Skip to main content

CASE REPORT article

Front. Neurol., 27 June 2018
Sec. Movement Disorders

Making a Difference—Positive Effect of Unilateral VIM Gamma Knife Thalamotomy in the Therapy of Tremor in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS)

\r\nPiotr Alster*Piotr Alster1*Dariusz M. KoziorowskiDariusz M. Koziorowski1Miros&#x;aw Za&#x;bekMirosław Za̧bek2Sebastian Dzierz&#x;ckiSebastian Dzierzȩcki2Jacek Ma&#x;dryJacek Ma̧dry1Karolina Duszy&#x;ska-Wa&#x;sKarolina Duszyńska-Wa̧s1Hanna GrygarowiczHanna Grygarowicz1Justyna ZielonkoJustyna Zielonko1Leszek KrlickiLeszek Królicki3Andrzej FriedmanAndrzej Friedman1
  • 1Department of Neurology, Medical University of Warsaw, Warsaw, Poland
  • 2Department of Neurosurgery, Medical Centre for Postgraduate Education, Warsaw, Poland
  • 3Nuclear Medicine, Medical University of Warsaw, Warsaw, Poland

Fragile X Tremor Ataxia Syndrome (FXTAS) is a syndrome based on expansion of the repeats of CGG triplets. The symptoms include action tremor and cerebellar gait ataxia. Additionally symptomatology of FXTAS may be associated to parkinsonism, executive function deficits, dementia, neuropathy and dysautonomia. We present a case of a patient who after 20 year history of progressive tremor and ataxia, was diagnosed after genetic examination as mutation of FXTAS. For the treatment of tremor the patient underwent Gamma Knife (GK) thalamotomy. Reduced tremor on the right side and improvement in everyday activities were observed in the outcome of the treatment. GK thalamotomy, in the context of this patient, did not significantly affect the ataxia.

Introduction

Fragile X-Associated Tremor Ataxia Syndrome (FXTAS) is an adult-onset neurodegenerative disorder which is often associated with action tremor and cerebellar gait ataxia (1). Clinical features of FXTAS include parkinsonism, executive function deficits, dementia, neuropathy, and dysautonomia. These symptoms, especially when combined, are completely disabling and can cause severe detriment to the quality of life of patients. A T2-weighted magnetic resonance imaging (MRI) of affected individuals usually reveals the Middle Cerebellar Peduncle (MCP) sign, which is a marked symmetric bilateral hyperintensity within the middle cerebellar peduncle. Other areas observed as hyperintense include the splenium of the corpus callosum, pons, insula, and periventricular white matter. Pharmacotherapies are currently unsuccessful in making a substantial improvement in the quality of lives of those suffering with FXTAS.

Background

Non-pharmacological interventions for the treatment of FXTAS include: Deep Brain Stimulation (DBS), Gamma Knife Radiosurgery (GK), Focal Ultrasound (FUS) and Radiofrequency (213) with DBS and Radiofrequency the most popular amongst current literature (26, 13). With respect to positive outcomes of these treatments, bilateral stimulation with DBS of the ventro-oralis posterior (VOP) thalamic nucleus and zona incerta (ZI) have been documented (14).

Bilateral stimulation of the ventral intermediate thalamus (VIM) has shown to alleviate tremor and ataxia in FXTAS in a long-term analysis (2). Further, although unsustained, similar outcomes were observed intraoperatively with an additional DBS lead into the ventralis oralis anterior (VOA) nucleus and the VOP region (26). Insertion of a second VIM DBS lead has shown to worsen gait (26), whereas stimulating the posterior subthalamic area has shown the contrary (4). A study on a Polish family affected by FXTAS, confirmed by molecular analysis, highlighted the possible outcome of the deterioration of cognitive abilities after DBS surgery (7). Needless to say, the risks of side effects due to DBS for the treatment of FXTAS cannot be eliminated. However, it does seem that DBS presents an optimistic approach in the treatment of FXTAS (26).

GK radiosurgery has a documented efficacy in the treatment of tremor (810), and Higuchi et al. specifically propose disabling tremors as an indication for GK in their recent article (8). Unilateral GK treatment seems to be regarded as most effective in the literature (810), whereas for patients with bilateral tremor GK is regarded as unbeneficial. The efficacy of GK in the treatment of intractable tremor is estimated at 70–90% (8). The maximum dose of radiation in GK is estimated as 120–180 Gy. Bilateral thalamotomy remains insufficiently researched and lacks publication in contemporary literature (8). One publication has focused on GK treatment for a patient with refractory Parkinson's disease (PD) tremor, with tremor assessment measured by the Fahn-Tolosa-Marin Rating Scale (FTRS) (9). Results showed that 70.0% of examined patients experienced full tremor relief, while an optimistic 93.9% had a significant reduction of tremor (9). Although GK has great potential in the treatment of symptoms associated with various syndromes, there remains the standing issue of a 3-6 month delay of tumor suppression.

MRI-guided focused ultrasound ablation (MRI-FUS), although only approved for the treatment of tremors associated with refractory essential tremor (ET), has been analyzed in the context of several other indications such as tremor in PD, dystonia, epilepsy, brain tumor and neuropathic pain (11, 12). The low risk of side effects after repeated treatments using this method, as well as possible reversible effect on neural function, are noted advantages of MRI-FUS (12). As an FDA-approved method for the treatment of ET, this method of lesioning presents a significant angle in the therapy of various diseases including FXTAS cases.

Case Presentation

A 73-year-old male patient was admitted to the Department of Neurology due to tremors of the head, neck, and upper limbs, and moderate tremor of lower limbs. Initial symptoms appeared 20 years prior, primarily as a kinetic tremor of the left upper and lower limbs. During a neurological examination, the patient additionally presented dysarthria, paresis of the right facial nerve, brisk reflexes on the right side, bilateral dysmetria, dysdiadochokinesis, truncal ataxia, ataxia of lower limbs which was more prominent on the left side, and unstable gait. Psychological examination exposed mild cognitive impairment and deficits of executive functions. An MRI in 2016 revealed bilateral hyperintensity in the MCP and white matter of cerebellar hemispheres (Figure 1).

FIGURE 1
www.frontiersin.org

Figure 1. Hyperintensities in the brain and cerebellum (left), postprocedural lesion (right).

The combination of intention tremor, ataxia, the MCP sign, and gait instability of patient's son and daughter instigated diagnosis of FXTAS. Use of the Amplide X FMR1 PCR kit (Asuragen) for extended molecular examination revealed permutations in the FMR1 gene (between 60 and 85 ± 5 repeats of CGG), and confirmed the diagnosis of FXTAS with expansion of CGG repeats in the FMR1 gene.

Due to insufficient effects of pharmacological treatments (primidone and propranolol) to treat the tremors, radiosurgical thalamotomy using GK on the VIM of the left thalamus was performed. The Leksell Model G stereotactic coordinate frame (Elekta AB, Sweden) was attached to the patient's head. High-resolution MRI were acquired using a 1.5T scanner, and contrast-enhanced T1 and T2 images taken at 1 mm. The anterior commissure (AC), the posterior commissure (PC), and the third ventricle were identified (Figure 1).

Stereotactic radiosurgical thalamotomy was performed using the Leksell Gamma Knife Perfexion model (Elekta AB, Sweden). The target was localized to the VIM nucleus of the left thalamus. Final isocenter coordinates were selected by means of GammaPlan Software (Elekta AB, Sweden), and were set in the following manner: (x coordinate) 16 mm lateral to the AC-PC line which constituted 50% of the width of the III ventricle plus 11 mm; (y coordinate) 8 mm anterior to the PC; and (z coordinate) 3 mm superior to the AC-PC line.

Final optimization of the x coordinate was safely adjusted in order not to exceed the 18 Gy dose in the posterior limb of the internal capsule. A maximum dose of 130 Gy was delivered with a single, fully opened 4-mm collimator. Control examination was done 6 months after GK thalamotomy. Improvement was observed 4 months after the procedure.

Comparison of tremor intensity before and after the procedure was done using the FTRS and the Tremor Rating Scale (TRS) (Table 1). The case presented in this study showed improvement in both rating scales (FTRS 54 – before and 44 – after, TRS – 28 – before and 14,5 after). The improvement was observed in the right side corresponding to the lesion (Videos 1, 2). This represents the most significant change in the context of the head tremor, postural tremor of the upper extremity and daily activities. Neurological examination showed that features such as dysarthria, central paresis of right facial nerve, bilateral dysmetria, dysdiadochokinesis, lower limb ataxia remained unchanged or insignificantly changed.

TABLE 1
www.frontiersin.org

Table 1. Fahn-Tolosa-Marin Tremor Rating Scale (FTRS) motor score and Tremor Rating Scale (TRS) changes.

Psychological examination did not present any relevant changes. Physiotherapist's examination revealed certain changes in the period before (2016) and after thalamotomy (2017). In the timed up and go (TUG) test before GK the patient did not present any abnormalities. After GK thalamotomy TUG showed dynamic imbalance. Examination also demonstrated static imbalance after GK thalamotomy, which was not observed before the procedure. Deterioration in certain features of the examination performed by the physiotherapist were associated with the progressive nature of FXTAS. This could also be observed during MRI, in the form of an increased signal in T2-weighted image within both hemispheres of cerebellum and bilaterally within middle cerebellar pedunculi, rather than side effects of GK thalamotomy (13). Approval of the Ethical Committee was not necessary for preparation of this article, as this work is a case study.

Discussion

According to our best knowledge, this is the first case study of a patient with tremor in FXTAS treated with GK thalamotomy. Certainly, this method of therapy shows certain limitations such as retardation of effect and lack of the possibility of bilateral GK thalamotomy. On one hand, it should be stressed that this method does not enable a neurological assessment during the procedure. However, in this study, GK was used to treat FXTAS with tremors in a case where pharmacotherapy effects were insufficient. Extended analysis of a larger group of patients and a longer observation period could highlight late side effects associated with this treatment. Nevertheless, GK in FXTAS seems to be a promising alternative to DBS in the nonpharmacological treatment of tremor.

Concluding Remarks

A decrease in the intensity of the tremor on the contralateral to the lesion side was observed after GK treatment. The examination was done 6 months after the procedure. Assessments using the FTRS motor score and TRS revealed improvements in the context of tremor on the right side and everyday activities such as pouring, drawing, and writing. There was no significant effect on the ipsilateral side. GK may represent another possibility for safe treatment of tremor in FXTAS cases. The use of this method on a larger group of patients may provide valuable information about the safety and efficacy of FXTAS treatment.

Ethics Statement

Ethical approval not required. This work is a case report. The case of the patient was analyzed retrospectively after the procedure.

Ethical Standards

The mentioned patient gave informed consent prior to the procedure. Written informed consent was obtained from the participant for the publication of this case report and the video in a publicly accessible journal.

Author Contributions

The contribution of each author was as following: PA study design, data collection, data interpretation, acceptance of final manuscript version, literature search. DK and AF study design, data collection, data interpretation, acceptance of final manuscript version. MZ, SD, JM, KD-W, HG, JZ, LK data collection, acceptance of final manuscript version.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

Research supported by internal funds.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fneur.2018.00512/full#supplementary-material

References

1. Kong HE, Zhao J, Xu S, Jin P, Jin Y. Fragile X-associated tremor/ataxia syndrome: from molecular pathogenesis to development of therapeutics. Front Cell Neurosci. (2017) 11:128. doi: 10.3389/fncel.2017.00128

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Weiss D, Mielke C, Wächter T, Bender B, Liscic RM, Scholten M, et al. Long-term outcome of deep brain stimulation in fragile X-associated tremor/ataxia syndrome. Parkinsonism Relat Disord. (2015) 21:310–3. doi: 10.1016/j.parkreldis.2014.12.015

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Hoshlag JAH, Neef N, Beudel M, Drost G, Oterdoom DLM, Kremer NI, et al. Deep brain stimulation for essential tremor: a comparison of targets. World Neurosurg. (2017) 110:e580–4. doi: 10.1016/j.wneu.2017.11.064

CrossRef Full Text | Google Scholar

4. Oyama G, Umemura A, Shimo Y, Nishikawa N, Nakajima A, Jo T, et al. Posterior subthalamic area deep brain stimulation for fragile X–associated tremor/ataxia syndrome. Neuromodulation (2014) 17:721–3. doi: 10.1111/ner.12150

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Senova S, Jarraya B, Iwamuro H, Tani N, Ouerchefani N, Lepetit H, et al. Uni- lateral thalamic stimulation safely improved fragile X-associated tremor ataxia: a case report. Mov Disord. (2012) 27:797–9. doi: 10.1002/mds.24923

CrossRef Full Text | Google Scholar

6. Xie T, Goodman R, Browner N, Haberfeld E, Winfield L, Goldman J, et al. Treatment of fragile X-associated tremor/ataxia syndrome with unilateral deep brain stimulation. Mov Disord. (2012) 27:799–800. doi: 10.1002/mds.24958

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Koziorowski D, Rajkiewicz M, Sułek-Piatkowska A, Zaremba J, Kaca-Orynska M, Mandat T, et al. Familial occurrence of FXTAS caused by premutation in the FMR1 gene. Neurol Neurochir Pol. (2011) 45:391–8.

PubMed Abstract | Google Scholar

8. Higuchi Y, Matsuda S, Serizawa T. Gamma knife radiosurgery in movement diorders: indications and limitations. Mov Disord. (2017) 32:28–35. doi: 10.1002/mds.26625

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Raju S, Niranjan A, Monaco EA III, Flickinger JC, Lunsford LD. Stereotactic radiosurgery for intractable tremor-dominant parkinson disease a retrospective analysis. Stereotact Funct Neurosurg. (2017) 95:291–7. doi: 10.1159/000479236

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Zesiewicz TA. Evidence-based guideline update: treatment of essential tremor: report of the quality standards subcommittee of the american academy of neurology. Neurology (2011) 77:1752–5. doi: 10.1212/WNL.0b013e318236f0fd

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Krishna V, Sammartino F, Rezai A. A review of the current therapies, challenges, and future directions of transcranial focused ultrasound technology advances in diagnosis and treatment. JAMA Neurol. (2018) 75:246–54. doi: 10.1001/jamaneurol.2017.3129

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Fasano A, Lozano AM, Cubo E. New neurosurgical approaches for tremor and Parkinson's disease. Curr Opin Neurol. (2017) 30:435–46. doi: 10.1097/WCO.0000000000000465

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Tamás G, Kovács N, Varga NÁ, Barsi P, Eross L, Molnár MJ, et al. Deep brain stimulation or thalamotomy in fragile X-associated tremor/ataxia syndrome? Case report. Neurol Neurochir Pol. (2016) 50:303–8. doi: 10.1016/j.pjnns.2016.04.004

PubMed Abstract | CrossRef Full Text | Google Scholar

14. dos Santos Ghilardi MG, Cury RG, dos Ângelos JS, Barbosa DC, Barbosa ER, Teixeira MJ, et al. Long-term improvement of tremor and ataxia after bilateral DBS of VoP/zona incerta in FXTAS. Neurology (2015) 84:1904–6. doi: 10.1212/WNL.0000000000001553

CrossRef Full Text | Google Scholar

Keywords: FXTAS, tremor, gamma knife (GK), radiosurgery, thalamotomy

Citation: Alster P, Koziorowski DM, Za̧bek M, Dzierzȩcki S, Ma̧dry J, Duszyńska-Wa̧s K, Grygarowicz H, Zielonko J, Królicki L and Friedman A (2018) Making a Difference—Positive Effect of Unilateral VIM Gamma Knife Thalamotomy in the Therapy of Tremor in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS). Front. Neurol. 9:512. doi: 10.3389/fneur.2018.00512

Received: 10 March 2018; Accepted: 11 June 2018;
Published: 27 June 2018.

Edited by:

Maria Fiorella Contarino, Leiden University Medical Center, Netherlands

Reviewed by:

Gertrud Tamas, Semmelweis University, Hungary
Matteo Bologna, Sapienza Università di Roma, Italy
Erich Talamoni Fonoff, Universidade de São Paulo, Brazil

Copyright © 2018 Alster, Koziorowski, Za̧bek, Dzierzȩcki, Ma̧dry, Duszyńska-Wa̧s, Grygarowicz, Zielonko, Królicki and Friedman. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Piotr Alster, piotr.alster@gmail.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.