Literature DB >> 14601143

Detection and quantification of a wide range of fMRI temporal responses using a physiologically-motivated basis set.

Michael P Harms1, Jennifer R Melcher.   

Abstract

The temporal dynamics of fMRI responses can span a broad range, indicating a rich underlying physiology, but also posing a significant challenge for detection. For instance, in human auditory cortex, prolonged sound stimuli ( approximately 30 sec) can evoke responses ranging from sustained to highly phasic (i.e., characterized by prominent peaks just after sound onset and offset). In the present study, we developed a method capable of detecting a wide variety of responses, while simultaneously extracting information about individual response components, which may have different neurophysiological underpinnings. Specifically, we implemented the general linear model using a novel set of basis functions chosen to reflect temporal features of cortical fMRI responses. This physiologically-motivated basis set (the "OSORU" basis set) was tested against (1) the commonly employed "sustained-only" basis "set" (i.e., a single smoothed "boxcar" function), and (2) a sinusoidal basis set, which is capable of detecting a broad range of responses, but lacks a direct relationship to individual response components. On data that included many different temporal responses, the OSORU basis set performed far better overall than the sustained-only set, and as well or better than the sinusoidal basis set. The OSORU basis set also proved effective in exploring brain physiology. As an example, we demonstrate that the OSORU basis functions can be used to spatially map the relative amount of transient vs. sustained activity within auditory cortex. The OSORU basis set provides a powerful means for response detection and quantification that should be broadly applicable to any brain system and to both human and non-human species. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 14601143      PMCID: PMC1866291          DOI: 10.1002/hbm.10136

Source DB:  PubMed          Journal:  Hum Brain Mapp        ISSN: 1065-9471            Impact factor:   5.038


  46 in total

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Authors:  M E Ravicz; J R Melcher
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2.  Specified-resolution wavelet analysis of activation patterns from BOLD contrast fMRI.

Authors:  V von Tscharner; K R Thulborn
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3.  Post-stimulus response in hemodynamics observed by functional magnetic resonance imaging--difference between the primary sensorimotor area and the supplementary motor area.

Authors:  T Nakai; K Matsuo; C Kato; Y Takehara; H Isoda; T Moriya; T Okada; H Sakahara
Journal:  Magn Reson Imaging       Date:  2000-12       Impact factor: 2.546

4.  A new statistical approach to detecting significant activation in functional MRI.

Authors:  J L Marchini; B D Ripley
Journal:  Neuroimage       Date:  2000-10       Impact factor: 6.556

5.  Spatiotemporal pattern of neural processing in the human auditory cortex.

Authors:  Erich Seifritz; Fabrizio Esposito; Franciszek Hennel; Henrietta Mustovic; John G Neuhoff; Deniz Bilecen; Gioacchino Tedeschi; Klaus Scheffler; Francesco Di Salle
Journal:  Science       Date:  2002-09-06       Impact factor: 47.728

6.  Time series analysis in the time domain and resampling methods for studies of functional magnetic resonance brain imaging.

Authors:  J J Locascio; P J Jennings; C I Moore; S Corkin
Journal:  Hum Brain Mapp       Date:  1997       Impact factor: 5.038

7.  Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.

Authors:  K K Kwong; J W Belliveau; D A Chesler; I E Goldberg; R M Weisskoff; B P Poncelet; D N Kennedy; B E Hoppel; M S Cohen; R Turner
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-15       Impact factor: 11.205

8.  Multidimensional wavelet analysis of functional magnetic resonance images.

Authors:  M J Brammer
Journal:  Hum Brain Mapp       Date:  1998       Impact factor: 5.038

9.  Quantification in functional magnetic resonance imaging: fuzzy clustering vs. correlation analysis.

Authors:  R Baumgartner; C Windischberger; E Moser
Journal:  Magn Reson Imaging       Date:  1998       Impact factor: 2.546

10.  Empirical analyses of BOLD fMRI statistics. I. Spatially unsmoothed data collected under null-hypothesis conditions.

Authors:  E Zarahn; G K Aguirre; M D'Esposito
Journal:  Neuroimage       Date:  1997-04       Impact factor: 6.556

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  25 in total

1.  Analysis of time and space invariance of BOLD responses in the rat visual system.

Authors:  Christopher J Bailey; Basavaraju G Sanganahalli; Peter Herman; Hal Blumenfeld; Albert Gjedde; Fahmeed Hyder
Journal:  Cereb Cortex       Date:  2012-01-31       Impact factor: 5.357

2.  Whole-brain, time-locked activation with simple tasks revealed using massive averaging and model-free analysis.

Authors:  Javier Gonzalez-Castillo; Ziad S Saad; Daniel A Handwerker; Souheil J Inati; Noah Brenowitz; Peter A Bandettini
Journal:  Proc Natl Acad Sci U S A       Date:  2012-03-19       Impact factor: 11.205

3.  Effects of sound level on fMRI activation in human brainstem, thalamic and cortical centers.

Authors:  Irina S Sigalovsky; Jennifer R Melcher
Journal:  Hear Res       Date:  2006-04-27       Impact factor: 3.208

4.  Calibration of BOLD fMRI using breath holding reduces group variance during a cognitive task.

Authors:  Moriah E Thomason; Lara C Foland; Gary H Glover
Journal:  Hum Brain Mapp       Date:  2007-01       Impact factor: 5.038

5.  Cortical FMRI activation to sequences of tones alternating in frequency: relationship to perceived rate and streaming.

Authors:  E Courtenay Wilson; Jennifer R Melcher; Christophe Micheyl; Alexander Gutschalk; Andrew J Oxenham
Journal:  J Neurophysiol       Date:  2007-01-03       Impact factor: 2.714

6.  Complex spatio-temporal dynamics of fMRI BOLD: A study of motor learning.

Authors:  Eugene Duff; Jinhu Xiong; Binquan Wang; Ross Cunnington; Peter Fox; Gary Egan
Journal:  Neuroimage       Date:  2006-11-01       Impact factor: 6.556

7.  BOLD responses in human auditory cortex are more closely related to transient MEG responses than to sustained ones.

Authors:  Alexander Gutschalk; Matti S Hämäläinen; Jennifer R Melcher
Journal:  J Neurophysiol       Date:  2010-01-27       Impact factor: 2.714

Review 8.  Beyond BOLD: optimizing functional imaging in stroke populations.

Authors:  Michele Veldsman; Toby Cumming; Amy Brodtmann
Journal:  Hum Brain Mapp       Date:  2014-12-02       Impact factor: 5.038

9.  Task Dependence, Tissue Specificity, and Spatial Distribution of Widespread Activations in Large Single-Subject Functional MRI Datasets at 7T.

Authors:  Javier Gonzalez-Castillo; Colin W Hoy; Daniel A Handwerker; Vinai Roopchansingh; Souheil J Inati; Ziad S Saad; Robert W Cox; Peter A Bandettini
Journal:  Cereb Cortex       Date:  2014-07-01       Impact factor: 5.357

10.  Characterisation of the BOLD response time course at different levels of the auditory pathway in non-human primates.

Authors:  Simon Baumann; Timothy D Griffiths; Adrian Rees; David Hunter; Li Sun; Alexander Thiele
Journal:  Neuroimage       Date:  2010-01-04       Impact factor: 6.556

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