. Effects of presentation rate of stimuli on response inhibition in ADHD children with and without tics. Percept Mot Skills 1995;81:259-262.
crossref pmid pdf
62. Just MA, Keller TA, Malave VL, Kana RK, Varma S. Autism as a neural systems disorder: a theory of frontal-posterior underconnectivity. Neurosci Biobehav Rev 2012;36:1292-1313.
crossref pmid pmc
63. Minshew NJ, Goldstein G, Siegel DJ. Neuropsychologic functioning in autism: profile of a complex information processing disorder. J Int Neuropsychol Soc 1997;3:303-316.
crossref pmid
64. Williams DL, Minshew NJ, Goldstein G. Further understanding of complex information processing in verbal adolescents and adults with autism spectrum disorders. Autism 2015;19:859-867.
crossref pmid pdf
65. Zapparrata NM, Brooks PJ, Ober TM. Slower processing speed in autism spectrum disorder: a meta-analytic investigation of time-based tasks. J Autism Dev Disord 2023;53:4618-4640.
crossref pmid pdf
66. Rommelse N, Luman M, Kievit R. Slow processing speed: a cross-disorder phenomenon with significant clinical value, and in need of further methodological scrutiny. Eur Child Adolesc Psychiatry 2020;29:1325-1327.
crossref pmid pdf
67. Cook NE, Braaten EB, Surman CBH. Clinical and functional correlates of processing speed in pediatric attention-deficit/hyperactivity disorder: a systematic review and meta-analysis. Child Neuropsychol 2018;24:598-616.
crossref pmid
68. Stephenson KG, Beck JS, South M, Norris M, Butter E. Validity of the WISC-V in youth with autism spectrum disorder: factor structure and measurement invariance. J Clin Child Adolesc Psychol 2021;50:669-681.
crossref pmid
69. Grondhuis SN, Mulick JA. Comparison of the Leiter International Performance Scale-Revised and the Stanford-Binet Intelligence Scales, 5th Edition, in children with autism spectrum disorders. Am J Intellect Dev Disabil 2013;118:44-54.
crossref pmid pdf
70. Calhoun SL, Mayes SD. Processing speed in children with clinical disorders. Psychol Sch 2005;42:333-343.
crossref
71. Pan Z, Park C, Brietzke E, Zuckerman H, Rong C, Mansur RB, et al. Cognitive impairment in major depressive disorder. CNS Spectr 2019;24:22-29.
crossref pmid
72. Martin EM, Rupprecht S, Schrenk S, Kattlun F, Utech I, Radscheidt M, et al. A hypoarousal model of neurological post-COVID syndrome: the relation between mental fatigue, the level of central nervous activation and cognitive processing speed. J Neurol 2023;270:4647-4660.
crossref pmid pmc pdf
73. Williams D, Botting N, Boucher J. Language in autism and specific language impairment: where are the links? Psychol Bull 2008;134:944-963.
crossref pmid
74. Vogindroukas I, Stankova M, Chelas EN, Proedrou A. Language and speech characteristics in autism. Neuropsychiatr Dis Treat 2022;18:2367-2377.
crossref pmid pmc pdf
75. Rapin I, Dunn M. Update on the language disorders of individuals on the autistic spectrum. Brain Dev 2003;25:166-172.
crossref pmid
76. Tager-Flusberg H. On the nature of linguistic functioning in early infantile autism. J Autism Dev Disord 1981;11:45-56.
crossref pmid pdf
77. Sainsbury WJ, Carrasco K, Whitehouse AJ, McNeil L, Waddington H. Age of diagnosis for co-occurring autism and attention deficit hyperactivity disorder during childhood and adolescence: a systematic review. Rev J Autism Dev Disord 2023;10:563-575.
crossref pdf


ABOUT
AUTHOR INFORMATION
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
Editorial Office
#522, G-five Central Plaza, 27 Seochojungang-ro 24-gil, Seocho-gu, Seoul 06601, Korea
Tel: +82-2-537-6171  Fax: +82-2-537-6174    E-mail: psychiatryinvest@gmail.com                

Copyright © 2026 by Korean Neuropsychiatric Association.

Developed in M2PI

Close layer
prev next