Parkinson's disease: From human genetics to clinical trials

Sci Transl Med. 2015 Sep 16;7(305):205ps20. doi: 10.1126/scitranslmed.aaa8280.

Abstract

Combining genetic insights into the pathogenesis of Parkinson's disease (PD) with findings from animal and cellular models of this disorder has advanced our understanding of the pathways that lead to the characteristic degeneration of dopaminergic neurons in the brain's nigrostriatal pathway. This has fueled an increase in candidate compounds designed to modulate these pathways and to alter the processes underlying neuronal death in this disorder. Using mitochondrial quality control and the macroautophagy/lysosomal pathways as examples, we discuss the pipeline from a comprehensive genetic architecture for PD through to clinical trials for drugs targeting pathways linked to neurodegeneration in PD. We also identify opportunities and pitfalls on the road to a clinically effective disease-modifying treatment for this disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Clinical Trials as Topic
  • Dopamine / metabolism
  • Dopaminergic Neurons / metabolism
  • Drug Design
  • Gene Expression Regulation
  • Genetic Predisposition to Disease
  • Humans
  • Lysosomes / metabolism
  • Mitochondria / metabolism
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / physiopathology
  • Parkinson Disease / drug therapy*
  • Parkinson Disease / genetics*
  • Substantia Nigra / metabolism
  • Substantia Nigra / physiopathology

Substances

  • Biomarkers
  • Dopamine