Literature DB >> 35970558

Non-neural factors influencing BOLD response magnitudes within individual subjects.

Jan W Kurzawski1, Omer Faruk Gulban2,3, Keith Jamison4, Jonathan Winawer5, Kendrick Kay6.   

Abstract

To what extent is the size of the blood-oxygen-level-dependent (BOLD) response influenced by factors other than neural activity? In a re-analysis of three neuroimaging datasets (male and female human participants), we find large systematic inhomogeneities in the BOLD response magnitude in primary visual cortex (V1): stimulus-evoked BOLD responses, expressed in units of percent signal change, are up to 50% larger along the representation of the horizontal meridian than the vertical meridian. To assess whether this surprising effect can be interpreted as differences in local neural activity, we quantified several factors that potentially contribute to the size of the BOLD response. We find relationships between BOLD response magnitude and cortical thickness, curvature, depth and macrovasculature. These relationships are consistently found across subjects and datasets and suggest that variation in BOLD response magnitudes across cortical locations reflects, in part, differences in anatomy and vascularization. To compensate for these factors, we implement a regression-based correction method and show that after correction, BOLD responses become more homogeneous across V1. The correction reduces the horizontal/vertical difference by about half, indicating that some of the difference is likely not due to neural activity differences. We conclude that interpretation of variation in BOLD response magnitude across cortical locations should consider the influence of the potential confounding factors of thickness, curvature, depth and vascularization.SIGNIFICANCE STATEMENTThe magnitude of the BOLD signal is often used as a surrogate of neural activity, but the exact factors that contribute to its strength have not been studied on a voxel-wise level. Here, we examined several anatomical and measurement-related factors to assess their relationship with BOLD signal magnitude. We find that BOLD magnitude correlates with cortical anatomy, depth and macrovasculature. To remove the contribution of these factors, we propose a simple, data-driven correction method that can be used in any functional magnetic resonance imaging (fMRI) experiment. After accounting for the confounding factors, BOLD magnitude becomes more spatially homogenous. Our correction method improves the ability to make more accurate inferences about local neural activity from fMRI data.
Copyright © 2022 the authors.

Entities:  

Year:  2022        PMID: 35970558      PMCID: PMC9512576          DOI: 10.1523/JNEUROSCI.2532-21.2022

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.709


  65 in total

1.  Echo time dependence of BOLD contrast and susceptibility artifacts.

Authors:  Maria Luisa Gorno-Tempini; Chloe Hutton; Oliver Josephs; Ralf Deichmann; Cathy Price; Robert Turner
Journal:  Neuroimage       Date:  2002-01       Impact factor: 6.556

Review 2.  The neural basis of functional brain imaging signals.

Authors:  David Attwell; Costantino Iadecola
Journal:  Trends Neurosci       Date:  2002-12       Impact factor: 13.837

Review 3.  The neural basis of the blood-oxygen-level-dependent functional magnetic resonance imaging signal.

Authors:  Nikos K Logothetis
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-08-29       Impact factor: 6.237

4.  Global and local fMRI signals driven by neurons defined optogenetically by type and wiring.

Authors:  Jin Hyung Lee; Remy Durand; Viviana Gradinaru; Feng Zhang; Inbal Goshen; Dae-Shik Kim; Lief E Fenno; Charu Ramakrishnan; Karl Deisseroth
Journal:  Nature       Date:  2010-06-10       Impact factor: 49.962

5.  Laminar imaging of positive and negative BOLD in human visual cortex at 7T.

Authors:  Alessio Fracasso; Peter R Luijten; Serge O Dumoulin; Natalia Petridou
Journal:  Neuroimage       Date:  2017-02-14       Impact factor: 6.556

6.  Compressive spatial summation in human visual cortex.

Authors:  Kendrick N Kay; Jonathan Winawer; Aviv Mezer; Brian A Wandell
Journal:  J Neurophysiol       Date:  2013-04-24       Impact factor: 2.714

7.  Tesla gradient recalled echo characteristics of photic stimulation-induced signal changes in the human primary visual cortex.

Authors:  R S Menon; S Ogawa; D W Tank; K Uğurbil
Journal:  Magn Reson Med       Date:  1993-09       Impact factor: 4.668

8.  Measuring the thickness of the human cerebral cortex from magnetic resonance images.

Authors:  B Fischl; A M Dale
Journal:  Proc Natl Acad Sci U S A       Date:  2000-09-26       Impact factor: 11.205

9.  Anticipatory haemodynamic signals in sensory cortex not predicted by local neuronal activity.

Authors:  Yevgeniy B Sirotin; Aniruddha Das
Journal:  Nature       Date:  2009-01-22       Impact factor: 49.962

Review 10.  Separating vascular and neuronal effects of age on fMRI BOLD signals.

Authors:  Kamen A Tsvetanov; Richard N A Henson; James B Rowe
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2020-11-16       Impact factor: 6.237

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.