21
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Comparing Risperidone and Olanzapine to Tetrabenazine for the Management of Chorea in Huntington Disease: An Analysis from the Enroll‐HD Database

      research-article

      Read this article at

      ScienceOpenPublisherPMC
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          Introduction

          Huntington's chorea (HC) is commonly managed with neuroleptic medications, though there is little evidence to support their use. This study aimed to perform a real‐world comparison of the efficacy of risperidone and olanzapine to tetrabenazine (TBZ) for HC.

          Methods

          The Enroll‐HD database was used to perform a propensity score‐matched comparison of risperidone and olanzapine to TBZ, regarding their efficacy in controlling chorea. Participants with motor manifest Huntington's disease (HD) were grouped according to their use of risperidone, olanzapine, or TBZ. For the three groups, independent propensity score matching was performed on participants’ baseline total functional score (TFC), baseline total motor score (TMS), disease burden score, CAG repeat length, baseline age, region, sex, and body mass index. Independent samples t test was used to calculate the differences between the groups in the annual rate of change of the TMS from the baseline to the second available visit.

          Results

          The risperidone (n = 72) and olanzapine groups (n = 77) had annualized increases (worsening) in the TMS of only 1.47 points and 3.20 points, respectively, compared to 5.70 points in the two matched TBZ groups (n = 72) ( P = 0.019) and (n = 77) ( P = 0.143), respectively.

          Conclusions

          In the absence of prospective data, this analysis of the Enroll‐HD database found that the neuroleptics risperidone and olanzapine seemed to at least be comparable to TBZ at controlling HC. These results demonstrate that neuroleptics may have comparable efficacy to TBZ for the treatment of HC. Further prospective studies are needed to confirm these findings.

          Related collections

          Most cited references17

          • Record: found
          • Abstract: found
          • Article: not found

          A randomized evaluation of the effects of six antipsychotic agents on QTc, in the absence and presence of metabolic inhibition.

          Many drugs have been associated with QTc prolongation and, in some cases, this is augmented by concomitant administration with metabolic inhibitors. The effects of 6 antipsychotics on the QTc interval at and around the time of estimated peak plasma/serum concentrations in the absence and presence of metabolic inhibition were characterized in a prospective, randomized study in which patients with psychotic disorders reached steady-state on either haloperidol 15 mg/d (n = 27), thioridazine 300 mg/d (n = 30), ziprasidone 160 mg/d (n = 31), quetiapine 750 mg/d (n = 27), olanzapine 20 mg/d (n = 24), or risperidone 6-8 mg/d increased to 16 mg/d (n = 25/20). Electrocardiograms (ECGs) were done at estimated Cmax at steady-state on both antipsychotic monotherapy and after concomitant administration of appropriate cytochrome P-450 (CYP450) inhibitor(s). Mean QTc intervals did not exceed 500 milliseconds in any patient taking any of the antipsychotics studied, in the absence or presence of metabolic inhibition. The mean QTc interval change was greatest in the thioridazine group, both in the presence and absence of metabolic inhibition. The presence of metabolic inhibition did not significantly augment QTc prolongation associated with any agent. Each of the antipsychotics studied was associated with measurable QTc prolongation at steady-state peak plasma concentrations, which was not augmented by metabolic inhibition. The theoretical risk of cardiotoxicity associated with QTc prolongation should be balanced against the substantial clinical benefits associated with atypical antipsychotics and the likelihood of other toxicities.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found

            Body weight is a robust predictor of clinical progression in Huntington disease.

            Unintended weight loss is a hallmark of Huntington disease (HD), but it is unknown to what extent weight loss impacts the rate of disease progression. Therefore, using longitudinal data from the Enroll-HD study, we assessed the association between baseline body mass index (BMI) and the rate of clinical progression in 5,821 HD mutation carriers. We found that high baseline BMI was associated with a significantly slower rate of functional, motor, and cognitive deterioration (all p < 0.001), independent of mutant HTT CAG repeat size. Our findings provide strong rationale for exploration of systemic metabolism as a therapeutic target in HD. Ann Neurol 2017;82:479-483.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Current Pharmacological Approaches to Reduce Chorea in Huntington’s Disease

              There are currently no effective pharmacological agents available to stop or prevent the progression of Huntington’s disease (HD), a rare hereditary neurodegenerative disorder. In addition to psychiatric symptoms and cognitive impairments, HD causes progressive motor disturbances, in particular choreiform movements, which are characterized by unwanted contractions of the facial muscles, trunk and extremities. Management of choreiform movements is usually advised if chorea interferes with daily functioning, causes social isolation, gait instability, falls, or physical injury. Although drugs to reduce chorea are available, only few randomized controlled studies have assessed the efficacy of these drugs, resulting in a high variety of prescribed drugs in clinical practice. The current pharmacological treatment options to reduce chorea in HD are outlined in this review, including the latest results on deutetrabenazine, a newly developed pharmacological agent similar to tetrabenazine, but with suggested less peak dose side effects. A review of the existing literature was conducted using the PubMed, Cochrane and Medline databases. In conclusion, mainly tetrabenazine, tiapride (in European countries), olanzapine, and risperidone are the preferred first choice drugs to reduce chorea among HD experts. In the existing literature, these drugs also show a beneficial effect on motor symptom severity and improvement of psychiatric symptoms. Generally, it is recommended to start with a low dose and increase the dose with close monitoring of any adverse effects. New interesting agents, such as deutetrabenazine and pridopidine, are currently under development and more randomized controlled trials are warranted to assess the efficacy on chorea severity in HD.
                Bookmark

                Author and article information

                Contributors
                Jordan-schultz@uiowa.edu
                Journal
                Mov Disord Clin Pract
                Mov Disord Clin Pract
                10.1002/(ISSN)2330-1619
                MDC3
                Movement Disorders Clinical Practice
                John Wiley and Sons Inc. (Hoboken )
                2330-1619
                30 November 2018
                February 2019
                : 6
                : 2 ( doiID: 10.1002/mdc3.2019.6.issue-2 )
                : 132-138
                Affiliations
                [ 1 ] Department of Psychiatry The University of Iowa Hospitals and Clinics Iowa City IA United States
                [ 2 ] Department of Neurology The University of Iowa Hospitals and Clinics Iowa City IA United States
                [ 3 ] Department of Pharmaceutical Care The University of Iowa Hospitals and Clinics Iowa City IA United States
                [ 4 ] Stead Family Department of Pediatrics The University of Iowa Hospitals and Clinics Iowa City IA United States
                [ 5 ] The Veteran's Affairs Medical Center Iowa City IA United States
                Author notes
                [*] [* ] Correspondence to: Jordan L. Schultz, PharmD, MSCS, BCACP, Assistant Professor of Psychiatry & Neurology, The Carver College of Medicine at the University of Iowa, 200 Hawkins Drive, 8921 JPP, Iowa City, IA 52242; Jordan-schultz@ 123456uiowa.edu
                Article
                PMC6384174 PMC6384174 6384174 MDC312706
                10.1002/mdc3.12706
                6384174
                30838312
                1422378c-609b-4691-b0a9-6ee2f3eeb694
                © 2018 International Parkinson and Movement Disorder Society
                History
                : 16 April 2018
                : 09 October 2018
                : 30 October 2018
                Page count
                Figures: 1, Tables: 4, Pages: 20, Words: 5002
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                mdc312706
                February 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.5.9 mode:remove_FC converted:21.02.2019

                chorea,olanzapine,tetrabenazine,Enroll‐HD,risperidone,Huntington's disease

                Comments

                Comment on this article