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Unraveling the Heterogeneity of ALS-A Call to Redefine Patient Stratification for Better Outcomes in Clinical Trials.
Tzeplaeff, Laura; Jürs, Alexandra V; Wohnrade, Camilla; Demleitner, Antonia F.
Afiliação
  • Tzeplaeff L; Department of Neurology, Rechts der Isar Hospital, Technical University of Munich, 81675 München, Germany.
  • Jürs AV; Translational Neurodegeneration Section "Albrecht Kossel", Department of Neurology, University Medical Center Rostock, 18057 Rostock, Germany.
  • Wohnrade C; Department of Neurology, Hannover Medical School, 30625 Hannover, Germany.
  • Demleitner AF; Department of Neurology, Rechts der Isar Hospital, Technical University of Munich, 81675 München, Germany.
Cells ; 13(5)2024 Mar 05.
Article em En | MEDLINE | ID: mdl-38474416
ABSTRACT
Despite tremendous efforts in basic research and a growing number of clinical trials aiming to find effective treatments, amyotrophic lateral sclerosis (ALS) remains an incurable disease. One possible reason for the lack of effective causative treatment options is that ALS may not be a single disease entity but rather may represent a clinical syndrome, with diverse genetic and molecular causes, histopathological alterations, and subsequent clinical presentations contributing to its complexity and variability among individuals. Defining a way to subcluster ALS patients is becoming a central endeavor in the field. Identifying specific clusters and applying them in clinical trials could enable the development of more effective treatments. This review aims to summarize the available data on heterogeneity in ALS with regard to various aspects, e.g., clinical, genetic, and molecular.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Revista: Cells Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Lateral Amiotrófica Limite: Humans Idioma: En Revista: Cells Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Alemanha