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Stereotact Funct Neurosurg. 2009 August; 87(4): 229–240.
Published online 2009 June 26. doi:  10.1159/000225976
PMCID: PMC2836941

Automated 3-Dimensional Brain Atlas Fitting to Microelectrode Recordings from Deep Brain Stimulation Surgeries



Deep brain stimulation (DBS) surgeries commonly rely on brain atlases and microelectrode recordings (MER) to help identify the target location for electrode implantation. We present an automated method for optimally fitting a 3-dimensional brain atlas to intraoperative MER and predicting a target DBS electrode location in stereotactic coordinates for the patient.


We retrospectively fit a 3-dimensional brain atlas to MER points from 10 DBS surgeries targeting the subthalamic nucleus (STN). We used a constrained optimization algorithm to maximize the MER points correctly fitted (i.e., contained) within the appropriate atlas nuclei. We compared our optimization approach to conventional anterior commissure-posterior commissure (AC/PC) scaling, and to manual fits performed by four experts. A theoretical DBS electrode target location in the dorsal STN was customized to each patient as part of the fitting process and compared to the location of the clinically defined therapeutic stimulation contact.


The human expert and computer optimization fits achieved significantly better fits than the AC/PC scaling (80, 81, and 41% of correctly fitted MER, respectively). However, the optimization fits were performed in less time than the expert fits and converged to a single solution for each patient, eliminating interexpert variance.

Conclusions and Significance

DBS therapeutic outcomes are directly related to electrode implantation accuracy. Our automated fitting techniques may aid in the surgical decision-making process by optimally integrating brain atlas and intraoperative neurophysiological data to provide a visual guide for target identification.

Key Words: Deep brain stimulation, Brain atlas, Microelectrode recordings, Stereotactic neurosurgery, Stereotactic target location


Deep brain stimulation (DBS) is a surgical intervention that uses electrical stimulation to treat the symptoms of medically refractory neurological disorders such as Parkinson's disease (PD) [1,2,3,4]. The surgical strategy for DBS varies among centers [1, 5, 6], but generally involves the integration of multiple data types. These can include various imaging modalities, intraoperative electrophysiological mapping [i.e., x, y, and z microelectrode recording (MER) coordinate points] [5,6,7,8,9], and standardized anatomical atlases [10] to define the DBS electrode trajectory and target implantation location [1, 3].

A fundamental purpose of MER is to verify the stereotactic location of the target brain region for electrode implantation. A neurophysiologist records neural activity as a microelectrode is advanced through stereotactic brain space and identifies specific nuclei based on the properties of the neural signals recorded [3,5,6,7,11,12,13]. While not performed at all DBS centers, this verification process can help alleviate two limitations. First, the surgical target cannot always be directly identified on preoperative imaging data [14]. Second, the intracranial pressure changes once the burr hole is drilled, resulting in a possible shift of the subcortical structures, thereby altering the position of the target point in stereotactic space [15,16,17].

Brain atlases are commonly employed to assist in the definition of the initial target point and interpret the MER [10]. However, standard 2-dimensional atlas planes seldom correspond to the oblique trajectories used, which along with the limited resolution and discontinuity of the atlas slices may delay the atlas-to-MER fitting process and/or increase the number of subsequent electrode tracks required to define the optimal implantation location [18, 19]. Thus, DBS surgical navigation systems that better integrate the various data sets used in electrode implantation are currently under development [6, 7, 14, 19, 20]. Additionally, 3-dimensional atlases have been created by interpolating between 2-dimensional slices [14, 21] or by generating maps that show the functional borders of target nuclei [6, 7, 14, 20, 22]. However, commercial surgical navigation systems do not currently provide an option to refit the brain atlas to the MER after it has been fitted to the preoperative imaging data, or entail a manual refitting, which requires precious time in the operating room and may be inconsistent across users. To address these limitations, we present a method that automatically fits a 3-dimensional brain atlas to patient-specific intraoperative MER using our academic DBS research software system, Cicerone [19].


Subject Population

Ten subthalamic nucleus (STN) DBS patients were retrospectively selected from a database of patients who had undergone surgery at the Cleveland Clinic. Unilateral implantation of a DBS electrode (Model 3387 or 3389, Medtronic Inc., Minneapolis, Minn., USA) was performed on the left side of the brain in 4 patients (patients 1, 4–6; table table1)1) and on the right side of the brain in 6 patients (patients 2, 3, 7–10). Each patient had idiopathic PD that responded to dopamine replacement therapy; however, the patients exhibited a wide spectrum of therapeutic DBS outcomes (see Maks et al. [23] for additional documentation on these 10 patients). This diverse patient population was selected to provide a realistic representation of the variability encountered with STN DBS for PD. This study was approved by the Cleveland Clinic Institutional Review Board.

Table 1
Fit comparison

Microelectrode Recordings

The technical aspects of MER acquisition are presented elsewhere [5]. Briefly, MER were performed with platinum-iridium microelectrodes (FHC Inc., Bowdoinham, Me., USA) that exhibited typical impedances in the range of 0.3–0.6 MΩ. Electrodes were inserted using a microTargeting® microdrive (FHC Inc.) attached to a stereotactic frame (Leksell model G, Elekta Corp., Stockholm, Sweden). An initial MER track was directed towards an MR image-based target. If the neural recordings in this penetration did not suggest an optimal location (e.g. less than 5 mm thickness, no somatosensory driving, low-threshold microstimulation effects suggesting proximity to internal capsule or central track of oculomotor nerve), then additional penetrations were required to refine the target location. This patient population received an average of 4.8 ± 1.3 microelectrode tracks oriented with ring angles of 62.8 ± 6.8° and arc angles of 8.5 ± 2.6 or 15.4 ± 2.8° from the vertical for left and right implants, respectively. Tracks had an average of 22 ± 12 clinically recorded MER sites. Each MER site (fig. (fig.1c,1c, d) was analyzed and classified intraoperatively by one of three experienced neurophysiologists (J.L.V., S.E.C., B.L.W.) using standard criteria [5, 8].

Fig. 1
Graphical user interface. a Stereotactic frame and AC/PC definition based on the patient's preoperative MRI. b–d Manual brain atlas fitting interface as seen by each of the human experts. b Control panel for manipulation of the brain atlas to ...

Brain Atlas

The 3-dimensional brain atlas used in this study was originally developed by Surgical Navigation Technologies (Medtronic Inc.) and Jaimie Henderson (Stanford University, Palo Alto, Calif., USA). Additional details on the origin of the brain atlas can be found in the methods of Butson et al. [24]. Briefly, 3-dimensional surfaces representing visible subcortical nuclei (e.g. thalamus) were segmented from a high-resolution MRI. These surfaces were then aligned with 2-dimensional Schaltenbrand and Wahren slices [10] to define outlines of nonvisible nuclei (e.g. STN) and lofted to create the additional 3-dimensional surfaces. For the purposes of this study, we used atlas representations of the thalamus and STN (fig. (fig.22).

Fig. 2
The brain atlas is a collection of nuclei, where each nucleus is formed by a 3-dimensional polygonal surface (wireframe). Anterior view of the left thalamus (light gray) and STN (dark gray) is shown.

Traditional Brain Atlas Fits

We fit the brain atlas to each patient using anterior commissure-posterior commissure (AC/PC) scaling and human expert-defined fits. Each patient data set (imaging data and MER points) was registered into stereotactic space using fiducial markers [19] to obtain an explicit definition of the coordinates of the AC, PC, and each MER site in a rigid coordinate system (fig. (fig.1).1). For the AC/PC scaling, the brain atlas was seeded into stereotactic space by orienting it to the midline and scaling it along the anteroposterior axis such that the atlas AC/PC line matched that of each patient. Manual fits of the 3-dimensional brain atlas to the MER points were performed by four experienced human experts (J.L.V., S.E.C., B.L.W., C.C.M.). A custom software application (derived from Cicerone [19]) was developed to enable the human users to interactively fit the brain atlas to the MER points. This application presented the expert users with three interactive views of the MER points and brain atlas. The first view was a 3-dimensional rendering of the atlas nuclei and all of the MER points (fig. (fig.1c).1c). The second and third views, respectively, were 2-dimensional 1-mm-thick oblique sagittal and oblique coronal views parallel to the actual microelectrode trajectory (fig. (fig.1d).1d). These views showed only MER points on that oblique plane. The users could manipulate the fit of the brain atlas to the MER points via a control panel (fig. (fig.1b),1b), and could interactively move through different slices in various planes to view the data in a more traditional 2-dimensional format. The viewing windows interactively showed the transformed brain atlas as the user translated, scaled, and rotated the brain atlas (9 degrees of freedom). The human experts spent time familiarizing themselves with the controls of the software using data from a practice patient prior to this study. Once the users were comfortable with the task, they were allowed a maximum of 15 min to perform the fit of each patient using the same transformation ranges available to the optimization algorithm.

Optimized Brain Atlas Fit

The goal of the optimization algorithm was to define a set of linear transformations that maximized the number of neurophysiologically identified MER sites inside their respective atlas-defined nuclei (i.e., thalamus and STN) and minimized inclusion of MER points from other areas of the brain (e.g. substantia nigra, zona incerta). Additionally, the optimization algorithm minimized the overall euclidean distance between the surfaces of the atlas nuclei and their corresponding MER points not contained by the atlas. The original anatomical relationships between atlas nuclei were maintained throughout the fit process (i.e., nuclei were scaled, translated and rotated together, not independently).

The optimal location of the brain atlas with respect to the MER was found by minimizing a cost function (see Appendix) that depended on the current set of bounded linear transformations [25]. The cost function was defined by two terms: (1) the weighted sum of the squared minimum euclidean distances between neurophysiologically identified MER points and the surfaces of their corresponding nuclei (fig. (fig.3),3), and (2) the weighted sum of MER points incorrectly fit by the atlas. The MER-to-atlas euclidean distances were defined as zero when MER points were contained within their corresponding nuclei. The terms in the cost function were weighted according to their specific nucleus. Larger weights for the STN (WSTN = 20) were used to assign a higher priority to fitting the STN over other nuclei (WTHA = 2). The cost function was calculated for different sets of transformations obtained by the optimization algorithm over a transformation space defined by a maximum rotation of ±10°, a maximum translation of ±10 mm, and a maximum scaling of ±20% for each axis from the initial condition. These bounds allow for a large degree of interpatient variability without creating an excessively large search space for the solution.

Fig. 3
Schematic representation of an STN MER site and its closest polygon on the surface of the atlas STN. The plane of the polygon given by the three vertices (V1, V2, and V3) separates the inside and outside of the nucleus with respect to the MER site. In ...

DBS Target Electrode Location

We determined a target location for the active DBS electrode contact with respect to the atlas STN. This target, selected only as an illustrative example, was defined 2 mm dorsal to the geometric centroid of the STN in the original brain atlas geometry (fig. (fig.4).4). This region has been previously identified as a general target location for therapeutic DBS in PD [12, 23,26,27,28], and could be suggested as an ideal location to place contact 2 of the clinical DBS electrode.

Fig. 4
Theoretical DBS electrode target (dark dot) in the dorsal STN. a Coronal view. b Sagittal view. The arrows show the dorsolateral (D-L) and dorsoposterior (D-P) directions.

The stereotactic location of this theoretical target point was transformed for each patient as the brain atlas was fit to their MER data. We then compared the location of the transformed target point to the stereotactic coordinates of the monopolar DBS electrode contact used for therapeutic stimulation in each patient (i.e., active contact). The therapeutic contact was determined by traditional postoperative clinical programming and the actual stereotactic location of the DBS electrode was confirmed by coregistration of the postoperative CT into stereotactic space prior to this study [23].

Fit Evaluation

We evaluated each of the three fitting techniques (AC/PC scaling, human expert, and optimization algorithm) by comparing five metrics: (1) the percentage of MER points correctly contained (i.e., fit) within their respective nuclei, (2) the percentage of MER points incorrectly contained within any nuclei, (3) the summed distance of unfitted MER points to their corresponding nuclei surfaces (fitting error), (4) the fitting time, and (5) euclidean distance from the active DBS electrode contact to the atlas-defined target electrode location. The percentage of MER points correctly and incorrectly contained by the atlas quantified the goodness of fit for each method. The fitting error discriminated between fits for which the atlases contained the same percentage of MER points but for which different transformations were used. We performed one-way ANOVA using Origin 7.5 (OriginLab Corporation, Northampton, Mass., USA) to determine statistical significance.

Sensitivity Analysis

We performed a sensitivity analysis to address the effects of changing the STN weights from 1 to 20 times the weight associated with the thalamus. Additionally, we evaluated the ability of the brain atlas fit to accommodate all of the MER points acquired in a patient, while incrementally adding individual tracks to the optimization algorithm. This evaluation was performed from one up to the maximum number of tracks recorded for each patient (i.e., up to six tracks) in the order in which these tracks were acquired clinically.


The fitting error (i.e., atlas-to-MER summed distance) was significantly smaller for the optimization method (10 ± 10 mm) than for the human expert (35 ± 22 mm, p < 0.005) and AC/PC scaling (183 ± 124 mm, p < 0.001) methods (fig. (fig.5d).5d). The human expert and optimization fits resulted in a brain atlas that correctly fit an average of 80 ± 10 and 81 ± 9% of the MER points, respectively (fig. (fig.5b),5b), while AC/PC scaling only fit 42 ± 22% (table (table1).1). The percentage of MER points correctly fit by AC/PC scaling was significantly smaller (p < 0.001) than the human expert and optimization fits. The correctly fit MER points for the optimized and human expert fits were not statistically different (p = 0.7). The human expert and optimization fits differed only in the percentages of MER points incorrectly fit (fig. (fig.5c).5c). The percentages of MER points incorrectly fit by the human expert (0.5%) fittings were significantly smaller than those of the optimization (2.2%, p < 0.04) and AC/PC fittings (3.5%, p < 0.005). There were no significant differences between the optimized and AC/PC fittings with respect to incorrectly fit MER points (p = 0.3).

Fig. 5
Fit comparison. a Visualization of the metrics used to determine goodness of fit. The ovals show thalamic and STN MER points correctly fit by the atlas. The circle shows an MER point from the substantia nigra that was incorrectly fitted in the atlas STN. ...

The human expert and optimization fits were effectively equivalent from a qualitative perspective (i.e., both fits captured the electrophysiology of the patients in a comparable way). However, the optimization fits were achieved in 0.4 ± 0.4 min on a 1.32-GHz Lenovo laptop computer with 2 GB of RAM (Lenovo, Morrisville, N.C., USA) running Windows XP (Microsoft Co., Redmond, Wash., USA), while the human experts used 8.6 ± 1.8 min to achieve their fits (fig. (fig.5e).5e). The optimization algorithm always generated the same fit for a specific data set (i.e., MER points), indicating a unique solution given the parameters of the algorithm. In contrast, the human expert fits exhibited a noticeable degree of variability in their fits for the same data (fig. (fig.66).

Fig. 6
Fit comparison. Oblique sagittal views of a single patient's left side atlas fittings to the MER points for the AC/PC scaling method (a), optimization-based fitting (b), and expert-defined fittings (c–f). The atlas-defined volumes of the thalamus ...

The average distance from the atlas-based target to the location of the active electrode contact for the human expert, optimization, and AC/PC fitting methods were 1.9 ± 0.8, 1.9 ± 0.7, and 3.8 ± 0.9 mm, respectively (table (table2;2; fig. fig.5f).5f). The distance from the target with the AC/PC fit to the clinically defined therapeutic contact was significantly larger (p < 0.01) than the distance generated by the other two fitting methods.

Table 2
Geometric distance between the therapeutic stimulation contact and the model-predicted location of the active therapeutic contact for the expert-defined, optimized, and conventional AC/PC methods

Increasing the optimization weight associated with fitting STN MER points in the STN increased the percentage of correctly fit STN MER by an average of 8% while decreasing the percentage of correctly fit thalamic MER by 7%. However, STN weights larger than 10 times the thalamus weights did not improve the percentage of correctly fit STN MER any further (i.e., it reached a plateau). The percentages of incorrectly fit MER, and the overall summed distance were not significantly affected by the weights across the ranges evaluated (p > 0.05).

The optimization algorithm required a minimum of two tracks of useful MER information to provide an appropriate fit (e.g. more than 61% of all MER points acquired in the patient were correctly fit with less than 1.8% of MER incorrectly fit). With three tracks, the mean percentage of MER fit correctly increased to over 70% without increasing the percentage of incorrectly fit MER (1.5%). Although the fits obtained with our optimization algorithm depended on the number of microelectrode tracks, incorporating more than three MER tracks did not have a significant effect in the percentages of MER correctly/incorrectly fit (p > 0.1), or the summed distance of MER points outside of their respective nuclei (fig. (fig.77).

Fig. 7
Influence of the number of tracks on the fit. The optimization algorithm was incrementally given MER points from tracks in the order they were collected in the operating room. After the addition of each track, the brain atlas fit to all of the MER points ...


Precise placement of DBS electrodes can facilitate maximal therapeutic outcomes with minimal side effects [13, 29]. As such, DBS surgical targeting continues to evolve and become more precise with new advances in imaging, neurophysiology, and brain atlas technology. This proof of principle study presents a technique to automate the alignment of a generic 3-dimensional brain atlas to intraoperative MER, and thereby assist in the definition of a stereotactic target location for implantation of the DBS electrode.

Recent advances in MRI make it possible to directly define target locations by direct visualization of nuclei such as the STN [30]. However, contrast and resolution limitations in mainstream MR scanners deter many from only using imaging data to make DBS implantation decisions [6, 7, 12, 14]. As such, current techniques for electrode placement typically require indirect probabilistic targeting [1, 14, 22, 31, 32]. Furthermore, the large anatomical variability across patients provides motivation for the use of additional techniques that characterize the topography within the nucleus [5] and refine the implant location for the DBS electrode [3, 15].

One traditional technique for integrating the multiple data sets used in DBS surgery is the manual overlay of 2-dimensional brain atlas slices that approximate specific regions of the brain onto graphs of MER points [5, 31, 33]. However, this process can be taxing given that the patient's MR images, brain atlas, and MER points are typically not coplanar, or are not available in a common visualization platform. Thus, strict adherence to the stereotactic coordinate system is typically lost, thereby limiting accuracy of the data analysis and target predictions. This study provides an example of how multiple data sets can be used together within the same stereotactic coordinate system.

Our results showed significantly larger distances between therapeutic electrode contacts and theoretical targets predicted by the conventional AC/PC method compared to the human expert and optimization fitting methods. Previous studies have proposed that there are no additional benefits from using sophisticated computer systems and high-field MRI for DBS target identification when compared to traditional indirect AC/PC-based methods [34]. In contrast, our results suggest that AC/PC-based target identification does not adequately account for the substantial variability in patient brain geometry [30].

In general, brain atlases are associated with numerous limitations. Commonly used atlases are constructed from a single brain that may not be representative of the broader patient population or disease state. In addition, even after an atlas is fit to a patient's brain the atlas may be misleading to the true anatomy of the patient. We restricted our atlas fits to the use of linear transformations (i.e., atlas is nondeformable) to maintain the original anatomical relationships between brain nuclei. One advantage of this method is that it limits the degrees of freedom and can be used with any 3-dimensional brain atlas. However, advances in nonlinear brain atlas deformation algorithms could increase correctly fitted MER percentages, and provide better adherence to the neuroanatomy visible in the MRI [14, 35]. It might also be useful to include additional constraints from image-based landmarks and/or weighting schemes to account for known locations of side effects identified by macro/ microstimulation to further improve the optimization-based fit [3].

Our optimization algorithm performed as well as experienced human experts, but in less time and without interexpert variability. Although the human expert fits achieved similar percentages of correctly fitted MER, the transformations required to position the brain atlas with respect to each patient's MER were significantly different (p < 0.05), particularly in three degrees of freedom: dorsoventral translation (tz), rotation about the dorsoventral (vertical) axis, and scaling along the medial-lateral direction. Thus, while the strategies followed by individual experts may provide a similar overall outcome, small differences in the fitting process can add variance to the analysis and determination of a target location. Larger fitting error variance in the human expert fit (σ2 = 475 mm2) than in the optimization fit (σ2 = 106 mm2) suggests that the optimization algorithm provides more consistent fits.

Algorithms, similar to that presented in this study, could be developed to suggest stereotactic trajectories for MER that maximize the probability of gathering information to constrain the fit. Such an advance could reduce the number of penetrations required for target identification. For example, after a single MER track the fit between a brain atlas and the MER points is relatively unconstrained (fig. (fig.7);7); however, acquisition of data along specific trajectories can substantially limit the possible permutations of the brain atlas to fit the data. Computational assistance in subsequent track selection could offer a degree of standardization that might benefit less experienced users by improving consistency across procedures and maximizing the amount of information gained by each track.

Human interpretation remains the gold standard for neurophysiological identification of MER points and nuclei borders. However, the fitting performance and speed of the optimization algorithm create a realistic opportunity for its clinical use during DBS surgeries. The basic goal would be to assist human experts in their decision-making process. Although traditional (manual) atlas fitting techniques can be performed while the microelectrode is being retracted and readied for the next track, fast automated atlas fits (which can be updated as each new MER point is acquired) allow the surgical team to dedicate more time to critical decision-making instead of manual atlas fits.

The results of this study support the concept that computational refinement of DBS target locations based on 3-dimensional brain atlases and MER can assist electrode placement. The atlas fitting and targeting method presented here, coupled with advanced DBS surgical navigation software tools [6, 7, 19, 20, 27], should improve the management of data and allow for selection of an optimal DBS electrode location in a reduced amount of time. As DBS applications and target sites continue to expand, 3-dimensional renderings of atlases and trajectories may improve opportunities to optimize the stimulation of targeted brain regions with novel electrode placement strategies.


This work was supported by grants from the National Institutes of Health (R21 NS050449, R01 NS059736) and the W.H. Coulter Foundation. The authors thank Jaimie Henderson for providing the 3-dimensional atlas surfaces used in this study. J.L.L., C.R.B., and C.C.M. authored intellectual property related to this project. C.C.M. and C.R.B. hold company shares in IntElect Medical Inc. C.C.M., C.R.B., J.L.L. and A.M.N. are paid consultants of IntElect Medical Inc.


The 3-dimensional brain atlas (fig. (fig.2)2) was linearly transformed to fit the patient-specific MER (fig. (fig.1)1) using an optimal set of linear transformations. These linear transformations were defined with the set of rotations α, β, and γ (about the x, y, and z axes, respectively), translations (tx,ty and tz), and scaling (sx, sy, and sz) of the three independent axes (fig. (fig.8)8) with respect to the mid-commissural point (MCP in fig. fig.1c).1c). The 3-dimensional transformations were applied to the brain atlas as a series of matrix multiplications of the form A′ = STA, where A and A′ are 4xn matrices (containing the affine coordinates of n vertices forming the atlas surfaces) representing the original and transformed atlases, respectively; T represents the affine transformation matrix that includes rotations (applied sequentially about the y, x, and z axes) and translations, and S represents the scalingmatrix transform.

Fig. 8
x, y, and z axes with the mid-commissural point as the origin. Also shown are the corresponding anterior-posterior (AP), left-right (L-R), and dorso-ventral (D-V) directions. α, β, and γ are the angles of rotation for the x, y ...

The optimal set of linear transformations was obtained by minimizing a cost function (eq. 1). The first term inside the sum calculates the weighted squared sum of the minimum euclidean distances (eq. 2) between the neurophysiologically identified MER points and the surface of their corresponding atlas nuclei. The second term calculates and weights the number of MER incorrectly fit by any nuclei (eq. 3).


where u corresponds to the set of transformations, which allowed a maximum translation and rotation of 10 mm and 10°, respectively, in each direction, and a maximum scaling of ±20% along each axis; i and l are nuclei indices describing the nucleus type (e.g. STN = 1, thalamus = 2), and j is a unique index to each MER point; W and V are weights that allow us to prioritize the fit of different nuclei; Iij and Llj are boolean operators used to penalize the cost function for missed MER points (i.e., MER point outside its corresponding nucleus) and MER fitted within an incorrect nucleus. For this study, the STN weights (W1, V1) were set to 20 and the weights of the thalamus (W2, V2) were set to 2.

To estimate the cost function for each transformation set, we first determined if the MER points were contained within their corresponding atlas nuclei. To do so, we found the polygon on the nucleus surface with the smallest euclidean distance (eq. 4) between the centroid of the polygon and its corresponding (i.e., of the same type) MER points (fig. (fig.8).8). We then calculated, for this polygon, the angle (eq. 5) between the vector formed from the MER point to the centroid of the polygon (eq. 4) and the vector normal to the polygon.


If the angle between these two vectors was smaller than or equal to 90°, the MER was contained within the nucleus and did not contribute to the fit error (i.e., atlas-to-MER summed distance) (eq. 2; by setting Iij = 0). On the other hand, if this angle (eq. 5) was larger than 90°, the MER was outside its nucleus and its distance to the nucleus surface (eq. 4) was added to the cost function (setting Iij = 1).

Alternatively, atlas transformations that resulted in nuclei containing MER points of a type other than their own (i.e., STN MER points contained within the thalamus) resulted in penalties to the cost function. This time, the cost function for this atlas transformation was increased by a factor of Vi (by setting Llj = 1) if the MER was contained within nucleus (i.e., angle ≤90°). The cost function was not penalized (Llj = 0) if the MER was outside the nucleus (i.e., angle >90°).

The optimization algorithm was implemented using the Matlab® Optimization Toolbox's fmincon function (The MathWorks Inc., Natick, Mass., USA), which finds a local minimum of a constrained nonlinear multivariable function using sequential quadratic programming. Details on sequential quadratic programming can be found in the literature [36,37,38,39]. The optimization was initialized by using the conventional AC/PC fit for each patient. Optimization was performed for a maximum of 1,000 iterations and 3,500 function evaluations, with a constraint tolerance of 0.1, an objective function optimality tolerance of 0.1 and a transformation parameter tolerance of 0.01. The parameter search direction (given by the second derivative of the cost function, also known as hessian [40]) was updated according to the steepest descent method [25]. All other optimization parameters were set to their default fmincon values.


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