Evidence map›Paper›PMID 42491388›Full record

ArticleImaging neuroscience (Cambridge, Mass.)

Assessing the efficacy and reproducibility of four common repetitive transcranial magnetic stimulation protocols: A sham-controled study.

Brice Passera, Peter J Fried, Justine Magnuson, Stephanie S Buss, Alvaro Pascual-Leone, Recep A Ozdemir, Mouhsin M Shafi

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Brice PasseraBerenson-Allen Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, United States.ORCID https://orcid.org/0000-0001-9821-1970
Peter J FriedBerenson-Allen Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Justine MagnusonDepartment of Psychology, University of British Columbia Okanagan, Kelowna, BC, Canada.
Stephanie S BussBerenson-Allen Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Alvaro Pascual-LeoneDepartment of Neurology, Harvard Medical School, Boston, MA, United States.
Recep A OzdemirBerenson-Allen Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Mouhsin M ShafiBerenson-Allen Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, United States.

Funding

The Role of Inflammation in the Pathophysiology of Delirium and its Associated Long-Term Cognitive DeclineP01AG031720 · NIA · HEBREW REHABILITATION CENTER FOR AGED · PI INOUYE, SHARON K. · 2010 to 2022
$26.7M
Personalized brain activity modulation to improve balance and cognition in elderly fallersR01AG059089 · NIA · HEBREW REHABILITATION CENTER FOR AGED · PI MANOR, BRADLEY D. · 2018 to 2022
$3.2M
Repetitive TMS-induced modulation of cortical excitability in ADR01MH115949 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SHAFI, MOUHSIN · 2018 to 2022
$3.2M
Treating hyperexcitability in Alzheimer’s disease with levetiracetam to improve brain function and cognitionR01AG060987 · NIA · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SHAFI, MOUHSIN · 2019 to 2023
$3.0M
Multifocal transcranial current stimulation for cognitive and motor dysfunction in dementiaR01AG076708 · NIA · HEBREW REHABILITATION CENTER FOR AGED · PI MANOR, BRADLEY D., PASCUAL-LEONE, ALVARO · 2022 to 2024
$2.3M
Enhancing robotic head and neck surgical skills using stimulated simulationR01EB032820 · NIBIB · FLORIDA STATE UNIVERSITY · PI Suvranu De, Ernest Dennis Gomez · 2023 to 2026
$1.8M
System biology approach to decode molecular mechanism of glucose metabolism in AD and dementiaR03AG072233 · NIA · HEBREW REHABILITATION CENTER FOR AGED · PI JEONG, SOHYUN · 2022 to 2023
$320k
NIA NIH HHS P01 AG031720NIA NIH HHS R01 AG059089NIA NIH HHS R01 AG060987NIA NIH HHS R01 AG076708NIA NIH HHS R03 AG072233NIBIB NIH HHS R01 EB032820NIMH NIH HHS R01 MH115949
6 · The paper itself

Abstract

Repetitive transcranial magnetic stimulation (rTMS) has been widely used in both clinical and research settings to modulate brain activity and assess brain plasticity. The effects of rTMS are generally believed to involve modulation of cortical excitability; protocols such as 10 Hz and iTBS increase cortical excitability, while 1 Hz and cTBS are considered inhibitory. However, recent meta-analyses and studies have shown a wide array of interindividual responses to each protocol and poor reliability of the results. Here, we applied two sessions of the four most commonly used rTMS protocols (iTBS, cTBS, 10 Hz, 1 Hz) and sham to the primary motor cortex and assessed their neurophysiological and behavioral effects. We hypothesized that relative to sham, 10 Hz and iTBS would increase motor excitability and modulate motor response times, while 1 Hz and cTBS would have opposite effects. We recorded single-pulse TMS-EEG-EMG pre-rTMS and 5 and 25 minutes post-rTMS. Participants performed a sequential finger-tapping task (SFTT) 20 minutes pre-rTMS and 15 minutes post-rTMS. Our main outcome measures were P30 amplitude, early LMFP (15-75 ms) area under-the-curve, MEP, and SFTT completion time. We calculated the Intra-Class Correlation between each session for each measure. For each protocol, we found no consistent protocol-dependent group effect on MEPs, TEPs, or behavior, with high intra-individual variability across sessions. An increase in SFTT completion time occurred for all active protocols but also sham. The test-retest reliability of rTMS effects was low (ICC < 0.5) for almost all protocols and metrics. This study is the first comprehensive assessment of the effects and reliability of the most commonly used rTMS protocols on cortical excitability and behavior. Our results suggest that rTMS effects are not reliable, at least at the single-session level, and that the inclusion of sham rTMS is essential for identifying protocol-specific effects. These results also suggest that a fundamental and unbiased re-evaluation of potential rTMS mechanisms is necessary.

Indexed as

cortical excitabilityelectroencephalographymotor taskplasticityrepetitive transcranial magnetic stimulationreproducibilityTMS-evoked potential

Identifiers

PMID42491388
PMCPMC13377501

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.