Efficacy of repetitive transcranial magnetic stimulation in cognitive impairment of neurodegenerative diseases: a systematic review and meta-analysis

Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation target...

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Published inBMC neurology Vol. 25; no. 1; pp. 295 - 14
Main Authors Zhang, Yu, Xu, Ke, Wang, Yulin, Shen, Yiwei, Liu, Zhengnan, Zhang, Chengguang, Zhou, Yan, Lv, Peizhu, Bai, Yan, Wang, Shun
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Published England BioMed Central Ltd 17.07.2025
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Abstract Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND. For two common types of ND Alzheimer's disease (AD) and Parkinson's disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson's disease, Alzheimer's disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC. We screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48). rTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.
AbstractList Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND.OBJECTIVECurrently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND.For two common types of ND Alzheimer's disease (AD) and Parkinson's disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson's disease, Alzheimer's disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC.METHODSFor two common types of ND Alzheimer's disease (AD) and Parkinson's disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson's disease, Alzheimer's disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC.We screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48).RESULTSWe screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48).rTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.CONCLUSIONrTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.
ObjectiveCurrently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND.MethodsFor two common types of ND Alzheimer’s disease (AD) and Parkinson’s disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson’s disease, Alzheimer’s disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC.ResultsWe screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48).ConclusionrTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.
Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND. For two common types of ND Alzheimer's disease (AD) and Parkinson's disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson's disease, Alzheimer's disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC. We screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48). rTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.
Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND. For two common types of ND Alzheimer's disease (AD) and Parkinson's disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson's disease, Alzheimer's disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC. We screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48). rTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.
Abstract Objective Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND. Methods For two common types of ND Alzheimer’s disease (AD) and Parkinson’s disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson’s disease, Alzheimer’s disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC. Results We screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48). Conclusion rTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution.
Objective Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and emotional domains of neurodegenerative diseases (ND), leading to the absence of a unified and effective rTMS treatment protocol or stimulation targets. This systematic review and meta-analysis summarizes existing evidence to evaluate the efficacy of rTMS targeting the dorsolateral prefrontal cortex (DLPFC) and non-DLPFC in the cognitive and emotional aspects of ND. Methods For two common types of ND Alzheimer's disease (AD) and Parkinson's disease (PD), we included 17 relevant randomized controlled trials (RCTs) from five databases. Search terms included rTMS, Parkinson's disease, Alzheimer's disease, cognitive impairment, and randomized controlled studies. Two independent reviewers assessed the risk of bias in the included literature, performed data extraction, and evaluated the evidence. Treatment effects were assessed using the Montreal Cognitive Assessment (MoCA), the Mini-Mental State Examination (MMSE), the Hamilton Depression Rating Scale (HAMD), the Hamilton Anxiety Rating Scale (HAMA), and Activities of Daily Living (ADL). Data were analyzed using R software to evaluate effect sizes and 95% confidence interval (CI). Heterogeneity tests were conducted to assess differences in treatment effects between DLPFC and non-DLPFC. Results We screened 3,467 articles and identified 17 studies that met the inclusion criteria. The pooled results showed significant effects: MoCA (MD: 2.13, 95% CI [0.75, 3.52], p < 0.001); MMSE (MD: 1.16, 95% CI [0.91, 1.41], p = 0.0075); HAMD (MD: -2.63, 95% CI [-6.45, -1.20], p = 0.14); HAMA (SMD: -0.62, 95% CI [-0.91, -0.33], p < 0.001); ADL (MD: -0.56, 95% CI [-1.10, 2.22], p = 0.48). Conclusion rTMS has a positive effect on cognitive impairment and emotional abnormalities associated with ND. There is a significant difference in MoCA scores between rTMS applied to DLPFC and non-DLPFC. DLPFC may serve as a reliable stimulation target for treating non-motor symptoms related to ND (such as cognitive and emotional issues), which is beneficial for developing an rTMS treatment protocol with broad applicability for ND. However, due to the small number of included studies and the indirect nature of the comparison methods, we should interpret these results with caution. Keywords: RTMS, Neurodegenerative diseases, Alzheimer's disease, Parkinson's disease, DLPFC/non-DLPFC, Meta-analysis, Cognitive and emotional disorders
ArticleNumber 295
Audience Academic
Author Zhou, Yan
Wang, Shun
Xu, Ke
Zhang, Yu
Shen, Yiwei
Liu, Zhengnan
Wang, Yulin
Lv, Peizhu
Bai, Yan
Zhang, Chengguang
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/40676541$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1177/1545968321104131
10.1002/alz.13016
10.1016/j.brs.2022.02.011
10.1016/j.heliyon.2023.e18364
10.1097/WCO.0000000000000795
10.1016/j.jelekin.2021.102622
10.3233/JPD-212978
10.1016/j.brs.2020.09.010
10.1080/00207454.2018.1486837
10.1016/j.brs.2009.10.005
10.3171/2019.6.JNS191224
10.1101/cshperspect.a023705
10.3390/ijms232112854
10.1172/JCI158453
10.3389/fnagi.2024.1363115
10.1001/jamanetworkopen.2024.9220
10.1212/WNL.0000000000003279
10.1136/bmj.d5928
10.1177/15500594211042708
10.1001/jamapsychiatry.2017.3292
10.4103/0366-6999.247217
10.1016/j.jad.2023.04.085
10.1016/j.neucli.2006.08.003
10.1017/S1461145707007961
10.1016/j.parkreldis.2020.07.006
10.1002/jcp.29248
10.4103/1673-5374.276329
10.1093/brain/awac322
10.1016/j.brs.2021.01.012
10.1002/gps.5974
10.18632/oncotarget.13060
10.1186/s12984-023-01123-w
10.1016/j.cell.2022.12.032
10.1101/cshperspect.a028035
10.1016/S0140-6736(21)00218-X
10.2147/NDT.S403002
10.1016/j.clinph.2019.11.002
10.1016/j.brs.2021.11.007
10.1016/j.biopsych.2024.06.016
10.3389/fnagi.2024.1354455
10.1016/j.jclinepi.2010.07.017
10.1159/000445296
10.1093/scan/nsaa082
10.1016/j.brs.2022.11.009
10.1016/j.arr.2023.101919
10.3390/ijms19103082
10.1101/cshperspect.a033118
10.1016/j.neulet.2021.136337
10.1016/j.psychres.2022.114721
10.1016/j.cger.2019.09.012
10.1136/bmj.g7647
10.1155/2018/8584653
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Issue 1
Keywords Cognitive and emotional disorders
Parkinson's disease
DLPFC/non-DLPFC
Neurodegenerative diseases
Alzheimer's disease
RTMS
Meta-analysis
Language English
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References DM Cammisuli (4292_CR52) 2020; 15
S Ray (4292_CR56) 2020; 36
G Nasios (4292_CR13) 2018; 2018
TC Cheng (4292_CR35) 2022; 12
M Li (4292_CR27) 2022; 15
EM Khedr (4292_CR40) 2020; 38
JP Higgins (4292_CR31) 2011; 343
NI Bradfield (4292_CR12) 2023; 54
S Komaitis (4292_CR51) 2020; 133
S Golriz Khatami (4292_CR8) 2020; 33
4292_CR4
4292_CR3
4292_CR5
4292_CR2
A Miller (4292_CR49) 2023; 38
W Song (4292_CR43) 2024; 16
Y Hu (4292_CR37) 2022; 15
4292_CR10
X Li (4292_CR50) 2023; 334
Y Zhang (4292_CR15) 2024; 16
A Makkos (4292_CR42) 2016; 73
M Jiang (4292_CR53) 2022; 3
W He (4292_CR36) 2021; 35
GH Guyatt (4292_CR32) 2011; 64
JP Lefaucheur (4292_CR55) 2020; 131
L Wei (4292_CR20) 2022; 315
JC Rothwell (4292_CR14) 1991; 43
BR Bloem (4292_CR47) 2021; 397
C Bagattini (4292_CR33) 2020; 13
JM Hoogendam (4292_CR19) 2010; 3
J Zhao (4292_CR25) 2017; 8
EF Cardoso (4292_CR34) 2008; 11
X Zhou (4292_CR45) 2022; 766
DM Wilson 3rd (4292_CR1) 2023; 186
T Zhang (4292_CR48) 2023; 19
S Jiang (4292_CR38) 2023; 9
M Brys (4292_CR57) 2016; 87
AU Khan (4292_CR11) 2019; 129
Y Gao (4292_CR16) 2023; 87
G Pateraki (4292_CR18) 2022; 62
4292_CR7
NS Philip (4292_CR54) 2018; 3
M Duggan (4292_CR6) 2020; 235
4292_CR9
YH Jung (4292_CR39) 2024; 7
Z Moussavi (4292_CR26) 2022; 145
J Li (4292_CR41) 2020; 80
JP Lefaucheur (4292_CR24) 2006; 36
YC Lin (4292_CR28) 2018; 131
X Wu (4292_CR44) 2022; 15
MKP Joyce (4292_CR23) 2025; 97
X Li (4292_CR17) 2021; 14
MM Pulopulos (4292_CR21) 2022; 17
L Shamseer (4292_CR29) 2015; 350
M Cumpston (4292_CR30) 2019; 10
S Kumar (4292_CR22) 2017; 74
S Zhuang (4292_CR46) 2020; 2020
M Pastore-Wapp (4292_CR58) 2023; 20
References_xml – volume: 35
  start-page: 986
  issue: 11
  year: 2021
  ident: 4292_CR36
  publication-title: Neurorehabil Neural Repair
  doi: 10.1177/1545968321104131
– ident: 4292_CR10
  doi: 10.1002/alz.13016
– volume: 15
  start-page: 437
  issue: 2
  year: 2022
  ident: 4292_CR27
  publication-title: Brain Stimul
  doi: 10.1016/j.brs.2022.02.011
– volume: 9
  start-page: e18364
  issue: 8
  year: 2023
  ident: 4292_CR38
  publication-title: Heliyon
  doi: 10.1016/j.heliyon.2023.e18364
– volume: 2020
  start-page: 7295414
  year: 2020
  ident: 4292_CR46
  publication-title: Parkinsons Dis.
– volume: 33
  start-page: 249
  issue: 2
  year: 2020
  ident: 4292_CR8
  publication-title: Curr Opin Neurol
  doi: 10.1097/WCO.0000000000000795
– volume: 62
  start-page: 102622
  year: 2022
  ident: 4292_CR18
  publication-title: J Electromyogr Kinesiol
  doi: 10.1016/j.jelekin.2021.102622
– volume: 12
  start-page: 723
  issue: 2
  year: 2022
  ident: 4292_CR35
  publication-title: J Parkinsons Dis
  doi: 10.3233/JPD-212978
– volume: 13
  start-page: 1655
  issue: 6
  year: 2020
  ident: 4292_CR33
  publication-title: Brain Stimul
  doi: 10.1016/j.brs.2020.09.010
– volume: 43
  start-page: 29
  year: 1991
  ident: 4292_CR14
  publication-title: Electroencephalogr Clin Neurophysiol Suppl
– volume: 129
  start-page: 55
  issue: 1
  year: 2019
  ident: 4292_CR11
  publication-title: Int J Neurosci
  doi: 10.1080/00207454.2018.1486837
– volume: 3
  start-page: 95
  issue: 2
  year: 2010
  ident: 4292_CR19
  publication-title: Brain Stimul
  doi: 10.1016/j.brs.2009.10.005
– volume: 133
  start-page: 1503
  issue: 5
  year: 2020
  ident: 4292_CR51
  publication-title: J Neurosurg
  doi: 10.3171/2019.6.JNS191224
– ident: 4292_CR2
  doi: 10.1101/cshperspect.a023705
– ident: 4292_CR9
  doi: 10.3390/ijms232112854
– ident: 4292_CR7
  doi: 10.1172/JCI158453
– volume: 3
  start-page: 211
  issue: 3
  year: 2018
  ident: 4292_CR54
  publication-title: Biol Psychiatry Cogn Neurosci Neuroimaging
– volume: 16
  start-page: 1363115
  year: 2024
  ident: 4292_CR15
  publication-title: Front Aging Neurosci
  doi: 10.3389/fnagi.2024.1363115
– volume: 7
  start-page: e249220
  issue: 5
  year: 2024
  ident: 4292_CR39
  publication-title: JAMA Netw Open
  doi: 10.1001/jamanetworkopen.2024.9220
– volume: 87
  start-page: 1907
  issue: 18
  year: 2016
  ident: 4292_CR57
  publication-title: Neurology
  doi: 10.1212/WNL.0000000000003279
– volume: 343
  start-page: d5928
  year: 2011
  ident: 4292_CR31
  publication-title: BMJ
  doi: 10.1136/bmj.d5928
– volume: 54
  start-page: 4
  issue: 1
  year: 2023
  ident: 4292_CR12
  publication-title: Clin EEG Neurosci
  doi: 10.1177/15500594211042708
– volume: 74
  start-page: 1266
  issue: 12
  year: 2017
  ident: 4292_CR22
  publication-title: JAMA Psychiatry
  doi: 10.1001/jamapsychiatry.2017.3292
– volume: 10
  start-page: Ed000142
  issue: 10
  year: 2019
  ident: 4292_CR30
  publication-title: Cochrane Database Syst Rev
– volume: 131
  start-page: 2899
  issue: 24
  year: 2018
  ident: 4292_CR28
  publication-title: Chin Med J (Engl)
  doi: 10.4103/0366-6999.247217
– volume: 334
  start-page: 180
  year: 2023
  ident: 4292_CR50
  publication-title: J Affect Disord
  doi: 10.1016/j.jad.2023.04.085
– volume: 36
  start-page: 125
  issue: 3
  year: 2006
  ident: 4292_CR24
  publication-title: Neurophysiol Clin
  doi: 10.1016/j.neucli.2006.08.003
– volume: 11
  start-page: 173
  issue: 2
  year: 2008
  ident: 4292_CR34
  publication-title: Int J Neuropsychopharmacol
  doi: 10.1017/S1461145707007961
– volume: 80
  start-page: 113
  year: 2020
  ident: 4292_CR41
  publication-title: Parkinsonism Relat Disord
  doi: 10.1016/j.parkreldis.2020.07.006
– volume: 235
  start-page: 3131
  issue: 4
  year: 2020
  ident: 4292_CR6
  publication-title: J Cell Physiol
  doi: 10.1002/jcp.29248
– volume: 15
  start-page: 1650
  issue: 9
  year: 2020
  ident: 4292_CR52
  publication-title: Neural Regen Res
  doi: 10.4103/1673-5374.276329
– volume: 145
  start-page: 3730
  issue: 11
  year: 2022
  ident: 4292_CR26
  publication-title: Brain
  doi: 10.1093/brain/awac322
– volume: 14
  start-page: 503
  issue: 3
  year: 2021
  ident: 4292_CR17
  publication-title: Brain Stimul
  doi: 10.1016/j.brs.2021.01.012
– volume: 38
  start-page: e5974
  issue: 8
  year: 2023
  ident: 4292_CR49
  publication-title: Int J Geriatr Psychiatry
  doi: 10.1002/gps.5974
– volume: 8
  start-page: 33864
  issue: 20
  year: 2017
  ident: 4292_CR25
  publication-title: Oncotarget
  doi: 10.18632/oncotarget.13060
– volume: 20
  start-page: 2
  issue: 1
  year: 2023
  ident: 4292_CR58
  publication-title: J Neuroeng Rehabil
  doi: 10.1186/s12984-023-01123-w
– volume: 186
  start-page: 693
  issue: 4
  year: 2023
  ident: 4292_CR1
  publication-title: Cell
  doi: 10.1016/j.cell.2022.12.032
– volume: 38
  start-page: 55
  issue: 1
  year: 2020
  ident: 4292_CR40
  publication-title: Restor Neurol Neurosci
– ident: 4292_CR4
  doi: 10.1101/cshperspect.a028035
– volume: 397
  start-page: 2284
  issue: 10291
  year: 2021
  ident: 4292_CR47
  publication-title: Lancet
  doi: 10.1016/S0140-6736(21)00218-X
– volume: 19
  start-page: 1477
  year: 2023
  ident: 4292_CR48
  publication-title: Neuropsychiatr Dis Treat
  doi: 10.2147/NDT.S403002
– volume: 131
  start-page: 474
  issue: 2
  year: 2020
  ident: 4292_CR55
  publication-title: Clin Neurophysiol
  doi: 10.1016/j.clinph.2019.11.002
– volume: 15
  start-page: 35
  issue: 1
  year: 2022
  ident: 4292_CR44
  publication-title: Brain Stimul
  doi: 10.1016/j.brs.2021.11.007
– volume: 97
  start-page: 359
  issue: 4
  year: 2025
  ident: 4292_CR23
  publication-title: Biol Psychiatry
  doi: 10.1016/j.biopsych.2024.06.016
– volume: 16
  start-page: 1354455
  year: 2024
  ident: 4292_CR43
  publication-title: Front Aging Neurosci
  doi: 10.3389/fnagi.2024.1354455
– volume: 3
  start-page: 100308
  issue: 6
  year: 2022
  ident: 4292_CR53
  publication-title: Innov (Camb)
– volume: 64
  start-page: 407
  issue: 4
  year: 2011
  ident: 4292_CR32
  publication-title: J Clin Epidemiol
  doi: 10.1016/j.jclinepi.2010.07.017
– volume: 73
  start-page: 169
  issue: 3
  year: 2016
  ident: 4292_CR42
  publication-title: Neuropsychobiology
  doi: 10.1159/000445296
– volume: 17
  start-page: 109
  issue: 1
  year: 2022
  ident: 4292_CR21
  publication-title: Soc Cogn Affect Neurosci
  doi: 10.1093/scan/nsaa082
– volume: 15
  start-page: 1530
  issue: 6
  year: 2022
  ident: 4292_CR37
  publication-title: Brain Stimul
  doi: 10.1016/j.brs.2022.11.009
– volume: 87
  start-page: 101919
  year: 2023
  ident: 4292_CR16
  publication-title: Ageing Res Rev
  doi: 10.1016/j.arr.2023.101919
– ident: 4292_CR3
  doi: 10.3390/ijms19103082
– ident: 4292_CR5
  doi: 10.1101/cshperspect.a033118
– volume: 766
  start-page: 136337
  year: 2022
  ident: 4292_CR45
  publication-title: Neurosci Lett
  doi: 10.1016/j.neulet.2021.136337
– volume: 315
  start-page: 114721
  year: 2022
  ident: 4292_CR20
  publication-title: Psychiatry Res
  doi: 10.1016/j.psychres.2022.114721
– volume: 36
  start-page: 93
  issue: 1
  year: 2020
  ident: 4292_CR56
  publication-title: Clin Geriatr Med
  doi: 10.1016/j.cger.2019.09.012
– volume: 350
  start-page: g7647
  year: 2015
  ident: 4292_CR29
  publication-title: BMJ
  doi: 10.1136/bmj.g7647
– volume: 2018
  start-page: 8584653
  year: 2018
  ident: 4292_CR13
  publication-title: Behav Neurol.
  doi: 10.1155/2018/8584653
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Snippet Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and...
Objective Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive...
ObjectiveCurrently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the cognitive and...
Abstract Objective Currently, there is a lack of reliable evidence to prove the effectiveness of repetitive transcranial magnetic stimulation (rTMS) in the...
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SubjectTerms Activities of daily living
Alzheimer Disease - psychology
Alzheimer Disease - therapy
Alzheimer's disease
Analysis
Bias
Care and treatment
Clinical trials
Cognitive ability
Cognitive Dysfunction - etiology
Cognitive Dysfunction - therapy
Degeneration
Dementia
Depression, Mental
Diagnosis
Disease
DLPFC/non-DLPFC
Electrophysiology
Emotions
Evidence-based medicine
Handbooks
Humans
Intervention
Magnetic brain stimulation
Magnetic fields
Memory
Meta-analysis
Methods
Movement disorders
Nervous system
Neural networks
Neurodegenerative diseases
Neurodegenerative Diseases - complications
Neurodegenerative Diseases - psychology
Neurodegenerative Diseases - therapy
Parkinson Disease - complications
Parkinson Disease - psychology
Parkinson Disease - therapy
Parkinson's disease
Patient outcomes
Prefrontal cortex
Randomized Controlled Trials as Topic - methods
RTMS
Systematic review
Transcranial magnetic stimulation
Transcranial Magnetic Stimulation - methods
Treatment Outcome
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Title Efficacy of repetitive transcranial magnetic stimulation in cognitive impairment of neurodegenerative diseases: a systematic review and meta-analysis
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