ACC Glu/GABA ratio is decreased in euthymic bipolar disorder I patients: possible in vivo neurometabolite explanation for mood stabilization

Author(s):  
Estêvão Scotti-Muzzi ◽  
Thais Chile ◽  
Ricardo Moreno ◽  
Bruno Fraccini Pastorello ◽  
Cláudia da Costa Leite ◽  
...  
2009 ◽  
Vol 2 (2) ◽  
Author(s):  
Thomas Martin Doring ◽  
Tadeu Takao Almodovar Kubo ◽  
Juliana Rodrigues Doring ◽  
Jiosef Fainberg ◽  
Mario Juruena ◽  
...  

2007 ◽  
Vol 116 (6) ◽  
pp. 467-472 ◽  
Author(s):  
A. Fornito ◽  
G. S. Malhi ◽  
J. Lagopoulos ◽  
B. Ivanovski ◽  
S. J. Wood ◽  
...  

2019 ◽  
Vol 45 (6) ◽  
pp. 1367-1378 ◽  
Author(s):  
Ellen Ji ◽  
Pamela Guevara ◽  
Miguel Guevara ◽  
Antoine Grigis ◽  
Nicole Labra ◽  
...  

Abstract Schizophrenia (SZ) and bipolar disorder (BD) are often conceptualized as “disconnection syndromes,” with substantial evidence of abnormalities in deep white matter tracts, forming the substrates of long-range connectivity, seen in both disorders. However, the study of superficial white matter (SWM) U-shaped short-range tracts remained challenging until recently, although findings from postmortem studies suggest they are likely integral components of SZ and BD neuropathology. This diffusion weighted imaging (DWI) study aimed to investigate SWM microstructure in vivo in both SZ and BD for the first time. We performed whole brain tractography in 31 people with SZ, 32 people with BD and 54 controls using BrainVISA and Connectomist 2.0. Segmentation and labeling of SWM tracts were performed using a novel, comprehensive U-fiber atlas. Analysis of covariances yielded significant generalized fractional anisotropy (gFA) differences for 17 SWM bundles in frontal, parietal, and temporal cortices. Post hoc analyses showed gFA reductions in both patient groups as compared with controls in bundles connecting regions involved in language processing, mood regulation, working memory, and motor function (pars opercularis, insula, anterior cingulate, precentral gyrus). We also found increased gFA in SZ patients in areas overlapping the default mode network (inferior parietal, middle temporal, precuneus), supporting functional hyperconnectivity of this network evidenced in SZ. We thus illustrate that short U-fibers are vulnerable to the pathological processes in major psychiatric illnesses, encouraging improved understanding of their anatomy and function.


2019 ◽  
Vol 88 (3) ◽  
pp. 171-176 ◽  
Author(s):  
Samuel Sarrazin ◽  
Cyril Poupon ◽  
Achille Teillac ◽  
Jean-François Mangin ◽  
Mircea Polosan ◽  
...  

2015 ◽  
Vol 77 (6) ◽  
pp. 581-588 ◽  
Author(s):  
Unn K. Haukvik ◽  
Lars T. Westlye ◽  
Lynn Mørch-Johnsen ◽  
Kjetil N. Jørgensen ◽  
Elisabeth H. Lange ◽  
...  
Keyword(s):  

2018 ◽  
Vol 14 (1) ◽  
pp. 37-45 ◽  
Author(s):  
Germano Orrù ◽  
Mauro Giovanni Carta

Background:Bipolar Disorder (BD), along with depression and schizophrenia, is one of the most serious mental illnesses, and one of the top 20 causes of severe impairment in everyday life. Recent molecular studies, using both traditional approaches and new procedures such as Whole-Genome Sequencing (WGS), have suggested that genetic factors could significantly contribute to the development of BD, with heritability estimates of up to 85%. However, it is assumed that BD is a multigenic and multifactorial illness with environmental factors that strongly contribute to disease development/progression, which means that progress in genetic knowledge of BD might be difficult to interpret in clinical practice.Objective:The aim of this study is to provide a synthetic description of the main SNPs variants identified/confirmed by recent extensive WGS analysis as well as by reconstruction in anin vitromechanism or by amygdala activation protocolin vivo.Method:Bibliographic data, genomic and protein Data Banks were consulted so as to carry out a cross genomic study for mutations, SNPs and chromosomal alterations described in these studies in BD patients.Results:Fifty-five different mutations have been described in 30 research papers by different genetic analyses including recent WGS analysis. Many of these studies have led to the discovery of the most probable susceptibility genes for BD, including ANK3, CACNA1C, NCAN, ODZ4, SYNE1, and TRANK1. Exploration has started the role of several of these mutations in BD pathophysiology usingin vitroand animal models.Conclusion:Although new genomic research technology in BD opens up new possibilities, the current results for common variants are still controversial because of four broad conditions: analytical validity, clinical validity, clinical utility and a reasonable cost for genetic analysis are not yet accessible.


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