|Year : 2023 | Volume
| Issue : 1 | Page : 13-20
Advancements in repetitive transcranial magnetic Stimulation for ischemic stroke rehabilitation
Yongfang Li1, Ji-Xian Wang2, Guo-Yuan Yang3
1 Department of Rehabilitation Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine; Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China
2 Department of Rehabilitation Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
3 Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China
|Date of Submission||07-Jun-2022|
|Date of Decision||03-Jan-2023|
|Date of Acceptance||03-Jan-2023|
|Date of Web Publication||28-Mar-2023|
MD, PhD, Med-X Research Institute and School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai
Department of Rehabilitation Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai
Source of Support: None, Conflict of Interest: None
Despite significant improvements in acute stroke management, numerous stroke patients continue to experience wide-ranging disabilities, posing a severe global healthcare problem. Effective neuro-rehabilitation is critical for reduction of disability and improvement of life quality after stroke. Rapid developments in several post-ischemic stroke rehabilitation techniques, including magnetic, ultrasonic, optogenetic and electronic modalities, have been achieved in recent years. Repetitive transcranial magnetic stimulation has shown promising therapeutic efficacy in ischemic stroke rehabilitation during the last two decades. This review provides a detailed summary of the development, safety and efficacy of transcranial magnetic stimulation devices, current experimental models and mechanisms of repetitive transcranial magnetic stimulation in the context of ischemic stroke rehabilitation.
Keywords: cellular mechanism; ischemia; rehabilitation; stroke; transcranial magnetic stimulation
|How to cite this article:|
Li Y, Wang JX, Yang GY. Advancements in repetitive transcranial magnetic Stimulation for ischemic stroke rehabilitation. Brain Netw Modulation 2023;2:13-20
|How to cite this URL:|
Li Y, Wang JX, Yang GY. Advancements in repetitive transcranial magnetic Stimulation for ischemic stroke rehabilitation. Brain Netw Modulation [serial online] 2023 [cited 2023 Dec 2];2:13-20. Available from: http://www.bnmjournal.com/text.asp?2023/2/1/13/372307
| Introduction|| |
Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation and neural regulation technique. It regulates cortical excitability in the stimulated and distant sites via electrical current generated by the rapid time-varying electromagnetic field, ultimately modulating neuroplasticity and brain function to achieve therapeutic effects (Rossi et al., 2009). Single-pulse TMS has been employed as a tool for neurophysiological experiments, especially for assessment of corticospinal function, since 1985 (Barker et al., 1985; Rossi et al., 2009). Subsequently, repetitive TMS (rTMS) gained increasing research interest in application evaluation of different diseases following the demonstration of its potential therapeutic effect on depression in 1995 (Fleischmann et al., 1995; Wassermann, 1998; Rossi et al., 2009). Over the past two decades, the applications of rTMS have been expanded to a range of fields including pain relief, mild cognitive impairments, movement disorders, ischemia stroke, Alzheimer’s disease, Parkinson’s disease, multiple sclerosis, consciousness disorders, tinnitus, substance abuse and addiction, schizophrenia and miscellaneous psychiatric conditions (Rossi et al., 2009; Lefaucheur et al., 2020).
Both TMS and transcranial direct current stimulation (tDCS) require close proximity to the scalp. However, compared with tDCS, the magnetic field of TMS can pass through the scalp and skull with almost no attenuation, does not stimulate the scalp and has better tolerance. Since the size and configuration of TMS coils can be specially designed, rTMS exhibits greater focality and spatial resolution than tDCS, potentially reaching areas of ~25 mm2. Moreover, rTMS has a higher temporal resolution higher than tDCS and is easier for doctors and physiotherapists to handle in clinical settings. Based on these characteristics, rTMS provides a suitable tool for probing and stimulation of specific brain circuits (Priori et al., 2009). Overall, rTMS represents a promising therapeutic modality with low risk of severe side-effects and high safety (Lefaucheur et al., 2020; Camacho-Conde et al., 2022).
Ischemic stroke is an acute cerebrovascular disorder with high morbidity, disability and mortality rates associated with significant healthcare costs (GBD 2016 Stroke Collaborators, 2019; Hollist et al., 2021). The stroke patients often live with varying degrees of dysfunction in movement, speech, swallowing, sensation, cognition, balance, emotional control, and so on. The combination of physical therapy, occupational therapy, speech therapy and cognitive rehabilitation is routinely applied to help rehabilitate patients after stroke in clinical practice. Clinical studies and trials of novel rehabilitation therapies including rTMS, tDCS, ultrasound stimulation, deep brain stimulation, virtual reality, robot-assisted therapy and brain-computer interface are in progress to explore the potentials of their future clinical application in management of stroke (Chen et al., 2021; Pruvost-Robieux et al., 2021; Sehle et al., 2021; Singh et al., 2021; Guo et al., 2022). Considerable progress in the development of rTMS for stroke therapy, in particular, post-stroke patient rehabilitation, has been reported over the past two decades (Lefaucheur et al., 2020; Starosta et al., 2022).
In this review, we focus on current advancements in rTMS for stroke rehabilitation, including the development of latest TMS devices, experimental models and contributory mechanisms to the therapeutic effects of rTMS.
Development of Advanced Transcranial Magnetic Stimulation Devices
TMS device systems are relatively large and heavy due to the need of producing fairly rapid time-varying current and high voltage in the coils, which limit the portability of TMS. New TMS devices are designed by advancing hardware and software configurations, adding new complementary technologies based on the old ones (Rossi et al., 2021). With continual development, the TMS devices are getting progressively smaller in size, the pulsed electric field and stimulation focality are getting more controllable. Several TMS devices have been approved for treatment of depression and obsessive-compulsive disorder by the US Food and Drug Administration since 2008 (Gattinger et al., 2012; Paulus et al., 2013; Cohen et al., 2022). These articles may be consulted for more detailed information on TMS device development (Rossi et al., 2021; Zhong et al., 2021; Cohen et al., 2022). Although no TMS devices have been approved for ischemic stroke rehabilitation to date, the possibility of implementing TMS into routine ischemic stroke clinical rehabilitation is under investigation (Smith and Stinear, 2016). As a result of unremitting and ongoing research efforts, improvements in TMS devices and up-to-date treatment indications are continuously being achieved.
Safety of Repetitive Transcranial Magnetic Stimulation
The technical design, manufacturing process, usage and maintenance of TMS require optimization to ensure safety of both subjects and operators. Procedures to enhance the lifetime of the device should be considered, which include insulating high voltage, reducing the heating, friction and vibration of the coils, and generating reliable magnetic fields (Rossi et al., 2021; Zeng et al., 2022). Technical safety may be enhanced by improving the targeting accuracy, response detection sensitivity, efficiency of threshold and dose algorithms of the device (Marjenin et al., 2020; Rossi et al., 2021).
Both the therapeutic and side-effects of TMS mainly depend on the stimulating protocol and device quality. Control of the stimulation dose is the key to minimize side-effects while maximizing the therapeutic effect (Zhong et al., 2021). The most severe side-effect of TMS is seizures, with a recorded overall rate of 0.31 per 10,000 sessions and 0.71 per 1000 patients (Taylor et al., 2021). The intensity, number, patterns, frequency and waveforms of the pulse, distribution of E-field, and individual differences induce alterations in the seizure threshold. Operators should therefore pay attention to these parameters when conducting TMS (Rossi et al., 2021). The lowest parameters for TMS-induced seizures using conventional devices are a single train with 25 Hz frequency and 100% maximal stimulator output continuing for up to 10 seconds. Under optimal parameters of TMS, including the dose and intensity of stimulus, duration, frequency, pulse number and session paradigms, the occurrence of seizures is relatively low (Rossi et al., 2009, 2021).
Experimental Ischemic Models Used in Repetitive Transcranial Magnetic Stimulation Application Investigation
Research on rTMS in ischemic stroke has been performed using rodent and primate models or tissues and cells in vitro (Tang et al., 2017). For ischemic stroke rodent model, mice or rats were subjected to transient or permanent middle cerebral artery occlusion (Peng et al., 2019; Park et al., 2020; Deng et al., 2021), photothrombosis of the cortical area of interest (Zong et al., 2020a, b) or common carotid artery occlusion (Fujiki et al., 2003). For central post-stroke pain, a primate model of unilateral hemorrhage of ventral posterolateral nucleus of the thalamus was used and the effects of rTMS treatment on the ipsilesional primary motor cortex were examined (Kadono et al., 2021). For in vitro studies, hippocampal organotypic culture was incubated with artificial cerebral fluid under hypoxic conditions (Ogiue-Ikeda et al., 2005) or brain cells were exposed to oxygen-glucose deprivation (Hong et al., 2020; Li et al., 2020a).
The cellular and molecular mechanisms underlying efficacy of rTMS in ischemic stroke
Investigations on the cellular mechanisms underlying the therapeutic activity of rTMS in ischemic stroke mainly include: 1) neuronal pathways by which rTMS affects axonal membrane and action potentials and potential alterations in specific biological functions, architecture and neuroplasticity, and 2) whether brain cells other than neurons are affected and the associated pathways (Camacho-Conde et al., 2022; Starosta et al., 2022).
In neurons, rTMS and the induced electric field could activate voltage-dependent calcium channels (Luo et al., 2019; Xia et al., 2021), N-methyl-D-aspartate receptor (Tokay et al., 2014; Natale et al., 2021) and calmodulin-dependent protein kinase II (Xia et al., 2021), along with promoting changes in the release of dopamine, glutamate and gamma-aminobutyric acid (Kanno et al., 2004; Yue et al., 2009; Zhang et al., 2022). These alterations elicit Ca2+ influx, excitatory postsynaptic potential, inhibitory postsynaptic potential and activation of molecular pathways critical for plasticity, such as Akt/mammalian target of rapamycin, mitogen-activated protein kinase/extracellular signal-regulated protein kinase 1/2 and ribosomal protein S6 (Vlachos et al., 2012; Tan et al., 2013; Fujiki et al., 2020). These changes in the synaptic dendrites induce long-term potentiation or long-term depression (Yang et al., 1999), alteration of gene expression and structural remodeling of dendritic spines, further contributing to the plasticity of synapses, neurons and brain (Vlachos et al., 2012; Tokay et al., 2014; Lenz et al., 2015, 2016; Ikeda et al., 2018; Cambiaghi et al., 2021; Tang et al., 2021). For example, cumulative stimulation of rTMS enhanced dentate gyrus neuronal excitability in neonatal mice (Zhu et al., 2021). rTMS additionally upregulated genes associated with synaptic plasticity and downregulated genes associated with inflammation in ischemic rats (Hong et al., 2021, 2022). rTMS could drive structural synaptic plasticity in young and aged mice (Tang et al., 2021), which was related to the improvement of cognition. Moreover, rTMS promoted the secretion of glial cell-derived neurotrophic factor from dopaminergic neurons (Yang et al., 2021). In a rat photothrombotic stroke model, 5 days of exposure to theta-burst rTMS reduced synaptic loss and neuronal degeneration, concomitant with inhibition of the inflammatory response, preservation of mitochondrial membrane integrity and suppression of apoptosis (Zong et al., 2020b). In addition, rTMS pre-treatment induced ischemic tolerance and protected neurons against delayed death, which was associated with the protection of neuronal function and induction of a particular gene set (Fujiki et al., 2003; Ogiue-Ikeda et al., 2005).
High-frequency rTMS (HF-rTMS) was shown to promote neural stem cell (NSC) proliferation possibly via brain-derived neurotrophic factor/Akt signaling and inhibition of inflammation (Zhao et al., 2019; Luo et al., 2022a). rTMS also stimulated NSC migration via the stromal cell-derived factor 1α/C-X-C chemokine receptor 4 axis after ischemic stroke (Deng et al., 2021). Another earlier report suggests that rTMS enhances NSC differentiation into neurons via Ca2+ influx and MAPK signaling after hemorrhagic stroke (Cui et al., 2019). In addition, rMS enhanced miR-106b expression to promote NSC proliferation (Liu et al., 2018).
In astrocytes, rMS could promote astrocytic intracellular calcium release and alters glial fibrillary acidic protein and inflammatory gene expression in vitro (Clarke et al., 2017; Hong et al., 2020). In a rat chronic neuropathic pain model, 20 Hz rTMS suppressed proliferation of astrocytes and downregulated the expression of neuronal nitric oxide synthase, which could potentially contribute to its beneficial effects on neuropathic pain relief (Yang et al., 2018). In a rat photothrombosis stroke model, intermittent theta-burst stimulation (iTBS) beginning 3 hours after stroke for 6 days promoted hypoxia-inducible factor 1-alpha signaling, shifted astrocyte polarization to A2, and increased vascular endothelial growth factor (VEGF) and transforming growth factor beta expression levels, which may partially underlie its activities in reducing blood-brain barrier permeability, increasing angiogenesis, and preserving neuronal and synaptic structure integrity and neurofunction (Zong et al., 2020a). In a rat model of depression, 10 Hz rTMS induced an increase in the number of astrocytes, fibroblast growth factor 2 expression in astrocytes, and activation of the fibroblast growth factor 2/fibroblast growth factor receptor 2/extracellular signal-regulated protein kinase signaling pathway (Yan et al., 2022).
In microglia, long-term low-frequency rTMS (LF-rTMS) stimulation promoted their polarization to M2 phenotype without affecting the proliferation of microglia after ischemia in spontaneously hypertensive rats (Luo et al., 2022a). In a rat photothrombosis stroke model, rTMS also promoted microglia polarization from M1 to M2 phenotype along with decreased interleukin (IL)-1 beta, IL-6, and tumor necrosis factor-α expression (Zong et al., 2020b). Recent studies showed that this effect of TMS on microglia was partially due to inhibition of nuclear factor kappa B and signal transducer and activator of transcription 6 pathway (Luo et al., 2022a), and the toll-like receptor 4/nuclear factor kappa B/NOD-like receptor 3 signaling pathway (Luo et al., 2022b). In addition, iTBS application for 4 weeks suppressed microglia activation and enhanced IL-10 expression at demyelinated lesions in mice (Yang et al., 2020). Stimulation with 25 Hz rTMS for 8 weeks in rat spinal cord injury lesions reduced the expression of ionized calcium binding adapter molecule 1 by ~30% (Kim et al., 2013).
In oligodendrocytes (OLs), 14 consecutive days of iTBS exposure led to an increase in the number of promyelinating and myelinating OLs via promoting OL survival, but had no effect on OL precursor cell (OPC) proliferation or differentiation in normal mouse cortex (Cullen et al., 2019). In vitro, stimulation OPCs with 40 Hz low-field rMS for 5 consecutive days enhanced their differentiation into OLs via activation of transforming growth factor beta 1, Akt and extracellular signal-regulated protein kinase 1/2 pathways (Dolgova et al., 2021). In a mouse model of multiple sclerosis, LF-rTMS stimulation was also shown to promote the expression of myelin basic protein, myelin OL glycoprotein and transforming growth factor beta, finally improving cognitive function (Wang et al., 2021). However, the precise effects of rTMS on OLs and OPCs after stroke remain to be elaborated.
iTBS treatment for 6 days attenuated the apoptosis of both existing and newborn endothelial cells and increased platelet-derived growth factor receptor βexpression in brain microvasculature but had no obvious effect on endothelial cell proliferation at 6 and 22 days following stroke in a rat model of photothrombosis stroke (Zong et al., 2020a).
Recently, the effects of rTMS on the brain glymphatic drainage system have attracted considerable research interest. In a mouse model of Alzheimer’s disease, 14 consecutive days of rTMS exposure enhanced the glymphatic and meningeal lymphatic drainage efficiency of Aβwithout affecting lymphagenesis and further reduced microglia and astrocyte activation, with the improvement of neuronal activity (Lin et al., 2021). In normal wild-type mice, application of continuous theta burst stimulation (cTBS) induced an increase in the diameters of glymphatic and meningeal lymphatic vessels and expression of VEGF-C in the meninges, which were abolished upon inhibition of the VEGF-C/VEGF receptor 3 pathway (Li et al., 2020b). The cellular and molecular mechanisms of rTMS implicated in the treatment of ischemic stroke are summarized in [Figure 1].
|Figure 1: The cellular and molecular mechanisms of rTMS in ischemic stroke.|
Note: rTMS stimulation can act on different brain cells including neurons and other brain cells to promote post-ischemic rehabilitation. rTMS activated voltage-dependent calcium channels and CaMKII, altered neurotransmitter release and gene expression, finally contributed to LTP/LTD, increased neural activity, synaptic plasticity and survival, and decreased neural apoptosis. rTMS could activate BDNF/Akt, SDF-1α/CXCR4 pathway and increase miR-106 level to promote the proliferation, migration and differentiation of NSCs. For astrocytes, rTMS increased intracellular calcium level, VEGF, transforming growth factor beta and fibroblast growth factor 2 expression, inhibited astrocyte proliferation and promoted the A2 polarization. Similarly, rTMS reduced microglia activation but enhanced M2 polarization, decreased the expression of IL-1β, IL-6 and increased IL-10 expression, which was associated with the inhibition of NF-κB/STAT 6 and TLR4/NFκB/NLRP3 pathways. rTMS could promoted angiogenesis through enhance the survival of existing and newborn endothelial cells. However, the effects of rTMS on OLs/OPCs and brain gramphatic system have not yet been investigated in ischemic stroke. BDNF: Brain derived neurotrophic factor; CaMKII: calmodulin-dependent protein kinase II; ERK1/2: extracellular signal-regulated protein kinase 1/2; FGF 2: fibroblast growth factor 2; GDNF: glial cell-derived neurotrophic factor; IL: interleukin; LTD: long-term depression; LTP: long-term potentiation; MBP: myelin basic protein; MOG: myelin oligodendrocyte glycoprotein; NF-κB/STAT 6: nuclear factor kappa B and signal transducer and activator of transcription 6; nNOS: neuronal nitric oxide synthase; NSC: neural stem cell; OL: oligodendrocyte; OPC: oligodendrocyte precursor cell; PDFGR-β: platelet-derived growth factor receptor β; rTMS: repetitive transcranial magnetic stimulation; SDF-1α/CXCR4: stromal cell-derived factor 1α/C-X-C chemokine receptor 4; TLR4/NFκB/NLRP3: Toll-like receptor 4/nuclear factor kappa B/NOD-like receptor 3; TNF-α: tumor necrosis factor-α; VEGF: vascular endothelial growth factor. Created with BioRender.
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The neural circuit mechanisms of rTMS in ischemic stroke
After ischemic stroke, the ipsilateral excitability is reduced, while the contralateral hemisphere is relatively overexcited, in turn further inhibits the ipsilateral excitability (Gerges et al., 2022). This phenomenon, initially reported in 1996, is known as “interhemispheric inhibition” (Boroojerdi et al., 1996). The biphasic balance recovery model links balanced hemispheres and functional recovery with structural integrity after brain injury (Di Pino et al., 2014). The intermispheric inhibition model postulates that patients with less significant injury and greater neural structure integrity have better functional recovery. Currently, this concept is commonly accepted as a theoretical model for rTMS application in ischemic stroke with relatively sufficient structural reservation (Di Pino et al., 2014; Lefaucheur et al., 2020). Based on this theoretical model, application of LF-rTMS/cTBS to inhibit contralateral excitability or HF-rTMS/iTBS to enhance ipsilateral excitability could benefit functional recovery. For these patients, the more balanced excitability between the two hemispheres, the better for the brain functional recovery. Another theoretical model is the variation theory where activity in the ipsilateral brain networks is severely damaged, which usually needs to stimulate the contralateral hemisphere to compensate the functional loss of the ipsilateral hemisphere after ischemic stroke (Finger, 2010; Di Pino et al., 2014). For patients with severe injury and lower neural structure integrity, increased excitability of the contralateral hemisphere may be more conducive to functional recovery, which compensates the function of affected hemisphere. Based on this model, HF-rTMS/iTBS could be applied to increase contralateral excitability for functional recovery under conditions of severe structural damage.
The stimulatory effects and after-effects of rTMS in stroke patients are not limited to the target brain area but also affect the distant interconnected brain circuit and spinal networks (Liew et al., 2014; Klomjai et al., 2015; Charalambous et al., 2016). Moreover, the effects of rTMS depend on the stimulation patterns including frequency, duration and intensity, stimulation loci, lesion location (dominant hemisphere, cortex or subcortex) and stroke stage (Ameli et al., 2009; Lefaucheur et al., 2020; Starosta et al., 2022). The after-effects of rTMS could be sustained from 4 to 12 weeks after stroke treatment (Emara et al., 2010; Lefaucheur et al., 2020; Rossi et al., 2021). Neuroimaging and neurophysiological techniques, such as functional magnetic resonance imaging, single-photon emission computerized tomography, functional near-infrared spectroscopy and electroencephalography, could be effectively used to ascertain the activities of different neural circuits and networks (Liew et al., 2014; Caparelli et al., 2022; Li et al., 2022; Walia et al., 2022). However, our current understanding of the mechanisms by which rTMS affects the stimulated region and interconnected networks remains limited.
Excitatory stimulation patterns with HF-rTMS/iTBS initially increase the excitability of the affected primary motor cortex (M1) and subsequently enhance the activity of supplementary motor area, contralateral corticospinal tract, spinal interneurons and motor neurons, which are responsible for voluntary movement (Hsu et al., 2012; Hannah, 2020). Moreover, rTMS in the affected M1 modulates the connection efficiency between M1, basal ganglia and thalamus (Liew et al., 2014). In contrast, inhibitory LF-rTMS/cTBS to unaffected M1 balances abnormal tanscallosal inhibition and facilitates excitability of the affected M1 and supplementary motor area (Takeuchi et al., 2005; Grefkes et al., 2010; Lefaucheur et al., 2020). A meta-analysis of the effects of rTMS on motor functions in stroke patients showed that both excitatory stimulation of the affected primary motor cortex and inhibitory stimulation of the unaffected hemisphere enhance motor function outcomes of patients (Hsu et al., 2012). However, cTBS stimulation of the contralateral M1 in chronic subcortical stroke patients led to decreased ipsilateral M1 excitability and upper limb function (Ackerley et al., 2010). These inconsistent results highlight the complexity of the neural circuit response after rTMS stimulation, showing variations with stroke stage and location. The neural circuit mechanisms implicated in rTMS therapy for ischemic stroke are briefly summarized in [Figure 2].
|Figure 2: The brief neural circuit mechanisms of rTMS in ischemic stroke.|
Note: In intermispheric inhibition model where the structural reservation is relatively sufficient, using LF-rTMS and/or cTBS to inhibit the unaffected hemisphere, using HF-rTMS and/or iTBS to excite the affected hemisphere, could both increase the excitability of M1, SMA, corticospinal tract, basal ganglia and thalamus. In variation model where the functional structure is severely damaged, using HF-rTMS and/or iTBS to excite the affected hemisphere could facilitate the excitability of the affected M1 and SMA to alternatively activate the affected corticospinal tract. Therefore, choosing appropriate rTMS stimulation protocols according to the actual situation is critical to the functional recovery in post-stroke rehabilitation. cTBS: Continuous theta burst stimulation; HF-rTMS: high-frequency rTMS; iTBS: intermittent theta burst stimulation; LF-rTMS: low-frequency rTMS; M1: primary motor cortex; rTMS: repetitive transcranial magnetic stimulation; SMA: supplementary motor area. Created with BioRender.
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| Conclusion|| |
The safety guidelines for the application of TMS in research and clinical settings is continuously updated and advanced every 10 years proposed by the international consensus conference (Rossi et al., 2009, 2021). In October 2018, the Siena (Italy) consensus conference proposed updating of the 10 safety guidelines for application of TMS in research and clinical settings (Rossi et al., 2009, 2021). Although TMS is used in routine clinical rehabilitation, safety issues require careful consideration. The above conference focused on the safety of available TMS devices and pulse configurations, duties and responsibilities of device manufactures, novel scenarios of TMS applications (such as in the neuroimaging context or imaging-guided and robot-guided TMS), combined effects of TMS interleaved with tDCS, safety during paired associative stimulation interventions, and risks of TMS inducing therapeutic seizures. These revised operational guidelines should facilitate establishment of criteria for appropriate use of TMS in stroke rehabilitation. The ongoing investigation of the underlying mechanisms of rTMS has advanced our understanding of the therapeutic effects of rTMS in post-stroke rehabilitation. Our review summarizes the current underlying mechanisms of rTMS application in stroke rehabilitation. However, the specific parameters and protocols of rTMS and the advanced application of rTMS combined with other therapies are not addressed in this review. We believe the increasing and more specific mechanism studies of rTMS will promote the development of rTMS application in stroke rehabilitation.
YFL conceived and drafted the manuscript and figures. GYY conducted critical revision of this manuscript. JXW contributed the design, discussion, correction and proofread the manuscript. All authors reviewed and approved the final version of the manuscript.
Conflicts of interest
The authors declare that they have no competing interest.
Editor note: JXW, and GYY are Editorial Board members of Brain Network and Modulation. They were blinded from reviewing or making decisions on the manuscript. The article was subject to the journal’s standard procedures, with peer review handled independently of these Editorial Board members and their research groups.
Data availability statement
No additional data are available.
Open access statement
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