The Effects of Extended-Release Stimulant Medication on Sleep in Children with ADHD
Penny Corkum1,2,3, Esmot Ara Begum1, Benjamin Rusak1,2
1Department of Psychology and Neuroscience, Dalhousie University, Nova Scotia.
Insights
Extended-release methylphenidate hydrochloride (MPH) significantly reduced total sleep time and increased sleep onset latency in children with Attention-Deficit/Hyperactivity Disorder (ADHD). This sleep disruption may impact daytime functioning.
Area of Science:
- Pediatric Sleep Medicine
- Neuroscience
- Pharmacology
Background:
- Stimulant medications like methylphenidate hydrochloride (MPH) effectively treat Attention-Deficit/Hyperactivity Disorder (ADHD) core symptoms.
- However, MPH may negatively impact sleep patterns in children.
Purpose of the Study:
- To investigate the acute effects of extended-release MPH on children's sleep.
- Utilized both actigraphy and polysomnography (PSG) for comprehensive sleep assessment.
Main Methods:
- A crossover trial involving 26 newly diagnosed, medication-naïve children with ADHD.
- Compared 2 weeks of placebo with 2 weeks of extended-release MPH treatment.
- Analyzed sleep variables using repeated measures MANOVAs.
Main Results:
- Actigraphy revealed a 30-minute reduction in total sleep time and a 30-minute increase in sleep onset latency with MPH (p<0.001).
- No significant differences in sleep efficiency were observed.
- PSG data showed trends consistent with actigraphy, and a significant increase in N3 sleep percentage (3.2%, p<0.05) with MPH.
Conclusions:
- Increased sleep onset latency and reduced total sleep time are potential adverse effects of MPH.
- These sleep disturbances may necessitate management strategies to optimize treatment outcomes in children with ADHD.
Objective:
Although stimulant medications, such as methylphenidate hydrochloride (MPH), are effective at reducing the core symptoms of Attention-Deficit/Hyperactivity Disorder (ADHD), they may also disrupt children's sleep. This study aimed to investigate the acute impact of extended-release MPH on sleep using both actigraphy and polysomnography (PSG).
Method:
Participants were 26 medication-naïve newly and rigorously diagnosed children with ADHD (23 males; 3 females) with a mean age of 8 years, 8 months (SD = 24.5mos) who were enrolled in a clinically-administered crossover medication trial with 2 conditions: 2 weeks of placebo and 2 weeks of MPH treatment. The effect of condition on sleep variables as measured by actigraphy (primary outcome) and PSG (secondary outcome) was analyzed using repeated measures MANOVAs.
Results:
Based on actigraphy data, total sleep time was significantly reduced by 30 minutes and sleep onset latency was significantly increased by 30 minutes in the MPH condition compared to the placebo condition (p<0.001). No differences were found in sleep efficiency. No statistically significant differences were found for the same variables assessed by PSG; however, the means were in the same direction as the actigraphy data. There was a significant increase in the relative percentage of stage N3 sleep by 3.2% during MPH treatment (p<0.05).
Conclusions:
Increased sleep onset latency resulting in reduced total sleep time, which has been linked to poorer daytime functioning, is a potential adverse effect of stimulant medication which may require management to optimize outcome.
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