Subcortical Structures and Neuropsychiatric Illness

1996 ◽  
Vol 2 (1) ◽  
pp. 66-75 ◽  
Author(s):  
Stephen Salloway ◽  
Jeffrey Cummings

Subcortical structures play an important role in modulating mood, drive, memory, executive functions, and cognitive timing. Subcortical structures are intimately linked with the frontal lobe and limbic system. Key subcortical structures regulating behavior include the caudate nucleus, the ventral striatum, the ventral pallidum, and the dorsomedial and reticular nuclei of the thalamus. Some degenerative diseases affect subcortical nuclear and white matter structures, causing involuntary movements and abnormal behavior. Primary psychiatric illnesses, such as obsessive-compulsive disorder, have been proposed to arise from dysfunction in the frontostriatal-thalamic circuits. The neuroanatomical and neurochemical organization of these subcortical systems mediating complex behaviors and the interactions between behavioral and motor systems are increasingly well understood. Undoubtedly, our newer understanding of subcortical systems will help us to unravel the pathophysiology of some neuropsychiatric disorders.

2009 ◽  
Vol 12 (2) ◽  
pp. 142-148 ◽  
Author(s):  
Yoon-Mi Hur

AbstractA growing literature suggests that personality traits may be endophenotype markers for psychiatric illnesses. Although the phenotypic relationships between obsessive–compulsive disorder (OCD) and high neuroticism and low extraversion have been well documented, underlying genetic and environmental contributions to these associations have not been explored previously. Five hundred and twenty-four monozygoitc (MZ) and 228 dizygotic (DZ) pairs of adolescent and young adult twins (aged 13–24 years) drawn from the South Korean Twin Registry completed the Maudsley Obsessive Compulsive Inventory (MOCI) and the Neuroticism and Extraversion scale of the Eysenck Personality Scale by mail. The total score of MOCI (MOCIT) was significantly and positively correlated with Neuroticism (r= .44), but only weakly and negatively related to Extraversion (r= –.10). A trivariate Cholesky model was applied to the data. The additive genetic correlations in the best-fitting model were .51 between Neuroticism and MOCIT and –.17 between Extraversion and MOCIT, suggesting that additive genetic factors that lead to high neuroticism and low extraversion overlap with those genetic factors influencing high OC symptoms. These findings add to the cumulative evidence of the shared genetic etiology for the associations between a personality profile of high neuroticism and low extraversion and mental illnesses.


2015 ◽  
Vol 25 (11) ◽  
pp. 1898-1905 ◽  
Author(s):  
Yoshinari Abe ◽  
Yuki Sakai ◽  
Seiji Nishida ◽  
Takashi Nakamae ◽  
Kei Yamada ◽  
...  

2019 ◽  
Vol 9 (9) ◽  
pp. 220 ◽  
Author(s):  
Baldermann ◽  
Bohn ◽  
Hammes ◽  
Schüller ◽  
Visser-Vandewalle ◽  
...  

Recent approaches have suggested that deep brain stimulation (DBS) for obsessive-compulsive disorder relies on distributed networks rather than local brain modulation. However, there is insufficient data on how DBS affects brain metabolism both locally and globally. We enrolled three patients with treatment-refractory obsessive-compulsive disorder with ongoing DBS of the bilateral ventral capsule/ventral striatum. Patients underwent resting-state 18F-fluorodeoxyglucose and positron emission tomography in both stimulation ON and OFF conditions. All subjects showed relative hypometabolism in prefronto-basal ganglia-thalamic networks compared to a healthy control cohort when stimulation was switched OFF. Switching the stimulation ON resulted in differential changes in brain metabolism. Locally, volumes of activated tissue at stimulation sites (n = 6) showed a significant increase in metabolism during DBS ON compared to DBS OFF (Mean difference 4.5 % ± SD 2.8; p = 0.012). Globally, differential changes were observed across patients encompassing prefrontal increase in metabolism in ON vs. OFF condition. Bearing in mind limitations of the small sample size, we conclude that DBS of the ventral capsule/ventral striatum for obsessive-compulsive disorder increases brain metabolism locally. Across distributed global networks, DBS appears to exert differential effects, possibly depending on localization of stimulation sites and response to the intervention.


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