scholarly journals Inflammatory monocyte gene expression: trait or state marker in bipolar disorder?

Author(s):  
K. Becking ◽  
B. C. M. Haarman ◽  
R. F. Riemersma van der Lek ◽  
L. Grosse ◽  
W. A. Nolen ◽  
...  
2007 ◽  
Vol 1 (S1) ◽  
Author(s):  
Na Li ◽  
Baolin Wu ◽  
Peng Wei ◽  
Benhuai Xie ◽  
Yang Xie ◽  
...  

2010 ◽  
Vol 70 (8) ◽  
pp. 3034-3041 ◽  
Author(s):  
Hyun Goo Woo ◽  
Jeong-Hoon Lee ◽  
Jung-Hwan Yoon ◽  
Chung Yong Kim ◽  
Hyo-Suk Lee ◽  
...  

2020 ◽  
Vol 20 (7) ◽  
pp. 518-523
Author(s):  
Rugül Köse Çinar

Objective: Neuroserpin is a serine protease inhibitor predominantly expressed in the nervous system functioning mainly in neuronal migration and axonal growth. Neuroprotective effects of neuroserpin were shown in animal models of stroke, brain, and spinal cord injury. Postmortem studies confirmed the involvement of neuroserpin in Alzheimer’s disease. Since altered adult neurogenesis was postulated as an aetiological mechanism for bipolar disorder, the possible effect of neuroserpin gene expression in the disorder was evaluated. Methods: Neuroserpin mRNA expression levels were examined in the peripheral blood of bipolar disorder type I manic and euthymic patients and healthy controls using the polymerase chain reaction method. The sample comprised of 60 physically healthy, middle-aged men as participants who had no substance use disorder. Results: The gene expression levels of neuroserpin were found lower in the bipolar disorder patients than the healthy controls (p=0.000). The neuroserpin levels did not differ between mania and euthymia (both 96% down-regulated compared to the controls). Conclusion: Since we detected differences between the patients and the controls, not the disease states, the dysregulation in the neuroserpin gene could be interpreted as a result of the disease itself.


2014 ◽  
Vol 24 ◽  
pp. S155-S156
Author(s):  
C. Schartner ◽  
C.J. Scholz ◽  
H. Weber ◽  
L. Weissflog ◽  
A. Reif

Epigenomics ◽  
2021 ◽  
Author(s):  
Beatriz Garcia-Ruiz ◽  
Manuel Castro de Moura ◽  
Gerard Muntané ◽  
Lourdes Martorell ◽  
Elena Bosch ◽  
...  

Aim: To investigate DDR1 methylation in the brains of bipolar disorder (BD) patients and its association with DDR1 mRNA levels and comethylation with myelin genes. Materials & methods: Genome-wide profiling of DNA methylation (Infinium MethylationEPIC BeadChip) corrected for glial composition and DDR1 gene expression analysis in the occipital cortices of individuals with BD (n = 15) and healthy controls (n = 15) were conducted. Results: DDR1 5-methylcytosine levels were increased and directly associated with DDR1b mRNA expression in the brains of BD patients. We also observed that DDR1 was comethylated with a group of myelin genes. Conclusion: DDR1 is hypermethylated in BD brain tissue and is associated with isoform expression. Additionally, DDR1 comethylation with myelin genes supports the role of this receptor in myelination.


Sign in / Sign up

Export Citation Format

Share Document