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Effectiveness of anti-psychotics and related drugs in the Huntington French-speaking group cohort.
Désaméricq, Gaëlle; Dolbeau, Guillaume; Verny, Christophe; Charles, Perrine; Durr, Alexandra; Youssov, Katia; Simonin, Clémence; Azulay, Jean-Philippe; Tranchant, Christine; Goizet, Cyril; Damier, Philippe; Broussolle, Emmanuel; Demonet, Jean-François; Morgado, Graca; Cleret de Langavant, Laurent; Macquin-Mavier, Isabelle; Bachoud-Lévi, Anne-Catherine; Maison, Patrick.
Affiliation
  • Désaméricq G; Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Service de Pharmacologie Clinique, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France ; Département d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France.
  • Dolbeau G; Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Unité de recherche clinique, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Verny C; Centre de référence des maladies neurogénétiques, service de neurologie, CHU d'Angers, Angers, France ; UMR CNRS 6214 - INSERM U1083, Angers, France.
  • Charles P; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France ; Département de génétique, Hôpital de la salpêtrière, AP-HP, Paris, France.
  • Durr A; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Youssov K; Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Département d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France ; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Simonin C; Departement of Neurology and Movement Disorders, CHRU Lille, Lille, France ; UMR837 INSERM - JPArc Team 6, Lille, France ; University Lille 2/Law & Health, Lille, France.
  • Azulay JP; Service de Neurologie et pathologie du mouvement, Hôpital de la Timone, Marseille, France.
  • Tranchant C; Service de Neurologie, CHU Hautepierre, Strasbourg, France ; Université de Strasbourg, Strasbourg, France.
  • Goizet C; Université Bordeaux Segalen, Laboratoire Maladies Rares: Génétique et Métabolisme (MRGM), EA4576, CHU Bordeaux, Service de Génétique médicale, Bordeaux, France.
  • Damier P; Centre d'Investigation Clinique 004, Inserm, Nantes, France.
  • Broussolle E; Faculté de Médecine et de Maïeutique Lyon Sud Charles Mérieux, Université Lyon I, Lyon, France ; Service de Neurologie C, Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Lyon, France ; Centre de Neurosciences Cognitives, UMR5229, CNRS, Bron, France.
  • Demonet JF; Centre Leenaards de la Mémoire, Département des Neurosciences Cliniques, CHUV, Lausanne, Switzerland.
  • Morgado G; Faculté de médecine, Université Paris Est, Créteil, France ; Centre d'Investigation Clinique 006, Inserm, Créteil, France ; Pôle Recherche clinique Santé Publique, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Cleret de Langavant L; Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Département d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France ; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Macquin-Mavier I; Faculté de médecine, Université Paris Est, Créteil, France ; Service de Pharmacologie Clinique, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Bachoud-Lévi AC; Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Département d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France ; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
  • Maison P; Equipe 01, U955, Inserm, Créteil, France ; Faculté de médecine, Université Paris Est, Créteil, France ; Département d'Etudes Cognitives, Ecole Normale Supérieure, Paris, France ; Centre de référence Maladie de Huntington, Hôpital H. Mondor - A. Chenevier, AP-HP, Créteil, France.
PLoS One ; 9(1): e85430, 2014.
Article in En | MEDLINE | ID: mdl-24454865
ABSTRACT

PURPOSE:

Huntington's disease is a rare condition. Patients are commonly treated with antipsychotics and tetrabenazine. The evidence of their effect on disease progression is limited and no comparative study between these drugs has been conducted. We therefore compared the effectiveness of antipsychotics on disease progression.

METHODS:

956 patients from the Huntington French Speaking Group were followed for up to 8 years between 2002 and 2010. The effectiveness of treatments was assessed using Unified Huntington's Disease Rating Scale (UHDRS) scores and then compared using a mixed model adjusted on a multiple propensity score.

RESULTS:

63% of patients were treated with antipsychotics during the survey period. The most commonly prescribed medications were dibenzodiazepines (38%), risperidone (13%), tetrabenazine (12%) and benzamides (12%). There was no difference between treatments on the motor and behavioural declines observed, after taking the patient profiles at the start of the drug prescription into account. In contrast, the functional decline was lower in the dibenzodiazepine group than the other antipsychotic groups (Total Functional Capacity 0.41 ± 0.17 units per year vs. risperidone and 0.54 ± 0.19 vs. tetrabenazine, both p<0.05). Benzamides were less effective than other antipsychotics on cognitive evolution (Stroop interference, Stroop color and Literal fluency p<0.05).

CONCLUSIONS:

Antipsychotics are widely used to treat patients with Huntington's disease. Although differences in motor or behavioural profiles between patients according to the antipsychotics used were small, there were differences in drug effectiveness on the evolution of functional and cognitive scores.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antipsychotic Agents / Huntington Disease Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: PLoS One Year: 2014 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Antipsychotic Agents / Huntington Disease Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Country/Region as subject: Europa Language: En Journal: PLoS One Year: 2014 Document type: Article