Torben Ellegaard Lund

Dr. Torben Ellegaard Lund

orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 December 2007 in Neuron
Verified
Journal Article
Closed access
AGAnne-Lise Giraud
Anne-Lise Giraud
AKAndreas Kleinschmidt
Andreas Kleinschmidt
DPDavid Poeppel
David Poeppel
TLTorben Ellegaard Lund
Torben Ellegaard Lund
RFRichard S.J. Frackowiak
Richard S.J. Frackowiak
HLHelmut Laufs
Helmut Laufs

1 January 2006 in NeuroImage
Verified
Journal Article
Closed access
TLTorben Ellegaard Lund
Torben Ellegaard Lund
KMKristoffer Hougaard Madsen
Kristoffer Hougaard Madsen
KSKaram Sidaros
Karam Sidaros
WLWen-Lin Luo
Wen-Lin Luo
TNThomas E. Nichols
Thomas E. Nichols

1 July 2007 in Magnetic Resonance Imaging
Verified
Journal Article
Closed access
LLLouis Lemieux
Louis Lemieux
ASAfraim Salek-Haddadi
Afraim Salek-Haddadi
TLTorben Ellegaard Lund
Torben Ellegaard Lund
HLHelmut Laufs
Helmut Laufs
DCDavid Carmichael
David Carmichael

1 July 2005 in NeuroImage
Verified
Journal Article
Closed access
TLTorben Ellegaard Lund
Torben Ellegaard Lund
MNMinna D. Nørgaard
Minna D. Nørgaard
EREgill Rostrup
Egill Rostrup
JRJames B. Rowe
James B. Rowe
OPOlaf Bjarne Paulson
Olaf Bjarne Paulson

28 May 2017 in Brain
Verified
Journal Article
Open access
PDF file
PPPeter Parbo
Peter Parbo
RIRola Ismail
Rola Ismail
KHKim V. Hansen
Kim V. Hansen
AAAli Amidi
Ali Amidi
FMFrederik H. Mårup
Frederik H. Mårup
DBDavid Brooks
David Brooks
See Kreisl (doi: 10.1093/awx151 ) for a scientific commentary on this article. Subjects with mild cognitive impairment associated with cortical amyloid-β have a greatly increased risk of progressing to Alzheimer’s disease. We hypothesized that neuroinflammation occurs early in Alzheimer’s disease and would be present in most amyloid-positive mild cognitive impairment cases. 11C-Pittsburgh compound B and 11C-(R)-PK11195 positron emission tomography was used to determine the amyloid load and detect the extent of neuroinflammation (microglial activation) in 42 mild cognitive impairment cases. Twelve age-matched healthy control subjects had 11C-Pittsburgh compound B and 10 healthy control subjects had 11C-(R)-PK11195 positron emission tomography for comparison. Amyloid-positivity was defined as 11C-Pittsburgh compound B target-to-cerebellar ratio above 1.5 within a composite cortical volume of interest. Supervised cluster analysis was used to generate parametric maps of 11C-(R)-PK11195 binding potential. Levels of 11C-(R)-PK11195 binding potential were measured in a selection of cortical volumes of interest and at a voxel level. Twenty-six (62%) of 42 mild cognitive impairment cases showed a raised cortical amyloid load compared to healthy controls. Twenty-two (85%) of the 26 amyloid-positive mild cognitive impairment cases showed clusters of increased cortical microglial activation accompanying the amyloid. There was a positive correlation between levels of amyloid load and 11C-(R)-PK11195 binding potentials at a voxel level within subregions of frontal, parietal and temporal cortices. 11C-(R)-PK11195 positron emission tomography reveals increased inflammation in a majority of amyloid positive mild cognitive impairment cases, its cortical distribution overlapping that of amyloid deposition.

1 July 2020 in NeuroImage
Verified
Journal Article
Open access
TMTomas E. Matthews
Tomas E. Matthews
MWMaria A.G. Witek
Maria A.G. Witek
TLTorben Ellegaard Lund
Torben Ellegaard Lund
PVPeter Vuust
Peter Vuust
VPVirginia B. Penhune
Virginia B. Penhune
The sensation of groove has been defined as the pleasurable desire to move to music, suggesting that both motor timing and reward processes are involved in this experience. Although many studies have investigated rhythmic timing and musical reward separately, none have examined whether the associated cortical and subcortical networks are engaged while participants listen to groove-based music. In the current study, musicians and non-musicians listened to and rated experimentally controlled groove-based stimuli while undergoing functional magnetic resonance imaging. Medium complexity rhythms elicited higher ratings of pleasure and wanting to move and were associated with activity in regions linked to beat perception and reward, as well as prefrontal and parietal regions implicated in generating and updating stimuli-based expectations. Activity in basal ganglia regions of interest, including the nucleus accumbens, caudate and putamen, was associated with ratings of pleasure and wanting to move, supporting their important role in the sensation of groove. We propose a model in which different cortico-striatal circuits interact to support the mechanisms underlying groove, including internal generation of the beat, beat-based expectations, and expectation-based affect. These results show that the sensation of groove is supported by motor and reward networks in the brain and, along with our proposed model, suggest that the basal ganglia are crucial nodes in networks that interact to generate this powerful response to music.