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Transcranial Direct Current Stimulation of the Temporoparietal Junction in Autism Spectrum Disorder: Results of a Phase‐IIa Randomized, Double‐Blind, Sham‐Controlled Feasibility Study

经颅直流电刺激 自闭症谱系障碍 颞顶交界 心理学 神经科学 听力学 自闭症 刺激 相(物质) 双盲 随机对照试验 医学 发展心理学 物理 认知 内科学 病理 替代医学 量子力学 前额叶皮质 安慰剂
作者
Christina Luckhardt,Magdalena Schütz,Andreas M. Mühlherr,Sara Boxhoorn,Christine Ecker,Hanna Mössinger,Julia Siemann,Fabienne Schlechter,Miguel Castelo‐Branco,H. C. Pereira,Marianne Latinus,Camille Ricou,Frédérique Bonnet‐Brilhault,Ricardo Salvador,Giulio Ruffini,Rafał Nowak,Michael Siniatchkin,Astrid Dempfle,Christine M. Freitag
出处
期刊:Autism Research [Wiley]
卷期号:18 (9): 1861-1876 被引量:1
标识
DOI:10.1002/aur.70084
摘要

Activation of the temporoparietal junction (TPJ) is reduced in autism spectrum disorder (ASD) during social cognitive tasks. Therefore, anodal transcranial direct current stimulation (tDCS) of the TPJ may enhance social cognitive abilities in autistic individuals. In a multicenter, randomized, sham-controlled, double-blind parallel-group Phase-IIa trial, we investigated feasibility, safety, and effect sizes of 10 sessions of anodal tDCS of the bilateral TPJ at 2 mA as an add-on to computer-based social cognitive training in 10- to 17-year-old youth with autism. Feasibility of recruitment was low, with only 11% of screened individuals being randomized to tDCS (N = 12) or sham (N = 12). In contrast, retention in the study, data collection, intervention adherence, and technical feasibility were mostly excellent. No serious adverse events occurred, and stimulation was well tolerated. There were no differences in the prespecified primary outcome social responsiveness between sham and tDCS immediately after the intervention (standardized estimated effect size [ES] = 0.098; 95%-confidence interval [95% CI] -1.043;1.240), but the sham group showed a trend for better social responsiveness at the 4 week follow-up (ES = 1.106; 95% CI -0.054; 2.270). Secondary outcomes including questionnaires and event-related potentials showed improved compulsive behavior and quality of life by tDCS. High technical feasibility, participant retention, and safety highlight the potential of tDCS in autism and may inform future improvements in the feasibility of recruitment. The differential pattern of effect estimates indicates positive, but also potential negative effects of tDCS, which may vary due to tDCS stimulation parameters. The trial was prospectively registered in the German Clinical Trials Register (Deutsches Register für klinische Studien, DRKS, DRKS00014732).
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