Interaction of systemic oxidative stress and mesial temporal network degeneration in Parkinson's disease with and without cognitive impairment

被引:21
作者
Chiang, Pi-Ling [1 ]
Chen, Hsiu-Ling [1 ]
Lu, Cheng-Hsien [2 ]
Chen, Yueh-Sheng [1 ]
Chou, Kun-Hsien [3 ]
Hsu, Tun-Wei [4 ]
Chen, Meng-Hsiang [1 ]
Tsai, Nai-Wen [2 ]
Li, Shau-Hsuan [5 ]
Lin, Wei-Che [1 ]
机构
[1] Chang Gung Univ, Dept Diagnost Radiol, Kaohsiung Chang Gung Mem Hosp, Coll Med, 123 Ta Pei Rd, Kaohsiung 83305, Taiwan
[2] Chang Gung Univ, Coll Med, Dept Neurol, Kaohsiung Chang Gung Mem Hosp, Kaohsiung, Taiwan
[3] Natl Yang Ming Univ, Brain Res Ctr, Taipei, Taiwan
[4] Taipei Vet Gen Hosp, Dept Radiol, Taipei, Taiwan
[5] Chang Gung Univ, Kaohsiung Chang Gung Mem Hosp, Dept Hematol & Oncol, Coll Med, Kaohsiung, Taiwan
关键词
Parkinson's disease; Systemic oxidative stress; Lymphocyte apoptosis; Mesial temporal network; Gray matter volume; Functional connectivity; Cognitive impairment; ALZHEIMERS-DISEASE; DIAGNOSTIC-CRITERIA; ALPHA-SYNUCLEIN; MATTER ATROPHY; BRAIN NETWORKS; DEMENTIA; INFLAMMATION; CONNECTIVITY; ACTIVATION;
D O I
10.1186/s12974-018-1317-z
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: To identify the vulnerable areas associated with systemic oxidative stress and further disruption of these vulnerable areas by measuring the associated morphology and functional network alterations in Parkinson's disease (PD) patients with and without cognitive impairment. Methods: This prospective study was approved by the institutional review board of KCGMH, and written informed consent was obtained. Between December 2010 and May 2015, 41 PD patients with different levels of cognitive functions and 29 healthy volunteers underwent peripheral blood sampling to quantify systemic oxidative stress, as well as T1W volumetric and resting state functional MRI (rs-fMRI) scans. Rs-fMRI was used to derive the healthy intrinsic connectivity patterns seeded by the vulnerable areas associated with any of the significant oxidative stress markers. The two groups were compared in terms of the functional connectivity correlation coefficient (fc-CC) and gray matter volume (GMV) of the network seeded by the vulnerable areas. Results: The levels of oxidative stress markers, including leukocyte apoptosis and adhesion molecules, were significantly higher in the PD group. Using whole-brain VBM-based correlation analysis, the bilateral mesial temporal lobes (MTLs) were identified as the most vulnerable areas associated with lymphocyte apoptosis (P < 0.005). We found that the MTL network of healthy subjects resembled the PD-associated atrophy pattern. Furthermore, reduced fc-CC and GMV were further associated with the aggravated cognitive impairment. Conclusion: The MTLs are the vulnerable areas associated with peripheral lymphocyte infiltration, and disruptions of the MTL functional network in both architecture and functional connectivity might result in cognitive impairments in Parkinson's disease.
引用
收藏
页数:11
相关论文
共 42 条
[1]  
Baba M, 1998, AM J PATHOL, V152, P879
[2]   Resting-State Functional Brain Networks in Parkinson's Disease [J].
Baggio, Hugo C. ;
Segura, Barbara ;
Junque, Carme .
CNS NEUROSCIENCE & THERAPEUTICS, 2015, 21 (10) :793-801
[3]   Cognitive Impairment and Resting-State Network Connectivity in Parkinson's Disease [J].
Baggio, Hugo-Cesar ;
Segura, Barbara ;
Sala-Llonch, Roser ;
Marti, Maria-Jose ;
Valldeoriola, Francesc ;
Compta, Yaroslau ;
Tolosa, Eduardo ;
Junque, Carme .
HUMAN BRAIN MAPPING, 2015, 36 (01) :199-212
[4]   Oxidative-stress-induced apoptosis in PBLs of two patients with Parkinson disease secondary to alpha-synuclein mutation [J].
Battisti, Carla ;
Forinichi, Patrizia ;
Radi, Elena ;
Federico, Antonio .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2008, 267 (1-2) :120-124
[5]   Longitudinal Inflammation, Cognitive Decline, and Alzheimer's Disease: A Mini-Review [J].
Bettcher, B. M. ;
Kramer, J. H. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2014, 96 (04) :464-469
[6]   Infiltration of CD4+ lymphocytes into the brain contributes to neurodegeneration in a mouse model of Parkinson disease [J].
Brochard, Vanessa ;
Combadiere, Behazine ;
Prigent, Annick ;
Laouar, Yasmina ;
Perrin, Aline ;
Beray-Berthat, Virginie ;
Bonduelle, Olivia ;
Alvarez-Fischer, Daniel ;
Callebert, Jacques ;
Launay, Jean-Marie ;
Duyckaerts, Charles ;
Flavell, Richard A. ;
Hirsch, Etienne C. ;
Hunot, Stephane .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (01) :182-192
[7]   Gray matter atrophy associated with mild cognitive impairment in Parkinson's disease [J].
Chen, Fu-Xiang ;
Kang, De-Zhi ;
Chen, Fu-Yong ;
Liu, Ying ;
Wu, Gang ;
Li, Xun ;
Yu, Liang-Hong ;
Lin, Yuan-Xiang ;
Lin, Zhang-Ya .
NEUROSCIENCE LETTERS, 2016, 617 :160-165
[8]   Plasma DNA Mediate Autonomic Dysfunctions and White Matter Injuries in Patients with Parkinson's Disease [J].
Chen, Meng-Hsiang ;
Chen, Pei-Chin ;
Lu, Cheng-Hsien ;
Chen, Hsiu-Ling ;
Chao, Yi-Ping ;
Li, Shau-Hsuan ;
Chen, Yi-Wen ;
Lin, Wei-Che .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2017, 2017
[9]   Associations among Cognitive Functions, Plasma DNA, and White Matter Integrity in Patients with Early-Onset Parkinson's Disease [J].
Chen, Yueh-Sheng ;
Chen, Meng-Hsiang ;
Lu, Cheng-Hsien ;
Chen, Pei-Chin ;
Chen, Hsiu-Ling ;
Yang, I-Hsiao ;
Tsai, Nai-Wen ;
Lin, Wei-Che .
FRONTIERS IN NEUROSCIENCE, 2017, 11
[10]   White matter damage and systemic inflammation in Parkinson's disease [J].
Chiang, Pi-Ling ;
Chen, Hsiu-Ling ;
Lu, Cheng-Hsien ;
Chen, Pei-Chin ;
Chen, Meng-Hsiang ;
Yang, I. -Hsiao ;
Tsai, Nai-Wen ;
Lin, Wei-Che .
BMC NEUROSCIENCE, 2017, 18