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纹状体多巴胺系统对哌甲酯的反应性——针对注意缺陷/多动障碍男性儿童和青少年的一项I-123-β-CIT单光子发射计算机断层扫描(SPECT)受试者内研究

Responsivity of the Striatal Dopamine System to Methylphenidate-A Within-Subject I-123-β-CIT-SPECT Study in Male Children and Adolescents With Attention-Deficit/Hyperactivity Disorder.

作者信息

Aster Hans-Christoph, Romanos Marcel, Walitza Susanne, Gerlach Manfred, Mühlberger Andreas, Rizzo Albert, Andreatta Marta, Hasenauer Natalie, Hartrampf Philipp E, Nerlich Kai, Reiners Christoph, Lorenz Reinhard, Buck Andreas K, Deserno Lorenz

机构信息

Department of Child and Adolescent Psychiatry, Psychotherapy and Psychosomatics, University of Würzburg, Würzburg, Germany.

Department of Neurology, University of Würzburg, Würzburg, Germany.

出版信息

Front Psychiatry. 2022 Apr 14;13:804730. doi: 10.3389/fpsyt.2022.804730. eCollection 2022.

DOI:10.3389/fpsyt.2022.804730
PMID:35492708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9046584/
Abstract

BACKGROUND

Methylphenidate (MPH) is the first-line pharmacological treatment of attention-deficit/hyperactivity disorder (ADHD). MPH binds to the dopamine (DA) transporter (DAT), which has high density in the striatum. Assessments of the striatal dopamine transporter by single positron emission computed tomography (SPECT) in childhood and adolescent patients are rare but can provide insight on how the effects of MPH affect DAT availability. The aim of our within-subject study was to investigate the effect of MPH on DAT availability and how responsivity to MPH in DAT availability is linked to clinical symptoms and cognitive functioning.

METHODS

Thirteen adolescent male patients (9-16 years) with a diagnosis of ADHD according to the DSM-IV and long-term stimulant medication (for at least 6 months) with MPH were assessed twice within 7 days using SPECT after application of I-123-β-CIT to examine DAT binding potential (DAT BP). SPECT measures took place in an on- and off-MPH status balanced for order across participants. A virtual reality continuous performance test was performed at each time point. Further clinical symptoms were assessed for baseline off-MPH.

RESULTS

On-MPH status was associated with a highly significant change (-29.9%) of striatal DAT BP as compared to off-MPH ( = -4.12, = 0.002). A more pronounced change in striatal DAT BP was associated with higher off-MPH attentional and externalizing symptom ratings (Pearson = 0.68, = 0.01). Striatal DAT BP off-MPH, but not on-MPH, was associated with higher symptom ratings (Pearson = 0.56, = 0.04).

CONCLUSION

Our findings corroborate previous reports from mainly adult samples that MPH changes striatal DAT BP availability and suggest higher off-MPH DAT BP, likely reflecting low baseline DA levels, as a marker of symptom severity.

摘要

背景

哌甲酯(MPH)是治疗注意力缺陷多动障碍(ADHD)的一线药物。MPH与多巴胺(DA)转运体(DAT)结合,DAT在纹状体中密度较高。在儿童和青少年患者中,通过单光子发射计算机断层扫描(SPECT)评估纹状体多巴胺转运体的情况较为少见,但可以深入了解MPH的作用如何影响DAT的可用性。我们的受试者内研究旨在调查MPH对DAT可用性的影响,以及DAT可用性对MPH的反应性如何与临床症状和认知功能相关联。

方法

13名年龄在9至16岁、根据《精神疾病诊断与统计手册》第四版(DSM-IV)诊断为ADHD且长期使用MPH进行刺激治疗(至少6个月)的青少年男性患者,在应用I-123-β-CIT后7天内使用SPECT进行两次评估,以检查DAT结合潜力(DAT BP)。SPECT测量在MPH用药状态和停药状态下进行,参与者的顺序保持平衡。在每个时间点进行虚拟现实持续操作测试。在MPH停药基线时评估进一步的临床症状。

结果

与MPH停药状态相比,MPH用药状态与纹状体DAT BP的高度显著变化(-29.9%)相关(t = -4.12,p = 0.002)。纹状体DAT BP更明显的变化与更高的MPH停药时注意力和外化症状评分相关(Pearson r = 0.68,p = 0.01)。MPH停药时的纹状体DAT BP,而非MPH用药时的纹状体DAT BP,与更高的症状评分相关(Pearson r = 0.56,p = 0.04)。

结论

我们的研究结果证实了之前主要来自成人样本的报告,即MPH会改变纹状体DAT BP的可用性,并表明MPH停药时较高的DAT BP可能反映了低基线DA水平,可作为症状严重程度的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/218193156140/fpsyt-13-804730-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/45ff534b15f6/fpsyt-13-804730-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/031947ba2846/fpsyt-13-804730-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/74123246ca3e/fpsyt-13-804730-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/51ca78d54a1e/fpsyt-13-804730-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/de0ec8f140a0/fpsyt-13-804730-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/218193156140/fpsyt-13-804730-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/45ff534b15f6/fpsyt-13-804730-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/031947ba2846/fpsyt-13-804730-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/74123246ca3e/fpsyt-13-804730-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/51ca78d54a1e/fpsyt-13-804730-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/de0ec8f140a0/fpsyt-13-804730-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c6e/9046584/218193156140/fpsyt-13-804730-g0006.jpg

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