4.5 Article

Meynert nucleus-related cortical thinning in Parkinson's disease with mild cognitive impairment

期刊

出版社

AME PUBL CO
DOI: 10.21037/qims-20-444

关键词

Parkinson's disease (PD); cholinergic system; cognitive impairment; nucleus basalis of Meynert; cortical thickness

资金

  1. National Natural Science Foundation of China [82071419, 81501112]
  2. Guangzhou Municipal People's Livelihood Science and Technology Project [201803010085]
  3. High-level Hospital Construction Project [DFJH201907]
  4. Supporting Research Funds for Outstanding Young Medical Talents in Guangdong Province [KJ012019442]
  5. Medical Research Fund of Guangdong Province, China [A2017317]
  6. National Key R&D Program of China [2017YFC1310200]

向作者/读者索取更多资源

The study found a positive correlation between NBM/Ch4 volume and cortical thickness in PD-MCI patients, particularly in the bilateral posterior cingulate, parietal, and frontal regions as well as the left insular region. The stronger correlation between NBM/Ch4 volume loss and cortical thinning in PD-MCI patients suggests a potentially important role of NBM/Ch4 in PD cognitive impairment.
Background: Cognitive impairment in Parkinson's disease (PD) involves the cholinergic system and cholinergic neurons, especially the nucleus basalis of Meynert (NBM/Ch4) located in the basal forebrain (BF). We analyzed associations between NBM/Ch4 volume and cortical thickness to determine whether the NBM/Ch4-innervated neocortex shows parallel atrophy with the NBM/Ch4 as disease progresses in PD patients with cognitive impairment (PD-MCI). Methods: We enrolled 35 PD-MCI patients, 48 PD patients with normal cognition (PD-NC), and 33 ageand education-matched healthy controls (HCs), with all participants undergoing neuropsychological assessment and structural magnetic resonance imaging (MRI). Correlation analyses between NBM/Ch4 volume and cortical thickness and correlation coefficient comparisons were conducted within and across groups. Results: In the PD-MCI group, NBM/Ch4 volume was positively correlated with cortical thickness in the bilateral posterior cingulate, parietal, and frontal and left insular regions. Based on correlation coefficient comparisons, the atrophy of NBM/Ch4 was more correlated with the cortical thickness of right posterior cingulate and precuneus, anterior cingulate and medial orbitofrontal lobe in PD-MCI versus HC, and the right medial orbitofrontal lobe and anterior cingulate in PD-NC versus HC. Further partial correlations between cortical thickness and NBM/Ch4 volume were significant in the right medial orbitofrontal (PD NC: r=0.3, P=0.045; PD-MCI: r=0.51, P=0.003) and anterior cingulate (PD-NC: r=0.41, P=0.006; PD-MCI: r=0.43, P=0.013) in the PD groups and in the right precuneus (r=0.37, P=0.04) and posterior cingulate (r=0.46, P=0.008) in the PD-MCI group. Conclusions: The stronger correlation between NBM/Ch4 and cortical thinning in PD-MCI patients suggests that NBM/Ch4 volume loss may play an important role in PD cognitive impairment.

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