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Consensus guidelines on the construct validity of rodent models of restless legs syndrome.
Salminen, Aaro V; Clemens, Stefan; García-Borreguero, Diego; Ghorayeb, Imad; Li, Yuqing; Manconi, Mauro; Ondo, William; Rye, David; Siegel, Jerome M; Silvani, Alessandro; Winkelman, John W; Allen, Richard P; Ferré, Sergi.
Afiliação
  • Salminen AV; Institute of Neurogenomics, Helmholtz Zentrum München GmbH - German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Clemens S; Institute of Human Genetics, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany.
  • García-Borreguero D; Department of Physiology, Brody School of Medicine, East Carolina University, Greenville, NC 27834, USA.
  • Ghorayeb I; Sleep Research Institute, 28036 Madrid, Spain.
  • Li Y; Département de Neurophysiologie Clinique, Pôle Neurosciences Cliniques, CHU de Bordeaux, 33076 Bordeaux, France.
  • Manconi M; Université de Bordeaux, Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, UMR 5287, 33076 Bordeaux, France.
  • Ondo W; CNRS, Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, UMR 5287, 33076 Bordeaux, France.
  • Rye D; Department of Neurology, Norman Fixel Institute for Neurological Diseases, College of Medicine, University of Florida, Gainesville, FL 32610, USA.
  • Siegel JM; Sleep Medicine Unit, Regional Hospital of Lugano, Neurocenter of Southern Switzerland, 6900 Lugano, Switzerland.
  • Silvani A; Faculty of Biomedical Sciences, Università della Svizzera Italiana, 6900 Lugano, Switzerland.
  • Winkelman JW; Department of Neurology, University Hospital Inselspital, 3010 Bern, Switzerland.
  • Allen RP; Houston Methodist Hospital Neurological Institute, Weill Cornell Medical School, Houston, TX 77070, USA.
  • Ferré S; Department of Neurology, Emory University School of Medicine, Atlanta, GA 30322, USA.
Dis Model Mech ; 15(8)2022 08 01.
Article em En | MEDLINE | ID: mdl-35946581
ABSTRACT
Our understanding of the causes and natural course of restless legs syndrome (RLS) is incomplete. The lack of objective diagnostic biomarkers remains a challenge for clinical research and for the development of valid animal models. As a task force of preclinical and clinical scientists, we have previously defined face validity parameters for rodent models of RLS. In this article, we establish new guidelines for the construct validity of RLS rodent models. To do so, we first determined and agreed on the risk, and triggering factors and pathophysiological mechanisms that influence RLS expressivity. We then selected 20 items considered to have sufficient support in the literature, which we grouped by sex and genetic factors, iron-related mechanisms, electrophysiological mechanisms, dopaminergic mechanisms, exposure to medications active in the central nervous system, and others. These factors and biological mechanisms were then translated into rodent bioequivalents deemed to be most appropriate for a rodent model of RLS. We also identified parameters by which to assess and quantify these bioequivalents. Investigating these factors, both individually and in combination, will help to identify their specific roles in the expression of rodent RLS-like phenotypes, which should provide significant translational implications for the diagnosis and treatment of RLS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome das Pernas Inquietas Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Animals Idioma: En Revista: Dis Model Mech Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome das Pernas Inquietas Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Limite: Animals Idioma: En Revista: Dis Model Mech Ano de publicação: 2022 Tipo de documento: Article