Synaptosomal-Associated Protein 25 Gene Polymorphisms Affect Treatment Efficiency of Methylphenidate in Children With
Jie Li1,2, Wen-Jie Yan1, Yan Wu1
1Department of Developmental and Behavioral Pediatrics, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Insights
Methylphenidate (MPH) treatment efficacy in children with ADHD varies. The study found that the SNAP-25 gene MnlI T/T genotype shows improved prefrontal function and ADHD symptom reduction with MPH, unlike G allele carriers.
Area of Science:
- Neuroscience
- Genetics
- Pediatrics
Background:
- Methylphenidate (MPH) is a first-line ADHD treatment, but individual responses vary.
- Synaptosomal-associated protein 25 (SNAP-25) gene MnlI polymorphisms are linked to MPH efficacy.
- The impact of SNAP-25 MnlI polymorphisms on brain hemodynamic responses to MPH is unclear.
Purpose of the Study:
- To investigate the interaction between MPH treatment-induced prefrontal functional changes and SNAP-25 gene MnlI genotype in children with ADHD.
- To explore if SNAP-25 MnlI genotype influences hemodynamic responses and behavioral outcomes following MPH treatment.
Main Methods:
- Functional near-infrared spectroscopy (fNIRS) monitored prefrontal hemodynamic changes during a go/no-go task in 38 children with ADHD.
- Participants were genotyped for SNAP-25 MnlI polymorphisms (T/T vs. G allele carriers).
- Changes in oxygenated hemoglobin ([Δavg oxy-Hb]) and deoxyhemoglobin ([Δavg deoxy-Hb]) were measured pre- and post-MPH treatment (1.5h and 4 weeks). SNAP-IV scores were also assessed.
Main Results:
- Children with the SNAP-25 T/T genotype showed significantly increased [Δavg oxy-Hb] in the dorsolateral prefrontal cortex after 4 weeks of MPH treatment, unlike G allele carriers.
- The T/T genotype group demonstrated improved accuracy on the go/no-go task and a significant reduction in SNAP-IV scores post-MPH treatment.
- G allele carriers showed no significant changes in hemodynamic responses, task accuracy, or SNAP-IV scores after MPH treatment.
Conclusions:
- SNAP-25 MnlI polymorphism influences MPH treatment outcomes in children with ADHD.
- fNIRS combined with SNAP-25 MnlI genotyping may serve as a biomarker for predicting MPH treatment response.
- This approach can help personalize ADHD treatment strategies based on genetic profiles.
Abstract:
Methylphenidate (MPH) is the first-line drug for the treatment of children with attention-deficit hyperactivity disorder (ADHD); however, individual curative effects of MPH vary. Many studies have demonstrated that synaptosomal-associated protein 25 (SNAP-25) gene MnlI polymorphisms may be related to the efficacy of MPH. However, the association between SNAP-25MnlI polymorphisms and changes in brain hemodynamic responses after MPH treatment is still unclear. This study used functional near-infrared spectroscopy (fNIRS) to preliminarily investigate the interaction of MPH treatment-related prefrontal inhibitory functional changes with the genotype status of the SNAP-25 gene in children with ADHD. In total, 38 children with ADHD aged 6.76-12.08 years were enrolled in this study and divided into the following two groups based on SNAP-25 gene MnlI polymorphisms: T/T genotype group (wild-type group, 27 children) and G allele carrier group (mutation group, 11 children). The averaged oxygenated hemoglobin concentration changes [Δavg oxy-Hb] and deoxyhemoglobin concentration changes [Δavg deoxy-Hb] in the frontal cortex before MPH treatment and after 1.5 h (post-MPH1.5h) and 4 weeks (post-MPH4w) of MPH treatments were monitored using fNIRS during the go/no-go task. SNAP-IV scores were evaluated both pre-MPH and post-MPH4w treatments. In the T/T genotype group, [Δavg oxy-Hb] in the dorsolateral prefrontal cortex was significantly higher after 4 weeks of MPH (post-MPH4W) treatment than pre-treatment; however, in the G allele group, no significant differences in [Δavg oxy-Hb] were observed between pre- and post-treatments. In the go/no-go task, the accuracy was significantly increased post-MPH4w treatment in the T/T genotype group, while no significant differences were observed in response time and accuracy of the "go" sand no-go task in the G allele group for pre-MPH, post-MPH1.5h, and post-MPH4w treatments. The T/T genotype group exhibited a significant decrease in SNAP-IV scores after MPH treatment, while the G allele group showed no significant difference. In conclusion, fNIRS data combined with SNAP-25 MnlI polymorphism analysis may be a useful biomarker for evaluating the effects of MPH in children with ADHD.
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