TY - JOUR
T1 - Altered thalamo-cortical white matter connectivity
T2 - Probabilistic tractography study in clinical-high risk for psychosis and first-episode psychosis
AU - Cho, Kang Ik K.
AU - Shenton, Martha E.
AU - Kubicki, Marek
AU - Jung, Wi Hoon
AU - Lee, Tae Young
AU - Yun, Je Yeon
AU - Kim, Sung Nyun
AU - Kwon, Jun Soo
N1 - Publisher Copyright:
© The Author 2015. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Disrupted thalamo-cortical connectivity is regarded as a core psychopathology in patients diagnosed with schizophrenia. However, whether the thalamo-cortical white matter connectivity is disrupted before the onset of psychosis is still unknown. To determine this gap in knowledge, the strength of thalamo-cortical white matter anatomical connectivity in subjects at clinical-high risk for psychosis (CHR) was compared to that of first-episode psychosis (FEP) and healthy controls. A total of 37 CHR, 21 FEP, and 37 matched healthy controls underwent diffusion-weighted magnetic resonance imaging to examine the number of probabilistic tractography "counts" representing thalamo-cortical white matter connectivity. We also investigated the relationship with psychopathology. For FEP, the connectivity between the thalamus and parietal cortex was significantly increased (F = 5.65, P <. 05) compared to that of healthy controls. However, the connectivity between thalamus and orbitofrontal cortex was significantly reduced compared to both healthy controls (F = 11.86, P <. 005) and CHR (F = 6.63, P <. 05). Interestingly, CHR exhibited a similar pattern as FEP, albeit with slightly reduced magnitude. Compared to healthy controls, there was a significant decrease (F = 4.16, P <. 05) in CHR thalamo-orbitofrontal connectivity. Also, the strength of the thalamo-orbitofrontal connectivity was correlated with the Global Assessment of Functioning score in CHR (r =. 35, P <. 05). This observed pattern of white matter connectivity disruptions in FEP and in CHR suggests that this pattern of disconnectivity not only highlights the involvement of thalamus but also might be useful as an early biomarker for psychosis.
AB - Disrupted thalamo-cortical connectivity is regarded as a core psychopathology in patients diagnosed with schizophrenia. However, whether the thalamo-cortical white matter connectivity is disrupted before the onset of psychosis is still unknown. To determine this gap in knowledge, the strength of thalamo-cortical white matter anatomical connectivity in subjects at clinical-high risk for psychosis (CHR) was compared to that of first-episode psychosis (FEP) and healthy controls. A total of 37 CHR, 21 FEP, and 37 matched healthy controls underwent diffusion-weighted magnetic resonance imaging to examine the number of probabilistic tractography "counts" representing thalamo-cortical white matter connectivity. We also investigated the relationship with psychopathology. For FEP, the connectivity between the thalamus and parietal cortex was significantly increased (F = 5.65, P <. 05) compared to that of healthy controls. However, the connectivity between thalamus and orbitofrontal cortex was significantly reduced compared to both healthy controls (F = 11.86, P <. 005) and CHR (F = 6.63, P <. 05). Interestingly, CHR exhibited a similar pattern as FEP, albeit with slightly reduced magnitude. Compared to healthy controls, there was a significant decrease (F = 4.16, P <. 05) in CHR thalamo-orbitofrontal connectivity. Also, the strength of the thalamo-orbitofrontal connectivity was correlated with the Global Assessment of Functioning score in CHR (r =. 35, P <. 05). This observed pattern of white matter connectivity disruptions in FEP and in CHR suggests that this pattern of disconnectivity not only highlights the involvement of thalamus but also might be useful as an early biomarker for psychosis.
KW - clinical high risk
KW - first-episode psychosis
KW - schizophrenia
KW - thalamus
KW - tractographythalamocortical
UR - http://www.scopus.com/inward/record.url?scp=84966295056&partnerID=8YFLogxK
U2 - 10.1093/schbul/sbv169
DO - 10.1093/schbul/sbv169
M3 - Article
C2 - 26598740
AN - SCOPUS:84966295056
SN - 0586-7614
VL - 42
SP - 723
EP - 731
JO - Schizophrenia Bulletin
JF - Schizophrenia Bulletin
IS - 3
ER -