Biological Bases of Empathy and Social Cognition in Patients with Attention-Deficit/Hyperactivity Disorder: A Focus on Treatment with Psychostimulants
Abstract
:1. Introduction
1.1. Empathy and Related Constructs
1.2. Social Cognition in ADHD
1.3. The Systematic Review
2. Materials and Methods
2.1. Search Strategy
2.2. Screening Procedure
- (1)
- Study design: any type of clinical trial;
- (2)
- Comparison: either case versus control, drug versus placebo or pre-to peri-/post-treatment;
- (3)
- Participants: patients non-retrospectively diagnosed with ADHD according to the international classification systems DSM-IV, ICD-9, or later versions; no restriction for participants’ age, gender, or IQ;
- (4)
- Intervention: either one-day, single-dose administration or prolonged daily administration of psychostimulants (e.g., Methylphenidate) or nonstimulant drugs (e.g., Atomoxetine);
- (5)
- Measures: any type of measurement (i.e., tasks, rating scales, and parent- or self-rated questionnaires) assessing empathy, theory of mind, and emotion recognition.
2.3. Data Collection
3. Results
3.1. Empathy and Theory of Mind
3.2. Emotion Recognition
4. Discussion
5. Conclusions
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Study | N | Gender | Age | ADHD | Comorbidity | Treatment | Assessment | Outcome |
---|---|---|---|---|---|---|---|---|
Coelho et al., 2017 [65] | 60 ADHD (30 C, 30 I) | 48/12 | 7–14 (unimodal group = 10.13) (multimodal group = 10.2) | no other medications when recruited | ID excluded | unimodal-medication only vs. multimodal medication + CBT for 20 weeks (prolonged release-MPH 20 mg) | Children’s Social Skills Multimedia System | Multimodal treatment showed more improvement in frequency indicators on empathy. |
Demirci and Erdogan, 2016 [58] | 60 ADHD (21 C, 17 H/I, 22 I) 60 HCs | 35/25 ADHD 35/25 HCs | 8–15 (ADHD = 10.8) (HCs = 10.8) | drug-naive | ID, ASD, CD excluded | pharmacological treatment for 12 weeks: −38 OROS-MPH (final dose 1.2 mg/kg/day) −32 ATX (final dose 1.2 mg/kg/day) | RMET | The ADHD sample had significantly lower scores in RMET than HCs. ADHD-H/I had a lower number of correct answers in the RMET than ADHD-I. After OROS-MPH/ATX treatment, the ADHD sample showed a significant improvement in RMET. |
Fantozzi et al., 2021 [62] | 61 ADHD (50 C, 11 I) | 51/10 | 6–17 (10.3) | drug-naive | ID, ASD excluded 14 SLD; 9 ODD; 4 MD; 2 LD; 1 AD; 1 tics; 1 dyspraxia | MPH treatment for 6 months (final dosage 31.6 ± 15.1 mg/day) | BES | Significant improvement in AE and CE. Changes in attention symptoms predicted changes in AE but not in CE. |
Golubchik and Weizman, 2017 [59] | 52 ADHD | 8–18 | psychostimulant-medication naive | ID, ASD, schizophrenia, bipolar disorder, suicidal ideation excluded 26 ODD | MPH treatment for 12 weeks (0.5–1 mg/kg/day) | EQ-C | Significant improvement in EQ scores in both groups (ADHD and ADHD/ODD). Only in the ADHD group, a significant correlation between changes in ADHD-RS and in EQ-C was found. | |
Golubchik and Weizman, 2019 [66] | 25 ADHD | 21/4 | 7–17 (10.8) | ID, ASD, psychosis, bipolar disorder excluded | single dose of MPH (1 mg/kg) | RMET | No improvement of RMET. | |
Gumustas et al., 2017 [60] | 65 ADHD 61 HCs | 53/12 ADHD 46/15 HCs | 8–14 (ADHD = 10.86) (HCs = 11.21) | drug-naive | ID, ASD, psychosis, mood disorders, anxiety disorders, ODD excluded | OROS-MPH treatment for 12 weeks (0.83 ± 0.21 mg/kg/day) | BEI (trait empathy) GEM-PR (trait empathy) ERT (state empathy) | No significant statistical differences in trait and in state empathy skills in the two groups. Following the MPH treatment, the ADHD group showed a significant increase in the ERT (state empathy) interpretation sub-score. |
Levi-Shachar et al., 2019 [61] | 50 ADHD 40 HCs | 28/22 ADHD 22/18 HCs | 6–12 (ADHD = 9.42) (HCs = 8.95) | psychotropic medication free | psychosis, affective disorders, CD, substance abuse disorder excluded | single dose of short-acting MPH (0.3–0.5 mg/kg) | ToM test | The ADHD sample displayed significantly poorer ToM performance compared with HCs. Following MPH administration, the ToM performance of the ADHD sample normalized. |
Levi-Shachar et al., 2021 [67] | 50 ADHD | 28/22 ADHD | 6–12 (ADHD = 9.42) | psychotropic medication free | psychosis, affective disorders, CD, substance abuse disorder excluded | single dose of short-acting MPH (0.3–0.5 mg/kg) | ToM test FPR | Negative association between severity of behavioral ADHD domains and impairment in ToM. Administration of MPH improved ToM performance, with the greatest improvement in children with more severe behavioral symptoms. |
Maoz et al., 2013 [47] | 24 ADHD (11 C, 13 I) | 16/8 | 6–12 (10.2) | ID, psychosis, bipolar disorder, major depression, DBD, substance abuse disorder excluded | single-dose of long-acting MPH | IRI FRP TCT | Significant improvement in ToM performance. | |
Maoz et al., 2019 [46] | 24 ADHD 36 HCs | 6/8 ADHD 19/17 HCs | 6–12 (ADHD = 10.29) (HCs = 9.37) | psychotropic medication free | ID, psychosis, bipolar disorder, major depression, CD, substance abuse disorder excluded | single dose of long-acting MPH | IRIFRP | The ADHD sample showed lower levels of self-reported empathy and FRP scores compared with HCs. In ADHD sample, MPH administration improved FRP scores to a level equal to that in HCs. |
Study | N | Gender | Age | ADHD | Comorbidity | Treatment | Assessment | Outcome |
---|---|---|---|---|---|---|---|---|
Demrici and Erdogan, 2016 [58] | 60 ADHD (21 C, 17 H/I, 22 I) 60 HCs | 35/25 ADHD 35/25 HCs | 8–15 years (ADHD = 10.8) (HCs = 10.8) | drug-naive | ID, ASD, CD excluded | pharmacological treatment for 12 weeks: −38 OROS-MPH (final dose 1.2 mg/kg/day) −32 ATX (final dose 1.2 mg/kg/day) | BFRT | ADHD sample had significantly lower scores in BFRT than HCs. ADHD-H/I had a lower number of correct answers in BRFT than ADHD-C and I. After OROS-MPH/ATX treatment, the ADHD sample showed a significant improvement in BFRT. |
Gumustas et al., 2017a [60] | 65 ADHD 61 HCs | 53/12 ADHD 46/15 HCs | 8–14 years (ADHD = 10.86)(HCs = 11.21) | drug-naive | ID, ASD, psychosis, mood disorders, anxiety disorders, ODD excluded | OROS-MPH treatment for 12 weeks (0.83 ± 0.21 mg/kg/day) | DANVA-2 | No significant statistical differences in facial expression recognition skills in the two groups. Following the MPH treatment, the ADHD group showed a significant decrease in the recognition error of anger and sadness expressions. |
Hall et al., 1999 [68] | 15 ADHD (13 C, 2 H/I) 15 ADHD/LD (14 C, 1 H/I) 15 no ADHD or LD | 36/9 | 7–10 years | the ADHD sample was taken MPH (Ritalin) for at least a month at the time of the study | ID excluded | the DANVA was administered twice to each child in the ADHD and ADHD/LD groups: once while the ADHD and ADHD/LD participants were on medication and once off medication | DANVA SPBRS | The ADHD/LD group demonstrated significant difficulty in comparison to their peers in perceiving paralanguage cues effectively. The ADHD/LD group showed significant improvement on the Postures and Paralanguage subtests during on-medication conditions. |
Schulz et al., 2018 [69] | 25 ADHD (17C, 8I) | 14/9 | 19–52 years (34.8 ± 9.8) | 2 participants were on medication at intake, 9 had a history of previous stimulant treatment (2 of whom had also previously been treated with nonstimulant medication) | psychosis, BD, PTSD, substance use disorderexcluded | 3 to 4 weeks of LDX (mean maintenance dose = 64 mg/day–SD = 13 mg) treatment and 3 weeks of medication in a randomized, counterbalanced, hybrid crossover design | participants were scanned twice with event-related fMRI while performing an emotional go/no-go task | No significant differences between the two treatment arms. LDX was associated with an increase in fMRI activation in the right amygdala and reduced interactions with the orbital aspect of the left inferior frontal gyrus specifically for responses to sad faces. |
Schwenck et al., 2013 [70] | 56 ADHD (10C,2H/I,44I) 28 ADHD-MD− 28 ADHD-MD+ 28 CG | 19/9 | 8.2–17.3 years (MD− = 12.36) (MD+ = 12.31) (CG = 12.49) | 47 children in the ADHD group were taken MPH at the time of the study (one child was additionally taken ATX), 6 drug-naive | ID, ASD, ODD, CD excluded | cross-sectional design study | MT | No differences found between ADHD-MD−, ADHD-MD+ and CG on emotion recognition. |
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Fantozzi, P.; Sesso, G.; Muratori, P.; Milone, A.; Masi, G. Biological Bases of Empathy and Social Cognition in Patients with Attention-Deficit/Hyperactivity Disorder: A Focus on Treatment with Psychostimulants. Brain Sci. 2021, 11, 1399. https://doi.org/10.3390/brainsci11111399
Fantozzi P, Sesso G, Muratori P, Milone A, Masi G. Biological Bases of Empathy and Social Cognition in Patients with Attention-Deficit/Hyperactivity Disorder: A Focus on Treatment with Psychostimulants. Brain Sciences. 2021; 11(11):1399. https://doi.org/10.3390/brainsci11111399
Chicago/Turabian StyleFantozzi, Pamela, Gianluca Sesso, Pietro Muratori, Annarita Milone, and Gabriele Masi. 2021. "Biological Bases of Empathy and Social Cognition in Patients with Attention-Deficit/Hyperactivity Disorder: A Focus on Treatment with Psychostimulants" Brain Sciences 11, no. 11: 1399. https://doi.org/10.3390/brainsci11111399
APA StyleFantozzi, P., Sesso, G., Muratori, P., Milone, A., & Masi, G. (2021). Biological Bases of Empathy and Social Cognition in Patients with Attention-Deficit/Hyperactivity Disorder: A Focus on Treatment with Psychostimulants. Brain Sciences, 11(11), 1399. https://doi.org/10.3390/brainsci11111399