Concepedia

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Nonlinear event‐related responses in fMRI

640

Citations

20

References

1998

Year

TLDR

Volterra series extend linear convolution to model the hemodynamic response function nonlinearly, enabling representation of stimulus‑rate effects and stimulus interactions. The study aims to describe and validate a Volterra‑series approach for characterizing evoked fMRI hemodynamic responses and to discuss its implications for experimental design. The method estimates Volterra kernels that map stimulus presentation to hemodynamic responses, allowing nonlinear system identification. Nonlinear components were statistically significant, validated in an independent experiment, and revealed stimulus‑specific modulation, saturation, and inverted‑U behavior at high rates, suggesting BOLD‑specific refractoriness.

Abstract

Abstract This paper presents an approach to characterizing evoked hemodynamic responses in fMRI based on nonlinear system identification, in particular the use of Volterra series. The approach employed enables one to estimate Volterra kernels that describe the relationship between stimulus presentation and the hemodynamic responses that ensue. Volterra series are essentially high‐order extensions of linear convolution or “smoothing.” These kernels, therefore, represent a nonlinear characterization of the hemodynamic response function that can model the responses to stimuli in different contexts (in this work, different rates of word presentation) and interactions among stimuli. The nonlinear components of the responses were shown to be statistically significant, and the kernel estimates were validated using an independent event‐related fMRI experiment. One important manifestation of these nonlinear effects is a modulation of stimulus‐specific responses by preceding stimuli that are proximate in time. This means that responses at high‐stimulus presentation rates saturate and, in some instances, show an inverted U behavior. This behavior appears to be specific to BOLD effects (as distinct from evoked changes in cerebral blood flow) and may represent a hemodynamic “refractoriness.” The aim of this paper is to describe the theory and techniques upon which these conclusions were based and to discuss the implications for experimental design and analysis.

References

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