A novel model incorporating two variability sources for describing motor evoked potentials.

Journal Article (Journal Article)

OBJECTIVE: Motor evoked potentials (MEPs) play a pivotal role in transcranial magnetic stimulation (TMS), e.g., for determining the motor threshold and probing cortical excitability. Sampled across the range of stimulation strengths, MEPs outline an input-output (IO) curve, which is often used to characterize the corticospinal tract. More detailed understanding of the signal generation and variability of MEPs would provide insight into the underlying physiology and aid correct statistical treatment of MEP data. METHODS: A novel regression model is tested using measured IO data of twelve subjects. The model splits MEP variability into two independent contributions, acting on both sides of a strong sigmoidal nonlinearity that represents neural recruitment. Traditional sigmoidal regression with a single variability source after the nonlinearity is used for comparison. RESULTS: The distribution of MEP amplitudes varied across different stimulation strengths, violating statistical assumptions in traditional regression models. In contrast to the conventional regression model, the dual variability source model better described the IO characteristics including phenomena such as changing distribution spread and skewness along the IO curve. CONCLUSIONS: MEP variability is best described by two sources that most likely separate variability in the initial excitation process from effects occurring later on. The new model enables more accurate and sensitive estimation of the IO curve characteristics, enhancing its power as a detection tool, and may apply to other brain stimulation modalities. Furthermore, it extracts new information from the IO data concerning the neural variability-information that has previously been treated as noise.

Full Text

Duke Authors

Cited Authors

  • Goetz, SM; Luber, B; Lisanby, SH; Peterchev, AV

Published Date

  • 2014

Published In

Volume / Issue

  • 7 / 4

Start / End Page

  • 541 - 552

PubMed ID

  • 24794287

Pubmed Central ID

  • PMC4108579

Electronic International Standard Serial Number (EISSN)

  • 1876-4754

Digital Object Identifier (DOI)

  • 10.1016/j.brs.2014.03.002


  • eng

Conference Location

  • United States