Comparison of cerebral blood flow in patients with major depressive disorder and Parkinson’s disease with depression

2017 ◽  
Vol 381 ◽  
pp. 802
Author(s):  
Y.D. Kim ◽  
S. In-Uk
2009 ◽  
Vol 25 (1) ◽  
pp. 44-49 ◽  
Author(s):  
Takeshi Inoue ◽  
Mayumi Kitagawa ◽  
Teruaki Tanaka ◽  
Shin Nakagawa ◽  
Tsukasa Koyama

2020 ◽  
Author(s):  
Angela A Tran ◽  
Myra De Smet ◽  
Gary D. Grant ◽  
Tien K. Khoo ◽  
Dean L Pountney

Major depressive disorder (MDD) affects more than cognition, having a temporal relationship with neuroinflammatory pathways of Parkinson’s disease (PD). Although this association is supported by epidemiological and clinical studies, the underlying mechanisms are unclear. Microglia and astrocytes play crucial roles in the pathophysiology of both MDD and PD. In PD, these cells can be activated by misfolded forms of the protein α-synuclein to release cytokines that can interact with multiple different physiological processes to produce depressive symptoms, including monoamine transport and availability, the hypothalamus-pituitary axis, and neurogenesis. In MDD, glial cell activation can be induced by peripheral inflammatory agents that cross the blood brain barrier and/or c-Fos signaling from neurons. The resulting neuroinflammation can cause neurodegeneration due to oxidative stress and glutamate excitotoxicity, contributing to PD pathology. Astrocytes are another major link due to their recognised role in the glymphatic clearance mechanism. Research suggesting that MDD causes astrocytic destruction or structural atrophy highlight the possibility that accumulation of α-synuclein in the brain is facilitated as the brain cannot adequately clear the protein aggregates. This review examines research into the overlapping pathophysiology of MDD and PD with particular focus on the roles of glial cells and neuroinflammation.


2017 ◽  
Vol 41 (S1) ◽  
pp. S225-S225
Author(s):  
Z. Hou ◽  
Z. Wang ◽  
W. Jiang ◽  
Y. Yin ◽  
Y. Yue ◽  
...  

ObjectiveThe potential pattern of regional cerebral blood flow (rCBF) in major depressive disorder (MDD) underlies different response to antidepressants medication remain unclear. This study aimed to investigate the differences of rCBF between patients with different treatment response.MethodsEighty MDD patients [(44 treatment-responsive depression (RD) and 36 non-responding depression (NRD)] and 42 healthy controls (HC) underwent pulsed arterial spin labeling (PASL) scans in magnetic resonance imaging and clinical estimates. The exact rCBF values of each groups were obtained via quantification evaluation.ResultsCompared to NRD, the RD patients showed decreased rCBF values in frontal sensorimotor network (i.e. left paracentral lobule, left medial frontal gyrus, right superior frontal gyrus and right middle frontal gyrus), and further receiver operating curve (ROC) analyses demonstrated that the altered rCBF in these four regions exhibited outstanding performance on distinguishing NRD from RD. The NRD also exhibited reduced rCBF in bilateral cerebellum posterior lobe and right middle occipital gyrus and elevated rCBF in right postcentral gyrus and right middle frontal gyrus as compared to HC.ConclusionsThe decreased rCBF in frontal sensorimotor network appeared to be distinct characteristics for NRD, and might be severed as promising neuroimaging markers to differentiate depressed patients with weak early response to antidepressant medication. These findings expand our understanding of neural substrate underlying the antidepressant efficacy.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2013 ◽  
Vol 25 (4) ◽  
pp. 343-345 ◽  
Author(s):  
Domenico De Berardis ◽  
Michele Fornaro ◽  
Nicola Serroni ◽  
Luigi Olivieri ◽  
Stefano Marini ◽  
...  

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