scholarly journals Structural Brain MR Imaging Changes Associated with Obsessive-Compulsive Disorder in Patients with Multiple Sclerosis

2012 ◽  
Vol 34 (2) ◽  
pp. 305-309 ◽  
Author(s):  
E. Tinelli ◽  
A. Francia ◽  
E.M. Quartuccio ◽  
M. Morreale ◽  
G.M. Contessa ◽  
...  
1994 ◽  
Vol 11 (1) ◽  
pp. 26-27 ◽  
Author(s):  
Aideen Freyne ◽  
Rory K Shelley

AbstractA patient who developed obsessive compulsive disorder within a year of developing multiple sclerosis is described. Possible reasons for an association between these two conditions are discussed. The role of serotonergic pathway dysfunction in obsessive compulsive disorder is also suggested by the pharmacological response in this case.


Author(s):  
Rabia Bilici ◽  
Nuray Türksoy Karalı ◽  
Nevin Sütlaş ◽  
Demet Kuşçu ◽  
Rıdvan Bilici

2020 ◽  
Author(s):  
Ali Sepehrinezhad ◽  
Ali Bozorgmehr ◽  
Sajad Sahab Negah ◽  
Minoo Karimi ◽  
Ali Shahbazi

Abstract Background: Multiple sclerosis (MS) is an autoimmune, inflammatory demyelinating, and disabling disorder of the central nervous system (CNS) with various clinical symptoms. Approximately 30% of the patients experience a variety of psychiatric problems during their disease course. Obsessive-compulsive disorder (OCD) is correlated with MS, but little is known about common molecular mechanisms of two diseases. Methods: In this study, after a comprehensive review of the existing literature, we collected almost all the genes involved in MS and OCD, and then analyzed the common genes between MS and OCD. Next, the connections and functional interactions between these three gene sets were investigated in the STRING database and analyzed in 3 separate networks by Cytoscape software. Eventually, after a multi-part enrichment analysis, we found the main molecular and cellular pathways, biological processes, brain areas, and, more importantly, cells/tissue related to the shared genes between MS and OCD. Results: Three genes of brain-derived neurotrophic factor (BDNF), tumor necrosis factor-alpha (TNFα), and neurexin-1 (NRXN1) are the major genes that were common between MS and OCD. Also, the deficit in synaptogenesis and neurotransmitter release in the nervous system are the most common complications of MS and OCD. Signaling receptor activity and estrogen receptor activity are the most important signaling pathways that are disturbed. Moreover, the presynaptic membrane, membrane raft, and growth cone are the main microenvironments that are affected in MS and OCD.Conclusions: In addition to an enrichment analysis that showed physical and functional interactions of genes related to MS and OCD, we demonstrated and predicted some new genes and microRNAs that can be promising biomarkers/targets for future experimental studies. Also, our finding indicated that neuroinflammation and synaptic plasticity are two significant pathological processes that are affected in MS and OCD.


2009 ◽  
Vol 10 (4-3) ◽  
pp. 956-960 ◽  
Author(s):  
Athanassios Douzenis ◽  
Panayiota G. Michalopoulou ◽  
Constantine Voumvourakis ◽  
Maria Typaldou ◽  
Ioannis Michopoulos ◽  
...  

2004 ◽  
Vol 61 (7) ◽  
pp. 720 ◽  
Author(s):  
Jesús Pujol ◽  
Carles Soriano-Mas ◽  
Pino Alonso ◽  
Narcís Cardoner ◽  
José M. Menchón ◽  
...  

2003 ◽  
Vol 13 ◽  
pp. S456
Author(s):  
T. Sobanski ◽  
G. Wagner ◽  
U. Gruhn ◽  
A. Herwig ◽  
R. Tauber ◽  
...  

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