Literature DB >> 30017248

Impaired topographic organization in cognitively unimpaired drug-naïve patients with rigidity-dominant Parkinson's disease.

Yanbing Hou1, Qianqian Wei1, Ruwei Ou1, Jing Yang1, Wei Song1, Qiyong Gong2, Huifang Shang3.   

Abstract

BACKGROUND: Resting-state functional magnetic resonance imaging (fMRI) and graph theory approaches have been combined to investigate the topographic organization in Parkinson's disease (PD).
METHOD: Twenty cognitively unimpaired drug-naïve patients with rigidity-dominant PD (PDAR) and 20 age-, sex-, and education-matched healthy controls were included. Small-world profile and topographic properties (clustering coefficient (Cp), characteristic path length (Lp), local efficiency (Eloc), global efficiency (Eglob), nodal efficiency (Enod), nodal degree (NDeg), and nodal betweenness (NBet)) were measured and compared between two groups, with age, gender and education as covariates. Correlation analyses between topographic features and the unified PD rating scale part-III (UPDRS-III) scores, cognitive scores were performed.
RESULTS: PDAR patients presented the small-world property, and abnormalities at the nodal level (Enod, NDeg, and NBet) but not at the global level (Cp, Lp, Eloc, and Eglob). Our results revealed lower nodal centralities mainly in the occipital lobe and areas of the limbic system (including amygdala nucleus), and higher nodal centralities in distributed frontal and temporal regions. Notably, the decreased nodal efficiency of occipital regions (including the calcarine area, lingual area and superior occipital gyrus (SOG)) was negatively correlated with UPDRS-III scores. And the nodal efficiency of the calcarine area was positively correlated with visuospatial scores.
CONCLUSION: Our results may provide insights into the underlying pathophysiology of PDAR and aid the development of potential biomarkers of the disease progression and cognitive decline in PDAR patients.
Copyright © 2018. Published by Elsevier Ltd.

Entities:  

Keywords:  Graph theory; Parkinson's disease; Resting-state fMRI; Subtype

Mesh:

Year:  2018        PMID: 30017248     DOI: 10.1016/j.parkreldis.2018.06.021

Source DB:  PubMed          Journal:  Parkinsonism Relat Disord        ISSN: 1353-8020            Impact factor:   4.891


  8 in total

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  8 in total

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