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White matter damage and systemic inflammation in Parkinson’s disease
by
Lu, Cheng-Hsien
, Yang, I.-Hsiao
, Tsai, Nai-Wen
, Chiang, Pi-Ling
, Chen, Meng-Hsiang
, Chen, Pei-Chin
, Chen, Hsiu-Ling
, Lin, Wei-Che
in
Age
/ Aged
/ Animal Models
/ Anisotropy
/ Antigens
/ Apoptosis
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood-brain barrier
/ Brain
/ Brain - pathology
/ Care and treatment
/ Cell adhesion molecules
/ Cerebellum
/ Cloning
/ Cognitive ability
/ Cytokines
/ Demyelination
/ Diagnosis
/ Diffusion Tensor Imaging
/ Disease
/ Family medical history
/ Female
/ Humans
/ Inflammation
/ Inflammation - pathology
/ Magnetic resonance imaging
/ Male
/ Middle Aged
/ Movement disorders
/ Multiple sclerosis
/ Neurobiology
/ Neurobiology of disease
/ Neurodegenerative diseases
/ Neurology
/ Neurosciences
/ Parkinson disease
/ Parkinson Disease - pathology
/ Parkinson's disease
/ Peripheral blood
/ Research Article
/ Substantia alba
/ Systemic inflammation
/ Values
/ White blood cells
/ White Matter - pathology
/ White matter damage
/ Womens health
2017
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White matter damage and systemic inflammation in Parkinson’s disease
by
Lu, Cheng-Hsien
, Yang, I.-Hsiao
, Tsai, Nai-Wen
, Chiang, Pi-Ling
, Chen, Meng-Hsiang
, Chen, Pei-Chin
, Chen, Hsiu-Ling
, Lin, Wei-Che
in
Age
/ Aged
/ Animal Models
/ Anisotropy
/ Antigens
/ Apoptosis
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood-brain barrier
/ Brain
/ Brain - pathology
/ Care and treatment
/ Cell adhesion molecules
/ Cerebellum
/ Cloning
/ Cognitive ability
/ Cytokines
/ Demyelination
/ Diagnosis
/ Diffusion Tensor Imaging
/ Disease
/ Family medical history
/ Female
/ Humans
/ Inflammation
/ Inflammation - pathology
/ Magnetic resonance imaging
/ Male
/ Middle Aged
/ Movement disorders
/ Multiple sclerosis
/ Neurobiology
/ Neurobiology of disease
/ Neurodegenerative diseases
/ Neurology
/ Neurosciences
/ Parkinson disease
/ Parkinson Disease - pathology
/ Parkinson's disease
/ Peripheral blood
/ Research Article
/ Substantia alba
/ Systemic inflammation
/ Values
/ White blood cells
/ White Matter - pathology
/ White matter damage
/ Womens health
2017
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White matter damage and systemic inflammation in Parkinson’s disease
by
Lu, Cheng-Hsien
, Yang, I.-Hsiao
, Tsai, Nai-Wen
, Chiang, Pi-Ling
, Chen, Meng-Hsiang
, Chen, Pei-Chin
, Chen, Hsiu-Ling
, Lin, Wei-Che
in
Age
/ Aged
/ Animal Models
/ Anisotropy
/ Antigens
/ Apoptosis
/ Biomedical and Life Sciences
/ Biomedicine
/ Blood-brain barrier
/ Brain
/ Brain - pathology
/ Care and treatment
/ Cell adhesion molecules
/ Cerebellum
/ Cloning
/ Cognitive ability
/ Cytokines
/ Demyelination
/ Diagnosis
/ Diffusion Tensor Imaging
/ Disease
/ Family medical history
/ Female
/ Humans
/ Inflammation
/ Inflammation - pathology
/ Magnetic resonance imaging
/ Male
/ Middle Aged
/ Movement disorders
/ Multiple sclerosis
/ Neurobiology
/ Neurobiology of disease
/ Neurodegenerative diseases
/ Neurology
/ Neurosciences
/ Parkinson disease
/ Parkinson Disease - pathology
/ Parkinson's disease
/ Peripheral blood
/ Research Article
/ Substantia alba
/ Systemic inflammation
/ Values
/ White blood cells
/ White Matter - pathology
/ White matter damage
/ Womens health
2017
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White matter damage and systemic inflammation in Parkinson’s disease
Journal Article
White matter damage and systemic inflammation in Parkinson’s disease
2017
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Overview
Background
Systemic inflammation and white matter (WM) alterations have been noted as effects of Parkinson’s disease (PD). This study sought to evaluate WM integrity in PD patients using diffusion tensor imaging (DTI) and to assess its relationship with systemic inflammation.
Methods
Sixty-six patients with PD (23 men and 43 women) and 67 healthy volunteers (29 men and 38 women) underwent blood sampling to quantify inflammatory markers and DTI scans to determine fiber integrity. The inflammatory markers included leukocyte apoptosis, as well as cellular and serum adhesion molecules, in each peripheral blood sample. DTI-related indices [including fractional anisotropy (FA), axial diffusivity (AD), radial diffusivity (RD), and mean diffusivity (MD)] were derived from DTI scans. The resulting FA maps were compared using voxel-based statistics to determine differences between the PD and control groups. The differences in the DTI indices, clinical severity, and inflammatory markers were correlated.
Results
Exploratory group-wise comparison between the two groups revealed that the PD patients exhibited extensive DTI index differences. Low FA accompanied by high RD and MD, without significant differences in AD, suggesting a demyelination process, were found in the parietal, occipital, cerebellar, and insular WM of the PD patients. The declined DTI indices were significantly correlated with increased clinical disease severity, adhesion molecules, and leukocyte apoptosis.
Conclusions
Patients with PD experience WM integrity damage in vulnerable regions, and these impairments are associated with increased disease severity and systemic inflammation. The possible interactions among them may represent variant neuronal injuries and their consequent processes in PD.
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