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Tetrabenazine as anti-chorea therapy in Huntington Disease: an open-label continuation study. Huntington Study Group/TETRA-HD Investigators
© Frank; licensee BioMed Central Ltd. 2009
Received: 20 March 2009
Accepted: 18 December 2009
Published: 18 December 2009
The Erratum to this article has been published in BMC Neurology 2011 11:18
Tetrabenazine (TBZ) selectively depletes central monoamines by reversibly binding to the type-2 vesicular monoamine transporter. A previous double blind study in Huntington disease (HD) demonstrated that TBZ effectively suppressed chorea, with a favorable short-term safety profile (Neurology 2006;66:366-372). The objective of this study was to assess the long-term safety and effectiveness of TBZ for chorea in HD.
Subjects who completed the 13-week, double blind protocol were invited to participate in this open label extension study for up to 80 weeks. Subjects were titrated to the best individual dose or a maximum of 200 mg/day. Chorea was assessed using the Total Maximal Chorea (TMC) score from the Unified Huntington Disease Rating Scale.
Of the 75 participants, 45 subjects completed 80 weeks. Three participants terminated due to adverse events (AEs) including depression, delusions with associated previous suicidal behavior, and vocal tics. One subject died due to breast cancer. The other 26 subjects chose not to continue on with each ensuing extension for various reasons. When mild and unrelated AEs were excluded, the most commonly reported AEs (number of subjects) were sedation/somnolence (18), depressed mood (17), anxiety (13), insomnia (10), and akathisia (9). Parkinsonism and dysphagia scores were significantly increased at week 80 compared to baseline. At week 80, chorea had significantly improved from baseline with a mean reduction in the TMC score of 4.6 (SD 5.5) units. The mean dosage at week 80 was 63.4 mg (range 12.5-175 mg).
TBZ effectively suppresses HD-related chorea for up to 80 weeks. Patients treated chronically with TBZ should be monitored for parkinsonism, dysphagia and other side effects including sleep disturbance, depression, anxiety, and akathisia.
Clinicaltrials.gov registration number (initial study): NCT00219804
Huntington disease (HD) is a hereditary, progressive neurodegenerative disease clinically characterized by a triad of chorea, cognitive symptoms and behavioral changes. Although there is no established treatment to delay the onset or forestall the progression of HD, symptomatic treatment of chorea may be beneficial in some individuals as it may have a favorable impact on motor function, quality of life and safety [1, 2].
Many agents and surgical procedures have been evaluated in HD for their anti-choreic efficacy including dopamine depleting agents, dopamine antagonists, benzodiazepines, glutamate antagonists, acetylcholinesterase inhibitors, dopamine agonists, anti-seizure medications, cannabinoids, lithium, deep brain stimulation, and fetal cell transplantation [3–5]. A preponderance of the mostly uncontrolled studies to date supports the use of TBZ in patients with a variety of hyperkinetic movement disorders, including HD [6–8]. The efficacy of TBZ as an anti-choreic drug was convincingly demonstrated in a double-blind, placebo-controlled trial, which demonstrated clear short-term symptomatic relief of chorea . There is paucity of data on the long term use of TBZ, but a few studies have provided evidence of its long-term efficacy and tolerability [7, 10].
TBZ is a reversible dopamine depleting agent that is highly selective for the central vesicular monoamine transporter type 2 (VMAT2) . TBZ depletes dopamine more selectively over norepinephrine and serotonin by inhibiting transport into presynaptic vesicles [12, 13]. The highest binding density for TBZ is in the caudate nucleus, putamen and nucleus accumbens, areas known to bear the brunt of pathology in HD [14, 15]. VMAT2 binding and monoamine depletion by TBZ is reversible, lasts hours, and is not modified by chronic treatment [16, 17].
Far too little evidence is available to guide long term symptomatic treatment in HD. Double-blind and long-term studies assessing various treatment strategies in HD are urgently needed . The objective of this open-label extension study was to assess the long-term safety and efficacy of TBZ in the treatment of chorea in HD.
Patients with HD who were ambulatory, had a Total Functional Capacity (TFC) score of greater than 5 and a Total Maximal Chorea (TMC) score of greater than 9 from the Unified Huntington Disease Rating Scale (UHDRS), were initially enrolled in the thirteen-week, double-blind, placebo-controlled study [9, 19]. Subjects were excluded if they were taking concurrent dopamine depleting drugs, dopamine D2 receptor blockers, selective and non-selective monoamine-oxidase inhibitors, amantadine, levodopa, or dopamine agonists. Participants were permitted to be on antidepressants, antianxiety agents and other psychotropic medications at stable doses. Clinically, subjects could not have disabling dysarthria, dysphagia or depression present at screening or have an unstable or serious medical or psychiatric illness, untreated depression or lack of a caregiver.
Written informed consent was obtained from all study participants and accompanying caregivers. In compliance with the Declaration of Helsinki, this study was approved by the Research Subjects Review Board at the University of Rochester as the coordinating site and by the ethics review boards at all individual sites that enrolled subjects.
TBZ was titrated over a maximum of 12 weeks every 3-7 days to the best individual dose (maximum of 200 mg/day). All subjects started at 12.5 mg per day and were titrated upward at the end of each week by 12.5 mg increments to doses equal to or lower than 125 mg/day, and then by 25 mg increments for doses higher than 125 mg/day. If at any time during the titration phase, moderate to severe, possibly or probably drug-related AEs occurred, the dose of TBZ was decreased to the patient's previous well-tolerated dose. Study drug titration (up or down) was permitted only during the first 11 weeks of the study.
Participants were examined at the end of weeks 2, 6, 12, 24 and then every 12 weeks; and had a safety follow-up visit one week after the end of treatment. Characteristics of participants and non-participants were compared using chi-square tests and Kruskal-Wallis tests, as appropriate.
Analysis of Efficacy Endpoints
The primary efficacy endpoint was the TMC score from the UHDRS at week 80 compared with the baseline TMC score. TMC score at week 80 was also compared to week 81 (after washout) to determine the degree of re-emergent chorea. To determine if TBZ may have worsened overall underlying chorea over time, TMC at week 81 was compared with baseline. T-tests and analysis of covariance (ANCOVA), adjusted for site and baseline value, were used to determine significance. Secondary endpoints included the Clinical Global Impression scale and the individual sections of the UHDRS.
Analysis of Safety and Tolerability Endpoints
Tolerability was assessed using adverse events, UHDRS parkinsonism score (total of the following UHDRS motor items: finger taps, pronation/supination, rigidity, bradykinesia, gait, tandem gait and retropulsion pull test), Barnes Akathisia Scale (BAS) , Unified Parkinson's Disease Rating Scale (UPDRS) dysphagia and dysarthria scores , and the 17-item Hamilton Depression Measure (HAM) . Changes from baseline were assessed using t-tests.
Treatment emergent AEs were designated to be those AEs that emerged after the start of the open-label study, excluding those for which subjects had a prior history and those that had been present during the double-blind study, including those without resolution. Those AEs that carried over from the double-blind portion of the study were not considered new events as they have been previously reported . The time period examined for all AEs was baseline to last day on study medication, prior to initiation of washout.
The total number (%) of subjects experiencing at least one AE was calculated separately for the titration and maintenance periods. McNemar's test was used to compare the number of subjects experiencing at least one AE during the titration phase with the number experiencing at least one AE during the maintenance phase. AEs starting in the period from the date of baseline visit to week 12 were designated as having occurred during the titration period. AEs starting in the period from the first day of week 12 to week 24 were designated as having occurred during the maintenance period. AEs designated as mild and/or not related to study medication were excluded, and three subjects with fewer than 13.5 weeks in this study period were omitted from this analysis.
To determine if 12 additional weeks of exposure to study medication impacted chorea or HD, efficacy and safety measures were compared between subjects originally assigned to placebo and TBZ in the double-blind study using ANCOVA.
Baseline characteristics (n = 75)
Age (mean ± SD, range)
50.9 ± 11.5, 29.2-77.4
CAGn (mean ± SD, range)
44.5 ± 3.4, 39-54
Women, n (%)
Caucasian, n (%)
Affected Parent, n (%)
Years of Illness duration (mean ± SD, range)
8.5 ± 4.5, 1.9-25.9
History of Depression, n (%)
Twenty subjects terminated from the study. There was one death due to metastatic breast cancer. Three participants withdrew due to AEs attributed by the investigators to TBZ, including vocal tics, depression, and delusions. One subject terminated because of an elevated bilirubin level but also reported akathisia, while another subject experienced a significant increase in liver enzymes. One subject was started on exclusionary medications, and two subjects were non-compliant with study medications. One subject was institutionalized, one moved out of the state, and two were lost to follow-up. The remaining seven terminations were due to withdrawal of patient consent or by caregiver or physician request. An additional ten subjects decided not to continue in ensuing extension phases. Subjects who completed the study were more likely to be female (p < 0.01), have higher CAG repeat length (45 vs. 43.5, p < 0.05), and have a lower total functional assessment score at baseline (18.0 vs. 20.5, p < 0.02). There were no differences in race, affected parent, history of depression, chorea score, TFC, total motor score, age, years of education or duration of illness.
Treatment emergent AEs reported in >5% of subjects (3 or more), excluding mild and not related to treatment
# of Subjects
When mild or unrelated events were excluded, 39 subjects reported at least one AE during titration while 20 subjects reported at least one AE during maintenance (p < 0.001). Insomnia, somnolence and diarrhea emerged during titration and subsequently resolved during maintenance. The number of subjects with somnolence decreased from 36 to 11 (p < 0.0001), insomnia from 14 to 2 (p < 0.003) and diarrhea from 5 to 1 (p < 0.05) when comparing titration to maintenance phases.
Between baseline and week 80, the mean parkinsonism score increased 2.1 (SD 4.3) UHDRS units (p = 0.002) and the mean UPDRS dysarthria score increased 0.4 (SD 0.8) UPDRS units (p < 0.002). There were no significant changes in the HAM scale scores, UPDRS dysphagia score, or BAS. Marked or severe akathisia (4 or 5 on the BAS scale) was experienced by only one participant, who terminated due to elevated bilirubin, rather than akathisia. Three participants (4%) had mild or moderate akathisia at baseline. Ten other participants (13.3%) developed mild or moderate akathisia during the course of the study.
There were 3 participants with isolated elevation of AST, greater than 3 times the upper limit of normal. Two occurrences were at baseline and one at week 24. All abnormal liver tests returned to normal by week 80 or at the end of study participation except in one participant with >2 times upper limit of normal AST in isolation. No participant experienced clinical liver dysfunction, but one participant was terminated early due to elevated AST and ALT at baseline and one subject terminated due to elevated bilirubin without clear etiology.
At 48 weeks, chorea reduction in the 45 participants who completed 80 weeks was not significantly different compared to the 11 subjects who completed week 48 but did not complete the study. After adjusting for study site and baseline chorea score, there was no association with the effect of TBZ on chorea related to age, gender, trinucleotide repeat length, gender of affected parent, or baseline clinical global impression of severity. Baseline chorea score itself was a predictor for greater reduction in chorea (p = 0.013).
Secondary Efficacy Outcomes
At week 80, there was a significant change in the CGI score of 0.3 (SD 0.7, p = 0.0054). Of the 45 completers, there was improvement in 16 (36%) and worsening of 4 (9%) with the remainder unchanged compared to baseline.
Baseline scores and changes from baseline in efficacy outcome measures at weeks 24, 48 and 80 [Mean (SD)].
N = 75
N = 73
N = 57
N = 45
UHDRS Motor Score
-7.4 (9.8) *
-5.6 (12.1) *
-5.8 (5.0) *
-5.6 (5.5) *
-4.6 (5.5) *
2.1 (4.3) *
-1.1 (2.3) *
-2.6 (3.3) *
-2.4 (7.2) *
-4.4 (6.0) *
-7.0 (8.1) *
Behavioral Score (freq*severity)
3.4 (14.4) *
2.9 (9.3) *
-1.2 (4.8) *
N = 47
N = 45
N = 38
N = 30
Total Functional Capacity
-0.5 (1.5) *
-1.1 (1.4) *
-2.0 (2.3) *
-2.0 (5.6) *
-2.0 (5.8) *
-3.6 (7.9) *
-1.9 (4.7) *
-4.8 (10.3) *
-4.4 (9.5) *
-8.9 (11.4) *
-11.0 (14.8) *
-7.9 (15.4) *
-9.0 (17.4) *
-2.7 (7.1) *
-4.5 (7.0) *
-5.0 (10.4) *
Placebo vs. TBZ
When the groups initially randomized to placebo and TBZ were compared, there were no differences in numbers of subjects with AEs, change in TMC score, change in chorea after withdrawal, best dosage, or any of the secondary measures. There was a reduction in the total number of AEs (p < 0.002) and somnolence (p < 0.01) in maintenance for those subjects initially assigned to TBZ.
The double-blind, randomized controlled trial preceding this study demonstrated that TBZ reduced chorea associated with HD for up to 12 weeks with the main AEs including drowsiness and insomnia . In this open label extension study, TBZ continued to effectively suppress chorea for up to 80 weeks in HD. TBZ was generally well tolerated, but treatment emergent AEs included sleep disturbance, depression, anxiety, and akathisia. Akathisia in particular may be difficult to identify due to confusion with chorea combined with the lack of insight associated with HD. During initiation and titration of therapy, patients may be more prone to sedation, insomnia and gastrointestinal problems but these tend to improve over time. Although clinicians should screen for and treat depression in all patients with HD, those with pre-existing depression may be at higher risk for developing depression while taking TBZ [23, 24].
In this study, there were no completed suicides, but one attempt listed as a serious AE and an additional subject who expressed suicidal ideation. Depression was not assessed by formal psychiatric criteria, but depressed mood was screened for using the Hamilton Depression Scale and item 25 of the UHDRS. During the double-blind phase of this study, there was a completed suicide in a subject randomized to the TBZ group, despite scoring within the normal range on the Hamilton Depression Scale two weeks prior to the event . Clinicians should be cautious about the heightened risk of suicide in HD regardless of depression indexes or use of monoamine depleters, as overall completed suicide rates are estimated at 7.3% and up to 25% of patients may attempt suicide at some point in the illness [25, 26]. In patients already diagnosed with HD, there may be an increased risk of suicide particularly when patients enter stage 2 of the disease, a time when independence diminishes .
At the conclusion of this study, the majority of participants were taking either 50 or 75 mg of TBZ. Notably, even after subjects had been on TBZ for over one year, dosage adjustments continued. In two other open-label, long term studies of TBZ used for a variety of hyperkinetic conditions including HD, the mean doses after more than two years were 60.4 and 106.2 mg, respectively [6, 7].
Discontinuation of TBZ after 80 weeks of treatment appears to be safe and is associated with the return of chorea, without significant worsening compared to baseline. Participants with higher baseline chorea scores experienced a greater reduction in chorea. When TBZ was discontinued, no subject developed signs consistent with neuroleptic withdrawal such as nausea, excessive sweating, tachycardia or akathisia. We did not identify AEs related to the withdrawal of TBZ, but other studies have specifically examined subjects when TBZ is stopped [9, 28]. One subject withdrew due to the development of "vocal tics". This AE has not been previously reported and in fact TBZ has been found to be an effective treatment of tics . It is possible that the "vocal tic" described was not a TBZ-related AE, but the emergence of tourettism as a symptom of HD .
Participants did not demonstrate a faster than expected rate of motor or functional decline due to HD. Although parkinsonism and dysphagia were increased in subjects at week 80, this finding was likely a result of the natural progression of disease. Had the parkinsonism been due to a pharmacological impact of tetrabenazine, we would have anticipated that the signs would have emerged more quickly and found on exams throughout the study. TBZ does not appear to have an effect on cognition or function after two years of therapy. Participants experienced an overall improvement on TBZ as demonstrated by the CGI at week 80, but there was no correlation to support the association of global improvement with either motor or chorea change. The UHDRS measures of cognition and function while taking TBZ declined at a rate consistent with the natural history of HD. The TFC scale declined 1.6 ± 0.4 points over almost two years in those initially assigned to TBZ, consistent with previously published measures of TFC [31, 32]. Although TBZ is unlikely to accelerate any aspect of decline in HD, it also does not appear to have any clinical long-term neuroprotective role, despite some evidence of potential neuroprotective effects demonstrated in animal models of HD .
The main limitation of this open-label study was the loss of subjects at each extension phase. The reasons for the attrition were related to administrative issues and a decision not to continue rather than any specific AEs. The majority of patients elected to complete 80 weeks on therapy, and in fact, once the study concluded, some subjects refused to stop taking TBZ and found other sources of the study medication prior to its availability on the US market. The findings support the clinical impression that chorea suppression in this large cohort of patients can be valuable to patients and families. The unblinded nature of this study limits the degree to which we can make conclusions about effectiveness, but the reduction in chorea was consistent with that seen in the double-blind trial. Further investigation is needed to determine the effectiveness and adverse event profile, particularly regarding cognition, when TBZ is combined with other commonly used medications.
Chorea, the most striking physical manifestation of HD, may be disabling and stigmatizing. Frequent or large amplitude involuntary movements can cause embarrassment or frustration and physical harm due to direct injury or falls as well as impact quality of life. The impact of suppressing chorea on weight, gait, behavior and functioning deserves further study, as do the indications for suppressing chorea in the ambulatory high functioning patient and the more advanced patient in whom chorea may be injurious. In lieu of discovering therapy that modifies the global course of the disease, identifying targeted symptomatic treatments for HD, such as those for chorea, is a way to palliate some of the more disabling and stigmatizing aspects of the disorder. This study confirms efficacy in long term use and may guide clinicians in dosing and treatment emergent, long-term adverse effects.
The authors thank the following individuals for their contributions to the conduct of this study:
Jan Bausch, BS; Stephen Bean, RPH; Sue Henderson, AAS; Letty Laskowski, BA; Margot Lutz, RN; Karen Rothenburgh; Arthur Watts, BS; Earl Westerlund (University of Rochester); Peggy Laird; Ben Lewis, PhD; Marion Yonce, MS; Kathryn Zunich, MD; and Jocelyn Catalla, BS (Prestwick Pharmaceuticals Inc.); and Clinical Research Consultants Amy T. Fletcher (Milan, IN); Timothy D. Foster (College Station, TX); and Daniel A. Rooney, Jr., BS (Portland, OR).
They also acknowledge the members of the Independent Data and Safety Monitoring Committee for this trial: Anthony Lang, MD (chair, University of Toronto); Michael McDermott, PhD; Pierre Tariot, MD; and Saleem Ismail, MD (University of Rochester). Thank you to Marcy MacDonald, PhD at Massachusetts General Hospital, Charlestown Labs for performing the DNA testing.
Huntington Study Group/TETRA-HD Investigators
Steering Committee: Frederick J. Marshall, MD (principal investigator, University of Rochester School of Medicine and Dentistry); Francis Walker, MD (co-principal investigator, Wake Forest University School of Medicine); Samuel Frank, MD (author, medical monitor, Boston University School of Medicine); David Oakes, PhD (chief biostatistician, University of Rochester School of Medicine and Dentistry); Sandra Plumb, BS (senior project coordinator, University of Rochester School of Medicine and Dentistry); Stewart A. Factor, DO (Emory University); Stanley Fahn, MD (Neurological Institute, Columbia University Medical Center); Victoria P. Hunt, RN (Wake Forest University School of Medicine); Joseph Jankovic, MD (Baylor College of Medicine); Aileen Shinaman, JD (University of Rochester School of Medicine and Dentistry); Ira Shoulson, MD (University of Rochester School of Medicine and Dentistry).
Participating Investigators and Coordinators: Jody Goldstein, BS; Jody Corey-Bloom, MD, PhD (University of California, San Diego); Marcia McCall, MS; Juan Sanchez-Ramos, MD, PhD (University of South Florida); Nonna Stepanov, MD; Sandra Kostyk, MD, PhD (Ohio State University); Constance Nickerson, LPN; Donald Higgins, MD (Albany Medical College); Joann Belden, RN; Joanne Wojcieszek, MD (Indiana University School of Medicine); Margaret Marie Cox, RN; Andrew Feigin, MD (North Shore-LIJ Health System); Dawn Radtke, RN; Martha Nance, MD (Hennepin County Medical Center); Christine Hunter, RN; William Ondo, MD (Baylor College of Medicine); Joan Harrison, RN; Claudia Testa, MD, PhD (Emory University School of Medicine); Penny Stanton, CCRP; Tetsuo Ashizawa, MD (University of Texas Medical Branch At Galveston); Jeana Jaglin, RN; Kathleen Shannon, MD (Rush University Medical Center); Mary Matthews, RN; Amy Colcher, MD (University of Pennsylvania); Mira Guzijan, MA; Michael Geschwind, MD, PhD (University of California, San Francisco); Lynn Bartos, RN; Karen Blindauer, MD (Medical College of Wisconsin); Kelly Dustin, RN; Karen Anderson, MD (University of Maryland School of Medicine); Chinekwu Anyanwu, MD; Philip Hanna, MD (New Jersey Neuroscience Institute).
Coordination Center and Biostatistics: Patricia Lindsay; Shirley Eberly, MS; (University of Rochester School of Medicine and Dentistry).
Prestwick Pharmaceuticals Inc. Authors: David Stamler, MD; Lucinda Wilson.
- Frank S, Marshall F, Plumb S, Oakes D, Shoulson I, Kieburtz K, the CARE-HD Investigators of the Huntington Study Group: Functional decline due to chorea in Huntington's disease. Neurology. 2004, 56 (suppl 3):Google Scholar
- Verhagen ML, Morris MJ, Farmer C, Gillespie M, Mosby K, Wuu J, Chase T: Huntington's disease: a randomized, controlled trial using the NMDA-antagonist amantadine. Neurology. 2002, 59: 694-699.View ArticleGoogle Scholar
- Adam OR, Jankovic J: Symptomatic treatment of Huntington disease. Neurotherapeutics. 2008, 5: 181-197. 10.1016/j.nurt.2008.01.008.View ArticlePubMedGoogle Scholar
- Phillips W, Shannon KM, Barker RA: The current clinical management of Huntington's disease. Mov Disord. 2008, 23: 1491-1504. 10.1002/mds.21971.View ArticlePubMedGoogle Scholar
- Roze E, Saudou F, Caboche J: Pathophysiology of Huntington's disease: from huntingtin functions to potential treatments. Curr Opin Neurol. 2008, 21: 497-503. 10.1097/WCO.0b013e328304b692.View ArticlePubMedGoogle Scholar
- Jankovic J, Beach J: Long-term effects of tetrabenazine in hyperkinetic movement disorders. Neurology. 1997, 48: 358-362.View ArticlePubMedGoogle Scholar
- Kenney C, Hunter C, Jankovic J: Long-term tolerability of tetrabenazine in the treatment of hyperkinetic movement disorders. Mov Disord. 2007, 22: 193-197. 10.1002/mds.21222.View ArticlePubMedGoogle Scholar
- Ondo WG, Tintner R, Thomas M, Jankovic J: Tetrabenazine Treatment for Huntington's Disease-Associated Chorea. Clinical Neuropharmacology. 2002, 25: 300-302. 10.1097/00002826-200211000-00003.View ArticlePubMedGoogle Scholar
- Huntington Study Group: Tetrabenazine as antichorea therapy in Huntington disease: a randomized controlled trial. Neurology. 2006, 66: 366-372. 10.1212/01.wnl.0000198586.85250.13.View ArticleGoogle Scholar
- Fasano A, Cadeddu F, Guidubaldi A, Piano C, Soleti F, Zinzi P, Bentivoglio AR: The long-term effect of tetrabenazine in the management of Huntington disease. Clin Neuropharmacol. 2008, 31: 313-318. 10.1097/WNF.0b013e318166da60.View ArticlePubMedGoogle Scholar
- Scherman D, Jaudon P, Henry JP: Characterization of the monoamine carrier of chromaffin granule membrane by binding of [2-3H]dihydrotetrabenazine. Proc Natl Acad Sci USA. 1983, 80: 584-588. 10.1073/pnas.80.2.584.View ArticlePubMedPubMed CentralGoogle Scholar
- Bagchi SP: Differential interactions of phencyclidine with tetrabenazine and reserpine affecting intraneuronal dopamine. Biochem Pharmacol. 1983, 32: 2851-2856. 10.1016/0006-2952(83)90388-X.View ArticlePubMedGoogle Scholar
- Pettibone DJ, Pflueger AB, Totaro JA: Tetrabenazine-induced depletion of brain monoamines: mechanism by which desmethylimipramine protects cortical norepinephrine. Eur J Pharmacol. 1984, 102: 431-436. 10.1016/0014-2999(84)90563-6.View ArticlePubMedGoogle Scholar
- Mehvar R, Jamali F: Concentration-effect relationships of tetrabenazine and dihydrotetrabenazine in the rat. J Pharm Sci. 1987, 76: 461-465. 10.1002/jps.2600760610.View ArticlePubMedGoogle Scholar
- Thibaut F, Faucheux BA, Marquez J, Villares J, Menard JF, Agid Y, Hirsch EC: Regional distribution of monoamine vesicular uptake sites in the mesencephalon of control subjects and patients with Parkinson's disease: a postmortem study using tritiated tetrabenazine. Brain Res. 1995, 692: 233-243. 10.1016/0006-8993(95)00674-F.View ArticlePubMedGoogle Scholar
- Kenney C, Hunter C, Davidson A, Jankovic J: Short-term effects of tetrabenazine on chorea associated with Huntington's disease. Mov Disord. 2007, 22: 10-13. 10.1002/mds.21161.View ArticlePubMedGoogle Scholar
- Scherman D, Henry JP: Reserpine binding to bovine chromaffin granule membranes. Characterization and comparison with dihydrotetrabenazine binding. Mol Pharmacol. 1984, 25: 113-122.PubMedGoogle Scholar
- Bonelli RM, Wenning GK: Pharmacological management of Huntington's disease: an evidence-based review. Curr Pharm Des. 2006, 12: 2701-2720. 10.2174/138161206777698693.View ArticlePubMedGoogle Scholar
- Huntington Study Group: Unified Huntington's Disease Rating Scale: reliability and consistency. Mov Disord. 1996, 11: 136-142. 10.1002/mds.870110204.View ArticleGoogle Scholar
- Barnes TR: A rating scale for drug-induced akathisia. Br J Psychiatry. 1989, 154: 672-676. 10.1192/bjp.154.5.672.View ArticlePubMedGoogle Scholar
- Fahn S, Elton RL, Members of the UPDRS Developmental Committee: Unified Parkinson's Disease Rating Scale. Recent development in Parkinson's disease. Edited by: Fahn S, Marsden CD, Calne DB, Goldstein M. 1987, Florham Park, NJ: Macmillan Healthcare Information, 2: 153-163.Google Scholar
- Hamilton M: A rating scale for depression. J Neurol Neurosurg Psychiatry. 1960, 23: 56-62. 10.1136/jnnp.23.1.56.View ArticlePubMedPubMed CentralGoogle Scholar
- Kenney C, Hunter C, Mejia N, Jankovic J: Is history of depression a contraindication to treatment with tetrabenazine?. Clin Neuropharmacol. 2006, 29: 259-264. 10.1097/01.WNF.0000228369.25593.35.View ArticlePubMedGoogle Scholar
- Schreiber W, Krieg JC, Eichhorn T: Reversal of tetrabenazine induced depression by selective noradrenaline (norepinephrine) reuptake inhibition. J Neurol Neurosurg Psychiatry. 1999, 67: 550-10.1136/jnnp.67.4.550.View ArticlePubMedPubMed CentralGoogle Scholar
- Di ML, Squitieri F, Napolitano G, Campanella G, Trofatter JA, Conneally PM: Suicide risk in Huntington's disease. J Med Genet. 1993, 30: 293-295. 10.1136/jmg.30.4.293.View ArticleGoogle Scholar
- Farrer LA: Suicide and attempted suicide in Huntington disease: implications for preclinical testing of persons at risk. Am J Med Genet. 1986, 24: 305-311. 10.1002/ajmg.1320240211.View ArticlePubMedGoogle Scholar
- Paulsen JS, Hoth KF, Nehl C, Stierman L: Critical periods of suicide risk in Huntington's disease. Am J Psychiatry. 2005, 162: 725-731. 10.1176/appi.ajp.162.4.725.View ArticlePubMedGoogle Scholar
- Frank S, Ondo W, Fahn S, Hunter C, Oakes D, Plumb S, Marshall F, Shoulson I, Eberly S, Walker F, Factor S, Hunt V, Shinaman A, Jankovic J: A study of chorea after tetrabenazine withdrawal in patients with Huntington disease. Clin Neuropharmacol. 2008, 31: 127-133. 10.1097/WNF.0b013e3180ca77ea.View ArticlePubMedGoogle Scholar
- Kenney C, Hunter C, Mejia N, Jankovic J: Tetrabenazine in the treatment of Tourette syndrome. J Ped Neurol. 2007, 5: 9-13.Google Scholar
- Jankovic J, Ashizawa T: Tourettism associated with Huntington's disease. Mov Disord. 1995, 10: 103-105. 10.1002/mds.870100116.View ArticlePubMedGoogle Scholar
- Safety and tolerability of the free-radical scavenger OPC-14117 in Huntington's disease. The Huntington Study Group. Neurology. 1998, 50: 1366-1373.Google Scholar
- Huntington Study Group: A randomized, placebo-controlled trial of coenzyme Q10 and remacemide in Huntington's disease. Neurology. 2001, 57: 397-404.Google Scholar
- Tang TS, Chen X, Liu J, Bezprozvanny I: Dopaminergic signaling and striatal neurodegeneration in Huntington's disease. J Neurosci. 2007, 27: 7899-7910. 10.1523/JNEUROSCI.1396-07.2007.View ArticlePubMedPubMed CentralGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2377/9/62/prepub
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