TY - JOUR
T1 - Harmonization of resting-state functional MRI data across multiple imaging sites via the separation of site differences into sampling bias and measurement bias
AU - Yamashita, Ayumu
AU - Yahata, Noriaki
AU - Itahashi, Takashi
AU - Lisi, Giuseppe
AU - Yamada, Takashi
AU - Ichikawa, Naho
AU - Takamura, Masahiro
AU - Yoshihara, Yujiro
AU - Kunimatsu, Akira
AU - Okada, Naohiro
AU - Yamagata, Hirotaka
AU - Matsuo, Koji
AU - Hashimoto, Ryuichiro
AU - Okada, Go
AU - Sakai, Yuki
AU - Morimoto, Jun
AU - Narumoto, Jin
AU - Shimada, Yasuhiro
AU - Kasai, Kiyoto
AU - Kato, Nobumasa
AU - Takahashi, Hidehiko
AU - Okamoto, Yasumasa
AU - Tanaka, Saori C.
AU - Kawato, Mitsuo
AU - Yamashita, Okito
AU - Imamizu, Hiroshi
N1 - Publisher Copyright:
© 2019 Yamashita et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2019
Y1 - 2019
N2 - When collecting large amounts of neuroimaging data associated with psychiatric disorders, images must be acquired from multiple sites because of the limited capacity of a single site. However, site differences represent a barrier when acquiring multisite neuroimaging data. We utilized a traveling-subject dataset in conjunction with a multisite, multidisorder dataset to demonstrate that site differences are composed of biological sampling bias and engineering measurement bias. The effects on resting-state functional MRI connectivity based on pairwise correlations because of both bias types were greater than or equal to psychiatric disorder differences. Furthermore, our findings indicated that each site can sample only from a subpopulation of participants. This result suggests that it is essential to collect large amounts of neuroimaging data from as many sites as possible to appropriately estimate the distribution of the grand population. Finally, we developed a novel harmonization method that removed only the measurement bias by using a traveling-subject dataset and achieved the reduction of the measurement bias by 29% and improvement of the signal-to-noise ratios by 40%. Our results provide fundamental knowledge regarding site effects, which is important for future research using multisite, multidisorder resting-state functional MRI data.
AB - When collecting large amounts of neuroimaging data associated with psychiatric disorders, images must be acquired from multiple sites because of the limited capacity of a single site. However, site differences represent a barrier when acquiring multisite neuroimaging data. We utilized a traveling-subject dataset in conjunction with a multisite, multidisorder dataset to demonstrate that site differences are composed of biological sampling bias and engineering measurement bias. The effects on resting-state functional MRI connectivity based on pairwise correlations because of both bias types were greater than or equal to psychiatric disorder differences. Furthermore, our findings indicated that each site can sample only from a subpopulation of participants. This result suggests that it is essential to collect large amounts of neuroimaging data from as many sites as possible to appropriately estimate the distribution of the grand population. Finally, we developed a novel harmonization method that removed only the measurement bias by using a traveling-subject dataset and achieved the reduction of the measurement bias by 29% and improvement of the signal-to-noise ratios by 40%. Our results provide fundamental knowledge regarding site effects, which is important for future research using multisite, multidisorder resting-state functional MRI data.
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U2 - 10.1371/journal.pbio.3000042
DO - 10.1371/journal.pbio.3000042
M3 - Article
C2 - 30998673
AN - SCOPUS:85065016805
SN - 1544-9173
VL - 17
JO - PLoS Biology
JF - PLoS Biology
IS - 4
M1 - e3000042
ER -