Skip to main content
Download PDF
Download ePub

Effects of transcranial magnetic stimulation in modulating cortical excitability in patients with stroke: a systematic review and meta-analysis

Journal of NeuroEngineering and Rehabilitation volume 19, Article number: 24 (2022) Cite this article

Abstract

Background

Transcranial magnetic stimulation (TMS) has attracted plenty of attention as it has been proved to be effective in facilitating motor recovery in patients with stroke. The aim of this study was to systematically review the effects of repetitive TMS (rTMS) and theta burst stimulation (TBS) protocols in modulating cortical excitability after stroke.

Methods

A literature search was carried out using PubMed, Medline, EMBASE, CINAHL, and PEDro, to identify studies that investigated the effects of four rTMS protocols—low and high frequency rTMS, intermittent and continuous TBS, on TMS measures of cortical excitability in stroke. A random-effects model was used for all meta-analyses.

Results

Sixty-one studies were included in the current review. Low frequency rTMS was effective in decreasing individuals’ resting motor threshold and increasing the motor-evoked potential of the non-stimulated M1 (affected M1), while opposite effects occurred in the stimulated M1 (unaffected M1). High frequency rTMS enhanced the cortical excitability of the affected M1 alone. Intermittent TBS also showed superior effects in rebalancing bilateral excitability through increasing and decreasing excitability within the affected and unaffected M1, respectively. Due to the limited number of studies found, the effects of continuous TBS remained inconclusive. Motor impairment was significantly correlated with various forms of TMS measures.

Conclusions

Except for continuous TBS, it is evident that these protocols are effective in modulating cortical excitability in stroke. Current evidence does support the effects of inhibitory stimulation in enhancing the cortical excitability of the affected M1.

Background

Extensive investigations by means of transcranial magnetic stimulation (TMS) have provided pivotal insights into the cortical neurophysiology of patients who have suffered a stroke. Immediately after a stroke, impaired motor function accompanies substantial changes within the affected primary motor cortex (M1)—specifically, decreased corticospinal excitability, which can be reflected by the absence of recordable motor evoked potentials (MEPs)/decreased MEP amplitudes and increased resting/active motor thresholds (rMT/aMT) [1]. Besides, it is also evident that persistent disinhibition is detectable, regardless of chronicity [1], which is believed to have a facilitatory role in motor recovery [2]. For instance, the effects of rehabilitation training correlate with reduced intracortical inhibition, reflected by reduced short-interval intracortical inhibition (SICI) and long-interval intracortical inhibition [3, 4]. With respect to the cortical reorganization within the unaffected M1, as suggested by neuroimaging studies, the unaffected M1 in stroke patients became overactivated during movement execution of the affected hand [5]. Along with recovery of motor functions, stroke patients tend to regain the interhemispheric balance over the bilateral sensorimotor cortices [6]. However, meta-analyses found nonsignificant differences in a series of TMS measures, such as rMT, aMT and MEP amplitudes, compared to healthy controls [1].

In view of the association between cortical excitability and motor impairment of the hemiplegic arm, non-invasive brain modulation by repetitive TMS (rTMS) has attracted plenty of attention as it is effective in facilitating motor relearning and motor recovery after stroke. In accordance with the interhemispheric imbalance model, hemiparesis is caused not only by damaged corticospinal output from the affected M1, but also by excessive transcallosal inhibition from the unaffected to the affected M1 which can be measured by interhemispheric inhibition (IHI) and the ipsilateral silent period (iSP) [7]. Therefore, two unilateral modulatory approaches have been proposed—exciting or inhibiting the affected and unaffected M1—to counterbalance bilateral cortical excitability [8]. Early studies have revealed that both a single session of low frequency rTMS (LF-rTMS) and high frequency rTMS (HF-rTMS) were effective in improving the motor performance of the hemiparetic hand when they were applied to the unaffected and affected M1 [9, 10], respectively. From a neurophysiological perspective, LF-rTMS was shown to significantly reduce the MEPs of the unaffected M1 and the IHI from the unaffected to affected M1 [9, 10], while HF-rTMS had a direct facilitatory effect on the affected M1 [10].

Theta burst stimulation (TBS) is a unique form of rTMS that is usually delivered at subthreshold intensities over a short conditioning period [11, 12]. In healthy people, intermittent TBS (iTBS) was shown to enhance cortical excitability outlasting the stimulation period by almost 30 min, while opposite effects were shown after continuous TBS (cTBS) [13]. In stroke, iTBS to the affected M1 and cTBS to the unaffected M1 were shown to increase and decrease the MEPs, respectively [14]. Clinical studies suggested that both iTBS and cTBS were effective in modulating modulate the cortical excitability in patients with acute stroke [15]; iTBS, but not cTBS, was also able to change the cortical excitability in patients with chronic stroke [14, 16, 17].

Since the early introduction of TMS in the treatment of stroke [9], the clinical effects of various rTMS protocols have been well reviewed [18], and LF-rTMS to the unaffected M1 was shown to be the most effective form of treatment [19]. However, previous meta-analyses and reviews have generally focused only on clinical effects; effects from a neurophysiological perspective were less systematically and statistically reviewed [18]. Because of the inextricable relationship between cortical reorganization and motor recovery, it is necessary to consider how rTMS modulates cortical excitability, and whether the interhemispheric imbalance model is a valid hypothesis underlying the two therapeutic approaches. Therefore, the current systematic review and meta-analysis were conducted to evaluate the effects of four forms of rTMS (namely, LF-rTMS, HF-rTMS, iTBS, and cTBS) on a range of TMS measures of cortical excitability, including rMT, aMT, MEPs, SICI, intracortical facilitation (ICF), and iSP of bilateral M1s. Moreover, not only the accumulated effects of multiple sessions of rTMS, but also the effects of a single session of stimulation were evaluated. We also summarize the correlation between cortical excitability and motor improvement after multiple sessions of stimulation.

Methods

This study was reported in accordance with the preferred reporting items for systematic reviews and meta-analysis statements [20].

Search strategy

A systematic literature search was conducted by the first author using the following electronic databases: PubMed, Medline, EMBASE, CINAHL, and PEDro. The keyword combination of “((stroke) OR cerebrovascular accident) OR (hemiparesis) OR (hemiplegia)) AND ((transcranial magnetic stimulation) OR (TMS) OR (rTMS))” was used for the literature search. A manual search was also conducted, including screening the reference lists of previous systematic reviews and searching for the same keywords in Google Scholar. The last search was conducted on Jun 5, 2021.

Selection criteria and data extraction

This study concerns the effects of both a single session and multiple sessions of rTMS. Therefore, the applied inclusion criteria were: (1) for studies investigating multiple sessions of rTMS, appropriate control groups must be employed; for studies investigating a single session of rTMS, a comparison between pre-rTMS and post-rTMS measures was indispensable; (2) studies using rTMS targeting the M1; (3) studies enrolling adult patients with a unilateral stroke; (4) studies having TMS measures of cortical excitability; (5) studies were published in English. Studies were excluded if they met any of the following exclusion criteria: (1) rTMS was applied in combination with other techniques; (2) bilateral TMS protocols; (3) studies in which necessary data regarding TMS measures were missing.

Once the study selection was completed, two authors independently extracted relevant data which were entered into two customized forms. Any discrepancies regarding data extraction were resolved through discussion.

Quality assessment

A checklist proposed for critically appraising the quality of TMS procedures was used for all the studies [21]. Moreover, the Physiotherapy Evidence Database (PEDro) rating scale was used to appraise the general methodological quality of the studies with a parallel-group design [22].

Data analysis

With respect to those studies ineligible for meta-analysis (e.g., skewed data), their main findings were qualitatively analyzed and integrated with the results of the meta-analyses. If there were two or less studies identified for a single analysis objective, we would not perform a meta-analysis but qualitatively described the results only. Since most studies investigating a single session of rTMS normalized the post-rTMS MEP amplitude to the pre-rTMS value, expressed as a percentage and SD, our meta-analyses computed a pooled mean of the percentage and its 95% confidence intervals (CI). Otherwise, absolute change scores were used to compute Hedges’ g, which corrected the possible bias of the small sample sizes. The Higgins’ I2 statistic was used to check heterogeneity across studies; an I2 value below 50% was considered to reflect low levels of heterogeneity, while an I2 value above 50% indicated high levels of heterogeneity. Given that the characteristics among the included studies were not exactly identical, a random-effects model was used for all the meta-analyses [23]. Publication bias was statistically examined using Egger’s linear regression test and by visually inspecting the funnel plot. The level of significance was set at p < 0.05 for all statistical analyses. Comprehensive Meta-analysis 3.0 software (Englewood, NJ, USA) was used to perform all the meta-analyses in the current study.

Results

Study characteristics

The literature search process is presented in Fig. 1. Finally, 61 original studies were included, of which 45 studies were used for the meta-analyses. The characteristics of studies investigating a single session [9, 10, 14,15,16,17, 24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42] and multiple sessions [43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78] of rTMS are presented in Table 1 and Table 2, respectively.

Fig. 1
figure 1

PRISMA flow diagram

Full size image
Table 1 Characteristics of studies investigating the effects of a single session of rTMS
Full size table
Table 2 Characteristics of studies investigating the effects of multiple sessions of rTMS
Full size table

The methodological quality of the TMS procedures is presented in Supporting Information (Additional file 1: Tables S1 and S2). Overall, the characteristics of the participants, coil type, and intensity were well reported. However, medication, CNS drugs, coil orientation, current direction, pulse shape, time interval between MEPs, and subject attention were missing in most studies. In addition, only a few studies used a navigation system to monitor the real-time position of coils in relation to the head of the participants. The PEDro score indicated that the included studies with a parallel-group design had good general methodological quality (Table 3), with a mean score of 7.2 (SD = 1.18). The funnel plots used in the publication bias examination are presented in Supporting Information (Additional file 1: Figs. S1 to S17).

Table 3 PEDro scores of the included studies with a parallel-group design
Full size table

Low frequency rTMS to the unaffected M1

Pomeroy et al. applied one Hz rTMS to the affected M1, rather than to the unaffected M1, and found that MEP responses of the hemiparetic arm were more frequently evoked after receiving real rTMS than sham rTMS [46]. Recently, Wang et al. found that HF-rTMS applied to the unaffected M1 yielded greater improvement on the MEP amplitude than LF-rTMS, suggesting a compensatory role of the unaffected M1 in the motor recovery of severe-impaired patients [75].

The effects after a single session and multiple sessions of LF-rTMS were evaluated by 11 [9, 24,25,26, 28, 31, 32, 34, 36, 41, 42] and 24 [44, 46, 47, 49,50,51, 54,55,56,57,58,59,60, 62, 63, 65, 67,68,69,70,71, 74, 76, 78] studies, respectively. Dos Santos et al. found that 10 sessions of LF-rTMS increased the cortical excitability of the unaffected M1, measured using an intensity tracking measuring approach that the intensity inducing MEPs of 1 mV by a single-pulse TMS stimulation was determined in the study to represent corticospinal excitability [69]. Moreover, LF-rTMS was found to be effective in rebalancing bilateral excitability by increasing the MEP amplitude of the affected M1 and decreasing the MEP amplitude of the unaffected M1 [56].

Resting/active motor threshold

Previously, significant modulatory effects on rMT induced by a single session of LF-rTMS were not found [24, 28, 36]. However, our meta-analysis has shown the significant effect of multiple sessions of LF-rTMS in decreasing the rMT of the affected M1 (Hedges’ g = − 0.61, 95% CI = − 1.08 to − 0.14, p = 0.011, I2 = 66.21%; Fig. 2), and no publication bias was identified (p = 0.187). It suggested that the decreased rMT could be sustained for three months after the intervention [50, 62], while no significant long-term effects were also reported [58]. Likewise, multiple sessions of LF-rTMS also decreased the aMT of the affected M1 immediately [47, 71].

Fig. 2
figure 2

Meta-analyses indicating the effects of low frequency repetitive transcranial magnetic stimulation (LF-rTMS) to the unaffected M1 in modulating bilateral cortical excitability. The meta-analysis showed that LF-rTMS was significantly effective to decrease (a) and increase (b) rMT of the affected and unaffected M1 after multiple sessions of stimulation, respectively. Although LF-rTMS also tended to increase the aMT of the unaffected M1, the pooled Hedges’ g value was not significant (c). A single session of LF-rTMS significantly increased the MEP amplitude of the affected M1 by 22.14% (d); similar results were also found after multiple sessions of stimulation (f). Conversely, the MEP amplitude of the unaffected M1 significantly decreased by 21.29% immediately after a single session of LF-rTMS (e); similarly, the MEP amplitude of the unaffected M1 significantly decreased after multiple sessions of LF-rTMS (g). rMT resting motor threshold; aMT active motor threshold, MEP motor-evoked potentials

Full size image

Conversely, the rMT of the unaffected M1 significantly increased after multiple sessions of LF-rTMS (Hedges’ g = 0.579, 95% CI = 0.26—0.90, p < 0.001, I2 = 37.36%), but significant publication bias was identified (p < 0.001). Inconsistent findings were reported with respect to its long-term effects [50, 55, 58, 62]. Although LF-rTMS also tended to increase the aMT of the unaffected M1, the pooled Hedges’ g value was not significant (Hedges’ g = 1.25, 95% CI = − 0.03–2.53, p = 0.055, I2 = 88.40%); the publications bias was not significant (p = 0.422).

Amplitude of motor-evoked potentials

A single session of LF-rTMS significantly increased the MEP amplitude of the affected M1 by 22.14% (95% CI = 16.26%—28.01%, p < 0.001, I2 = 30.51%) and no publication bias was identified (p = 0.070). Similar results were also found after multiple sessions of stimulation (Hedges’ g = 0.81, 95% CI = 0.51—1.11, p < 0.001, I2 = 41.51%), although the publication bias was significant (p < 0.001). It was noted that the increased MEP amplitude could be sustained for almost three months [62, 63, 68].

Conversely, the MEP amplitude of the unaffected M1 decreased by 21.29% (95% CI = − 27.17% to − 15.41%, p < 0.001, I2 = 56.88%) immediately after a single session of LF-rTMS, in line with two other studies [41, 42]; however, the publication bias was significant (p = 0.040). Likewise, the MEP amplitude of the unaffected M1 decreased after multiple sessions of LF-rTMS (Hedges’ g = − 0.54, 95% CI = − 0.78 to − 0.30, p < 0.001, I2 = 26.05%), with no significant publication bias identified (p = 0.502). In terms of its long-term effects, the decreased MEP amplitude could be sustained for three to six months after the intervention [59, 62, 63].

Intracortical inhibition/facilitation

Despite the heterogeneity of the inter-stimulus intervals and intensities, four studies consistently found no significant changes in regard to the SICI [24, 26, 32, 36], cortical silent period [32, 36], and ICF [32] of the affected M1 after a single session of LF-rTMS. Similarly, no significant changes were found in the unaffected M1 [36, 55, 60]. Only one study conducted by Mello et al. revealed that the ICF of the unaffected M1 was upregulated after 10 sessions of LF-rTMS in patients with stroke at the acute/subacute stage [60].

Transcallosal inhibition

A limited number of studies have suggested that iSP recorded in the affected hand reduced immediately after a single session [9, 28] and 10 sessions [50] of LF-rTMS. For the unaffected hand, no significant effects on iSP were found [28, 32]. By measuring IHI, decreased inhibition from the unaffected to the affected M1 was also noted [32].

High frequency rTMS to the affected M1

Seven [10, 26, 29, 30, 33, 35, 41] and 13 [43, 45, 47, 48, 61,62,63, 66, 70, 73, 74, 76, 77] studies evaluated the effects of a single session and multiple sessions of HF-rTMS on the affected M1 in cortical excitability, respectively. Khedr et al. showed that more patients presented MEP responses after receiving 10 sessions of real HF-rTMS than sham [43]. However, this comparison did not yield statistical significance.

Resting/active motor threshold

A single session of HF-rTMS was shown to decrease the rMT [29] and aMT [47, 48] of the affected M1; a meta-analysis also supported the notion that multiple sessions of HF-rTMS could decrease the rMT of the affected M1 (Hedges’ g = − 1.27, 95% CI = − 2.28 to − 0.26, p = 0.014, I2 = 89.28%; Fig. 3) without evident publication bias (p = 0.454). The effects on the unaffected M1 were less investigated and inconsistent results were reported [47, 48, 62, 70].

Fig. 3
figure 3

Meta-analyses indicating the effects of high frequency repetitive transcranial magnetic stimulation (HF-rTMS) to the affected M1 in modulating bilateral cortical excitability. A meta-analysis indicated that multiple sessions of HF-rTMS applied to the affected M1 significantly decreased the rMT of the affected M1 (a). A single session of HF-rTMS significantly increases MEP amplitudes of the affected M1 by 73.11% (b). Multiple sessions of HF-rTMS also significantly increased MEP amplitudes of the affected M1 (c). However, multiple sessions of stimulation had no effects on the MEP amplitude of the unaffected M1 (d). rMT resting motor threshold, MEP motor-evoked potentials

Full size image

Amplitude of motor-evoked potentials

A single session of HF-rTMS did not show any effects on the MEP amplitude of the unaffected M1 [26, 41], while it significantly increased that of the affected M1 [10, 41]. A meta-analysis showed an MEP increment of 73.11% (95% CI = 11.76%–134.45%, p = 0.019, I2 = 94.85%); however, significant publication bias was identified (p = 0.027). Likewise, meta-analyses of multiple-session studies also supported the notion that HF-rTMS had no effects on the MEP amplitude of the unaffected M1 (Hedges’ g = 0.24, 95% CI = − 0.15–0.63, p = 0.235, I2 = 46.61%), but significantly increased that of the affected M1 (Hedges’ g = 0.73, 95% CI = 0.17 –1.28, p = 0.010, I2 = 73.38%). No publication bias was identified in the former (p = 0.412) and latter (p = 0.145) analyses.

Intracortical inhibition/facilitation

It was consistently found that a single session of HF-rTMS did not change the SICI or the ICF of the affected M1 [26, 29, 30].

Intermittent theta burst stimulation to the affected M1

The effects of a single session of iTBS were extensively studied [14,15,16,17, 27, 37,38,39,40], and four studies investigated the effects of multiple sessions of iTBS on cortical excitability [53, 54, 57, 64, 68]. iTBS was given at subthreshold intensities, and almost all the studies delivered 600 pulses, except the study by Hsu et al. in which patients received 1200 pulses [53].

Resting/active motor threshold

Meta-analyses indicated that a single session of iTBS tended to decrease the aMT (Hedges’ g = − 0.26, 95% CI = − 0.64 to 0.13, p = 0.189, I2 = 54.92%) and rMT (Hedges’ g = − 0.48, 95% CI =− 1.00 to 0.03, p = 0.063, I2 = 77.21%) of the affected M1, and increase the aMT (Hedges’ g = 0.14, 95% CI = − 0.10 to 0.38, p = 0.257, I2 < 0.001%) and rMT (Hedges’ g = 0.15, 95% CI = − 0.09 to 0.39, p = 0.215, I2 < 0.001%) of the unaffected M1; however, none of the pooled Hedges’ g values was significant (Fig. 4). No publication bias was identified in any of the meta-analyses (all p values > 0.05).

Fig. 4
figure 4

Meta-analyses indicating the effects of intermittent theta burst stimulation (iTBS) to the affected M1 in modulating bilateral cortical excitability. Meta-analyses indicated that a single session of iTBS tended to decrease the aMT (a) and rMT (c) of the affected M1 and increase the aMT (b) and rMT (d) of the unaffected M1. However, none of the pooled Hedges’ g values were significant. A single session of iTBS significantly increased the MEP amplitude of the affected M1 (e) and decreased that of the unaffected M1 (f). rMT resting motor threshold; aMT active motor threshold; MEP motor-evoked potentials

Full size image

For the effects of multiple sessions of stimulation, iTBS combined with physical therapy was beneficial to the rMT and aMT of the bilateral M1s [53, 54, 57, 64]. It is noteworthy that the post-iTBS measurements were conducted one day after the last session of the intervention in two studies [53, 64], rather than immediately after the stimulation in those studies investigating the effects of a single session of iTBS.

Amplitude of motor evoked potentials

A single session of iTBS significantly increased the MEP amplitude of the affected M1 (Hedges’ g = 0.44, 95% CI = 0.24 to 0.64, p < 0.001, I2 = 25.59%) and decreased that of the unaffected M1 (Hedges’ g = − 0.42, 95% CI = − 0.62 to − 0.21, p < 0.001, I2 < 0.001%). Significant publication bias was identified in the former analysis (p = 0.029), but not in the latter one (p = 0.241).

Largely inconsistent findings were reported regarding the MEP amplitudes of the bilateral M1s after multiple sessions of iTBS [53, 54, 57, 64]. For the long-term effects, a previous study revealed that iTBS had superior effects in sustaining the increased cortical excitability in the affected M1 for almost three months [68].

Intracortical inhibition

Preliminary evidence did not support the modulatory effects of iTBS on SICI [38] and the cortical silent period of the affected M1 in patients with stroke [40].

Continuous theta burst stimulation to the unaffected M1

A study conducted by Di Lazzaro et al. suggested that a single session of cTBS to the unaffected M1 had similar effects as iTBS to the affected M1, simultaneously increasing the rMT and aMT of the unaffected M1 and decreasing those of the affected M1 [15]. However, another study, also conducted by Di Lazzaro et al. showed that 10 sessions of cTBS did not effectively modulate cortical excitability, reflected by the nonsignificant changes in the rMT, aMT, and MEP amplitudes of the bilateral M1s [52]. These nonsignificant findings were also confirmed by Neva et al. in which neither the SICI, the ICF, nor the iSP of the bilateral M1s benefited from cTBS [72].

Correlation between the changes in TMS measures and motor improvement

A total of 12 studies performed various correlation analyses between TMS measures and motor impairment [43, 48,49,50, 56, 57, 59, 61,62,63, 70, 71, 75]. Cross-sectional analyses indicated positive correlations between the cortical excitability of the affected M1 and the severity of motor impairment of the hemiplegic arm [61, 63], while that of the unaffected M1 was negatively correlated with motor impairment of the hemiplegic arm [71]. Furthermore, motor improvement was significantly correlated with a reduction in the cortical excitability of the unaffected M1 [56, 57, 59]. The decrease in iSP from the unaffected to the affected M1 and the increase in MEP amplitudes in the affected M1 were correlated with arm motor improvement [50, 62]. A previous study has also shown the predictive value of MEP amplitudes for subsequent motor improvement [48].

Two studies conducted these analyses in patients with severe arm impairments. Positive correlation between the cortical excitability of the unaffected M1 and arm motor impairment was noted after receiving LF-rTMS [49]. The changes in MEP latency in the unaffected M1 were negatively correlated with motor improvement [75].

Discussion

The aim of the current study was to systematically review the effects of four commonly used rTMS protocols on the cortical excitability of patients with a unilateral stroke lesion. LF-rTMS to the unaffected M1 is the most extensively investigated one in the literature. Our meta-analyses indicated that it was effective in increasing the MEP amplitude and decreasing the rMT of the affected M1, with opposite effects regarding the unaffected M1. Applying HF-rTMS to the affected M1 increased cortical excitability of the stimulated M1, while no significant effects were found on that of the unaffected M1. Unlike the modulatory effects of HF-rTMS, iTBS not only increased the cortical excitability of the affected M1, but also decreased that of the unaffected M1. A limited number of studies investigated cTBS in stroke and a firm conclusion cannot be drawn. Motor impairment of the hemiplegic arm was significantly correlated with various forms of TMS measures.

The meta-analysis conducted by McDonnell et al. suggested that the unaffected M1 of patients with stroke was not hyperactivated during active contraction and resting, indicated by the nonsignificant differences on aMT, rMT, and MEPs compared with healthy controls [1]. Most recently, a longitudinal study revealed that the premovement IHI did not significantly differ from that of healthy controls at the acute/subacute stage of stroke, however, the premovement IHI was abnormally higher at the chronic stage [79]. Therefore, the authors argued that the excessive IHI in chronic stroke patients may be a consequence of cortical reorganization, but it was not causally associated with motor impairment [79]. To the best of our knowledge, this study suggested that motor impairment at the acute/subacute stage was not caused by excessive premovement. However, the study by Xu et al. [79] cannot rule out the possibility that the interhemispheric imbalance developed at the chronic stage, presumably caused by the maladaptation of cortical reorganization or learned non-use, may prevent the recovery of motor function, since many studies have supported the clinical effects of LF-rTMS to the unaffected M1 in chronic stroke patients. In our meta-analyses, we found that LF-rTMS to the unaffected M1 could significantly increase the cortical excitability of the affected M1, accompanied by decreased cortical excitability of the unaffected M1. A small number of studies also documented that reduced iSP and IHI after LF-rTMS were highly correlated with motor improvement [9, 28, 50], which would further reinforce the interhemispheric imbalance model.

In a large-scale randomized controlled trial by Harvey et al. [80], the authors failed to find superior effects of LF-rTMS applied to the unaffected M1 against sham stimulation in improving poststroke upper limb motor functions. The failure to reject the null hypothesis points out the importance of studying the characteristics of treatment responders to LF-rTMS. Carey et al. found that the responders to LF-rTMS (applied to the unaffected M1) had greater hand function and greater preservation volume of the ipsilesional posterior limb of the internal capsule at baseline, compared with the nonresponders [81]. Besides, disrupting either the unaffected M1 or the unaffected dorsal pre-motor cortex by TMS worsened the contralateral motor performance in stroke patients with severe motor impairment [82], and that HF-rTMS applied to the unaffected M1 could facilitate motor improvement in stroke patients with severe motor impairment [75]. These studies suggested that the unaffected hemisphere plays different roles in motor recovery according to the severity of motor impairment [75, 81, 82]. Di Pino et al. proposed a bimodal balance–recovery model to explain the differential roles of the unaffected hemisphere in poststroke motor recovery [8]. Patients with mild motor impairment can benefit from inhibitory brain stimulation applied to the unaffected hemisphere due to high level of structural preservation, whereas the unaffected hemisphere, because of substantial damage to the ipsilesional corticospinal tract, has a significant role for compensation. Recently, Lin et al. found that IHI from the unaffected to affected M1 was negatively correlated with upper limb function in less impaired patients, while positive correlation was found in more impaired patients [83]. This supports further the bimodal balance–recovery model. In our current systematic review, only one study in which HF-rTMS was applied to the unaffected M1 in patients with severe motor impairment, and this study showed that improvement in upper limb function was correlated with shortened latency of unaffected MEP [75]. Because MEPs from the affected M1 was not detectable [75], it remained unknown whether the excitability of the affected M1 was altered after HF-rTMS applied to the unaffected M1. Regarding the mechanism, recent studies are still debating the pathway of the unaffected M1 in facilitating motor recovery via callosal connections, or direct pathway from the unaffected hemisphere [84, 85]. Traditional measures of intracortical and interhemispheric excitability/inhibition rely highly on electromyography outputs, which are usually not detectable in patients with severe motor impairment. Alternatively, combining TMS and electroencephalography can directly probe the cortical reactivity after TMS pulses [86, 87], which might be useful in the investigation of interhemispheric communication for those patients with severe motor impairments.

As aforementioned, the neurophysiological effects of LF-rTMS to the unaffected M1 can be explained by the mechanism of rebalancing interhemispheric inhibition. It is necessary to understand whether hyperactivity or excessive inhibition flow from the unaffected M1 is a prerequisite for LF-rTMS applied to the unaffected M1 aiming to modulate the cortical excitability of the affected M1. Healthy people are assumed to have balanced interhemispheric inhibition. However, many previous studies have found that LF-rTMS and cTBS not only suppressed the MEP amplitude of the simulated M1, but also enhanced that of the non-stimulated M1 [88, 89]. Increased cortical excitability within the non-stimulated M1 is likely relevant to the elevated intrinsic excitability of the excitatory interneurons responsible for glutamatergic non-NMDA receptors [90]. Given the above findings in healthy people, it is reasonable to expect the cortical excitability of the affected M1 to benefit from inhibitory stimulation to the unaffected M1, even though the unaffected M1 is not hyperactivated or does not inhibit the affected M1 excessively during resting and premovement at the acute and subacute stages after stroke [1, 79]. If this is the case, the interhemispheric imbalance model may not be the unique hypothesis of inhibitory stimulation to the unaffected M1, and future studies are warranted.

A large body of evidence suggests that the cortical excitability of the affected M1 decreased after stroke, and motor improvement is associated with the increase of excitability in the affected M1 [1]. Our meta-analyses indicated that both HF-rTMS and iTBS are useful in increasing the cortical excitability of the unaffected M1. Furthermore, the effect of simultaneously suppressing the unaffected M1 was noted after iTBS, but not after HF-rTMS. For a direct comparison, a previous study has shown the superior effects of iTBS in increasing the MEPs of the stimulated M1, compared to HF-rTMS in healthy people [88], but comparable effects were also reported [91]. Animal studies suggested that different TMS protocols may have specifically different effects in modulating neurogenesis and protein expression, which may potentially account for the different effects across neurophysiological and clinical measures [92].

In addition to unilateral-hemispheric stimulation, some new protocols integrating these regular forms of rTMS have been studied in stroke. For instance, the dual-hemisphere stimulation consisting of inhibitory rTMS to the unaffected M1 and excitatory rTMS to the affected M1 was more effective in enhancing motor performance and cortical excitability [74] and reducing the SICI of the affected M1 than unilateral-hemispheric stimulation [26]. Another protocol, LF-rTMS primed with HF-rTMS, also showed encouraging effects in reducing intracortical inhibition within the affected M1 [32]. Besides, functional rTMS triggered by electromyogram may induce greater excitability changes than passive stimulation protocols [29].

Limitations

This review was not free from limitations. First, we must be cautious when interpreting the findings relevant to LF-rTMS. The high IHI elicited by paired-pulse TMS was found during the premovement period but the majority of previous TMS measures were conducted at rest. Therefore, the outcomes—paired-pulse induced IHI at rest and single-pulse induced iSP during sustained isometric contractions, in our review might not be conclusive in explaining excessive inhibition driving from the unaffected M1 [89]. Second, substantial heterogeneity and publication bias were identified in some meta-analyses, probably due to the small sample sizes in most included studies and the way in which the patient characteristics, TMS protocols, and methodologies were not identical. Third, the available studies mostly focused on the effects on TMS measures, which may limit our findings to patients with mild to moderate impairments only. This is because the MEPs of the affected M1 are usually not recordable in stroke patients with severe motor impairments.

Conclusions

The current study systematically reviewed existing research investigating the effects of four forms of rTMS in modulating the cortical excitability of bilateral M1s. LF-rTMS to the unaffected M1 is the most extensively studied protocol, while cTBS is the least studied one. Although recent studies have argued for the rationale of inhibitory stimulation applied to the unaffected M1, our analyses suggested that LF-rTMS not only suppressed the cortical excitability of the unaffected M1 but also simultaneously enhanced that of the affected M1. HF-rTMS enhanced the cortical excitability of the affected M1 only. Preliminary evidence also supported the effects of iTBS in rebalancing bilateral cortical excitability in stroke. Our findings support the bimodal balance–recovery model in patients with mild motor impairment, more studies are needed to investigate the neurophysiological effects of HF-rTMS applied to the unaffected M1 in patients with severe motor impairment.

Availability of data and materials

All data generated or analyzed during this study are included in this published article and its additional file.

Abbreviations

TMS:

Transcranial magnetic stimulation

M1:

Primary motor cortex

MEPs:

Motor evoked potentials

rMT:

Resting motor threshold

aMT:

Active motor threshold

rTMS:

Repetitive transcranial magnetic stimulation

SICI:

Short-interval intracortical inhibition

IHI:

Interhemispheric inhibition

iSP:

Ipsilateral silent period

LF-rTMS:

Low frequency rTMS

HF-rTMS:

High frequency rTMS

TBS:

Theta burst stimulation

iTBS:

Intermittent theta burst stimulation

cTBS:

Continuous theta burst stimulation

ICF:

Intracortical facilitation

References

  1. McDonnell MN, Stinear CM. TMS measures of motor cortex function after stroke: a meta-analysis. Brain Stimul. 2017;10:721–34.

    Article  PubMed  Google Scholar 

  2. Mooney RA, Ackerley SJ, Rajeswaran DK, Cirillo J, Barber PA, Stinear M, Byblow WD. The influence of primary motor cortex inhibition on upper limb impairment and function in chronic stroke: a multimodal study. Neurorehabil Neural Repair. 2019;33:130–40.

    Article  PubMed  Google Scholar 

  3. Fujiwara T, Honaga K, Kawakami M, Nishimoto A, Abe K, Mizuno K, Kodama M, Masakado Y, Tsuji T, Liu M. Modulation of cortical and spinal inhibition with functional recovery of upper extremity motor function among patients with chronic stroke. Restor Neurol Neurosci. 2015;33:883–94.

    CAS  PubMed  Google Scholar 

  4. Johnstone A, Levenstein JM, Hinson EL, Stagg CJ. Neurochemical changes underpinning the development of adjunct therapies in recovery after stroke: a role for GABA? J Cereb Blood Flow Metab. 2018;38:1564–83.

    Article  CAS  PubMed  Google Scholar 

  5. Grefkes C, Ward NS. Cortical reorganization after stroke: How much and how functional? Neuroscientist. 2014;20:56–70.

    Article  PubMed  Google Scholar 

  6. Tang Q, Li G, Liu T, Wang A, Feng S, Liao X, Jin Y, Guo Z, He B, McClure MA, et al. Modulation of interhemispheric activation balance in motor-related areas of stroke patients with motor recovery: systematic review and meta-analysis of fMRI studies. Neurosci Biobehav Rev. 2015;57:392–400.

    Article  PubMed  Google Scholar 

  7. Ward NS, Cohen LG. Mechanisms underlying recovery of motor function after stroke. Arch of Neurol. 2004;61:1844–8.

    Article  Google Scholar 

  8. Di Pino G, Pellegrino G, Assenza G, Capone F, Ferreri F, Formica D, Ranieri F, Tombini M, Ziemann U, Rothwell JC, et al. Modulation of brain plasticity in stroke: a novel model for neurorehabilitation. Nat Rev Neurol. 2014;10:597–608.

    Article  Google Scholar 

  9. Takeuchi N, Chuma T, Matsuo Y, Watanabe I, Ikoma K. Repetitive transcranial magnetic stimulation of contralesional primary motor cortex improves hand function after stroke. Stroke. 2005;36:2681–6.

    Article  PubMed  Google Scholar 

  10. Kim Y-H, You SH, Ko M-H, Park J-W, Lee KH, Jang SH, Yoo W-K, Hallett M. Repetitive transcranial magnetic stimulation-induced corticomotor excitability and associated motor skill acquisition in chronic stroke. Stroke. 2006;37:1471–6.

    Article  PubMed  Google Scholar 

  11. Suppa A, Huang Y-Z, Funke K, Ridding MC, Cheeran B, Di Lazzaro V, Ziemann U, Rothwell JC. Ten years of theta burst stimulation in humans: established knowledge, unknowns and prospects. Brain Stimul. 2016;9:323–35.

    Article  CAS  PubMed  Google Scholar 

  12. Huang Y-Z, Edwards MJ, Rounis E, Bhatia KP, Rothwell JC. Theta burst stimulation of the human motor cortex. Neuron. 2005;45:201–6.

    Article  CAS  PubMed  Google Scholar 

  13. Chung SW, Hill AT, Rogasch NC, Hoy KE, Fitzgerald PB. Use of theta-burst stimulation in changing excitability of motor cortex: a systematic review and meta-analysis. Neurosci Biobehav Rev. 2016;63:43–64.

    Article  PubMed  Google Scholar 

  14. Talelli P, Greenwood RJ, Rothwell JC. Exploring theta burst stimulation as an intervention to improve motor recovery in chronic stroke. Clin Neurophysiol. 2007;118:333–42.

    Article  CAS  PubMed  Google Scholar 

  15. Di Lazzaro V, Pilato F, Dileone M, Profice P, Capone F, Ranieri F, Musumeric G, Cianfoni A, Pasqualetti P, Tonali PA. Modulating cortical excitability in acute stroke: a repetitive TMS study. Clin Neurophysiol. 2008;119:715–23.

    Article  PubMed  Google Scholar 

  16. Ackerley SJ, Stinear CM, Barber PA, Byblow WD. Combining theta burst stimulation with training after subcortical stroke. Stroke. 2010;41:1568–72.

    Article  PubMed  Google Scholar 

  17. Ackerley SJ, Stinear CM, Barber PA, Byblow WD. Priming sensorimotor cortex to enhance task-specific training after subcortical stroke. Clin Neurophysiol. 2014;125:1451–8.

    Article  PubMed  Google Scholar 

  18. Lefaucheur JP, Aleman A, Baeken C, Benninger DH, Brunnelin J, Di Lazzaro V, Filipović SR, Grefkes C, Hasan A, Hummel FC, et al. Evidence-based guidelines on the therapeutic use of repetitive transcranial magnetic stimulation (rTMS): an update (2014–2018). Clin Neurophysiol. 2020;131:474–528.

    Article  PubMed  Google Scholar 

  19. Zhang L, Xing G, Fan Y, Guo Z, Chen H, Mu Q. Short-and long-term effects of repetitive transcranial magnetic stimulation on upper limb motor function after stroke: a systematic review and meta-analysis. Clin Rehabil. 2017;31:1137–53.

    Article  PubMed  Google Scholar 

  20. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann of Intern Med. 2009;151:264–9.

    Article  Google Scholar 

  21. Chipchase L, Schabrun S, Cohen L, Hodges P, Ridding M, Rothwell J, Taylor J, Ziemann U. A checklist for assessing the methodological quality of studies using transcranial magnetic stimulation to study the motor system: an international consensus study. Clin Neurophysiol. 2012;123:1698–704.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Moseley AM, Herbert RD, Sherrington C, Maher CG. Evidence for physiotherapy practice: a survey of the physiotherapy evidence database (PEDro). Aust J Physiother. 2002;48:43–9.

    Article  PubMed  Google Scholar 

  23. Borenstein M, Hedges LV, Higgins JP, Rothstein HR. A basic introduction to fixed-effect and random-effects models for meta-analysis. Res Synth Methods. 2010;1:97–111.

    Article  PubMed  Google Scholar 

  24. Takeuchi N, Tada T, Toshima M, Chuma T, Matsuo Y, Ikoma K. Inhibition of the unaffected motor cortex by 1 Hz repetitive transcranial magnetic stimulation enhances motor performance and training effect of the paretic hand in patients with chronic stroke. J Rehabil Med. 2008;40:298–303.

    Article  PubMed  Google Scholar 

  25. Jayaram G, Stinear JW. The effects of transcranial stimulation on paretic lower limb motor excitability during walking. J Clin Neurophysiol. 2009;26:272–9.

    Article  PubMed  Google Scholar 

  26. Takeuchi N, Tada T, Toshima M, Matsuo Y, Ikoma K. Repetitive transcranial magnetic stimulation over bilateral hemispheres enhances motor function and training effect of paretic hand in patients after stroke. J Rehabil Med. 2009;41:1049–54.

    Article  PubMed  Google Scholar 

  27. Di Lazzaro V, Profice P, Pilato F, Capone F, Ranieri F, Pasqualetti P, Colosimo C, Pravatà E, Cianfoni A, Dileone M. Motor cortex plasticity predicts recovery in acute stroke. Cereb Cortex. 2010;20:1523–8.

    Article  PubMed  Google Scholar 

  28. Takeuchi N, Tada T, Matsuo Y, Ikoma K. Low-frequency repetitive TMS plus anodal transcranial DCS prevents transient decline in bimanual movement induced by contralesional inhibitory rTMS after stroke. Neurorehabil Neural Repair. 2012;26:988–98.

    Article  PubMed  Google Scholar 

  29. Massie CL, Tracy BL, Malcolm MP. Functional repetitive transcranial magnetic stimulation increases motor cortex excitability in survivors of stroke. Clin Neurophysiol. 2013;124:371–8.

    Article  PubMed  Google Scholar 

  30. Massie CL, Tracy BL, Paxton RJ, Malcolm MP. Repeated sessions of functional repetitive transcranial magnetic stimulation increases motor cortex excitability and motor control in survivors of stroke. NeuroRehabilitation. 2013;33:185–93.

    Article  PubMed  Google Scholar 

  31. Vongvaivanichakul P, Tretriluxana J, Bovonsunthonchai S, Pakaprot N, Laksanakorn W. Reach-to-grasp training in individuals with chronic stroke augmented by low-frequency repetitive transcranial magnetic stimulation. J Med Assoc Thai. 2014;97:S45–9.

    PubMed  Google Scholar 

  32. Cassidy JM, Chu H, Anderson DC, Krach LE, Snow L, Kimberley TJ, Carey JR. A comparison of primed low-frequency repetitive transcranial magnetic stimulation treatments in chronic stroke. Brain Stimul. 2015;8:1074–84.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Goh HT, Chan HY, Abdul-Latif L. Aftereffects of 2 noninvasive brain stimulation techniques on corticospinal excitability in persons with chronic stroke: a pilot study. J Neurol Phys Ther. 2015;39:15–22.

    Article  PubMed  Google Scholar 

  34. Tretriluxana J, Kantak S, Tretriluxana S, Wu AD, Fisher BE. Improvement in paretic arm reach-to-grasp following low frequency repetitive transcranial magnetic stimulation depends on object size: a pilot study. Stroke Res Treat. 2015;2015:498169.

    PubMed  PubMed Central  Google Scholar 

  35. Uhm KE, Kim Y-H, Yoon KJ, Hwang JM, Chang WH. BDNF genotype influence the efficacy of rTMS in stroke patients. Neurosci Lett. 2015;594:117–21.

    Article  CAS  PubMed  Google Scholar 

  36. Bashir S, Vernet M, Najib U, Perez J, Alonso-Alonso M, Knobel M, Yoo W-K, Edwards D, Pascual-Leone A. Enhanced motor function and its neurophysiological correlates after navigated low-frequency repetitive transcranial magnetic stimulation over the contralesional motor cortex in stroke. Restor Neurol Neurosci. 2016;34:677–89.

    PubMed  PubMed Central  Google Scholar 

  37. Di Lazzaro V, Pellegrino G, Di Pino G, Ranieri F, Lotti F, Florio L, Capone F. Human motor cortex functional changes in acute stroke: gender effects. Front Neurosci. 2016;10:10.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Murdoch K, Buckley JD, McDonnell MN. The effect of aerobic exercise on neuroplasticity within the motor cortex following stroke. PLoS ONE. 2016;11:e0152377.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Diekhoff-Krebs S, Pool EM, Sarfeld AS, Rehme AK, Eickhoff SB, Fink GR, Grefkes C. Interindividual differences in motor network connectivity and behavioral response to iTBS in stroke patients. Neuroimage Clin. 2017;15:559–71.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Khan FR. Additive effects of sequential excitatory and inhibitory theta burst stimulation in improving cortical excitability following ischaemic stroke. Brain Inj. 2017;31:649–54.

    Article  PubMed  Google Scholar 

  41. Hanafi MH, Kassim NK, Ibrahim AH, Adnan MM, Ahmad WMAW, Idris Z, Larif LA. Cortical modulation after two different repetitive transcranial magnetic stimulation protocols in similar ischemic stroke patients. Malays J Med Sci. 2018;25:116–25.

    PubMed  PubMed Central  Google Scholar 

  42. Tretriluxana J, Thanakamchokchai J, Jalayondeja C, Pakaprot N, Tretriluxana S. The persisted effects of low-frequency repetitive transcranial magnetic stimulation to augment task-specific induced hand recovery following subacute stroke: extended study. Ann Rehabil Med. 2018;42:777–87.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Khedr EM, Ahmed MA, Fathy N, Rothwell JC. Therapeutic trial of repetitive transcranial magnetic stimulation after acute ischemic stroke. Neurology. 2005;65:466–8.

    Article  PubMed  Google Scholar 

  44. Fregni F, Boggio PS, Valle AC, Rocha RR, Duarte J, Ferreira MJL, Wagner T, Fecteau S, Rigonatti SP, Riberto M, et al. A sham-controlled trial of a 5-day course of repetitive transcranial magnetic stimulation of the unaffected hemisphere in stroke patients. Stroke. 2006;37:2115–22.

    Article  PubMed  Google Scholar 

  45. Malcolm MP, Triggs WJ, Light KE, Rothi LJG, Wu S, Reid K, Nadeau SE. Repetitive transcranial magnetic stimulation as an adjunct to constraint-induced therapy: an exploratory randomized controlled trial. Am J Phys Med Rehabil. 2007;86:707–15.

    Article  PubMed  PubMed Central  Google Scholar 

  46. Pomeroy VM, Cloud G, Tallis RC, Donaldson C, Nayak V, Miller S. Transcranial magnetic stimulation and muscle contraction to enhance stroke recovery: a randomized proof-of-principle and feasibility investigation. Neurorehabil Neural Repair. 2007;21:509–17.

    Article  PubMed  Google Scholar 

  47. Khedr EM, Abdel-Fadeil MR, Farghali A, Qaid M. Role of 1 and 3 Hz repetitive transcranial magnetic stimulation on motor function recovery after acute ischaemic stroke. Eur J Neurol. 2009;16:1323–30.

    Article  CAS  PubMed  Google Scholar 

  48. Khedr EM, Etraby AE, Hemeda M, Nasef AM, Razek AA. Long-term effect of repetitive transcranial magnetic stimulation on motor function recovery after acute ischemic stroke. Acta Neurol Scand. 2010;121:30–7.

    Article  CAS  PubMed  Google Scholar 

  49. Theilig S, Podubecka J, Bosl K, Wiederer R, Nowak DA. Functional neuromuscular stimulation to improve severe hand dysfunction after stroke: does inhibitory rTMS enhance therapeutic efficiency? Exp Neurol. 2011;230:149–55.

    Article  PubMed  Google Scholar 

  50. Avenanti A, Coccia M, Ladavas E, Provinciali L, Ceravolo MG. Low-frequency rTMS promotes use-dependent motor plasticity in chronic stroke: a randomized trial. Neurology. 2012;78:256–64.

    Article  CAS  PubMed  Google Scholar 

  51. Wang R-Y, Tseng HY, Liao K-K, Wang C-J, Lai K-L, Yang Y-R. RTMS combined with task-oriented training to improve symmetry of interhemispheric corticomotor excitability and gait performance after stroke: A randomized trial. Neurorehabil Neural Repair. 2012;26:222–30.

    Article  PubMed  Google Scholar 

  52. Di Lazzaro V, Rothwell JC, Talelli P, Capone F, Ranieri F, Wallace AC, Musumerci G, Dileone M. Inhibitory theta burst stimulation of affected hemisphere in chronic stroke: a proof of principle, sham-controlled study. Neurosci Lett. 2013;553:148–52.

    Article  PubMed  Google Scholar 

  53. Hsu Y-F, Huang Y-Z, Lin Y-Y, Tang C-W, Liao K-K, Lee P-L Tsai Y-A, Cheng H-L, Cheng H, Chern C-M, et al. Intermittent theta burst stimulation over ipsilesional primary motor cortex of subacute ischemic stroke patients: a pilot study. Brain Stimul. 2013;6:166–174.

  54. Sung W-H, Wang C-P, Chou C-L, Chen Y-C, Chang Y-C, Tsai P-Y. Efficacy of coupling inhibitory and facilitatory repetitive transcranial magnetic stimulation to enhance motor recovery in hemiplegic stroke patients. Stroke. 2013;44:1375–82.

    Article  PubMed  Google Scholar 

  55. Rose DK, Patten C, McGuirk TE, Lu X, Triggs WJ. Does inhibitory repetitive transcranial magnetic stimulation augment functional task practice to improve arm recovery in chronic stroke? Stroke Res Treat. 2014;2014:305236.

    PubMed  PubMed Central  Google Scholar 

  56. Wang C-C, Wang C-P, Tsai P-Y, Hsieh CY, Chan R-C, Yeh S-C. Inhibitory repetitive transcranial magnetic stimulation of the contralesional premotor and primary motor cortices facilitate poststroke motor recovery. Restor Neurol Neurosci. 2014;32:825–35.

    CAS  PubMed  Google Scholar 

  57. Wang C-P, Tsai P-Y, Yang T-F, Yang K-Y, Wang C-C. Differential effect of conditioning sequences in coupling inhibitory/facilitatory repetitive transcranial magnetic stimulation for poststroke motor recovery. CNS Neurosci Ther. 2014;20:355–63.

    Article  PubMed  PubMed Central  Google Scholar 

  58. Blesneag AV, Slăvoacă DF, Popa L, Stan AD, Jemna N, Moldovan FI, Muresanu DF. Low-frequency rTMS in patients with subacute ischemic stroke: clinical evaluation of short and long-term outcomes and neurophysiological assessment of cortical excitability. J Med Life. 2015;8:378–87.

    CAS  PubMed  PubMed Central  Google Scholar 

  59. Ludemann-Podubecka J, Bosl K, Theilig S, Wiederer R, Nowak DA. The effectiveness of 1 Hz rTMS over the primary motor area of the unaffected hemisphere to improve hand function after stroke depends on hemispheric dominance. Brain Stimul. 2015;8:823–30.

    Article  PubMed  Google Scholar 

  60. Mello EA, Cohen LG, Dos Anjos SM, Conti Juliana, Andrade KNF, Moll FT, Marins T, Fernandes CA, Jr WR, Conforto AB. Increase in short-interval intracortical facilitation of the motor cortex after low-frequency repetitive magnetic stimulation of the unaffected hemisphere in the subacute phase after stroke. Neural Plast. 2015;2015:407320.

  61. Srikumari V, Vengamma B, Parvathi G. Effect of repetitive transcranial magnetic stimulation on cortico motor-excitability and motor function of the afected hand in subjects with stroke. Indian J Physiother Occup Ther. 2015;9:120–6.

    Article  Google Scholar 

  62. Du J, Tian L, Liu W, Hu J, Xu G, Ma M, Fan X, Ye R, Jiang Y, Yin Q, et al. Effects of repetitive transcranial magnetic stimulation on motor recovery and motor cortex excitability in patients with stroke: a randomized controlled trial. Eur J Neurol. 2016;23:1666–72.

    Article  CAS  PubMed  Google Scholar 

  63. Du J, Yang F, Liu L, Hu J, Cai B, Liu W, Xu G, Liu X. Repetitive transcranial magnetic stimulation for rehabilitation of poststroke dysphagia: a randomized, double-blind clinical trial. Clin Neurophysiol. 2016;127:1907–13.

    Article  PubMed  Google Scholar 

  64. Volz LJ, Rehme AK, Michely J, Nettekoven C, Eickhoff SB, Fink GR, Grefkes C. Shaping early reorganization of neural networks promotes motor function after stroke. Cereb Cortex. 2016;26:2882–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Cha HG, Kim MK. Effects of strengthening exercise integrated repetitive transcranial magnetic stimulation on motor function recovery in subacute stroke patients: a randomized controlled trial. Technol Health Care. 2017;25:521–9.

    Article  PubMed  Google Scholar 

  66. Guan Y-Z, Li J, Zhang X-W, Wu S, Du H, Cui L-Y, Zhang W-H. Effectiveness of repetitive transcranial magnetic stimulation (rTMS) after acute stroke: a one-year longitudinal randomized trial. CNS Neurosci Ther. 2017;23:940–6.

    Article  PubMed  PubMed Central  Google Scholar 

  67. Huang Y-Z, Lin L-F, Chang K-H, Hu C-J, Liou T-H, Lin Y-N. Priming with 1-Hz repetitive transcranial magnetic stimulation over contralesional leg motor cortex does not increase the rate of regaining ambulation within 3 months of stroke: a randomized controlled trial. Am J Phys Med Rehabil. 2018;97:339–45.

    Article  PubMed  Google Scholar 

  68. Watanabe K, Kudo Y, Sugawara E, Nakamizo T, Amari K, Takahshi K, Tanaka O, Endo M, Hayakawa Y, Johkura K. Comparative study of ipsilesional and contralesional repetitive transcranial magnetic stimulations for acute infarction. J Neurol Sci. 2018;384:10–4.

    Article  PubMed  Google Scholar 

  69. Dos Santos RBC, Galvao SCB, Frederico LMP, Amaral NSL, Carnero MIS, de Moura Filho AG, Piscitelli D, Monte-Silva K. Cortical and spinal excitability changes after repetitive transcranial magnetic stimulation combined to physiotherapy in stroke spastic patients. Neurol Sci. 2019;40:1199–207.

    Article  PubMed  Google Scholar 

  70. Du J, Yang F, Hu J, Hu J, Xu Q, Cong N, Zhang Q, Liu L, Manrini D, Zhang Z, et al. Effects of high- and low-frequency repetitive transcranial magnetic stimulation on motor recovery in early stroke patients: evidence from a randomized controlled trial with clinical, neurophysiological and functional imaging assessments. Neuroimage Clin. 2019;21:101620.

    Article  PubMed  Google Scholar 

  71. El-Tamawy MS, Darwish MH, Elkholy SH, Moustafa EBS. Effect of repetitive transcranial magnetic stimulation on cortical and motor outcomes post stroke: a randomized controlled trial. Indian J Public Health Res Dev. 2019;10:1967–73.

    Article  Google Scholar 

  72. Neva JL, Brown KE, Wadden KP, Mang CS, Borich MR, Meehan SK, Boyd LA. The effects of five sessions of continuous theta burst stimulation over contralesional sensorimotor cortex paired with paretic skilled motor practice in people with chronic stroke. Restor Neurol Neurosci. 2019;37:273–90.

    CAS  PubMed  PubMed Central  Google Scholar 

  73. Wang RY, Wang FY, Huang SF, Yang YR. High-frequency repetitive transcranial magnetic stimulation enhanced treadmill training effects on gait performance in individuals with chronic stroke: a double-blinded randomized controlled pilot trial. Gait Posture. 2019;68:382–7.

    Article  PubMed  Google Scholar 

  74. Zhang C, Zheng X, Lu R, Yun W, Yun H, Zhou X. Repetitive transcranial magnetic stimulation in combination with neuromuscular electrical stimulation for treatment of post-stroke dysphagia. J Int Med Res. 2019;47:662–72.

    Article  PubMed  Google Scholar 

  75. Wang Q, Zhang D, Zhao YY, Hai H, Ma YW. Effects of high-frequency repetitive transcranial magnetic stimulation over the contralesional motor cortex on motor recovery in severe hemiplegic stroke: a randomized clinical trial. Brain Stimul. 2020;13:979–86.

    Article  PubMed  Google Scholar 

  76. Hassan AF, Hanafi MH, Idris Z, Abdullah JM, Nayan SA, Aziz NA. Corticomotor excitability after two different repetitive transcranial magnetic stimulation protocols in haemorrhagic stroke patients. Interdiscip Neurosurg. 2020;20:100670.

    Article  Google Scholar 

  77. Ke J, Zou X, Huang M, Huang Q, Li H, Zhou X. High-frequency rTMS with two different inter-train intervals improves upper limb motor function at the early stage of stroke. J Int Med Res. 2020;48:0300060520928737.

    Article  CAS  PubMed Central  Google Scholar 

  78. Gong Y, Long XM, Xu Y, Cai XY, Ye M. Effects of repetitive transcranial magnetic stimulation combined with transcranial direct current stimulation on motor function and cortex excitability in subacute stroke patients: a randomized controlled trial. Clin Rehabil. 2021;35:718–27.

    Article  PubMed  Google Scholar 

  79. Xu J, Branscheidt M, Schambra H, Schambra H, Steiner L, Widmer M, Diedrichsen J, Goldsmith J, Lindquist M, Kitago T, Luft AR, et al. Rethinking interhemispheric imbalance as a target for stroke neurorehabilitation. Ann Neurol. 2019;85:502–13.

    Article  PubMed  PubMed Central  Google Scholar 

  80. Harvey RL, Edwards D, Dunning K, Fregni F, Stein J, Laine J, Rogers LM, Vox F, Durand-Sanchez A, Bockbrader M, et al. Randomized sham-controlled trial of navigated repetitive transcranial magnetic stimulation for motor recovery in stroke. Stroke. 2018;49:2138–46.

    Article  PubMed  Google Scholar 

  81. Carey JR, Deng H, Gillick BT, Cassidy JM, Anderson DC, Zhang L, Thomas W. Serial treatments of primed low-frequency rTMS in stroke: characteristics of responders vs. nonresponders. Restor Neurol Neurosci. 2014;32:323–35.

    PubMed  PubMed Central  Google Scholar 

  82. Mohapatra S, Harrington R, Chan E, Dromerick AW, Breceda EY, Harris-Love M. Role of contralesional hemisphere in paretic arm reaching in patients with severe arm paresis due to stroke: A preliminary report. Neurosci Lett. 2016;617:52–8.

    Article  CAS  PubMed  Google Scholar 

  83. Lin Y-L, Potter-Baker KA, Cunningham DA, Li M, Sankarasubramanian V, Lee J, Jones S, Sakaie K, Wang X, Machado AG, et al. Stratifying chronic stroke patients based on the influence of contralesional motor cortices: an inter-hemispheric inhibition study. Clin Neurophysiol. 2020;131:2516–25.

    Article  PubMed  PubMed Central  Google Scholar 

  84. Hammerbeck U, Hoad D, Greenwood R, Rothwell JC. The unsolved role of heightened connectivity from the unaffected hemisphere to paretic arm muscles in chronic stroke. Clin Neurophysiol. 2019;130:781–8.

    Article  PubMed  Google Scholar 

  85. Chen Y-T, Li S, DiTommaso C, Zhou P, Li S. Possible contributions of ipsilateral pathways from the contralesional motor cortex to the voluntary contraction of the spastic elbow flexors in stroke survivors: a TMS study. Am J Phys Med Rehabil. 2019;98:558–65.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Tremblay S, Rogasch NC, Premoli I, Blumberger DM, Casarotto S, Chen R, Di Lazzaro V, Farzan F, Ferrarelli F, Fitzgerald PB, et al. Clinical utility and prospective of TMS-EEG. Clin Neurophysiol. 2019;130:802–44.

    Article  PubMed  Google Scholar 

  87. Bai Z, Zhang J, Fong KNK. Intermittent theta burst stimulation to the primary motor cortex reduces cortical inhibition: A TMS-EEG study. Brain Sci. 2021;11:1114.

    Article  PubMed  PubMed Central  Google Scholar 

  88. Di Lazzaro V, Dileone M, Pilato F, Capone F, Musumeci G, Ranieri F, Ricci V, Bria P, Di Iorio R, de Waure C, et al. Modulation of motor cortex neuronal networks by rTMS: Comparison of local and remote effects of six different protocols of stimulation. J Neurophysiol. 2011;105:2150–6.

    Article  PubMed  Google Scholar 

  89. Boddington LJ, Reynolds JNJ. Targeting interhemispheric inhibition with neuromodulation to enhance stroke rehabilitation. Brain Stimul. 2017;10:214–22.

    Article  CAS  PubMed  Google Scholar 

  90. Heide G, Witte OW, Ziemann U. Physiology of modulation of motor cortex excitability by low-frequency suprathreshold repetitive transcranial magnetic stimulation. Exp Brain Res. 2006;171:26–34.

    Article  CAS  PubMed  Google Scholar 

  91. Zafar N, Paulus W, Sommer M. Comparative assessment of best conventional with best theta burst repetitive transcranial magnetic stimulation protocols on human motor cortex excitability. Clin Neurophysiol. 2008;119:1393–9.

    Article  PubMed  Google Scholar 

  92. Luo J, Zheng H, Zhang L, Zhang Q, Li L, Pei Z, Hu X. High-frequency repetitive transcranial magnetic stimulation (rTMS) improves functional recovery by enhancing neurogenesis and activating BDNF/TrkB signaling in ischemic rats. Int J Mol Sci. 2017;18:455.

    Article  PubMed Central  Google Scholar 

Download references

Acknowledgements

Not applicable.

Study design

This is a systematic review and meta-analysis on the effects of transcranial magnetic stimulation on modulating cortical excitability in patients with stroke. It provides a relatively large literature on modulatory uses of TMS aimed at changing cortical motor excitability after stroke, which is an important issue of whether such modulation of excitability is useful in recovery of motor function.

Funding

This project was funded by the General Research Fund (GRF, Grant No.: 151059/19 M), Research Grants Council, University Grants Committee, Hong Kong SAR (http://www.ugc.edu.hk/eng/rgc/), the Shanghai Sailing Program (No.: 20YF1445100) and the Shanghai Municipal Science and Technology Major Project (No.: 2021SHZDZX0100), Shanghai, China.

Author information

Authors and Affiliations

  1. Department of Rehabilitation Sciences, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China

    Zhongfei Bai, Jiaqi Zhang & Kenneth N. K. Fong

  2. Department of Occupational Therapy, Shanghai YangZhi Rehabilitation Hospital (Shanghai Sunshine Rehabilitation Center), Shanghai, China

    Zhongfei Bai

  3. Department of Rehabilitation Sciences, Tongji University School of Medicine, Shanghai, China

    Zhongfei Bai

Authors
  1. Zhongfei Bai
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jiaqi Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Kenneth N. K. Fong
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

Study objective: ZB, KNKF. Literature search: ZB, JZ. Data extraction: ZB, JZ. Methodological quality assessment: ZB, JZ, KNKF. Critical review and approval of manuscript: ZB, JZ, KNKF. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Kenneth N. K. Fong.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1

The methodological quality of transcranial magnetic stimulation studies investigating the effects of a single session of simulation on cortical excitability. Table. S2 The methodological quality of transcranial magnetic stimulation studies investigating the effects of multiple sessions of simulation on cortical excitability. Figs. S1 to S17 The funnel plots for the meta-analysis regarding the effects of rTMS on various outcomes.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Bai, Z., Zhang, J. & Fong, K.N.K. Effects of transcranial magnetic stimulation in modulating cortical excitability in patients with stroke: a systematic review and meta-analysis. J NeuroEngineering Rehabil 19, 24 (2022). https://doi.org/10.1186/s12984-022-00999-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12984-022-00999-4

Keywords

  • Stroke
  • Transcranial magnetic stimulation
  • Cortical excitability
  • Motor-evoked potentials
  • Interhemispheric imbalance

Journal of NeuroEngineering and Rehabilitation

ISSN: 1743-0003

Contact us