Frontiers in Neurology (Mar 2019)

Why Is Aging a Risk Factor for Cognitive Impairment in Parkinson's Disease?—A Resting State fMRI Study

  • Atsuko Nagano-Saito,
  • Atsuko Nagano-Saito,
  • Pierre Bellec,
  • Pierre Bellec,
  • Alexandru Hanganu,
  • Alexandru Hanganu,
  • Alexandru Hanganu,
  • Alexandru Hanganu,
  • Stevan Jobert,
  • Béatriz Mejia-Constain,
  • Clotilde Degroot,
  • Clotilde Degroot,
  • Anne-Louise Lafontaine,
  • Anne-Louise Lafontaine,
  • Anne-Louise Lafontaine,
  • Anne-Louise Lafontaine,
  • Jennifer I. Lissemore,
  • Kelly Smart,
  • Chawki Benkelfat,
  • Oury Monchi,
  • Oury Monchi,
  • Oury Monchi,
  • Oury Monchi,
  • Oury Monchi,
  • Oury Monchi

DOI
https://doi.org/10.3389/fneur.2019.00267
Journal volume & issue
Vol. 10

Abstract

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Using resting-state functional MRI (rsfMRI) data of younger and older healthy volunteers and patients with Parkinson's disease (PD) with and without mild cognitive impairment (MCI) and applying two different analytic approaches, we investigated the effects of age, pathology, and cognition on brain connectivity. When comparing rsfMRI connectivity strength of PD patients and older healthy volunteers, reduction between multiple brain regions in PD patients with MCI (PD-MCI) compared with PD patients without MCI (PD-non-MCI) was observed. This group difference was not affected by the number and location of clusters but was reduced when age was included as a covariate. Next, we applied a graph-theory method with a cost-threshold approach to the rsfMRI data from patients with PD with and without MCI as well as groups of younger and older healthy volunteers. We observed decreased hub function (measured by degree and betweenness centrality) mainly in the medial prefrontal cortex (mPFC) in older healthy volunteers compared with younger healthy volunteers. We also found increased hub function in the posterior medial structure (precuneus and the cingulate cortex) in PD-non-MCI patients compared with older healthy volunteers and PD-MCI patients. Hub function in these posterior medial structures was positively correlated with cognitive function in all PD patients. Together these data suggest that overlapping patterns of hub modifications could mediate the effect of age as a risk factor for cognitive decline in PD, including age-related reduction of hub function in the mPFC, and recruitment availability of the posterior medial structure, possibly to compensate for impaired basal ganglia function.

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