Evidence map›Paper›PMID 30967835›Full record

ArticleFrontiers in neurology2019

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

Atsuko Nagano-Saito, Pierre Bellec, Alexandru Hanganu, Stevan Jobert, Béatriz Mejia-Constain, Clotilde Degroot, Anne-Louise Lafontaine, Jennifer I Lissemore, Kelly Smart, Chawki Benkelfat and 1 more

Abstract read
In one paragraph

Article in Frontiers in neurology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Atsuko Nagano-SaitoCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.
Pierre BellecCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.
Alexandru HanganuCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.
Stevan JobertCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.
Béatriz Mejia-ConstainCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.
Clotilde DegrootCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.
Anne-Louise LafontaineDepartment of Neurology & Neurosurgery, and Psychiatry, McGill University, Montreal, QC, Canada.
Jennifer I LissemoreDepartment of Neurology & Neurosurgery, and Psychiatry, McGill University, Montreal, QC, Canada.
Kelly SmartDepartment of Neurology & Neurosurgery, and Psychiatry, McGill University, Montreal, QC, Canada.
Chawki BenkelfatDepartment of Neurology & Neurosurgery, and Psychiatry, McGill University, Montreal, QC, Canada.
Oury MonchiCentre de Recherche, Institut Universitaire de Gériatrie de Montréal, Montreal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

agecognitionfunctional connectivitymild cognitive impairmentneuroimaging (functional)Parkinson's disease

Identifiers

PMID30967835
PMCPMC6438889

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.