Literature DB >> 22544535

Therapy in Huntington's disease: where are we?

Martha A Nance1.   

Abstract

As of 2012, almost 20 years after the discovery of the causative gene, clinical research has yet to find a disease-modifying treatment for Huntington's disease. However, both pharmacologic and nonpharmacologic therapies are available for many of the common symptoms of the disease. Recent studies of gene-positive patients in the prodromal, not clinically diagnosable, stages of the disease, are changing our perception of when the process of neurodegeneration begins. Once disease-modifying therapies become available, the approach to the diagnosis of Huntington's disease will likely shift from an examination-based clinical diagnosis, to one that includes a more complex combination of imaging, examination, and biomarker analysis.

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Year:  2012        PMID: 22544535     DOI: 10.1007/s11910-012-0277-4

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  58 in total

1.  Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres.

Authors:  Maartje C Van Rij; Marjan De Rademaeker; Céline Moutou; Jos C F M Dreesen; Martine De Rycke; Inge Liebaers; Joep P M Geraedts; Christine E M De Die-Smulders; Stéphane Viville
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

2.  Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data.

Authors:  Sarah J Tabrizi; Ralf Reilmann; Raymund A C Roos; Alexandra Durr; Blair Leavitt; Gail Owen; Rebecca Jones; Hans Johnson; David Craufurd; Stephen L Hicks; Christopher Kennard; Bernhard Landwehrmeyer; Julie C Stout; Beth Borowsky; Rachael I Scahill; Chris Frost; Douglas R Langbehn
Journal:  Lancet Neurol       Date:  2011-12-02       Impact factor: 44.182

3.  Efficacy and safety of the dopaminergic stabilizer Pridopidine (ACR16) in patients with Huntington's disease.

Authors:  Anders Lundin; Espen Dietrichs; Sara Haghighi; Marie-Louise Göller; Arvid Heiberg; Ghada Loutfi; Håkan Widner; Klas Wiktorin; Leif Wiklund; Anders Svenningsson; Clas Sonesson; Nicholas Waters; Susanna Waters; Joakim Tedroff
Journal:  Clin Neuropharmacol       Date:  2010 Sep-Oct       Impact factor: 1.592

4.  Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot study.

Authors:  Paola Zinzi; Dario Salmaso; Rosa De Grandis; Graziano Graziani; Stefano Maceroni; Annarita Bentivoglio; Paolo Zappata; Marina Frontali; Gioia Jacopini
Journal:  Clin Rehabil       Date:  2007-07       Impact factor: 3.477

5.  Two years' follow-up of rivastigmine treatment in Huntington disease.

Authors:  Marina de Tommaso; Olimpia Difruscolo; Vittorio Sciruicchio; Nicola Specchio; Paolo Livrea
Journal:  Clin Neuropharmacol       Date:  2007 Jan-Feb       Impact factor: 1.592

6.  Use of oral nutritional supplements in patients with Huntington's disease.

Authors:  Araceli Trejo; Marie-Catherine Boll; Ma Elisa Alonso; Adriana Ochoa; Leora Velásquez
Journal:  Nutrition       Date:  2005-09       Impact factor: 4.008

7.  Adherence to use of a home-based exercise DVD in people with Huntington disease: participants' perspectives.

Authors:  Hanan Khalil; Lori Quinn; Robert van Deursen; Richard Martin; Anne Rosser; Monica Busse
Journal:  Phys Ther       Date:  2011-09-29

8.  Fall risk assessment using the Tinetti mobility test in individuals with Huntington's disease.

Authors:  Anne D Kloos; Deb A Kegelmeyer; Gregory S Young; Sandra K Kostyk
Journal:  Mov Disord       Date:  2010-12-15       Impact factor: 10.338

9.  Falls and gait disturbances in Huntington's disease.

Authors:  Yvette A M Grimbergen; Mirjam J Knol; Bastiaan R Bloem; Berry P H Kremer; Raymund A C Roos; Marten Munneke
Journal:  Mov Disord       Date:  2008-05-15       Impact factor: 10.338

Review 10.  Therapeutic interventions for disease progression in Huntington's disease.

Authors:  Tiago Mestre; Joaquim Ferreira; Miguel M Coelho; Mário Rosa; Cristina Sampaio
Journal:  Cochrane Database Syst Rev       Date:  2009-07-08
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  5 in total

1.  Recent advances in the management of choreas.

Authors:  Jean-Marc Burgunder
Journal:  Ther Adv Neurol Disord       Date:  2013-03       Impact factor: 6.570

2.  Experimental models for identifying modifiers of polyglutamine-induced aggregation and neurodegeneration.

Authors:  Barbara Calamini; Donald C Lo; Linda S Kaltenbach
Journal:  Neurotherapeutics       Date:  2013-07       Impact factor: 7.620

Review 3.  Huntington Disease in Asia.

Authors:  Miao Xu; Zhi-Ying Wu
Journal:  Chin Med J (Engl)       Date:  2015-07-05       Impact factor: 2.628

Review 4.  A systematic review and meta-analysis of strength training in individuals with multiple sclerosis or Parkinson disease.

Authors:  Travis M Cruickshank; Alvaro R Reyes; Melanie R Ziman
Journal:  Medicine (Baltimore)       Date:  2015-01       Impact factor: 1.889

5.  The Q175 mouse model of Huntington's disease shows gene dosage- and age-related decline in circadian rhythms of activity and sleep.

Authors:  Dawn H Loh; Takashi Kudo; Danny Truong; Yingfei Wu; Christopher S Colwell
Journal:  PLoS One       Date:  2013-07-30       Impact factor: 3.240

  5 in total

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