Abstract:Establishing spatial correspondence between subject and template images is necessary in neuroimaging research and clinical applications such as brain mapping and stereotactic neurosurgery. Our anatomical fiducial (AFID) framework has recently been validated to serve as a quantitative measure of image registration based on salient anatomical features. In this study, we sought to apply the AFIDs protocol to the clinic, focusing on structural magnetic resonance images obtained from patients with Parkinson’s disea… Show more
“…A Wilcoxon signed-rank test revealed no significant differences between any LEs in all axes. Furthermore, we expanded our analysis to a subset of 24 patients who previously had AFIDs placed by five raters (Abbass et al, 2022; Lau et al, 2019; Taha et al, 2023). The median AFLE (IQR) ranged from 0.56 mm (0.40-0.69 mm) for AFID02 (PC) to 2.25 mm (1.49-2.75 mm) for AFID25 (right inferior anteromedial temporal horn).…”
Section: Resultsmentioning
confidence: 99%
“…We previously reported and openly released AFIDs annotations in a population of thirty-nine patients undergoing STN DBS for PD (Abbass et al, 2022; Taha et al, 2023). Briefly, 5 raters localized AFIDs on subject scans and on the MNI template.…”
Section: Methodsmentioning
confidence: 99%
“…The median AFLE (IQR) ranged from 0.56 mm (0.40-0.69 mm) for AFID02 (PC) to 2.25 mm (1.49-2.75 mm) for AFID25 (right inferior anteromedial temporal horn). See Abbass et al (2022) for more details.…”
Section: Localization Accuracymentioning
confidence: 99%
“…These voxel overlap measures are straightforward to obtain from common neuroimaging workflows, but are also relatively coarse metrics that do not capture focal misregistration (Rohlfing, 2012). Anatomically placed points (also referred to as fiducials or landmarks) can also be used to quantify registration accuracy measured as the millimetric distance between transformed points (Abbass et al, 2022; Lau et al, 2019; Schönecker et al, 2009). This motivated our group to identify and validate anatomical fiducials (AFIDs) which can be accurately and reliably placed.…”
Effects of deep brain stimulation (DBS) depend on millimetric accuracy and are commonly studied across populations by registering patient scans to a stereotactic space. Multiple factors contribute to estimates of electrode position, but the millimetric contributions of these factors remains poorly quantified. We previously validated 32 anatomical fiducials (AFIDs) to measure AFID registration error (AFRE), which can capture focal misregistration not observed using volume-based methods. To this end, we used the AFIDs framework to examine the effects of misregistration on electrode position in stereotactic space, leveraging a retrospective series of patients who underwent subthalamic nucleus DBS. Raters independently localized DBS electrodes and AFIDs on patient scans, which were non-linearly registered to a common stereotactic (MNI) space. AFIDs provided intuitive measures of registration accuracy, with AFREs ranging from 1.49 mm to 6.85 mm across brain regions. Subcortical AFIDs in proximity to the DBS target had AFREs that spatially covaried, suggesting consistent spatial patterns of misregistration to stereotactic space. These identified spatial patterns explained 28% of the variance in electrode position along the axis of maximum variance, corresponding to a median of 0.64 mm (range of 0.05 to 2.05 mm). To our knowledge, these represent the first millimetric estimates of registration accuracy in DBS, allowing uncoupling of registration-related factors from other sources of variance in electrode position. Furthermore, they can be employed for estimating registration-related variance in population studies, for quality control, and to provide a basis for comparison as well as optimization of registration parameters and software.
“…A Wilcoxon signed-rank test revealed no significant differences between any LEs in all axes. Furthermore, we expanded our analysis to a subset of 24 patients who previously had AFIDs placed by five raters (Abbass et al, 2022; Lau et al, 2019; Taha et al, 2023). The median AFLE (IQR) ranged from 0.56 mm (0.40-0.69 mm) for AFID02 (PC) to 2.25 mm (1.49-2.75 mm) for AFID25 (right inferior anteromedial temporal horn).…”
Section: Resultsmentioning
confidence: 99%
“…We previously reported and openly released AFIDs annotations in a population of thirty-nine patients undergoing STN DBS for PD (Abbass et al, 2022; Taha et al, 2023). Briefly, 5 raters localized AFIDs on subject scans and on the MNI template.…”
Section: Methodsmentioning
confidence: 99%
“…The median AFLE (IQR) ranged from 0.56 mm (0.40-0.69 mm) for AFID02 (PC) to 2.25 mm (1.49-2.75 mm) for AFID25 (right inferior anteromedial temporal horn). See Abbass et al (2022) for more details.…”
Section: Localization Accuracymentioning
confidence: 99%
“…These voxel overlap measures are straightforward to obtain from common neuroimaging workflows, but are also relatively coarse metrics that do not capture focal misregistration (Rohlfing, 2012). Anatomically placed points (also referred to as fiducials or landmarks) can also be used to quantify registration accuracy measured as the millimetric distance between transformed points (Abbass et al, 2022; Lau et al, 2019; Schönecker et al, 2009). This motivated our group to identify and validate anatomical fiducials (AFIDs) which can be accurately and reliably placed.…”
Effects of deep brain stimulation (DBS) depend on millimetric accuracy and are commonly studied across populations by registering patient scans to a stereotactic space. Multiple factors contribute to estimates of electrode position, but the millimetric contributions of these factors remains poorly quantified. We previously validated 32 anatomical fiducials (AFIDs) to measure AFID registration error (AFRE), which can capture focal misregistration not observed using volume-based methods. To this end, we used the AFIDs framework to examine the effects of misregistration on electrode position in stereotactic space, leveraging a retrospective series of patients who underwent subthalamic nucleus DBS. Raters independently localized DBS electrodes and AFIDs on patient scans, which were non-linearly registered to a common stereotactic (MNI) space. AFIDs provided intuitive measures of registration accuracy, with AFREs ranging from 1.49 mm to 6.85 mm across brain regions. Subcortical AFIDs in proximity to the DBS target had AFREs that spatially covaried, suggesting consistent spatial patterns of misregistration to stereotactic space. These identified spatial patterns explained 28% of the variance in electrode position along the axis of maximum variance, corresponding to a median of 0.64 mm (range of 0.05 to 2.05 mm). To our knowledge, these represent the first millimetric estimates of registration accuracy in DBS, allowing uncoupling of registration-related factors from other sources of variance in electrode position. Furthermore, they can be employed for estimating registration-related variance in population studies, for quality control, and to provide a basis for comparison as well as optimization of registration parameters and software.
“…Alternatively, Abbass et al recently reported utilization of anatomical fiducials in the brain for such a purpose. However, this method includes the placement of 32 fiducial points which is impractical for clinical application [35]. Therefore, as automated segmentation tools continue to evolve, efficient and reliable methods of QC are needed to make them more clinically relevant.…”
<b><i>Introduction:</i></b> Accurate and precise delineation of the globus pallidus pars interna (GPi) and subthalamic nucleus (STN) is critical for the clinical treatment and research of Parkinson’s disease (PD). Automated segmentation is a developing technology which addresses limitations of visualizing deep nuclei on MR imaging and standardizing their definition in research applications. We sought to compare manual segmentation with three workflows for template-to-patient nonlinear registration providing atlas-based automatic segmentation of deep nuclei. <b><i>Methods:</i></b> Bilateral GPi, STN, and red nucleus (RN) were segmented for 20 PD and 20 healthy control (HC) subjects using 3T MRIs acquired for clinical purposes. The automated workflows used were an option available in clinical practice and two common research protocols. Quality control (QC) was performed on registered templates via visual inspection of readily discernible brain structures. Manual segmentation using T1, proton density, and T2 sequences was used as “ground truth” data for comparison. Dice similarity coefficient (DSC) was used to assess agreement between segmented nuclei. Further analysis was done to compare the influences of disease state and QC classifications on DSC. <b><i>Results:</i></b> Automated segmentation workflows (CIT-S, CRV-AB, and DIST-S) had the highest DSC for the RN and lowest for the STN. Manual segmentations outperformed automated segmentation for all workflows and nuclei; however, for 3/9 workflows (CIT-S STN, CRV-AB STN, and CRV-AB GPi) the differences were not statically significant. HC and PD only showed significant differences in 1/9 comparisons (DIST-S GPi). QC classification only demonstrated significantly higher DSC in 2/9 comparisons (CRV-AB RN and GPi). <b><i>Conclusion:</i></b> Manual segmentations generally performed better than automated segmentations. Disease state does not appear to have a significant effect on the quality of automated segmentations via nonlinear template-to-patient registration. Notably, visual inspection of template registration is a poor indicator of the accuracy of deep nuclei segmentation. As automatic segmentation methods continue to evolve, efficient and reliable QC methods will be necessary to support safe and effective integration into clinical workflows.
Tools available for reproducible, quantitative assessment of brain correspondence have been limited. We previously validated the anatomical fiducial (AFID) placement protocol for point-based assessment of image registration with millimetric (mm) accuracy. In this data descriptor, we release curated AFID placements for some of the most commonly used structural magnetic resonance imaging datasets and templates. The release of our accurate placements allows for rapid quality control of image registration, teaching neuroanatomy, and clinical applications such as disease diagnosis and surgical targeting. We release placements on individual subjects from four datasets (N = 132 subjects for a total of 15,232 fiducials) and 14 brain templates (4,288 fiducials), totalling more than 300 human rater hours of annotation. We also validate human rater accuracy of released placements to be within 1 – 2 mm (using more than 45,000 Euclidean distances), consistent with prior studies. Our data is compliant with the Brain Imaging Data Structure allowing for facile incorporation into neuroimaging analysis pipelines.
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