126 results on '"Cheeran, B"'
Search Results
2. Stimulation genomics : probing the effects of genetic variation on human cortical plasticity and its clinical implications
- Author
-
Cheeran, B. J.
- Subjects
612.8 - Abstract
The studies presented in this thesis employ neurophysiological outcome measures and the application of artificially induced cortical stimulation plasticity paradigms to study the effects of human genetic variation on human cortical neuroplasticity. The introductory chapter includes a review of illustrative models of neuroplasticity. I also cover the principles, physiology and pharmacology of TMS and rTMS. With this background, I set out the scope and principles of such an approach applied to the study of human genetic variation, and define the field of Stimulation Genomics. I set out the case for such an approach, highlighting previous studies that have employed neurophysiological outcome measures and the application of artificially induced cortical stimulation plasticity paradigms to study the effects of disease-causing human genetic mutations. In the subsequent introductory chapters I have focused on the rationale of selecting the Brain Derived Neurotrophic Factor polymorphism Rs6265 (BDNF Val66 Met) as the candidate polymorphism for our studies, covering the molecular biology and physiological roles of this highly conserved protein, and with a particular focus on its diverse roles in neuroplasticity. The 1st experiment presented here used established rTMS and TDCS paradigms to probe the effects of the BDNF Val66Met SNP on cortical plasticity and metaplasticity. The results generated from this study, and particularly the results suggesting an effect on metaplasticity, formed the basis for the studies in patients. We investigated the influence of this SNP on the rate of onset of Levodopa-Induced Dyskinesia (LID) in patients with Parkinson's disease and on the penetrance of DYT1 Dystonia. The final experiment presented here was designed to confirm the effects of the BDNF Val66Met polymorphism on the iTBS paradigm, and quantify its effects alongside other variables thought to influence the response to rTMS paradigms. This study also provides some crucial insights into the iTBS paradigm itself.
- Published
- 2011
3. Design of the Remote Optimization Adjustment and Measurement for Deep Brain Stimulation (ROAM-DBS) randomized prospective outcomes study of remote programming
- Author
-
Tomlinson, T., primary, Feldman, M., additional, Gharabaghi, A., additional, Groppa, S., additional, Luo, L., additional, Lu, H., additional, Luca, C., additional, Marshall, V., additional, Merola, A., additional, Schnitzler, A., additional, Verhagen, L., additional, Walter, B., additional, Wu, C., additional, Zauber, S.E., additional, and Cheeran, B., additional
- Published
- 2023
- Full Text
- View/download PDF
4. Necessity and feasibility of remote tele-programming of deep brain stimulation systems in Parkinson’s disease
- Author
-
Esper, C., primary, Merola, A., additional, Himes, L., additional, Patel, N., additional, Bezchlibnyk, Y., additional, Falconer, D., additional, Weiss, D., additional, Luca, C., additional, Cheeran, B., additional, and Mari, Z., additional
- Published
- 2023
- Full Text
- View/download PDF
5. Reprogramming frequency in clinical practice: 6-months post-implantation of DBS for Parkinson’s disease subjects in ADROIT
- Author
-
Groppa, S., primary, Schnitzler, A., additional, Bezchlibnyk, Y., additional, Pilitsis, J., additional, Giordana, C., additional, Verhagen, L., additional, Frassica, M., additional, Cheeran, B., additional, and Chen, S.-Y., additional
- Published
- 2023
- Full Text
- View/download PDF
6. Ten Years of Theta Burst Stimulation in Humans: Established Knowledge, Unknowns and Prospects
- Author
-
Suppa, A., Huang, Y.-Z., Funke, K., Ridding, M.C., Cheeran, B., Di Lazzaro, V., Ziemann, U., and Rothwell, J.C.
- Published
- 2016
- Full Text
- View/download PDF
7. Directional Deep Brain Stimulation for Parkinson's Disease: Results of an International Crossover Study With Randomized, Double-Blind Primary Endpoint
- Author
-
Schnitzler, A, Mir, P, Brodsky, MA, Verhagen, L, Groppa, S, Alvarez, R, Evans, A, Blazquez, M, Nagel, S, Pilitsis, JG, Poetter-Nerger, M, Tse, W, Almeida, L, Tomycz, N, Jimenez-Shahed, J, Libionka, W, Carrillo, F, Hartmann, CJ, Groiss, SJ, Glaser, M, Defresne, F, Karst, E, Cheeran, B, Vesper, J, Schnitzler, A, Mir, P, Brodsky, MA, Verhagen, L, Groppa, S, Alvarez, R, Evans, A, Blazquez, M, Nagel, S, Pilitsis, JG, Poetter-Nerger, M, Tse, W, Almeida, L, Tomycz, N, Jimenez-Shahed, J, Libionka, W, Carrillo, F, Hartmann, CJ, Groiss, SJ, Glaser, M, Defresne, F, Karst, E, Cheeran, B, and Vesper, J
- Abstract
OBJECTIVE: Published reports on directional deep brain stimulation (DBS) have been limited to small, single-center investigations. Therapeutic window (TW) is used to describe the range of stimulation amplitudes achieving symptom relief without side effects. This crossover study performed a randomized double-blind assessment of TW for directional and omnidirectional DBS in a large cohort of patients implanted with a DBS system in the subthalamic nucleus for Parkinson's disease. MATERIALS AND METHODS: Participants received omnidirectional stimulation for the first three months after initial study programming, followed by directional DBS for the following three months. The primary endpoint was a double-blind, randomized evaluation of TW for directional vs omnidirectional stimulation at three months after initial study programming. Additional data recorded at three- and six-month follow-ups included stimulation preference, therapeutic current strength, Unified Parkinson's Disease Rating Scale (UPDRS) part III motor score, and quality of life. RESULTS: The study enrolled 234 subjects (62 ± 8 years, 33% female). TW was wider using directional stimulation in 183 of 202 subjects (90.6%). The mean increase in TW with directional stimulation was 41% (2.98 ± 1.38 mA, compared to 2.11 ± 1.33 mA for omnidirectional). UPDRS part III motor score on medication improved 42.4% at three months (after three months of omnidirectional stimulation) and 43.3% at six months (after three months of directional stimulation) with stimulation on, compared to stimulation off. After six months, 52.8% of subjects blinded to stimulation type (102/193) preferred the period with directional stimulation, and 25.9% (50/193) preferred the omnidirectional period. The directional period was preferred by 58.5% of clinicians (113/193) vs 21.2% (41/193) who preferred the omnidirectional period. CONCLUSION: Directional stimulation yielded a wider TW compared to omnidirectional stimulation and was preferred by
- Published
- 2022
8. Evaluation of outcome following revision of STN deep brain stimulation to GPi for an individual with Parkinsonʼs disease: 1192
- Author
-
Forrow, B., Joint, C., Bogdanovic, M., Cheeran, B., Fitzgerald, J., Green, A. L., and Aziz, T. Z.
- Published
- 2014
9. Abnormal synaptic depotentiation in treated PD precedes the onset of levodopa induced dyskinesia: 746
- Author
-
Cheeran, B., Lago-Rodriguez, A., Koch, G., Jenkinson, N., and Hu, M.
- Published
- 2014
10. BDNF val66met influences time to onset of levodopa induced dyskinesia in Parkinson's disease
- Author
-
Foltynie, T., Cheeran, B., Williams-Gray, C.H., Edwards, M.J., Schneider, S.A., Weinberger, D., Rothwell, J.C., Barker, R.A., and Bhatia, K.P.
- Subjects
Parkinson's disease -- Research ,Parkinson's disease -- Physiological aspects ,Dopa -- Usage ,Dopa -- Complications and side effects ,Brain-derived neurotrophic factor -- Research ,Brain-derived neurotrophic factor -- Physiological aspects ,Movement disorders -- Risk factors ,Health ,Psychology and mental health - Published
- 2009
11. Proceedings of the Seventh Annual Deep Brain Stimulation Think Tank: Advances in Neurophysiology, Adaptive DBS, Virtual Reality, Neuroethics and Technology
- Author
-
Ramirez-Zamora, A, Giordano, J, Gunduz, A, Alcantara, J, Cagle, JN, Cernera, S, Difuntorum, P, Eisinger, RS, Gomez, J, Long, S, Parks, B, Wong, JK, Chiu, S, Patel, B, Grill, WM, Walker, HC, Little, SJ, Gilron, R, Tinkhauser, G, Thevathasan, W, Sinclair, NC, Lozano, AM, Foltynie, T, Fasano, A, Sheth, SA, Scangos, K, Sanger, TD, Miller, J, Brumback, AC, Rajasethupathy, P, McIntyre, C, Schlachter, L, Suthana, N, Kubu, C, Sankary, LR, Herrera-Ferra, K, Goetz, S, Cheeran, B, Steinke, GK, Hess, C, Almeida, L, Deeb, W, Foote, KD, Okun, MS, Ramirez-Zamora, A, Giordano, J, Gunduz, A, Alcantara, J, Cagle, JN, Cernera, S, Difuntorum, P, Eisinger, RS, Gomez, J, Long, S, Parks, B, Wong, JK, Chiu, S, Patel, B, Grill, WM, Walker, HC, Little, SJ, Gilron, R, Tinkhauser, G, Thevathasan, W, Sinclair, NC, Lozano, AM, Foltynie, T, Fasano, A, Sheth, SA, Scangos, K, Sanger, TD, Miller, J, Brumback, AC, Rajasethupathy, P, McIntyre, C, Schlachter, L, Suthana, N, Kubu, C, Sankary, LR, Herrera-Ferra, K, Goetz, S, Cheeran, B, Steinke, GK, Hess, C, Almeida, L, Deeb, W, Foote, KD, and Okun, MS
- Abstract
The Seventh Annual Deep Brain Stimulation (DBS) Think Tank held on September 8th of 2019 addressed the most current: (1) use and utility of complex neurophysiological signals for development of adaptive neurostimulation to improve clinical outcomes; (2) Advancements in recent neuromodulation techniques to treat neuropsychiatric disorders; (3) New developments in optogenetics and DBS; (4) The use of augmented Virtual reality (VR) and neuromodulation; (5) commercially available technologies; and (6) ethical issues arising in and from research and use of DBS. These advances serve as both "markers of progress" and challenges and opportunities for ongoing address, engagement, and deliberation as we move to improve the functional capabilities and translational value of DBS. It is in this light that these proceedings are presented to inform the field and initiate ongoing discourse. As consistent with the intent, and spirit of this, and prior DBS Think Tanks, the overarching goal is to continue to develop multidisciplinary collaborations to rapidly advance the field and ultimately improve patient outcomes.
- Published
- 2020
12. Directional versus omnidirectional Deep Brain Stimulation: Results of a multi-cente prospective blinded crossover study
- Author
-
Schnitzler, A., primary, Mir, P., additional, Brodsky, M., additional, Verhagen, L., additional, Groppa, S., additional, Alvarez, R., additional, Evans, A., additional, Blazquez, M., additional, Nagel, S., additional, Pilitsis, J., additional, Pötter-Nerger, M., additional, Tse, W., additional, Almeida, L., additional, Tomycz, N., additional, Jimenez-Shahed, J., additional, Carrillo, F., additional, Hartmann, C., additional, Groiss, S., additional, Defresne, F., additional, Karst, E., additional, Cheeran, B., additional, and Vesper, J., additional
- Published
- 2020
- Full Text
- View/download PDF
13. Study design and rationale for an international study of DBS for movement disorders
- Author
-
Pahwa, R., primary, Pilitsis, J., additional, Groppa, S., additional, Fasano, A., additional, Ostrem, J., additional, Phibbs, F., additional, Lyons, K., additional, Jimenez-Shahed, J., additional, Pouratian, N., additional, Neimat, J., additional, Defresne, F., additional, Karst, E., additional, Cheeran, B., additional, and Schnitzler, A., additional
- Published
- 2020
- Full Text
- View/download PDF
14. Unexpected Complications of Novel Deep Brain Stimulation Treatments: Ethical Issues and Clinical Recommendations
- Author
-
Maslen, H, Cheeran, B, Pugh, J, Pycroft, L, Boccard, S, Prangnell, S, Green, AL, FitzGerald, J, Savulescu, J, and Aziz, T
- Abstract
BACKGROUND: Innovative neurosurgical treatments present a number of known risks, the natures and probabilities of which can be adequately communicated to patients via the standard procedures governing obtaining informed consent. However, due to their novelty, these treatments also come with unknown risks, which require an augmented approach to obtaining informed consent. OBJECTIVE: This paper aims to discuss and provide concrete procedural guidance on the ethical issues raised by serious unexpected complications of novel deep brain stimulation treatments. APPROACH: We illustrate our analysis using a case study of the unexpected development of recurrent stereotyped events in patients following the use of deep brain stimulation (DBS) to treat severe chronic pain. Examining these unexpected complications in light of medical ethical principles, we argue that serious complications of novel DBS treatments do not necessarily make it unethical to offer the intervention to eligible patients. However, the difficulty the clinician faces in determining whether the intervention is in the patient's best interests generates reasons to take extra steps to promote the autonomous decision making of these patients. CONCLUSION AND RECOMMENDATIONS: We conclude with clinical recommendations, including details of an augmented consent process for novel DBS treatment.
- Published
- 2018
15. Variability in response to non-invasive brain stimulation: basic physiology
- Author
-
Cheeran, B., Lopez-Alonso, V., and Del-Olmo, M.F.
- Published
- 2017
- Full Text
- View/download PDF
16. Sensorimotor adaptation as a behavioural biomarker of early spinocerebellar ataxia type 6
- Author
-
Panouillères, MTN, Joundi, RA, Benitez-Riveiro, S, Cheeran, B, Butler, CR, Németh, AH, Miall, RC, and Jenkinson, N
- Abstract
Early detection of the behavioural deficits of neurodegenerative diseases may help to describe the pathogenesis of such diseases and establish important biomarkers of disease progression. The aim of this study was to identify how sensorimotor adaptation of the upper limb, a cerebellar-dependent process restoring movement accuracy after introduction of a perturbation, is affected at the pre-clinical and clinical stages of spinocerebellar ataxia type 6 (SCA6), an inherited neurodegenerative disease. We demonstrate that initial adaptation to the perturbation was significantly impaired in the eighteen individuals with clinical motor symptoms but mostly preserved in the five pre-clinical individuals. Moreover, the amount of error reduction correlated with the clinical symptoms, with the most symptomatic patients adapting the least. Finally both pre-clinical and clinical individuals showed significantly reduced de-adaptation performance after the perturbation was removed in comparison to the control participants. Thus, in this large study of motor features in SCA6, we provide novel evidence for the existence of subclinical motor dysfunction at a pre-clinical stage of SCA6. Our findings show that testing sensorimotor de-adaptation could provide a potential predictor of future motor deficits in SCA6.
- Published
- 2017
17. Unexpected complications of novel deep brain stimulation treatments: ethical issues and clinical recommendations
- Author
-
Savulescu, J, Maslen, H, Cheeran, B, Pugh, J, Boccard, S, Green, A, FitzGerald, J, and Aziz, T
- Abstract
BACKGROUND: Innovative neurosurgical treatments present a number of known risks, the natures and probabilities of which can be adequately communicated to patients via the standard procedures governing obtaining informed consent. However, due to their novelty, these treatments also come with unknown risks, which require an augmented approach to obtaining informed consent. OBJECTIVE: This paper aims to discuss and provide concrete procedural guidance on the ethical issues raised by serious unexpected complications of novel deep brain stimulation treatments. APPROACH: We illustrate our analysis using a case study of the unexpected development of recurrent stereotyped events in patients following the use of DBS to treat severe chronic pain. Examining these unexpected complications in light of medical ethical principles, we argue that serious complications of novel DBS treatments do not necessarily make it unethical to offer the intervention to eligible patients. However, the difficulty the clinician faces in determining whether the intervention is in the patient’s best interests generates reasons to take extra steps to promote the autonomous decisionmaking of these patients. CONCLUSION AND RECOMMENDATIONS: We conclude with clinical recommendations, including details of an augmented consent process for novel DBS treatment.
- Published
- 2017
18. Transcranial magnetic stimulation: from neurophysiology to pharmacology, molecular biology and genomics
- Author
-
Cheeran, B., Koch, G., Stagg, C.J., Baig, F., and Teo, J.
- Subjects
Genetics -- Research ,Genetics -- Physiological aspects ,Neurophysiology -- Research ,Pharmacology -- Research ,Molecular biology -- Research ,Genomics -- Research ,Brain research -- Genetic aspects ,Adaptation (Physiology) -- Research ,Brain stimulation -- Usage ,Psychology and mental health - Published
- 2010
19. Bilateral adaptive deep brain stimulation is effective in Parkinson's disease
- Author
-
Little S, Beudel M, Zrinzo L, Foltynie T, Limousin P, Hariz M, Neal S, Cheeran B, Cagnan H, Gratwicke J, Tz, Aziz, Pogosyan A, and Peter Brown
- Subjects
Adult ,Male ,RETURN ,Aging ,Cerebral ,Deep Brain Stimulation ,Clinical Trials and Supportive Activities ,Bioengineering ,Neurodegenerative ,Medical and Health Sciences ,Double-Blind Method ,BRADYKINESIA ,Subthalamic Nucleus ,Clinical Research ,Humans ,OSCILLATORY ACTIVITY ,Dominance ,Aged ,Neurologic Examination ,Assistive Technology ,Parkinson's Disease ,Neurology & Neurosurgery ,Rehabilitation ,Psychology and Cognitive Sciences ,Neurosciences ,Videotape Recording ,Parkinson Disease ,Middle Aged ,SUBTHALAMIC NUCLEUS STIMULATION ,LOCAL-FIELD POTENTIALS ,Combined Modality Therapy ,TIME ,Brain Disorders ,BETA-ACTIVITY ,Treatment Outcome ,Neurological - Abstract
Introduction and objectives: Adaptive deep brain stimulation (aDBS) uses feedback from brain signals to guide stimulation. A recent acute trial of unilateral aDBS showed that aDBS can lead to substantial improvements in contralateral hemibody Unified Parkinson’s Disease Rating Scale (UPDRS) motor scores and may be superior to conventional continuous DBS in Parkinson’s disease (PD). We test whether potential benefits are retained with bilateral aDBS and in the face of concurrent medication. Methods: We applied bilateral aDBS in 4 patients with PD undergoing DBS of the subthalamic nucleus. aDBS was delivered bilaterally with independent triggering of stimulation according to the amplitude of β activity at the corresponding electrode. Mean stimulation voltage was 3.0±0.1 volts. Motor assessments consisted of double-blinded video-taped motor UPDRS scores that included both limb and axial features. Results: UPDRS scores were 43% (p=0.04; Cohen’s d=1.62) better with aDBS than without stimulation. Motor improvement with aDBS occurred despite an average time on stimulation (ToS) of only 45%. Levodopa was well tolerated during aDBS and led to further reductions in ToS. Conclusion: Bilateral aDBS can improve both axial and limb symptoms and can track the need for stimulation across drug states.
- Published
- 2016
- Full Text
- View/download PDF
20. TMS activation of interhemispheric pathways between the posterior parietal cortex and the contralateral motor cortex
- Author
-
Koch, G, Ruge, D, Cheeran, B, Fernandez Del Olmo, M, Pecchioli, C, Marconi, B, Versace, V, Lo Gerfo, E, Torriero, S, Oliveri, M, Caltagirone, C, Rothwell, JC, Koch, G, Ruge, D, Cheeran, B, Fernandez Del Olmo, M, Pecchioli, C, Marconi, B, Versace, V, LO GERFO, E, Torriero, S, Oliveri, M, Caltagirone, C, Rothwell, J, Lo Gerfo, E, and Rothwell, JC
- Subjects
Adult ,Male ,Physiology ,Long-Term Potentiation ,rhesus monkey ,human corpus-callosum ,NO ,Neural Pathway ,anterior intraparietal area ,Parietal Lobe ,Neural Pathways ,Humans ,world monkeys ,Neuronal Plasticity ,Motor Cortex ,dorsal premotor ,connections ,Transcranial Magnetic Stimulation ,inhibition ,Transcranial magnetic stimulation ,online adjustments ,humans ,TMS ,parietal cortex ,interhemispheric ,Female ,Settore MED/26 - Neurologia ,Nerve Net ,Neuroscience ,Human - Abstract
Using a twin coil transcranial magnetic stimulation (tc-TMS) approach we have previously demonstrated that facilitation may be detected in the primary motor cortex (M1) following stimulation over the ipsilateral caudal intraparietal sulcus (cIPS). Here we tested the interhemispheric interactions between the IPS and the contralateral motor cortex (M1). We found that conditioning the right cIPS facilitated contralateral M1 when the conditioning stimulus had an intensity of 90% resting motor threshold (RMT) but not at 70% or 110% RMT. Facilitation was maximal when the interstimulus interval (ISI) between cIPS and M1 was 6 or 12 ms. These facilitatory effects were mediated by interactions with specific groups of interneurons in the contralateral M1. In fact, short intracortical inhibition (SICI) was reduced following cIPS stimulation. Moreover, additional comparison of facilitation of responses evoked by anterior-posterior versus posterior-anterior stimulation of M1 suggested that facilitation was more effective on early I1/I2 circuits than on I3 circuits. In contrast to these effects, stimulation of anterior IPS (aIPS) at 90% RMT induced inhibition, instead of facilitation, of contralateral M1 at ISIs of 10-12 ms. Finally, we found similar facilitation between left cIPS and right M1 although the conditioning stimuli had to have a higher intensity compared with stimulation of right cIPS (110% instead of 90% RMT). These findings demonstrate that different subregions of the posterior parietal cortex (PPC) in humans exert both facilitatory and inhibitory effects towards the contralateral primary motor cortex. These corticocortical projections could contribute to a variety of motor tasks such as bilateral manual coordination, movement planning in space and grasping. © 2009 The Authors. Journal compilation © 2009 The Physiological Society.
- Published
- 2009
21. Tremor Reduction by Deep Brain Stimulation Is Associated With Gamma Power Suppression in Parkinson's Disease
- Author
-
Beudel, M, Little, S, Pogosyan, A, Ashkan, K, Foltynie, T, Limousin, P, Zrinzo, L, Hariz, M, Bogdanovic, M, Cheeran, B, Green, AL, Aziz, T, Thevathasan, W, Brown, P, Beudel, M, Little, S, Pogosyan, A, Ashkan, K, Foltynie, T, Limousin, P, Zrinzo, L, Hariz, M, Bogdanovic, M, Cheeran, B, Green, AL, Aziz, T, Thevathasan, W, and Brown, P
- Abstract
OBJECTIVES: Rest tremor is a cardinal symptom of Parkinson's disease (PD), and is readily suppressed by deep brain stimulation (DBS) of the subthalamic nucleus (STN). The therapeutic effect of the latter on bradykinesia and rigidity has been associated with the suppression of exaggerated beta (13-30 Hz) band synchronization in the vicinity of the stimulating electrode, but there is no correlation between beta suppression and tremor amplitude. In the present study, we investigate whether tremor suppression is related to suppression of activities at other frequencies. MATERIALS AND METHODS: We recorded hand tremor and contralateral local field potential (LFP) activity from DBS electrodes during stimulation of the STN in 15 hemispheres in 11 patients with PD. DBS was applied with increasing voltages starting at 0.5 V until tremor suppression was achieved or until 4.5 V was reached. RESULTS: Tremor was reduced to 48.9% ± 10.9% of that without DBS once stimulation reached 2.5-3 V (t14 = -4.667, p < 0.001). There was a parallel suppression of low gamma (31-45 Hz) power to 92.5% ± 3% (t14 = -2.348, p = 0.034). This was not seen over a band containing tremor frequencies and their harmonic (4-12 Hz), or over the beta band. Moreover, low gamma power correlated with tremor severity (mean r = 0.43 ± 0.14, p = 0.008) within subjects. This was not the case for LFP power in the other two bands. CONCLUSIONS: Our findings support a relationship between low gamma oscillations and PD tremor, and reinforce the principle that the subthalamic LFP is a rich signal that may contain information about the severity of multiple different Parkinsonian features.
- Published
- 2015
22. Further insights into the effect of BDNF genotype on non-invasive brain stimulation
- Author
-
Suppa, A., primary and Cheeran, B., additional
- Published
- 2015
- Full Text
- View/download PDF
23. A common polymorphism in the brain-derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS
- Author
-
Cheeran, B, Talelli, P, Mori, F, Koch, G, Suppa, A, Edwards, M, Houlden, H, Bhatia, K, Greenwood, R, and Rothwell, J
- Subjects
NO - Abstract
The brain-derived neurotrophic factor gene (BDNF) is one of many genes thought to influence synaptic plasticity in the adult brain and shows a common single nucleotide polymorphism (BDNF Val66Met) in the normal population that is associated with differences in hippocampal volume and episodic memory. It is also thought to influence possible synaptic changes in motor cortex following a simple motor learning task. Here we extend these studies by using new non-invasive transcranial magnetic stimulation (TMS) and transcranial direct current stimulation (TDCS) techniques that directly test the excitability and plasticity of neuronal circuits in human motor cortex in subjects at rest. We investigated whether the susceptibility to TMS probes of plasticity is significantly influenced by the BDNF polymorphism. Val66Met carriers were matched with Val66Val individuals and tested on the following protocols: continuous and intermittent theta burst TMS; median nerve paired associative stimulation; and homeostatic plasticity in the TDCS/1 Hz rTMS model. The response of Met allele carriers differed significantly in all protocols compared with the response of Val66Val individuals. We suggest that this is due to the effect of BNDF on the susceptibility of synapses to undergo LTP/LTD. The circuits tested here are implicated in the pathophysiology of movement disorders such as dystonia and are being assessed as potential new targets in the treatment of stroke. Thus the polymorphism may be one factor that influences the natural response of the brain to injury and disease. © 2008 The Author. Journal compilation © 2008 The Physiological Society.
- Published
- 2008
24. Mapping genetic influences on the corticospinal motor system in humans
- Author
-
Cheeran, B J, Ritter, C, Rothwell, J C, Siebner, H R, Cheeran, B J, Ritter, C, Rothwell, J C, and Siebner, H R
- Abstract
Udgivelsesdato: 2009-Nov, It is becoming increasingly clear that genetic variations account for a certain amount of variance in the acquisition and maintenance of different skills. Until now, several levels of genetic influences were examined, ranging from global heritability estimates down to the analysis of the contribution of single nucleotide polymorphisms (SNP) and variable number tandem repeats. In humans, the corticospinal motor system is essential to the acquisition of fine manual motor skills which require a finely tuned coordination of activity in distal forelimb muscles. Here we review recent brain mapping studies that have begun to explore the influence of functional genetic variation as well as mutations on function and structure of the human corticospinal motor system, and also the clinical implications of these studies. Transcranial magnetic stimulation of the primary motor hand area revealed a modulatory role of the common val66met polymorphism in the BDNF gene on corticospinal plasticity. Diffusion-sensitive magnetic resonance imaging has been employed to pinpoint subtle structural changes in corticospinal motor projections in individuals carrying a mutation in genes associated with motor neuron degeneration. These studies underscore the potential of non-invasive brain mapping techniques to characterize the genetic influence on the human corticospinal motor system.
- Published
- 2009
25. Hyperexcitability of parietal-motor functional connections in the intact left-hemisphere of patients with neglect
- Author
-
Koch, G, Oliveri, M, Cheeran, B, Ruge, D, LO GERFO, E, Salerno, S, Torriero, S, Marconi, B, Mori, F, Driver, J, Rothwell, J, Caltagirone, C, Torriero, Sara, Caltagirone, C., LO GERFO, EMANUELE, Koch, G, Oliveri, M, Cheeran, B, Ruge, D, LO GERFO, E, Salerno, S, Torriero, S, Marconi, B, Mori, F, Driver, J, Rothwell, J, Caltagirone, C, Torriero, Sara, Caltagirone, C., and LO GERFO, EMANUELE
- Abstract
Hemispatial neglect is common after unilateral brain damage, particularly to perisylvian structures in the right-hemisphere (RH). In this disabling syndrome, behaviour and awareness are biased away from the contralesional side of space towards the ipsilesional side. Theoretical accounts of this in terms of hemispheric rivalry have speculated that the intact left-hemisphere (LH) may become hyper-excitable after a RH lesion, due to release of inhibition from the damaged hemisphere. We tested this directly using a novel twin-coil transcranial magnetic stimulation (TMS) approach to measure excitability within the intact LH of neglect patients. This involved applying a conditioning TMS pulse over left posterior parietal cortex (PPC), in order to test its effect on the amplitude of motor evoked potentials (MEPs) produced by a subsequent test pulse over left motor cortex (M1). Twelve RH stroke patients with neglect, an age-matched group of eight RH stroke patients without neglect, and 10 healthy controls were examined. We found that excitability of left PPC-M1 circuits was higher in neglect patients than the other groups, and related to the degree of neglect on clinical cancellation tests. A follow-up found that 1 Hz repetitive TMS over left PPC normalized this over-excitability, and also ameliorated visual neglect on an experimental measure with chimeric objects. Our results provide 'direct' evidence for pathological over-excitability of the LH in the neglect syndrome, as quantified by left PPC influences on left M1, with implications for possible treatment. © The Author (2008). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.
- Published
- 2008
26. Immunotherapy-responsive chorea as the presenting feature of LGI1-antibody encephalitis
- Author
-
Tofaris, G. K., primary, Irani, S. R., additional, Cheeran, B. J., additional, Baker, I. W. S., additional, Cader, Z. M., additional, and Vincent, A., additional
- Published
- 2012
- Full Text
- View/download PDF
27. Human Theta Burst Stimulation Enhances Subsequent Motor Learning and Increases Performance Variability
- Author
-
Teo, J. T. H., primary, Swayne, O. B. C., additional, Cheeran, B., additional, Greenwood, R. J., additional, and Rothwell, J. C., additional
- Published
- 2010
- Full Text
- View/download PDF
28. P20-16 The Rodil Project: Understanding variability in the response to rTMS
- Author
-
Fernandez-del-Olmo, M., primary, Cheeran, B., additional, Gomez-Garre, P., additional, Lago, A., additional, Marquez, G., additional, Koch, G., additional, Teo, J.T.H., additional, Rothwell, J.C., additional, and Mir, P., additional
- Published
- 2010
- Full Text
- View/download PDF
29. Hyperexcitability of parietal-motor functional connections in the intact left-hemisphere of patients with neglect
- Author
-
Koch, G., primary, Oliveri, M., additional, Cheeran, B., additional, Ruge, D., additional, Gerfo, E. L., additional, Salerno, S., additional, Torriero, S., additional, Marconi, B., additional, Mori, F., additional, Driver, J., additional, Rothwell, J. C., additional, and Caltagirone, C., additional
- Published
- 2008
- Full Text
- View/download PDF
30. Functional Interplay between Posterior Parietal and Ipsilateral Motor Cortex Revealed by Twin-Coil Transcranial Magnetic Stimulation during Reach Planning toward Contralateral Space
- Author
-
Koch, G., primary, Del Olmo, M. F., additional, Cheeran, B., additional, Schippling, S., additional, Caltagirone, C., additional, Driver, J., additional, and Rothwell, J. C., additional
- Published
- 2008
- Full Text
- View/download PDF
31. Focal Stimulation of the Posterior Parietal Cortex Increases the Excitability of the Ipsilateral Motor Cortex
- Author
-
Koch, G., primary, Fernandez Del Olmo, M., additional, Cheeran, B., additional, Ruge, D., additional, Schippling, S., additional, Caltagirone, C., additional, and Rothwell, J. C., additional
- Published
- 2007
- Full Text
- View/download PDF
32. GASTRIC CANCER PRESENTING AS SUBACUTE COMBINED DEGENERATION OF THE SPINAL CORD.
- Author
-
Sircar, P., primary, Shetty, S., additional, Cheeran, B., additional, Akinyemi, E., additional, and Niranjan, S., additional
- Published
- 2007
- Full Text
- View/download PDF
33. 90 GASTRIC CANCER PRESENTING AS SUBACUTE COMBINED DEGENERATION OF THE SPINAL CORD.
- Author
-
Sircar, P., primary, Shetty, S., additional, Cheeran, B., additional, Akinyemi, E., additional, and Niranjan, S., additional
- Published
- 2007
- Full Text
- View/download PDF
34. Time Course of Functional Connectivity between Dorsal Premotor and Contralateral Motor Cortex during Movement Selection
- Author
-
Koch, G., primary, Franca, M., additional, Fernandez Del Olmo, M., additional, Cheeran, B., additional, Milton, R., additional, Alvarez Sauco, M., additional, and Rothwell, J. C., additional
- Published
- 2006
- Full Text
- View/download PDF
35. Stimulating at the right time: phase-specific deep brain stimulation
- Author
-
Cagnan, H, Pedrosa, D, Little, S, Pogosyan, A, Cheeran, B, Aziz, T, Green, A, Fitzgerald, J, Foltynie, T, Limousin, P, Zrinzo, L, Hariz, M, Friston, KJ, Denison, T, and Brown, P
- Subjects
Essential Tremor ,Deep Brain Stimulation ,1.1 Normal biological development and functioning ,6.3 Medical devices ,Neurodegenerative ,Medical and Health Sciences ,closed-loop stimulation ,Thalamus ,dystonic tremor ,Clinical Research ,Underpinning research ,Tremor ,Accelerometry ,Humans ,ventrolateral thalamus ,Parkinson's Disease ,Neurology & Neurosurgery ,Rehabilitation ,Psychology and Cognitive Sciences ,synchrony ,Neurosciences ,Evaluation of treatments and therapeutic interventions ,Brain Disorders ,nervous system diseases ,Dystonia ,Neurological - Abstract
See Moll and Engel (doi:10.1093/aww308) for a scientific commentary on this article Brain regions dynamically engage and disengage with one another to execute everyday actions from movement to decision making. Pathologies such as Parkinson's disease and tremor emerge when brain regions controlling movement cannot readily decouple, compromising motor function. Here, we propose a novel stimulation strategy that selectively regulates neural synchrony through phase-specific stimulation. We demonstrate for the first time the therapeutic potential of such a stimulation strategy for the treatment of patients with pathological tremor. Symptom suppression is achieved by delivering stimulation to the ventrolateral thalamus, timed according to the patient's tremor rhythm. Sustained locking of deep brain stimulation to a particular phase of tremor afforded clinically significant tremor relief (up to 87% tremor suppression) in selected patients with essential tremor despite delivering less than half the energy of conventional high frequency stimulation. Phase-specific stimulation efficacy depended on the resonant characteristics of the underlying tremor network. Selective regulation of neural synchrony through phase-locked stimulation has the potential to both increase the efficiency of therapy and to minimize stimulation-induced side effects.
36. Hyperexcitability of parietal-motor functional connections in the intact left-hemisphere of patients with neglect
- Author
-
Francesco Mori, Sara Torriero, Jon Driver, Diane Ruge, Silvia Salerno, Massimiliano Oliveri, Carlo Caltagirone, Emanuele Lo Gerfo, Binith Cheeran, Giacomo Koch, John C. Rothwell, Barbara Marconi, Koch, G, Oliveri, M, Cheeran, B, Ruge, D, LO GERFO, E, Salerno, S, Torriero, S, Marconi, B, Mori, F, Driver, J, Rothwell, J, Caltagirone, C, KOCH G, OLIVERI M, CHEERAN B, RUGE D, LO GERFO E, SALERNO S, TORRIERO S, MARCONI B, MORI F, DRIVER J, ROTHWELL JC, and CALTAGIRONE C
- Subjects
Male ,genetic structures ,medicine.medical_treatment ,Humans ,Stroke ,Aged ,Parietal Lobe ,Motor Cortex ,Evoked Potentials, Motor ,Adult ,Neural Pathways ,Middle Aged ,Psychomotor Performance ,Transcranial Magnetic Stimulation ,Female ,Functional Laterality ,Perceptual Disorders ,Parietal cortex ,rTMS ,Neglect syndrome ,Evoked Potentials ,media_common ,Connectivity ,neglect ,Parietal lobe ,Cortical excitability ,medicine.anatomical_structure ,Motor ,Settore MED/26 - Neurologia ,medicine.symptom ,Perceptual Disorder ,Psychology ,Motor cortex ,Human ,media_common.quotation_subject ,Posterior parietal cortex ,Article ,Lateralization of brain function ,rehabilitation ,Neglect ,NO ,Neural Pathway ,medicine ,Hemispatial neglect ,Transcranial magnetic stimulation ,neglect syndrome ,transcranial magnetic stimulation ,connectivity ,parietal cortex ,cortical excitability ,Unilateral neglect ,TMS ,Neurology (clinical) ,Neuroscience - Abstract
Hemispatial neglect is common after unilateral brain damage, particularly to perisylvian structures in the right-hemisphere (RH). In this disabling syndrome, behaviour and awareness are biased away from the contralesional side of space towards the ipsilesional side. Theoretical accounts of this in terms of hemispheric rivalry have speculated that the intact left-hemisphere (LH) may become hyper-excitable after a RH lesion, due to release of inhibition from the damaged hemisphere. We tested this directly using a novel twin-coil transcranial magnetic stimulation (TMS) approach to measure excitability within the intact LH of neglect patients. This involved applying a conditioning TMS pulse over left posterior parietal cortex (PPC), in order to test its effect on the amplitude of motor evoked potentials (MEPs) produced by a subsequent test pulse over left motor cortex (M1). Twelve RH stroke patients with neglect, an age-matched group of eight RH stroke patients without neglect, and 10 healthy controls were examined. We found that excitability of left PPC-M1 circuits was higher in neglect patients than the other groups, and related to the degree of neglect on clinical cancellation tests. A follow-up found that 1 Hz repetitive TMS over left PPC normalized this over-excitability, and also ameliorated visual neglect on an experimental measure with chimeric objects. Our results provide 'direct' evidence for pathological over-excitability of the LH in the neglect syndrome, as quantified by left PPC influences on left M1, with implications for possible treatment. © The Author (2008). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.
- Published
- 2016
37. Future directions in psychiatric neurosurgery: Proceedings of the 2022 American Society for Stereotactic and Functional Neurosurgery meeting on surgical neuromodulation for psychiatric disorders.
- Author
-
Hitti FL, Widge AS, Riva-Posse P, Malone DA Jr, Okun MS, Shanechi MM, Foote KD, Lisanby SH, Ankudowich E, Chivukula S, Chang EF, Gunduz A, Hamani C, Feinsinger A, Kubu CS, Chiong W, Chandler JA, Carbunaru R, Cheeran B, Raike RS, Davis RA, Halpern CH, Vanegas-Arroyave N, Markovic D, Bick SK, McIntyre CC, Richardson RM, Dougherty DD, Kopell BH, Sweet JA, Goodman WK, Sheth SA, and Pouratian N
- Subjects
- Humans, United States, Neurosurgical Procedures, Neurosurgery, Deep Brain Stimulation, Mental Disorders surgery, Psychosurgery
- Abstract
Objective: Despite advances in the treatment of psychiatric diseases, currently available therapies do not provide sufficient and durable relief for as many as 30-40% of patients. Neuromodulation, including deep brain stimulation (DBS), has emerged as a potential therapy for persistent disabling disease, however it has not yet gained widespread adoption. In 2016, the American Society for Stereotactic and Functional Neurosurgery (ASSFN) convened a meeting with leaders in the field to discuss a roadmap for the path forward. A follow-up meeting in 2022 aimed to review the current state of the field and to identify critical barriers and milestones for progress., Design: The ASSFN convened a meeting on June 3, 2022 in Atlanta, Georgia and included leaders from the fields of neurology, neurosurgery, and psychiatry along with colleagues from industry, government, ethics, and law. The goal was to review the current state of the field, assess for advances or setbacks in the interim six years, and suggest a future path forward. The participants focused on five areas of interest: interdisciplinary engagement, regulatory pathways and trial design, disease biomarkers, ethics of psychiatric surgery, and resource allocation/prioritization. The proceedings are summarized here., Conclusion: The field of surgical psychiatry has made significant progress since our last expert meeting. Although weakness and threats to the development of novel surgical therapies exist, the identified strengths and opportunities promise to move the field through methodically rigorous and biologically-based approaches. The experts agree that ethics, law, patient engagement, and multidisciplinary teams will be critical to any potential growth in this area., Competing Interests: Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests. Sarah Bick receives funding from the Neurosurgery Research and Career Development Program (K12 NS080223) and consulting honoraria from Varian Medical Systems. Rafael Carbunaru owns stock options and is an employee of Boston Scientific, a manufacturer of DBS devices. Jennifer Chandler receives funding from CIHR (Canadian Institutes of Health Research) through the ERANET-Neuron program. Binith Cheeran owns stock options and is an employee of Abbott, a manufacturer of DBS devices. Rachel Davis receives consulting honoraria from Medtronic and speaker fees from Baylor for an OCD conference. Darin Dougherty's research has been funded by the International OCD Foundation, Brain and Behavior Research Foundation, National Institute of Mental Health, Tiny Blue Dot Foundation and Medtronic; he has received honoraria and consultation fees from Medtronic, Sage, and Celanese and has equity in Neurable, Innercosmos, and Intrinsic Powers. Ashley Feinsinger receives funding from the NIH (RF1MH121373 and UH3NS103442), received honoraria for her work on the NIH Neuroethics Workgroup, she is on an advisory board of Vivani Medical Products (Orion Early Feasibility Study), and she is on the data safety monitoring board of R01 MH122431. Kelly Foote reported grants from the National Institutes of Health during the conduct of the study; nonfinancial support from Medtronic (donation of closed-loop DBS devices) outside the submitted work; and grants from Medtronic, Boston Scientific, and Functional Neuromodulation outside the submitted work. Wayne Goodman receives funding from NIH (UH3NS100459), the McNair Foundation, and Biohaven. WG receives royalties from Nview, LLC and OCDscales, LLC as well as consulting honoraria from Biohaven. Aysegul Gunduz receives investigational device donations from Medtronic under the NIH BRAIN Public-Private Partnership agreements, and her research is funded by NIH grants UH3NS095553, R01NS096008, UH3NS119844. Casey Halpern has patents related to sensing and brain stimulation for the treatment of neuropsychiatric disorders, and he works as a consultant for Boston Scientific Neuromodulation and Insightec. Brian Kopell has received consulting honoraria from Abbott and Medtronic. Cynthia Kubu receives grant funding from the NIH (5RO1MH114853, 5RC1NS068086, 3RF1MH123407-01S1) and participates on the data safety monitoring boards for studies investigating the use of DBS for pain (UHS3 BRIAN/UH3 HEAL, 3UH3NS113661). She is the president of the Society for Clinical Neuropsychology. Sarah Lisanby receives funding from the NIMH (1ZIAMH002955) and has a role on the Scientific Advisory Boards of the Aalto University School of Science and the German Center for Brain Stimulation. Cameron McIntyre is a paid consultant for Boston Scientific Neuromodulation, receives royalties from Hologram Consultants, Neuros Medical, Qr8 Health, and is a shareholder in the following companies: Hologram Consultants, Surgical Information Sciences, BrainDynamics, CereGate, Autonomic Technologies, Cardionomic, Enspire DBS. Michael Okun serves as Medical Advisor for the Parkinson's Foundation, and has received research grants from NIH, Parkinson's Foundation, the Michael J. Fox Foundation, the Parkinson Alliance, Smallwood Foundation, the Bachmann-Strauss Foundation, the Tourette Syndrome Association, and the UF Foundation. Michael Okun's research is supported by: NIHR01 NR014852, R01NS096008, UH3NS119844, U01NS119562. Michael Okun is PI of the NIH R25NS108939 Training Grant. Michael Okun has received royalties for publications with Demos, Manson, Amazon, Smashwords, Books4Patients, Perseus, Robert Rose, Oxford and Cambridge (movement disorders books). Nader Pouratian receives research funding from NIH (R24 MH114796, UH3 NS103442, UH3 NS103549, R01 NS097782, UH3 NS113661, R01 GM135420, RF1 MH121373), consulting/presentation honoraria from Abbott, Sensoria Therapeutics, Boston Scientific, and BrainLab. Nader Pouratian is on an advisory board at Abbott Laboratories and has leadership positions in the Congress of Neurological Surgeons and American Society of Stereotactic and Functional Neurosurgery. Robert Raike owns stock options and is an employee of Medtronic, a manufacturer of DBS devices. Patricio Riva-Posse has received honoraria for consulting for Janssen Pharmaceuticals, Abbott Neuromodulation, and LivaNova. Sameer Sheth received funding from the McNair Foundation for this work. SS receives consulting honoraria from Boston Scientific, Neuropace, Zimmer Biomet, and Koh Young. Nora Vanegas-Arroyave receives research funding from NIH and the Michael J. Fox foundation. Alik Widge has received honoraria for consulting for Abbott, he has received device donations from Medtronic, and he has unlicensed patents in the area of deep brain stimulation., (Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.)
- Published
- 2023
- Full Text
- View/download PDF
38. Directional Deep Brain Stimulation for Parkinson's Disease: Results of an International Crossover Study With Randomized, Double-Blind Primary Endpoint.
- Author
-
Schnitzler A, Mir P, Brodsky MA, Verhagen L, Groppa S, Alvarez R, Evans A, Blazquez M, Nagel S, Pilitsis JG, Pötter-Nerger M, Tse W, Almeida L, Tomycz N, Jimenez-Shahed J, Libionka W, Carrillo F, Hartmann CJ, Groiss SJ, Glaser M, Defresne F, Karst E, Cheeran B, and Vesper J
- Subjects
- Cross-Over Studies, Female, Humans, Male, Quality of Life, Treatment Outcome, Deep Brain Stimulation methods, Parkinson Disease drug therapy
- Abstract
Objective: Published reports on directional deep brain stimulation (DBS) have been limited to small, single-center investigations. Therapeutic window (TW) is used to describe the range of stimulation amplitudes achieving symptom relief without side effects. This crossover study performed a randomized double-blind assessment of TW for directional and omnidirectional DBS in a large cohort of patients implanted with a DBS system in the subthalamic nucleus for Parkinson's disease., Materials and Methods: Participants received omnidirectional stimulation for the first three months after initial study programming, followed by directional DBS for the following three months. The primary endpoint was a double-blind, randomized evaluation of TW for directional vs omnidirectional stimulation at three months after initial study programming. Additional data recorded at three- and six-month follow-ups included stimulation preference, therapeutic current strength, Unified Parkinson's Disease Rating Scale (UPDRS) part III motor score, and quality of life., Results: The study enrolled 234 subjects (62 ± 8 years, 33% female). TW was wider using directional stimulation in 183 of 202 subjects (90.6%). The mean increase in TW with directional stimulation was 41% (2.98 ± 1.38 mA, compared to 2.11 ± 1.33 mA for omnidirectional). UPDRS part III motor score on medication improved 42.4% at three months (after three months of omnidirectional stimulation) and 43.3% at six months (after three months of directional stimulation) with stimulation on, compared to stimulation off. After six months, 52.8% of subjects blinded to stimulation type (102/193) preferred the period with directional stimulation, and 25.9% (50/193) preferred the omnidirectional period. The directional period was preferred by 58.5% of clinicians (113/193) vs 21.2% (41/193) who preferred the omnidirectional period., Conclusion: Directional stimulation yielded a wider TW compared to omnidirectional stimulation and was preferred by blinded subjects and clinicians., (Copyright © 2022. Published by Elsevier Inc.)
- Published
- 2022
- Full Text
- View/download PDF
39. Benefits and Risks of a Staged-Bilateral VIM Versus Unilateral VIM DBS for Essential Tremor.
- Author
-
Prakash P, Deuschl G, Ozinga S, Mitchell KT, Cheeran B, Larson PS, Merola A, Groppa S, Tomlinson T, and Ostrem JL
- Abstract
Background: Despite over 30 years of clinical experience, high-quality studies on the efficacy of bilateral versus unilateral deep brain stimulation (DBS) of the ventral intermediate (VIM) nucleus of the thalamus for medically refractory essential tremor (ET) remain limited., Objectives: To compare benefits and risks of bilateral versus unilateral VIM DBS using the largest ET DBS clinical trial dataset available to date., Methods: Participants from the US St. Jude/Abbott pivotal ET DBS trial who underwent staged-bilateral VIM implantation constituted the primary cohort in this sub-analysis. Their assessments "on" DBS at six months after second-side VIM DBS implantation were compared to the assessments six months after unilateral implantation. Two control cohorts of participants with unilateral implantation only were also used for between-group comparisons., Results: The primary cohort consisted of n = 38 ET patients (22M/16F; age of 65.3 ± 9.5 years). The second side VIM-DBS resulted in a 29.6% additional improvement in the total motor CRST score ( P < 0.001), with a 64.1% CRST improvement in the contralateral side ( P < 0.001). An added improvement was observed in the axial tremor score (21.4%, P = 0.005), and CRST part B (24.8%, P < 0.001) score. Rate of adverse events was slightly higher after bilateral stimulation., Conclusions: In the largest ET DBS study to date, staged-bilateral VIM DBS was a highly effective treatment for ET with bilateral implantation resulting in greater reduction in total motor tremor scores when compared to unilateral stimulation alone., Competing Interests: Abbott (formerly St Jude Medical) was the sponsor of the original trial.13 This current sub‐analysis was conducted with in collaboration with Abbott. Abbott provided the raw clinical data and re‐analysis was performed by the Abbott clinical science team under the direction of non‐Abbott investigators. No specific funding was received for this sub‐analysis. Interpretation and manuscript preparation were conducted by the investigators independent of Abbott., (© 2022 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society.)
- Published
- 2022
- Full Text
- View/download PDF
40. Necessity and feasibility of remote tele-programming of deep brain stimulation systems in Parkinson's disease.
- Author
-
Esper CD, Merola A, Himes L, Patel N, Bezchlibnyk YB, Falconer D, Weiss D, Luca C, Cheeran B, and Mari Z
- Subjects
- Feasibility Studies, Humans, Treatment Outcome, Deep Brain Stimulation methods, Parkinson Disease therapy, Telemedicine methods
- Abstract
Introduction: Outcomes after deep brain stimulation (DBS) therapy are dependent on good surgical placement in the target nucleus and optimized stimulation parameters through multiple programming sessions. This often requires frequent travel to a specialized DBS center, which presents a challenge for those with limited access. Recently, the FDA approved a remote tele-programming solution for DBS. To determine if remote tele-programming of DBS systems is beneficial and useful for Parkinson's Disease (PD) patients, Parkinson's Foundation hosted a survey in collaboration with Abbott Labs., Methods: The survey was conducted to assess the need for telemedicine among PD patients with DBS and the usability of the telehealth interface for DBS teleprogramming. The survey included two validated instruments: The Effective Accessibility and Accommodation survey (EAA) and the Telehealth Usability Questionnaire (TUQ)., Results: 47 patients completed the EAA and 41 completed the TUQ. Results from the EAA revealed more than a third of PD patients cannot easily get to a clinic for various reasons, and more than a quarter reported difficulty contacting their clinic for advice. Results from the TUQ revealed overall satisfaction with the DBS remote programming telehealth interface and care provided. The majority of respondents reported that remote tele-programming visits are similar in quality to in-person visits., Conclusion: This study provides support for the use of telehealth and tele-programming for DBS management in PD patients. The ability to use remote technologies for care will increase access to DBS and mitigate the disparities that currently prevent access to care., (Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2022
- Full Text
- View/download PDF
41. Rapid development of an integrated remote programming platform for neuromodulation systems through the biodesign process.
- Author
-
Silburn P, DeBates S, Tomlinson T, Schwark J, Creek G, Patel H, Punnoose A, Cheeran B, Ross E, Lautner D, and Pathak YJ
- Abstract
Treating chronic symptoms for pain and movement disorders with neuromodulation therapies involves fine-tuning of programming parameters over several visits to achieve and maintain symptom relief. This, together with challenges in access to trained specialists, has led to a growing need for an integrated wireless remote care platform for neuromodulation devices. In March of 2021, we launched the first neuromodulation device with an integrated remote programming platform. Here, we summarize the biodesign steps taken to identify the unmet patient need, invent, implement, and test the new technology, and finally gain market approval for the remote care platform. Specifically, we illustrate how agile development aligned with the evolving regulatory requirements can enable patient-centric digital health technology in neuromodulation, such as the remote care platform. The three steps of the biodesign process applied for remote care platform development are: (1) Identify, (2) Invent, and (3) Implement. First, we identified the unmet patient needs through market research and voice-of-customer (VOC) process. Next, during the concept generation phase of the invention step, we integrated the results from the VOC into defining requirements for prototype development. Subsequently, in the concept screening phase, ten subjects with PD participated in a clinical pilot study aimed at characterizing the safety of the remote care prototype. Lastly, during the implementation step, lessons learned from the pilot experience were integrated into final product development as new features. Following final product development, we completed usability testing to validate the full remote care system and collected preliminary data from the limited market release experience. The VOC data, during prototype development, helped us identify thresholds for video quality and needs priorities for clinicians and patients. During the pilot study, one subject reported anticipated remote-care-related adverse events that were resolved without sequelae. For usability analysis following final product development, the failure rates for task completion for both user groups were about 1%. Lastly, during the initial 4 weeks of the limited market release experience, a total of 858 remote care sessions were conducted with a 93% success rate. Overall, we developed a remote care platform by adopting a user-centric approach. Although the system intended to address pre-COVID19 challenges associated with disease management, the unforeseen overlap of the study with the pandemic elevated the importance of such a system and an innovative development process enabled us to advance a patient-centric platform to gain regulatory approval and successfully launch the remote care platform to market., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
- View/download PDF
42. Reduced Risk of Reoperations With Modern Deep Brain Stimulator Systems: Big Data Analysis From a United States Claims Database.
- Author
-
Wu C, Nagel SJ, Agarwal R, Pötter-Nerger M, Hamel W, Sharan AD, Connolly AT, Cheeran B, and Larson PS
- Abstract
Objective: There have been significant improvements in the design and manufacturing of deep brain stimulation (DBS) systems, but no study has considered the impact of modern systems on complications. We sought to compare the relative occurrence of reoperations after de novo implantation of modern and traditional DBS systems in patients with Parkinson's disease (PD) or essential tremor (ET) in the United States. Design: Retrospective, contemporaneous cohort study. Setting: Multicenter data from the United States Centers for Medicare and Medicaid Services administrative claims database between 2016 and 2018. Participants: This population-based sample consisted of 5,998 patients implanted with a DBS system, of which 3,869 patients had a de novo implant and primary diagnosis of PD or ET. Follow-up of 3 months was available for 3,810 patients, 12 months for 3,561 patients, and 24 months for 1,812 patients. Intervention: Implantation of a modern directional (MD) or traditional omnidirectional (TO) DBS system. Primary and Secondary Outcome Measures: We hypothesized that MD systems would impact complication rates. Reoperation rate was the primary outcome. Associated diagnoses, patient characteristics, and implanting center details served as covariates. Kaplan-Meier analysis was performed to compare rates of event-free survival and regression models were used to determine covariate influences. Results: Patients implanted with modern systems were 36% less likely to require reoperation, largely due to differences in acute reoperations and intracranial lead reoperations. Risk reduction persisted while accounting for practice differences and implanting center experience. Risk reduction was more pronounced in patients with PD. Conclusions: In the first multicenter analysis of device-related complications including modern DBS systems, we found that modern systems are associated with lower reoperation rates. This risk profile should be carefully considered during device selection for patients undergoing DBS for PD or ET. Prospective studies are needed to further investigate underlying causes., Competing Interests: CW, SN, MP-N, WH, and PL are paid consultants for Abbott Laboratories. RA, AC, and BC are employees of Abbott Laboratories. The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The authors declare that this study received funding from Abbott Laboratories. The funder was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication., (Copyright © 2021 Wu, Nagel, Agarwal, Pötter-Nerger, Hamel, Sharan, Connolly, Cheeran and Larson.)
- Published
- 2021
- Full Text
- View/download PDF
43. Corrigendum: Proceedings of the Eighth Annual Deep Brain Stimulation Think Tank: Advances in Optogenetics, Ethical Issues Affecting DBS Research, Neuromodulatory Approaches for Depression, Adaptive Neurostimulation, and Emerging DBS Technologies.
- Author
-
Vedam-Mai V, Deisseroth K, Giordano J, Lazaro-Munoz G, Chiong W, Suthana N, Langevin JP, Gill J, Goodman W, Provenza NR, Halpern CH, Shivacharan RS, Cunningham TN, Sheth SA, Pouratian N, Scangos KW, Mayberg HS, Horn A, Johnson KA, Butson CR, Gilron R, de Hemptinne C, Wilt R, Yaroshinsky M, Little S, Starr P, Worrell G, Shirvalkar P, Chang E, Volkmann J, Muthuraman M, Groppa S, Kühn AA, Li L, Johnson M, Otto KJ, Raike R, Goetz S, Wu C, Silburn P, Cheeran B, Pathak YJ, Malekmohammadi M, Gunduz A, Wong JK, Cernera S, Hu W, Wagle Shukla A, Ramirez-Zamora A, Deeb W, Patterson A, Foote KD, and Okun MS
- Abstract
[This corrects the article DOI: 10.3389/fnhum.2021.644593.]., (Copyright © 2021 Vedam-Mai, Deisseroth, Giordano, Lazaro-Munoz, Chiong, Suthana, Langevin, Gill, Goodman, Provenza, Halpern, Shivacharan, Cunningham, Sheth, Pouratian, Scangos, Mayberg, Horn, Johnson, Butson, Gilron, de Hemptinne, Wilt, Yaroshinsky, Little, Starr, Worrell, Shirvalkar, Chang, Volkmann, Muthuraman, Groppa, Kühn, Li, Johnson, Otto, Raike, Goetz, Wu, Silburn, Cheeran, Pathak, Malekmohammadi, Gunduz, Wong, Cernera, Hu, Wagle Shukla, Ramirez-Zamora, Deeb, Patterson, Foote and Okun.)
- Published
- 2021
- Full Text
- View/download PDF
44. Proceedings of the Eighth Annual Deep Brain Stimulation Think Tank: Advances in Optogenetics, Ethical Issues Affecting DBS Research, Neuromodulatory Approaches for Depression, Adaptive Neurostimulation, and Emerging DBS Technologies.
- Author
-
Vedam-Mai V, Deisseroth K, Giordano J, Lazaro-Munoz G, Chiong W, Suthana N, Langevin JP, Gill J, Goodman W, Provenza NR, Halpern CH, Shivacharan RS, Cunningham TN, Sheth SA, Pouratian N, Scangos KW, Mayberg HS, Horn A, Johnson KA, Butson CR, Gilron R, de Hemptinne C, Wilt R, Yaroshinsky M, Little S, Starr P, Worrell G, Shirvalkar P, Chang E, Volkmann J, Muthuraman M, Groppa S, Kühn AA, Li L, Johnson M, Otto KJ, Raike R, Goetz S, Wu C, Silburn P, Cheeran B, Pathak YJ, Malekmohammadi M, Gunduz A, Wong JK, Cernera S, Hu W, Wagle Shukla A, Ramirez-Zamora A, Deeb W, Patterson A, Foote KD, and Okun MS
- Abstract
We estimate that 208,000 deep brain stimulation (DBS) devices have been implanted to address neurological and neuropsychiatric disorders worldwide. DBS Think Tank presenters pooled data and determined that DBS expanded in its scope and has been applied to multiple brain disorders in an effort to modulate neural circuitry. The DBS Think Tank was founded in 2012 providing a space where clinicians, engineers, researchers from industry and academia discuss current and emerging DBS technologies and logistical and ethical issues facing the field. The emphasis is on cutting edge research and collaboration aimed to advance the DBS field. The Eighth Annual DBS Think Tank was held virtually on September 1 and 2, 2020 (Zoom Video Communications) due to restrictions related to the COVID-19 pandemic. The meeting focused on advances in: (1) optogenetics as a tool for comprehending neurobiology of diseases and on optogenetically-inspired DBS, (2) cutting edge of emerging DBS technologies, (3) ethical issues affecting DBS research and access to care, (4) neuromodulatory approaches for depression, (5) advancing novel hardware, software and imaging methodologies, (6) use of neurophysiological signals in adaptive neurostimulation, and (7) use of more advanced technologies to improve DBS clinical outcomes. There were 178 attendees who participated in a DBS Think Tank survey, which revealed the expansion of DBS into several indications such as obesity, post-traumatic stress disorder, addiction and Alzheimer's disease. This proceedings summarizes the advances discussed at the Eighth Annual DBS Think Tank., Competing Interests: SG and MM were employed by companies Medtronic and Boston Scientific Neuromodulation respectively. The remaining 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., (Copyright © 2021 Vedam-Mai, Deisseroth, Giordano, Lazaro-Munoz, Chiong, Suthana, Langevin, Gill, Goodman, Provenza, Halpern, Shivacharan, Cunningham, Sheth, Pouratian, Scangos, Mayberg, Horn, Johnson, Butson, Gilron, de Hemptinne, Wilt, Yaroshinsky, Little, Starr, Worrell, Shirvalkar, Chang, Volkmann, Muthuraman, Groppa, Kühn, Li, Johnson, Otto, Raike, Goetz, Wu, Silburn, Cheeran, Pathak, Malekmohammadi, Gunduz, Wong, Cernera, Wagle Shukla, Ramirez-Zamora, Deeb, Patterson, Foote and Okun.)
- Published
- 2021
- Full Text
- View/download PDF
45. Steering the Volume of Tissue Activated With a Directional Deep Brain Stimulation Lead in the Globus Pallidus Pars Interna: A Modeling Study With Heterogeneous Tissue Properties.
- Author
-
Zhang S, Tagliati M, Pouratian N, Cheeran B, Ross E, and Pereira E
- Abstract
Objective: To study the effect of directional deep brain stimulation (DBS) electrode configuration and vertical electrode spacing on the volume of tissue activated (VTA) in the globus pallidus, pars interna (GPi). Background: Directional DBS leads may allow clinicians to precisely direct current fields to different functional networks within traditionally targeted brain areas. Modeling the shape and size of the VTA for various monopolar or bipolar configurations can inform clinical programming strategies for GPi DBS. However, many computational models of VTA are limited by assuming tissue homogeneity. Methods: We generated a multimodal image-based detailed anatomical (MIDA) computational model with a directional DBS lead (1.5 mm or 0.5 mm vertical electrode spacing) placed with segmented contact 2 at the ventral posterolateral "sensorimotor" region of the GPi. The effect of tissue heterogeneity was examined by replacing the MIDA tissues with a homogeneous tissue of conductance 0.3 S/m. DBS pulses (amplitude: 1 mA, pulse width: 60 μs, frequency: 130 Hz) were used to produce VTAs. The following DBS contact configurations were tested: single-segment monopole (2B-/Case+), two-segment monopole (2A-/2B-/Case+ and 2B-/3B-/Case+), ring monopole (2A-/2B-/2C-/Case+), one-cathode three-anode bipole (2B-/3A+/3B+/3C+), three-cathode three-anode bipole (2A-/2B-/2C-/3A+/3B+/3C+). Additionally, certain vertical configurations were repeated with 2 mA current amplitude. Results: Using a heterogeneous tissue model affected both the size and shape of the VTA in GPi. Electrodes with both 0.5 mm and 1.5 mm vertical spacing (1 mA) modeling showed that the single segment monopolar VTA was entirely contained within the GPi when the active electrode is placed at the posterolateral "sensorimotor" GPi. Two segments in a same ring and ring settings, however, produced VTAs outside of the GPi border that spread into adjacent white matter pathways, e.g., optic tract and internal capsule. Both stacked monopolar settings and vertical bipolar settings allowed activation of structures dorsal to the GPi in addition to the GPi. Modeling of the stacked monopolar settings with the DBS lead with 0.5 mm vertical electrode spacing further restricted VTAs within the GPi, but the VTA volumes were smaller compared to the equivalent settings of 1.5 mm spacing., (Copyright © 2020 Zhang, Tagliati, Pouratian, Cheeran, Ross and Pereira.)
- Published
- 2020
- Full Text
- View/download PDF
46. Comparing Current Steering Technologies for Directional Deep Brain Stimulation Using a Computational Model That Incorporates Heterogeneous Tissue Properties.
- Author
-
Zhang S, Silburn P, Pouratian N, Cheeran B, Venkatesan L, Kent A, and Schnitzler A
- Subjects
- Humans, Deep Brain Stimulation methods, Finite Element Analysis, Models, Neurological
- Abstract
Objective: A computational model that accounts for heterogeneous tissue properties was used to compare multiple independent current control (MICC), multi-stim set (MSS), and concurrent activation (co-activation) current steering technologies utilized in deep brain stimulation (DBS) on volume of tissue activated (VTA) and power consumption., Methods: A computational model was implemented in Sim4Life v4.0 with the multimodal image-based detailed anatomical (MIDA) model, which accounts for heterogeneous tissue properties. A segmented DBS lead placed in the subthalamic nucleus (STN). Three milliamperes of current (with a 90 μs pseudo-biphasic waveform) was distributed between two electrodes with various current splits. The laterality, directional accuracy, volume, and shape of the VTAs using MICC, MSS and co-activation, and their power consumption were computed and compared., Results: MICC, MSS, and coactivation resulted in less laterality of steering than single-segment activation. Both MICC and MSS show directional inaccuracy (more pronounced with MSS) during radial current steering. Co-activation showed greater directional accuracy than MICC and MSS at centerline between the two activated electrodes. MSS VTA volume was smaller and more compact with less current spread outside the active electrode plane than MICC VTA. There was no consistent pattern of power drain between MSS and MICC, but electrode co-activation always used less power than either fractionating paradigm., Conclusion: While current fractionalization technologies can achieve current steering between two segmented electrodes, this study shows that there are important limitations in accuracy and focus of tissue activation when tissue heterogeneity is accounted for., (© 2019 The Authors. Neuromodulation: Technology at the Neural Interface published by Wiley Periodicals, Inc. on behalf of International Neuromodulation Society.)
- Published
- 2020
- Full Text
- View/download PDF
47. Proceedings of the Seventh Annual Deep Brain Stimulation Think Tank: Advances in Neurophysiology, Adaptive DBS, Virtual Reality, Neuroethics and Technology.
- Author
-
Ramirez-Zamora A, Giordano J, Gunduz A, Alcantara J, Cagle JN, Cernera S, Difuntorum P, Eisinger RS, Gomez J, Long S, Parks B, Wong JK, Chiu S, Patel B, Grill WM, Walker HC, Little SJ, Gilron R, Tinkhauser G, Thevathasan W, Sinclair NC, Lozano AM, Foltynie T, Fasano A, Sheth SA, Scangos K, Sanger TD, Miller J, Brumback AC, Rajasethupathy P, McIntyre C, Schlachter L, Suthana N, Kubu C, Sankary LR, Herrera-Ferrá K, Goetz S, Cheeran B, Steinke GK, Hess C, Almeida L, Deeb W, Foote KD, and Okun MS
- Abstract
The Seventh Annual Deep Brain Stimulation (DBS) Think Tank held on September 8th of 2019 addressed the most current: (1) use and utility of complex neurophysiological signals for development of adaptive neurostimulation to improve clinical outcomes; (2) Advancements in recent neuromodulation techniques to treat neuropsychiatric disorders; (3) New developments in optogenetics and DBS; (4) The use of augmented Virtual reality (VR) and neuromodulation; (5) commercially available technologies; and (6) ethical issues arising in and from research and use of DBS. These advances serve as both "markers of progress" and challenges and opportunities for ongoing address, engagement, and deliberation as we move to improve the functional capabilities and translational value of DBS. It is in this light that these proceedings are presented to inform the field and initiate ongoing discourse. As consistent with the intent, and spirit of this, and prior DBS Think Tanks, the overarching goal is to continue to develop multidisciplinary collaborations to rapidly advance the field and ultimately improve patient outcomes., (Copyright © 2020 Ramirez-Zamora, Giordano, Gunduz, Alcantara, Cagle, Cernera, Difuntorum, Eisinger, Gomez, Long, Parks, Wong, Chiu, Patel, Grill, Walker, Little, Gilron, Tinkhauser, Thevathasan, Sinclair, Lozano, Foltynie, Fasano, Sheth, Scangos, Sanger, Miller, Brumback, Rajasethupathy, McIntyre, Schlachter, Suthana, Kubu, Sankary, Herrera-Ferrá, Goetz, Cheeran, Steinke, Hess, Almeida, Deeb, Foote and Okun.)
- Published
- 2020
- Full Text
- View/download PDF
48. Variability in non-invasive brain stimulation studies: Reasons and results.
- Author
-
Guerra A, López-Alonso V, Cheeran B, and Suppa A
- Subjects
- Humans, Long-Term Potentiation physiology, Motor Cortex surgery, Transcranial Magnetic Stimulation methods, Evoked Potentials, Motor physiology, Motor Cortex physiology, Neuronal Plasticity physiology, Transcranial Direct Current Stimulation
- Abstract
Non-invasive brain stimulation techniques (NIBS), such as Theta Burst Stimulation (TBS), Paired Associative Stimulation (PAS) and transcranial Direct Current Stimulation (tDCS), are widely used to probe plasticity in the human motor cortex (M1). Although TBS, PAS and tDCS differ in terms of physiological mechanisms responsible for experimentally-induced cortical plasticity, they all share the ability to elicit long-term potentiation (LTP) and depression (LTD) in M1. However, NIBS techniques are all affected by relevant variability in intra- and inter-subject responses. A growing number of factors contributing to NIBS variability have been recently identified and reported. In this review, we have readdressed the issue of variability in human NIBS studies. We have first briefly discussed the physiological mechanisms responsible for TBS, PAS and tDCS-induced cortical plasticity. Then, we have provided statistical measures of intra- and inter-subject variability, as calculated in previous studies. Finally, we have reported in detail known sources of variability by categorizing them into physiological, technical and statistical factors. Improving knowledge about sources of variability could lead to relevant advances in designing new tailored NIBS protocols in physiological and pathological conditions., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
49. Solutions for managing variability in non-invasive brain stimulation studies.
- Author
-
Guerra A, López-Alonso V, Cheeran B, and Suppa A
- Subjects
- Humans, Stereotaxic Techniques rehabilitation, Transcranial Direct Current Stimulation methods, Evoked Potentials, Motor physiology, Motor Cortex physiology, Neuronal Plasticity physiology, Transcranial Magnetic Stimulation methods
- Abstract
In the last three decades, a number of non-invasive brain stimulation (NIBS) protocols, capable of assessing and modulating plasticity in the human motor cortex (M1), have been described. For almost as long, NIBS has delivered the tantalising prospect of non-invasive neuromodulation as a therapeutic intervention for neurorehabilitation, psychiatry, chronic pain and other disease states. Apart from modest effects in depression, this early promise has not been realised since the symptomatic improvements produced by NIBS are generally weak. One key factor explaining this lack of clinical translation concerns variability in response to NIBS. Several studies have demonstrated a number of physiological, technical and statistical factors accounting for intra- and inter-subject variability. However, solutions to overcome this problem are still under debate. In the present review, we have provided a detailed description of methodological and technical solutions to control known factors influencing variability. We have also suggested potential strategies to strengthen and stabilize NIBS-induced after-effects. Finally, we propose new possible outcome variables which better reflect intrinsic cortical activity, allowing a more sensitive measurement and valid interpretation of responses to NIBS., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
50. Applying a Sensing-Enabled System for Ensuring Safe Anterior Cingulate Deep Brain Stimulation for Pain.
- Author
-
Huang Y, Cheeran B, Green AL, Denison TJ, and Aziz TZ
- Abstract
Deep brain stimulation (DBS) of the anterior cingulate cortex (ACC) was offered to chronic pain patients who had exhausted medical and surgical options. However, several patients developed recurrent seizures. This work was conducted to assess the effect of ACC stimulation on the brain activity and to guide safe DBS programming. A sensing-enabled neurostimulator (Activa PC + S) allowing wireless recording through the stimulating electrodes was chronically implanted in three patients. Stimulation patterns with different amplitude levels and variable ramping rates were tested to investigate whether these patterns could provide pain relief without triggering after-discharges (ADs) within local field potentials (LFPs) recorded in the ACC. In the absence of ramping, AD activity was detected following stimulation at amplitude levels below those used in chronic therapy. Adjustment of stimulus cycling patterns, by slowly ramping on/off (8-s ramp duration), was able to prevent ADs at higher amplitude levels while maintaining effective pain relief. The absence of AD activity confirmed from the implant was correlated with the absence of clinical seizures. We propose that AD activity in the ACC could be a biomarker for the likelihood of seizures in these patients, and the application of sensing-enabled techniques has the potential to advance safer brain stimulation therapies, especially in novel targets.
- Published
- 2019
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.