TY - JOUR
T1 - Towards HCP-Style macaque connectomes
T2 - 24-Channel 3T multi-array coil, MRI sequences and preprocessing
AU - Autio, Joonas A.
AU - Glasser, Matthew F.
AU - Ose, Takayuki
AU - Donahue, Chad J.
AU - Bastiani, Matteo
AU - Ohno, Masahiro
AU - Kawabata, Yoshihiko
AU - Urushibata, Yuta
AU - Murata, Katsutoshi
AU - Nishigori, Kantaro
AU - Yamaguchi, Masataka
AU - Hori, Yuki
AU - Yoshida, Atsushi
AU - Go, Yasuhiro
AU - Coalson, Timothy S.
AU - Jbabdi, Saad
AU - Sotiropoulos, Stamatios N.
AU - Kennedy, Henry
AU - Smith, Stephen
AU - Van Essen, David C.
AU - Hayashi, Takuya
N1 - Funding Information:
We thank technical help and comments from Yujie Hou, Kenneth Knoblauch, Stephen Frey, Nobuyoshi Tanki, Chiho Takeda, Akihiro Kawasaki, Reiko Kobayashi, Kenji Mitsui and Hanako Hirose for their technical help. This research is partially supported by the program for Brain/MINDS and Brain/MINDS-beyond from Japan Agency for Medical Research and development, AMED (JP18dm0207001, JP19dm0307006), by RIKEN Compass to Healthy Life Research Complex Program from Japan Science and Technology Agency, JST, by MEXT KAKENHI Grant (16H03300, 16H03306, 16H01626, 15K12779 (T.H.) and JP26640065, JP16H06531 (Y.G.), NIH F30 MH097312 (M.F.G.), T32 EB014855 (C.J.D.), and RO1 MH-060974 (D.C.V.E.), by the National Institutes of Natural Sciences (NINS) program for cross-disciplinary study (2013–2015) (Y.G.) and by Wellcome Trust (SMS, JS) and by LABEX CORTEX (ANR-11-LABX-0042) of Université de Lyon (ANR-11-IDEX-0007) operated by the French National Research Agency (ANR) (H. K.), ANR-11-BSV4-501, CORE-NETS (H.K.), ANR-14-CE13-0033, ARCHI-CORE (H.K.), ANR-15-CE32-0016, CORNET (H.K.), Chinese Academy of Sciences President's International Felloship Initiative. Grant No. 2018VBA0011 (H.K.). The author Yoshihiko Kawabata holds financial conflict of interest because the coil is produced by his company (Takashima Seisakusho Co. Ltd. Tokyo, Japan) and distributed through his collaboration company (Rogue Research, Montreal, Canada). The other authors have no conflicts of interest to declare.
Funding Information:
We thank technical help and comments from Yujie Hou, Kenneth Knoblauch, Stephen Frey, Nobuyoshi Tanki, Chiho Takeda, Akihiro Kawasaki, Reiko Kobayashi, Kenji Mitsui and Hanako Hirose for their technical help. This research is partially supported by the program for Brain/MINDS and Brain/MINDS-beyond from Japan Agency for Medical Research and development, AMED ( JP18dm0207001 , JP19dm0307006 ), by RIKEN Compass to Healthy Life Research Complex Program from Japan Science and Technology Agency, JST , by MEXT KAKENHI Grant ( 16H03300 , 16H03306 , 16H01626 , 15K12779 (T.H.) and JP26640065 , JP16H06531 (Y.G.), NIH F30 MH097312 (M.F.G.), T32 EB014855 (C.J.D.), and RO1 MH-060974 (D.C.V.E.), by the National Institutes of Natural Sciences (NINS) program for cross-disciplinary study (2013–2015) (Y.G.) and by Wellcome Trust (SMS, JS) and by LABEX CORTEX (ANR-11-LABX-0042) of Université de Lyon (ANR-11-IDEX-0007) operated by the French National Research Agency (ANR) (H. K.), ANR-11-BSV4-501, CORE-NETS (H.K.), ANR-14-CE13-0033, ARCHI-CORE (H.K.), ANR-15-CE32-0016, CORNET (H.K.), Chinese Academy of Sciences President’s International Felloship Initiative. Grant No. 2018VBA0011 (H.K.). The author Yoshihiko Kawabata holds financial conflict of interest because the coil is produced by his company (Takashima Seisakusho Co. Ltd., Tokyo, Japan) and distributed through his collaboration company (Rogue Research, Montreal, Canada). The other authors have no conflicts of interest to declare.
Publisher Copyright:
© 2020 The Author(s)
PY - 2020/7/15
Y1 - 2020/7/15
N2 - Macaque monkeys are an important animal model where invasive investigations can lead to a better understanding of the cortical organization of primates including humans. However, the tools and methods for noninvasive image acquisition (e.g. MRI RF coils and pulse sequence protocols) and image data preprocessing have lagged behind those developed for humans. To resolve the structural and functional characteristics of the smaller macaque brain, high spatial, temporal, and angular resolutions combined with high signal-to-noise ratio are required to ensure good image quality. To address these challenges, we developed a macaque 24-channel receive coil for 3-T MRI with parallel imaging capabilities. This coil enables adaptation of the Human Connectome Project (HCP) image acquisition protocols to the in-vivo macaque brain. In addition, we adapted HCP preprocessing methods to the macaque brain, including spatial minimal preprocessing of structural, functional MRI (fMRI), and diffusion MRI (dMRI). The coil provides the necessary high signal-to-noise ratio and high efficiency in data acquisition, allowing four- and five-fold accelerations for dMRI and fMRI. Automated FreeSurfer segmentation of cortex, reconstruction of cortical surface, removal of artefacts and nuisance signals in fMRI, and distortion correction of dMRI all performed well, and the overall quality of basic neurobiological measures was comparable with those for the HCP. Analyses of functional connectivity in fMRI revealed high sensitivity as compared with those from publicly shared datasets. Tractography-based connectivity estimates correlated with tracer connectivity similarly to that achieved using ex-vivo dMRI. The resulting HCP-style in vivo macaque MRI data show considerable promise for analyzing cortical architecture and functional and structural connectivity using advanced methods that have previously only been available in studies of the human brain.
AB - Macaque monkeys are an important animal model where invasive investigations can lead to a better understanding of the cortical organization of primates including humans. However, the tools and methods for noninvasive image acquisition (e.g. MRI RF coils and pulse sequence protocols) and image data preprocessing have lagged behind those developed for humans. To resolve the structural and functional characteristics of the smaller macaque brain, high spatial, temporal, and angular resolutions combined with high signal-to-noise ratio are required to ensure good image quality. To address these challenges, we developed a macaque 24-channel receive coil for 3-T MRI with parallel imaging capabilities. This coil enables adaptation of the Human Connectome Project (HCP) image acquisition protocols to the in-vivo macaque brain. In addition, we adapted HCP preprocessing methods to the macaque brain, including spatial minimal preprocessing of structural, functional MRI (fMRI), and diffusion MRI (dMRI). The coil provides the necessary high signal-to-noise ratio and high efficiency in data acquisition, allowing four- and five-fold accelerations for dMRI and fMRI. Automated FreeSurfer segmentation of cortex, reconstruction of cortical surface, removal of artefacts and nuisance signals in fMRI, and distortion correction of dMRI all performed well, and the overall quality of basic neurobiological measures was comparable with those for the HCP. Analyses of functional connectivity in fMRI revealed high sensitivity as compared with those from publicly shared datasets. Tractography-based connectivity estimates correlated with tracer connectivity similarly to that achieved using ex-vivo dMRI. The resulting HCP-style in vivo macaque MRI data show considerable promise for analyzing cortical architecture and functional and structural connectivity using advanced methods that have previously only been available in studies of the human brain.
KW - Cortex
KW - Diffusion
KW - Human connectome project
KW - Macaque
KW - Parallel imaging
KW - Primate
KW - Resting-state
UR - http://www.scopus.com/inward/record.url?scp=85083462975&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2020.116800
DO - 10.1016/j.neuroimage.2020.116800
M3 - Article
C2 - 32276072
AN - SCOPUS:85083462975
SN - 1053-8119
VL - 215
JO - NeuroImage
JF - NeuroImage
M1 - 116800
ER -