Reliability and sensitivity of two whole-brain segmentation approaches included in FreeSurfer – ASEG and SAMSEG
Donatas Sederevičius,
Didac Vidal-Piñeiro,
Øystein Sørensen,
Koen van Leemput,
Juan Eugenio Iglesias,
Adrian V. Dalca,
Douglas N. Greve,
Bruce Fischl,
Atle Bjørnerud,
Kristine B. Walhovd,
Anders M. Fjell
Affiliations
Donatas Sederevičius
Center for Lifespan Changes in Brain and Cognition, University of Oslo, Pb. 1094, Blindern, Oslo 0317, Norway; Corresponding author.
Didac Vidal-Piñeiro
Center for Lifespan Changes in Brain and Cognition, University of Oslo, Pb. 1094, Blindern, Oslo 0317, Norway
Øystein Sørensen
Center for Lifespan Changes in Brain and Cognition, University of Oslo, Pb. 1094, Blindern, Oslo 0317, Norway
Koen van Leemput
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, United States; Department of Health Technology, Technical University of Denmark, Denmark
Juan Eugenio Iglesias
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, United States; Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, United Kingdom; Computer Science and Artificial Intelligence Laboratory, MIT, United States
Adrian V. Dalca
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, United States; Computer Science and Artificial Intelligence Laboratory, MIT, United States
Douglas N. Greve
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, United States
Bruce Fischl
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, United States; Computer Science and Artificial Intelligence Laboratory, MIT, United States
Atle Bjørnerud
Division of Radiology and Nuclear Medicine, Oslo University Hospital, Norway
Kristine B. Walhovd
Center for Lifespan Changes in Brain and Cognition, University of Oslo, Pb. 1094, Blindern, Oslo 0317, Norway; Division of Radiology and Nuclear Medicine, Oslo University Hospital, Norway
Anders M. Fjell
Center for Lifespan Changes in Brain and Cognition, University of Oslo, Pb. 1094, Blindern, Oslo 0317, Norway; Division of Radiology and Nuclear Medicine, Oslo University Hospital, Norway
Accurate and reliable whole-brain segmentation is critical to longitudinal neuroimaging studies. We undertake a comparative analysis of two subcortical segmentation methods, Automatic Segmentation (ASEG) and Sequence Adaptive Multimodal Segmentation (SAMSEG), recently provided in the open-source neuroimaging package FreeSurfer 7.1, with regard to reliability, bias, sensitivity to detect longitudinal change, and diagnostic sensitivity to Alzheimer’s disease. First, we assess intra- and inter-scanner reliability for eight bilateral subcortical structures: amygdala, caudate, hippocampus, lateral ventricles, nucleus accumbens, pallidum, putamen and thalamus. For intra-scanner analysis we use a large sample of participants (n = 1629) distributed across the lifespan (age range = 4–93 years) and acquired on a 1.5T Siemens Avanto (n = 774) and a 3T Siemens Skyra (n = 855) scanners. For inter-scanner analysis we use a sample of 24 participants scanned on the day with three models of Siemens scanners: 1.5T Avanto, 3T Skyra and 3T Prisma. Second, we test how each method detects volumetric age change using longitudinal follow up scans (n = 491 for Avanto and n = 245 for Skyra; interscan interval = 1–10 years). Finally, we test sensitivity to clinically relevant change. We compare annual rate of hippocampal atrophy in cognitively normal older adults (n = 20), patients with mild cognitive impairment (n = 20) and Alzheimer’s disease (n = 20). We find that both ASEG and SAMSEG are reliable and lead to the detection of within-person longitudinal change, although with notable differences between age-trajectories for most structures, including hippocampus and amygdala. In summary, SAMSEG yields significantly lower differences between repeated measures for intra- and inter-scanner analysis without compromising sensitivity to changes and demonstrating ability to detect clinically relevant longitudinal changes.