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Peripheral mitochondrial function correlates with clinical severity in idiopathic Parkinson's disease.
Milanese, Chiara; Payán-Gómez, César; Galvani, Marta; Molano González, Nicolás; Tresini, Maria; Nait Abdellah, Soraya; van Roon-Mom, Willeke M C; Figini, Silvia; Marinus, Johan; van Hilten, Jacobus J; Mastroberardino, Pier G.
Afiliación
  • Milanese C; Department of Molecular Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Payán-Gómez C; Department of Molecular Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Galvani M; Faculty of Natural Sciences and Mathematics, Universidad del Rosario, Bogotá, Colombia.
  • Molano González N; Department of Mathematics, University of Pavia, Pavia, Italy.
  • Tresini M; Center for Autoimmune Diseases Research, School of Medicine and Health Sciences, Universidad del Rosario, Bogotá, Colombia.
  • Nait Abdellah S; Department of Molecular Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • van Roon-Mom WMC; Department of Molecular Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Figini S; Human Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Marinus J; Political and Social Sciences, University of Pavia, Pavia, Italy.
  • van Hilten JJ; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Mastroberardino PG; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
Mov Disord ; 34(8): 1192-1202, 2019 08.
Article en En | MEDLINE | ID: mdl-31136028
ABSTRACT

BACKGROUND:

Parkinson's disease is an intractable disorder with heterogeneous clinical presentation that may reflect different underlying pathogenic mechanisms. Surrogate indicators of pathogenic processes correlating with clinical measures may assist in better patient stratification. Mitochondrial function, which is impaired in and central to PD pathogenesis, may represent one such surrogate indicator.

METHODS:

Mitochondrial function was assessed by respirometry experiment in fibroblasts derived from idiopathic patients (n = 47) in normal conditions and in experimental settings that do not permit glycolysis and therefore force energy production through mitochondrial function. Respiratory parameters and clinical measures were correlated with bivariate analysis. Machine-learning-based classification and regression trees were used to classify patients on the basis of biochemical and clinical measures. The effects of mitochondrial respiration on α-synuclein stress were assessed monitoring the protein phosphorylation in permitting versus restrictive glycolysis conditions.

RESULTS:

Bioenergetic properties in peripheral fibroblasts correlate with clinical measures in idiopathic patients, and the correlation is stronger with predominantly nondopaminergic signs. Bioenergetic analysis under metabolic stress, in which energy is produced solely by mitochondria, shows that patients' fibroblasts can augment respiration, therefore indicating that mitochondrial defects are reversible. Forcing energy production through mitochondria, however, favors α-synuclein stress in different cellular experimental systems. Machine-learning-based classification identified different groups of patients in which increasing disease severity parallels higher mitochondrial respiration.

CONCLUSION:

The suppression of mitochondrial activity in PD may be an adaptive strategy to cope with concomitant pathogenic factors. Moreover, mitochondrial measures in fibroblasts are potential peripheral biomarkers to follow disease progression. © 2019 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Metabolismo Energético / Alfa-Sinucleína / Fibroblastos / Mitocondrias Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Parkinson / Metabolismo Energético / Alfa-Sinucleína / Fibroblastos / Mitocondrias Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2019 Tipo del documento: Article