Non-randomized clinical trial of repetitive transcranial magnetic stimulation in the treatment of children with Rett syndrome

WANG Chao, LI Hui-ping, ZHOU Bing-rui, LI Chun-yang, ZHANG Ying, DONG Ping

Chinese Journal of Child Health Care ›› 2019, Vol. 27 ›› Issue (7) : 771-774.

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Chinese Journal of Child Health Care ›› 2019, Vol. 27 ›› Issue (7) : 771-774. DOI: 10.11852/zgetbjzz2018-1810

Non-randomized clinical trial of repetitive transcranial magnetic stimulation in the treatment of children with Rett syndrome

  • WANG Chao1,2, LI Hui-ping1, ZHOU Bing-rui1, LI Chun-yang1, ZHANG Ying1, DONG Ping1
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Abstract

Objectives To investigate the efficacy of repetitive transcranial magnetic stimulation(rTMS) in the treatment of Rett syndrome(RTT),so as to provide reference for clinical treatment. Methods Totally 17 children with Rett syndrome who met the criterion were enrolled in this study from January 2015 to April 2018,and were non-randomly divided into the TMS group(n=7) and control group(n=10). The TMS group was given rTMS for 6 months,while the control group received routine follow-up. All children were tested for MECP2 gene and were assessed by Griffiths Mental Development Scale-Chinese Version(GDS-C),Peabody Development Motor Scales(PDMS),Children′s Sleep Habits Questionnaire(CSHQ),flash visual evoked potential(FVEP) and brainstem auditory evoked potential(BAEP) at admission and 6 months respectively. Results 1) The overall development and motor ability of the children in TMS group and control group showed obviously degenerative changes,but the differences between the two groups were not significant(P>0.05). 2) The sleep duration of children in TMS group and control group was shorter. After 6 months of rTMS intervention in TMS group,the average sleep duration of children in TMS group was longer than that of control group,but there was no significant difference between the two groups[ΔTMS group:(0.83±0.97) h vs. Δ control group:(-0.40±1.20) h,P>0.05]. 3) There were no significant changes on the results of FVEP and BAEP before and after treatment,so was the difference between the two groups(P>0.05). 4) rTMS was safe during treatment and no adverse events were reported. Conclusions Repeated transcranial magnetic stimulation may prolong the sleep duration and improve the quality of sleep in RTT children. Moreover,rTMS treatment has no significant effect on the progression of mental and motor developmental levels in RTT children,as well as the parameters of FVEP and BAEP. Meanwhile,there are no serious adverse reactions during the use of rTMS

Key words

repetitive transcranial magnetic stimulation / Rett syndrome / sleep duration / psychomotor development / visual evoked potential / auditory evoked potential

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WANG Chao, LI Hui-ping, ZHOU Bing-rui, LI Chun-yang, ZHANG Ying, DONG Ping. Non-randomized clinical trial of repetitive transcranial magnetic stimulation in the treatment of children with Rett syndrome[J]. Chinese Journal of Child Health Care. 2019, 27(7): 771-774 https://doi.org/10.11852/zgetbjzz2018-1810

References

[1] Neul JL,Kaufmann WE,Glaze DG,et al.Rett syndrome:revised diagnostic criteria and nomenclature[J].Ann Neurol,2010,68(6):944-950.
[2] Liyanage VR,Rastegar M.Rett syndrome and MeCP2[J].Neuromol Med,2014,16(2):231-264.
[3] Tillotson R,Selfridge J,Koerner MV,et al.Radically truncated MeCP2 rescues Rett syndrome-like neurological defects[J].Nature,2017,550(7676):398-401.
[4] Carrette LLG,BlumR,MaW,et al.Tsix-Mecp2 female mous e model for Rett syndrome reveals that low-level MECP2 expression extends life and improves neuromotor function[J].P National Acad Sci USA,2018,115(32):8185-8190.
[5] Balakrishnan S,Mironov SL.Rescue of hyperexcitability in hippocampal CA1 neurons from Mecp2(-/y)mouse through surface potential neutralization[J].PLoS One,2018,13(4):e0195094.
[6] Xiao L,Correll CU,Feng L,et al.Rhythmic low-field magnetic stimulation may improve depression by increasing brain-derived neurotrophic factor[J].CNS Spectr,2019,24(3):313-321.
[7] Landeros-Weisenberger A,Mantovani A,Motlagh MG,et al.Randomized sham controlled double-blind trial of repetitive transcranial magnetic stimulation for adults with severe tourette syndrome[J].Brain Stimul,2015,8(3):574-581.
[8] Lee YJ,Koo BH,Seo WS,et al.Repetitive transcranial magnetic stimulation of the supplementary motor area in treatment-resistant obsessive-compulsive disorder:an open-label pilot study[J].J Clin Neurosci,2017,44:264-268.
[9] Barahona-Correa JB,Velosa A,Chainho A,et al.Repetitive transcranial magnetic stimulation for treatment of autism spectrum disorder:a systematic review and meta Analysis[J].Front Integr Neurosci,2018,12:27.
[10] Eeíková A,Jech R, ejka V,et al.Benefits of pallidal stimulation in dystonia are linked to cerebellar volume and cortical inhibition[J].Sci Rep,2018,8(1):17218.
[11] Chou YH,Hickey PT,Sundman M,et al.Effects of repetitive transcranial magnetic stimulation on motor symptoms in Parkinson disease:a systematic review and meta-analysis[J].JAMA Neurol,2015,72(4):432-440.
[12] Yang C,Guo Z,Peng H,et al.Repetitive transcranial magnetic stimulation therapy for motor recovery in Parkinson′s disease:a Meta-analysis[J].Brain Behav,2018,8(11):e01132.
[13] Iimori T,Nakajima S,Miyazaki T,et al.Effectiveness of the prefrontal repetitive transcranial magnetic stimulation on cognitive profiles in depression,schizophrenia,and Alzheimer′s disease:a systematic review[J].Prog Neuro-Psychoph,2019,88:31-40.
[14] Zhang Y,Mao RR,Chen ZF,et al.Deep-brain magnetic stimulation promotes adult hippocampal neurogenesis and alleviates stress-related behaviors in mouse models for neuropsychiatric disorders[J].Mol Brain,2014,7:11.
[15] Hermiller MS,Vanhaerents S,Raij T,et al.Frequency-specific noninvasive modulation of memory retrieval and its relationship with hippocampal network connectivity[J].Hippocampus,2018.doi:10.1002/hipo.23054.
[16] Owen,JA,Spirito A,McGuinn M.The Children′s Sleep Habits Questionnaire(CSHQ):psyshome tric propen ties of a survey instrument for schoolaged children[J].Sleep,2000,23(8):1043-1051.
[17] 陈文娟,李锋,李生慧,等.常用儿童睡眠时间评估方法的比较研究[J].中华儿科杂志,2012,50(4):5.
[18] Liao W.Psychomotor dysfunction in Rett syndrome:insights into the neurochemical and circuit roots[J].Dev Neurobiol,2019,79(1):51-59.
[19] Wu Y,Cui N,Xing H,et al.Mecp2 disruption in rats causes reshaping in firing activity and patterns of brainstem respiratory neurons[J].Neuroscience,2019,397:107-115.
[20] Amaddeo A,Desanctis L,Arroyo JO,et al.Polysomnograp- hic findings in Rett syndrome[J].Eur J Paediatr Neurol,2019,23(1):214-221.
[21] Cappuccio G,Bernardo P,Raiano E,et al.Pain and sleep disturbances in Rett syndrome and other neurodevelopmental disorders[J].Acta Paediatr,2019,108(1):171-172.
[22] Nishida M,Kikuchi S,Nisijima K,et al.Actigraphy in patients with major depressive disorder undergoing repetitive transcranial magnetic stimulation:an open label pilot study[J].J ECT,2017,33(1):36-42.
[23] LeBlanc JJ,DeGregorio G,Centofante E,et al.Visual evok- ed potentials detect cortical processing deficits in Rett syndrome[J].Ann Neurol,2015,78(5):775-86.
[24] Foxe JJ,Burke KM,Andrade GN,et al.Automatic cortical representation of auditory pitch changes in Rett syndrome[J].J Neurodev Disord,2016,8(1):34.
[25] Pereira LS,Muller VT,da Mota Gomes M,et al.Safety of repetitive transcranial magnetic stimulation in patients with epilepsy:a systematic review[J].Epilepsy Behav,2016,57:167-176
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