TY - JOUR
T1 - Image data harmonization tools for the analysis of post-traumatic epilepsy development in preclinical multisite MRI studies
AU - Bhagavatula, Sweta
AU - Cabeen, Ryan
AU - Harris, Neil G.
AU - Gröhn, Olli
AU - Wright, David K.
AU - Garner, Rachael
AU - Bennett, Alexis
AU - Alba, Celina
AU - Martinez, Aubrey
AU - Ndode-Ekane, Xavier Ekolle
AU - Andrade, Pedro
AU - Paananen, Tomi
AU - Ciszek, Robert
AU - Immonen, Riikka
AU - Manninen, Eppu
AU - Puhakka, Noora
AU - Tohka, Jussi
AU - Heiskanen, Mette
AU - Ali, Idrish
AU - Shultz, Sandy R.
AU - Casillas-Espinosa, Pablo M.
AU - Yamakawa, Glenn R.
AU - Jones, Nigel C.
AU - Hudson, Matthew R.
AU - Silva, Juliana C.
AU - Braine, Emma L.
AU - Brady, Rhys D.
AU - Santana-Gomez, Cesar E.
AU - Smith, Gregory D.
AU - Staba, Richard
AU - O'Brien, Terence J.
AU - Pitkänen, Asla
AU - Duncan, Dominique
N1 - Funding Information:
This study was conducted with the support of the National Institute of Neurological Disorders and Stroke (NINDS) of the National Institutes of Health (NIH) under award numbers U54 NS100064 ( EpiBioS4Rx ), R01NS111744 , and R01NS127524 . RPC was supported by the CZI Imaging Scientist Award Program , under CZI grant DAF2021-225670 and grant DOI https://doi.org/10.37921/029224bgopor from the Chan Zuckerberg Initiative DAF, an advised fund of Silicon Valley Community Foundation (funder DOI 10.13039/100014989).
Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/9
Y1 - 2023/9
N2 - Preclinical MRI studies have been utilized for the discovery of biomarkers that predict post-traumatic epilepsy (PTE). However, these single site studies often lack statistical power due to limited and homogeneous datasets. Therefore, multisite studies, such as the Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx), are developed to create large, heterogeneous datasets that can lead to more statistically significant results. EpiBioS4Rx collects preclinical data internationally across sites, including the United States, Finland, and Australia. However, in doing so, there are robust normalization and harmonization processes that are required to obtain statistically significant and generalizable results. This work describes the tools and procedures used to harmonize multisite, multimodal preclinical imaging data acquired by EpiBioS4Rx. There were four main harmonization processes that were utilized, including file format harmonization, naming convention harmonization, image coordinate system harmonization, and diffusion tensor imaging (DTI) metrics harmonization. By using Python tools and bash scripts, the file formats, file names, and image coordinate systems are harmonized across all the sites. To harmonize DTI metrics, values are estimated for each voxel in an image to generate a histogram representing the whole image. Then, the Quantitative Imaging Toolkit (QIT) modules are utilized to scale the mode to a value of one and depict the subsequent harmonized histogram. The standardization of file formats, naming conventions, coordinate systems, and DTI metrics are qualitatively assessed. The histograms of the DTI metrics were generated for all the individual rodents per site. For inter-site analysis, an average of the individual scans was calculated to create a histogram that represents each site. In order to ensure the analysis can be run at the level of individual animals, the sham and TBI cohort were analyzed separately, which depicted the same harmonization factor. The results demonstrate that these processes qualitatively standardize the file formats, naming conventions, coordinate systems, and DTI metrics of the data. This assists in the ability to share data across the study, as well as disseminate tools that can help other researchers to strengthen the statistical power of their studies and analyze data more cohesively.
AB - Preclinical MRI studies have been utilized for the discovery of biomarkers that predict post-traumatic epilepsy (PTE). However, these single site studies often lack statistical power due to limited and homogeneous datasets. Therefore, multisite studies, such as the Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx), are developed to create large, heterogeneous datasets that can lead to more statistically significant results. EpiBioS4Rx collects preclinical data internationally across sites, including the United States, Finland, and Australia. However, in doing so, there are robust normalization and harmonization processes that are required to obtain statistically significant and generalizable results. This work describes the tools and procedures used to harmonize multisite, multimodal preclinical imaging data acquired by EpiBioS4Rx. There were four main harmonization processes that were utilized, including file format harmonization, naming convention harmonization, image coordinate system harmonization, and diffusion tensor imaging (DTI) metrics harmonization. By using Python tools and bash scripts, the file formats, file names, and image coordinate systems are harmonized across all the sites. To harmonize DTI metrics, values are estimated for each voxel in an image to generate a histogram representing the whole image. Then, the Quantitative Imaging Toolkit (QIT) modules are utilized to scale the mode to a value of one and depict the subsequent harmonized histogram. The standardization of file formats, naming conventions, coordinate systems, and DTI metrics are qualitatively assessed. The histograms of the DTI metrics were generated for all the individual rodents per site. For inter-site analysis, an average of the individual scans was calculated to create a histogram that represents each site. In order to ensure the analysis can be run at the level of individual animals, the sham and TBI cohort were analyzed separately, which depicted the same harmonization factor. The results demonstrate that these processes qualitatively standardize the file formats, naming conventions, coordinate systems, and DTI metrics of the data. This assists in the ability to share data across the study, as well as disseminate tools that can help other researchers to strengthen the statistical power of their studies and analyze data more cohesively.
KW - Epilepsy
KW - MRI
KW - Neuroimaging
KW - Preclinical research
KW - Rat model
KW - TBI
UR - http://www.scopus.com/inward/record.url?scp=85166962583&partnerID=8YFLogxK
U2 - 10.1016/j.eplepsyres.2023.107201
DO - 10.1016/j.eplepsyres.2023.107201
M3 - Article
C2 - 37562146
AN - SCOPUS:85166962583
SN - 0920-1211
VL - 195
JO - Epilepsy Research
JF - Epilepsy Research
M1 - 107201
ER -