l-Carnosine as Adjunctive Therapy in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial.
- 2018-06
- Journal of child and adolescent psychopharmacology 28(5)
- Alireza Ghajar
- Farinaz Aghajan-Nashtaei
- Mohsen Afarideh
- Mohammad-Reza Mohammadi
- Shahin Akhondzadeh
- PubMed: 29469593
- DOI: 10.1089/cap.2017.0157
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Population
- 56 drug-free children and adolescents aged 6-17 years old with a diagnosis of ADHD
- Methods
- Randomized, double-blind placebo-controlled study; l-carnosine (800 mg/d in two divided doses) or placebo plus methylphenidate (0.5-1.5 mg/kg/d) for 8 weeks
- Blinding
- Double-blind
- Duration
- 8 weeks
- Funding
- Unclear
Objectives
This study aimed to investigate the efficacy and tolerability of l-carnosine as an add-on to methylphenidate in management of children with attention-deficit/hyperactivity disorder (ADHD).Methods
This was an 8-week, randomized, double-blind placebo-controlled study. Fifty-six drug-free children and adolescents aged 6-17 years old with a diagnosis of ADHD entered the study. The patients were randomly assigned to l-carnosine (800 mg/d in two divided doses) or placebo plus methylphenidate (0.5-1.5 mg/kg/d) for 8 weeks. Children were assessed using the Teacher and Parent ADHD Rating Scale-IV (ADHD-RS-IV) at baseline and at weeks 4 and 8 postbaseline.Results
Fifty patients completed the study, and all had two postbaseline measurements. Using the general linear model repeated measures, significant effect was observed for time × treatment interaction on total and inattention subscales of the Parent ADHD-RS (Greenhouse-Geisser corrected: F = 3.783, df = 1.444, p = 0.041 and F = 4.032, df = 1.600, p = 0.030). Improvements in the Teacher ADHD-RS were not significantly different between the two groups in total (Greenhouse-Geisser corrected: F = 0.200, df = 1.218, p = 0.705), as well as inattention and hyperactivity subscale scores (p = 0.956 and 0.281, respectively). The frequency of side effects was not significantly different between the two treatment arms.Conclusions
l-carnosine, as a supplementary medication, might be beneficial in treatment of children with ADHD. However, further investigations and different doses of l-carnosine are required to replicate these findings in children with ADHD.Research Insights
Improvements in the Teacher ADHD-RS were not significantly different between the two groups in total, as well as inattention and hyperactivity subscale scores (p = 0.956 and 0.281, respectively)
- Effect
- Neutral
- Effect size
- Small
- Dose
- 800 mg/d in two divided doses
Improvements in the Teacher ADHD-RS were not significantly different between the two groups in total (Greenhouse-Geisser corrected: F = 0.200, df = 1.218, p = 0.705)
- Effect
- Neutral
- Effect size
- Small
- Dose
- 800 mg/d in two divided doses
Using the general linear model repeated measures, significant effect was observed for time × treatment interaction on total and inattention subscales of the Parent ADHD-RS (Greenhouse-Geisser corrected: F = 3.783, df = 1.444, p = 0.041 and F = 4.032, df = 1.600, p = 0.030).
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 800 mg/d in two divided doses
Improvements in the Teacher ADHD-RS were not significantly different between the two groups in total (Greenhouse-Geisser corrected: F = 0.200, df = 1.218, p = 0.705), as well as inattention and hyperactivity subscale scores (p = 0.956 and 0.281, respectively).
- Effect
- Neutral
- Effect size
- Small
- Dose
- 800 mg/d in two divided doses
Improvements in the Teacher ADHD-RS were not significantly different between the two groups in total, as well as inattention and hyperactivity subscale scores (p = 0.956 and 0.281, respectively)
- Effect
- Neutral
- Effect size
- Small
- Dose
- 800 mg/d in two divided doses
significant effect was observed for time × treatment interaction on total and inattention subscales of the Parent ADHD-RS (Greenhouse-Geisser corrected: F = 3.783, df = 1.444, p = 0.041 and F = 4.032, df = 1.600, p = 0.030).
- Effect
- Beneficial
- Effect size
- Moderate
- Dose
- 800 mg/d in two divided doses
Adverse Events Reported
The frequency of side effects was not significantly different between the two treatment arms.
- Finding
- No significant difference
- Significant
- No