Huaguang Yang1, Weiyin Vivian Liu2, Liang Li1, Zhi Wen1, Lanhua Hu1, XiaoGuang Luo3, and Yunfei Zha1
1Renmin Hospital of Wuhan University, Wuhan, China, 2MR Research, GE Healthcare, Wuhan, China, 3Department of Neurology, The First Affiliated Hospital of South University of Science and Technology, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, ShenZhen, China
Synopsis
Keywords: fMRI (resting state), Parkinson's Disease
Cerebellum
is responsible for posture and gait control. 65.93% of patients with multiple
system atrophy experienced FOG. Patients with the damaged cerebellar locomotor
region had gait-freezing-like symptoms, suggesting that the cerebellum may be
involved in the occurrence and development of FOG symptoms. This study
suggested that the cerebellum volume atrophy may be involved in FOG development
in MSA patients and subsequently induce functional abnormality in the
cerebellum-cerebral circuit. This study provided neuroimaging evidence for
clinical understanding of cerebellum role in MSA patients with FOG injury.
Introduction
Multiple
system atrophy (MSA) is a sporadic, adult-onset neurodegenerative disease
characterized by autonomic failure, parkinsonism, and cerebellar ataxia [1]. Freezing of gait(FOG)was
defined as “Brief, episodic absence or marked reduction of forward progression
of the feet despite the intention to walk [2].
Epidemiological studies reveal about 65.93% of MSA patients had experienced FOG
[3]. As one of the disabling gait
disorders, FOG may cause falls and in turn contributes to lower quality of
life. Identification of the neurological mechanism underpinning FOG will help
clinicians better understand FOG pathophysiology and
potentially select effective treatments
to alleviate symptoms. Neuroimaging studies found that the cerebellum, in
addition to pedunculopontine nucleus, is widely involved in fog regulation in
patients with Parkinson's disease [3]. A
recent study further found that patients with the damaged cerebellar locomotor
region had gait-freezing-like symptoms [4],
suggesting that the cerebellum may be involved in the occurrence and
development of FOG symptoms. Due to the key role of the cerebellum impairment
in MSA, the current study was to explore whether atrophy of cerebellar gray
matter volume and cerebellum-cerebral circuit related to FOG in multiple system
atrophy patients.Materials and Methods
43
MSA patients with FOG and 27 MSA patients without FOG diagnosed by clinic
doctors who specifies in Parkinson's disease and confirmed by the follow-up
study were included in this study,42 HCs were recruited
through advertisements but excluded after assessed exist of brain lesions based
on medical history and conventional MRI. All patients
underwent the resting state function magnetic resonance BOLD sequence and T1
BRAVO structural image 3.0T MRI scanner (Discovery MR750W, GE Healthcare). Volumes
of cerebellum subregions and cerebellum atrophy secondary cerebellum-cerebral
circuit were analyzed by SPM12 software embed in MATLAB. The relationship
between these changes and the severity of FOG score was further analyzed.Results
The
volume shrinkage in the right cerebellum VIII and
left cerebellum VI were the main manifestations in MSA patients with FOG
injury, an negative correlation was found between
FOG-Q scores and left cerebellum VI (Figure 1). A secondary FC analysis
based on the right cerebellum VIII and left
cerebellum VI as seeds revealed an increased FC
between lobule VIII and the left inferior
parietal lobule and left cerebellum
crus I; an increased FC between lobule VI and the bilateral
superior temporal gyrus, right medial frontal gyrus, left
rectus, left insula, right superior frontal
gyrus, left middle occipital gyrus and left middle cingulum cortex.Discussion
MSA
patients with or without fog showed significant different cerebellar gray
matter volume after controlling the interference of motor and non-motor
covariates. This suggested that cerebellar atrophy may be involved in the
regulation of FOG symptoms in MSA patients. MSA patients are distinct from
idiopathic PD patients with FOG injury. Our results were inconsistent with the
finding for patients with FOG of the abnormal cerebellar function rather than
cerebellar gray matter structure alteration. In present study, MSA patients
with FOG symptoms showed more widely damaged cerebellum subregions, including right
cerebellum VIII and cerebellum VI, than those without FOG. left cerebellum VI was the only cerebellum region
related to FOG severity in MSA patients. Furthermore, a second seed-based
functional connectivity method revealed the decreased cerebellar-cortical
“executive-control” and “visual-auditory” cortex. The relationship between the
FOG severity and decreased the cerebellum volume as well as weaker
cerebellum-cerebral circuit in the present study may explain that disturbances
of executive control in loading tasks can exacerbate the gait freezing.Conclusions
This
study suggested that the cerebellum volume atrophy may be involved in FOG
development in MSA patients and subsequently induce functional abnormality in
the cerebellum-cerebral circuit. This study provided neuroimaging evidence for
clinical understanding of cerebellum role in MSA patients with FOG injury.Acknowledgements
With
special thanks to Professor Xiaoguang Luo for her guidance on the conception of
the manuscript.References
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