The role of MRI tractography in stereotactic targeting for surgical treatment of Parkinson’s disease
DOI:
https://doi.org/10.25305/unj.350206Keywords:
Parkinson’s disease, deep brain stimulation, stereotactic radiofrequency lesioning, dentatorubrothalamic tractAbstract
Objective: To evaluate the clinical efficacy of surgical treatment of tremor-dominant Parkinson’s disease (PD) with regard to stereotactic target determination based on MRI tractography data, and to compare the outcomes of stereotactic radiofrequency (RF) thalamotomy of the ventral intermediate nucleus (Vim) with tractography-assisted lesioning of the dentatorubrothalamic tract (DRTT).
Materials and methods: This retrospective study included 25 patients with PD who underwent surgery between 2018 and 2025. Inclusion criteria were tremor-dominant clinical presentation, a progressive disease course, and insufficient response to pharmacological therapy. Patients were divided into two groups: the Vim group (n=19), in which stereotactic RF thalamotomy was performed using indirect target calculation, and the DRTT group (n=6), in which the surgical target was determined using MRI tractography based on diffusion tensor imaging (DTI). Surgical planning was performed using Element software (Brainlab, Germany). Clinical efficacy was assessed preoperatively and 12 months postoperatively using the Unified Parkinson’s Disease Rating Scale (UPDRS, part III), the Clinical Rating Scale for Tremor (CRST, parts A and C).
Results: In all patients, tremor of the contralateral limb was completely abolished immediately after surgery. At 12 months, the mean UPDRS III score decreased by 44%, from 83.2±8.7 to 46.7±4.18 points (p=0.04). A statistically significant improvement in UPDRS III scores was observed in the DRTT group (p=0.032), whereas the difference in the Vim group did not reach statistical significance. Tremor regression assessed by CRST-A and CRST-C was observed in both groups but was more pronounced in patients who underwent tractography-assisted lesioning. Postoperatively, a reduction in daily levodopa dosage was noted: by 23.4% in the Vim group and by 27.7% in the DRTT group. No intraoperative complications were recorded. Transient neurological adverse effects occurred more frequently in the Vim group and resolved completely during the early postoperative period.
Conclusions: The use of MRI tractography for stereotactic target selection in ablative surgery for PD enables individualized surgical planning and provides more precise targeting of pathophysiologically relevant neural pathways. Tractography-assisted lesioning of the DRTT is associated with more stable tremor control, a tendency toward greater improvement of accompanying motor symptoms, and a potentially lower risk of neurological adverse effects.
References
1. Krauss JK, Lipsman N, Aziz T, Boutet A, Brown P, Chang JW, Davidson B, Grill WM, Hariz MI, Horn A, Schulder M, Mammis A, Tass PA, Volkmann J, Lozano AM. Technology of deep brain stimulation: current status and future directions. Nat Rev Neurol. 2021 Feb;17(2):75-87. [CrossRef] [PubMed] [PubMed Central]
2. Hariz M, Blomstedt P. Deep brain stimulation for Parkinson's disease. J Intern Med. 2022 Nov;292(5):764-778. [CrossRef] [PubMed] [PubMed Central]
3. Higuchi Y, Matsuda S, Serizawa T. Gamma knife radiosurgery in movement disorders: Indications and limitations. Mov Disord. 2017 Jan;32(1):28-35. [CrossRef] [PubMed]
4. Taira T, Horisawa S, Takeda N, Ghate P. Stereotactic Radiofrequency Lesioning for Movement Disorders. Prog Neurol Surg. 2018;33:107-119. [CrossRef] [PubMed]
5. Fukutome K, Hirabayashi H, Osakada Y, Kuga Y, Ohnishi H. Bilateral Magnetic Resonance Imaging-Guided Focused Ultrasound Thalamotomy for Essential Tremor. Stereotact Funct Neurosurg. 2022;100(1):44-52. [CrossRef] [PubMed]
6. Giammalva GR, Maugeri R, Umana GE, Paolini F, Bonosi L, Meccio F, Scalia G, Palmisciano P, Gerardi RM, Iacopino DG. DBS, tcMRgFUS, and gamma knife radiosurgery for the treatment of essential tremor: a systematic review on techniques, indications, and current applications. J Neurosurg Sci. 2022 Dec;66(6):476-484. [CrossRef] [PubMed]
7. Kostiuk K. Stereotactic Staged Asymmetric Bilateral Radiofrequency Lesioning for Parkinson's Disease. Stereotact Funct Neurosurg. 2023;101(6):359-368. [CrossRef] [PubMed] [PubMed Central]
8. Haynes WI, Haber SN. The organization of prefrontal-subthalamic inputs in primates provides an anatomical substrate for both functional specificity and integration: implications for Basal Ganglia models and deep brain stimulation. J Neurosci. 2013 Mar 13;33(11):4804-14. [CrossRef] [PubMed] [PubMed Central]
9. Verlaat L, Rijks N, Dilai J, Admiraal M, Beudel M, de Bie RMA, van der Zwaag W, Schuurman R, van den Munckhof P, Bot M. 7-Tesla Magnetic Resonance Imaging Scanning in Deep Brain Stimulation for Parkinson's Disease: Improving Visualization of the Dorsolateral Subthalamic Nucleus. Mov Disord Clin Pract. 2024 Apr;11(4):373-380. [CrossRef] [PubMed] [PubMed Central]
10. Kremer NI, Roberts MJ, Potters WV, Dilai J, Mathiopoulou V, Rijks N, Drost G, van Laar T, van Dijk JMC, Beudel M, de Bie RMA, van den Munckhof P, Janssen MLF, Schuurman PR, Bot M. Dorsal subthalamic nucleus targeting in deep brain stimulation: microelectrode recording versus 7-Tesla connectivity. Brain Commun. 2023 Nov 11;5(6):fcad298. [CrossRef] [PubMed] [PubMed Central]
11. Little S, Brown P. Debugging Adaptive Deep Brain Stimulation for Parkinson's Disease. Mov Disord. 2020 Apr;35(4):555-561. [CrossRef] [PubMed] [PubMed Central]
12. Wang S, Zhu G, Shi L, Zhang C, Wu B, Yang A, Meng F, Jiang Y, Zhang J. Closed-Loop Adaptive Deep Brain Stimulation in Parkinson's Disease: Procedures to Achieve It and Future Perspectives. J Parkinsons Dis. 2023;13(4):453-471. [CrossRef] [PubMed] [PubMed Central]
13. Ramanathan PV, Salas-Vega S, Shenai MB. Directional Deep Brain Stimulation-A Step in the Right Direction? A Systematic Review of the Clinical and Therapeutic Efficacy of Directional Deep Brain Stimulation in Parkinson Disease. World Neurosurg. 2023 Feb;170:54-63.e1. [CrossRef] [PubMed]
14. Rajamani N, Friedrich H, Butenko K, Dembek T, Lange F, Navrátil P, Zvarova P, Hollunder B, de Bie RMA, Odekerken VJJ, Volkmann J, Xu X, Ling Z, Yao C, Ritter P, Neumann WJ, Skandalakis GP, Komaitis S, Kalyvas A, Koutsarnakis C, Stranjalis G, Barbe M, Milanese V, Fox MD, Kühn AA, Middlebrooks E, Li N, Reich M, Neudorfer C, Horn A. Deep brain stimulation of symptom-specific networks in Parkinson's disease. Nat Commun. 2024 May 31;15(1):4662. [CrossRef] [PubMed] [PubMed Central]
15. Coenen VA, Allert N, Paus S, Kronenbürger M, Urbach H, Mädler B. Modulation of the cerebello-thalamo-cortical network in thalamic deep brain stimulation for tremor: a diffusion tensor imaging study. Neurosurgery. 2014 Dec;75(6):657-69; discussion 669-70. [CrossRef] [PubMed]
16. Fahn S, Tolosa E, Marin C. Clinical rating scale for tremor. In: Jankovic J, Tolosa E, editors. Parkinson’s disease and movement disorders. Baltimore–Munich: Urban & Schwarzenberg; 1988. p. 225–234.
17. Goetz CG, Tilley BC, Shaftman SR, Stebbins GT, Fahn S, Martinez-Martin P, Poewe W, Sampaio C, Stern MB, Dodel R, Dubois B, Holloway R, Jankovic J, Kulisevsky J, Lang AE, Lees A, Leurgans S, LeWitt PA, Nyenhuis D, Olanow CW, Rascol O, Schrag A, Teresi JA, van Hilten JJ, LaPelle N; Movement Disorder Society UPDRS Revision Task Force. Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing results. Mov Disord. 2008 Nov 15;23(15):2129-70. [CrossRef] [PubMed]
18. Sammartino F, Krishna V, King NK, Lozano AM, Schwartz ML, Huang Y, Hodaie M. Tractography-Based Ventral Intermediate Nucleus Targeting: Novel Methodology and Intraoperative Validation. Mov Disord. 2016 Aug;31(8):1217-25. [CrossRef] [PubMed] [PubMed Central]
19. Rodriguez-Oroz MC, Martínez-Fernández R, Lipsman N, Horisawa S, Moro E. Bilateral Lesions in Parkinson's Disease: Gaps and Controversies. Mov Disord. 2025 Feb;40(2):231-240. [CrossRef] [PubMed] [PubMed Central]
20. Chintapalli R, Chang S, Kaprealian T, Savjani R, Tenn S, Bari A. Gamma knife versus linear accelerator thalamotomy for essential tremor and Parkinson's disease: A systematic review and meta-analysis. J Clin Neurosci. 2025 Mar;133:111050. [CrossRef] [PubMed]
21. Paschen S, Natera-Villalba E, Pineda-Pardo JA, Del Álamo M, Rodríguez-Rojas R, Hensler J, Deuschl G, Obeso JA, Helmers AK, Martínez-Fernández R. Comparative Study of Focused Ultrasound Unilateral Thalamotomy and Subthalamotomy for Medication-Refractory Parkinson's Disease Tremor. Mov Disord. 2025 May;40(5):823-833. [CrossRef] [PubMed] [PubMed Central]
22. Ranjan M, Elias GJB, Boutet A, Zhong J, Chu P, Germann J, Devenyi GA, Chakravarty MM, Fasano A, Hynynen K, Lipsman N, Hamani C, Kucharczyk W, Schwartz ML, Lozano AM, Hodaie M. Tractography-based targeting of the ventral intermediate nucleus: accuracy and clinical utility in MRgFUS thalamotomy. J Neurosurg. 2019 Sep 27;133(4):1002-1009. [CrossRef] [PubMed]
23. Muller J, Alizadeh M, Matias CM, Thalheimer S, Romo V, Martello J, Liang TW, Mohamed FB, Wu C. Use of probabilistic tractography to provide reliable distinction of the motor and sensory thalamus for prospective targeting during asleep deep brain stimulation. J Neurosurg. 2021 Oct 8;136(5):1371-1380. [CrossRef] [PubMed]
24. Nowacki A, Schlaier J, Debove I, Pollo C. Validation of diffusion tensor imaging tractography to visualize the dentatorubrothalamic tract for surgical planning. J Neurosurg. 2019 Jan 1;130(1):99-108. [CrossRef] [PubMed]
25. Coenen VA, Allert N, Mädler B. A role of diffusion tensor imaging fiber tracking in deep brain stimulation surgery: DBS of the dentato-rubro-thalamic tract (drt) for the treatment of therapy-refractory tremor. Acta Neurochir (Wien). 2011 Aug;153(8):1579-85; discussion 1585. [CrossRef] [PubMed]
26. Tsolaki E, Kashanian A, Chiu K, Bari A, Pouratian N. Connectivity-based segmentation of the thalamic motor region for deep brain stimulation in essential tremor: A comparison of deterministic and probabilistic tractography. Neuroimage Clin. 2024;41:103587. [CrossRef] [PubMed] [PubMed Central]
27. Rodrigues NB, Mithani K, Meng Y, Lipsman N, Hamani C. The Emerging Role of Tractography in Deep Brain Stimulation: Basic Principles and Current Applications. Brain Sci. 2018 Jan 29;8(2):23. [CrossRef] [PubMed] [PubMed Central]
28. Magara A, Bühler R, Moser D, Kowalski M, Pourtehrani P, Jeanmonod D. First experience with MR-guided focused ultrasound in the treatment of Parkinson's disease. J Ther Ultrasound. 2014 May 31;2:11. [CrossRef] [PubMed] [PubMed Central]
29. Hassler R, Riechert T. Indications and localization of stereotactic brain operations. Confin Neurol. 1954;14:1–15.
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