TY - JOUR
T1 - Associations of leptin and corticostriatal connectivity in bipolar disorder
AU - Wei, Shyh Yuh
AU - Tseng, Huai Hsuan
AU - Chang, Hui Hua
AU - Chang, Wei Hung
AU - Yang, Yen Kuang
AU - Chen, Po See
N1 - Funding Information:
The authors thank all the participants in this study and extend particular appreciation to Chien Ting Lin and Yi-Han Han from National Cheng Kung University for their technical and experimental assistance. They thank the Mind Research and Imaging Center (MRIC) at National Cheng Kung University for consultation and instrument availability. The MRIC is supported by the Ministry of Science and Technology.
Funding Information:
This work was supported by the National Science and Technology Council, Taiwan (MOST 108-2320-B-006-004, MOST 108-2314-B-006-045, MOST 110-2320-B-006-022, MOST 107-2314-B-006-082, MOST 108-2628-B-006-004, MOST 107-2320-B-006-071) and National Cheng Kung University Hospital (NCKUH-11004018).
Funding Information:
The authors thank all the participants in this study and extend particular appreciation to Chien Ting Lin and Yi-Han Han from National Cheng Kung University for their technical and experimental assistance. They thank the Mind Research and Imaging Center (MRIC) at National Cheng Kung University for consultation and instrument availability. The MRIC is supported by the Ministry of Science and Technology.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Bipolar disorder (BD) and metabolic disturbance represent a chronic state of low-grade inflammation and corticostriatal circuitry alterations. Herein, we aimed to investigate whether plasma leptin, an adipokine that plays a key role in the interplay of metabolism and inflammation, is associated with corticostriatal connectivity in patients with BD. Twenty-eight BD I patients, 36 BD II patients and 66 healthy controls were enrolled and completed the Hamilton Depression Rating Scale, the Young Mania Rating Scale, and the Recent Life Change Questionnaire. Fasting plasma leptin and C-reactive protein (CRP) levels were measured, and corticostriatal connectivity was examined using functional magnetic resonance imaging (fMRI). The relationships between leptin, CRP and body mass index (BMI) identified in the controls and BD II patients were absent in the BD I patients. We did not find a significant group difference in the leptin level; nevertheless, the negative correlation between leptin level and corticostriatal connectivity (ventrolateral prefrontal cortex and inferior temporal gyrus) observed in the healthy controls was absent in the BD patients. The disproportionate increase in leptin level with increasing BMI in BD indicated a potential inflammatory role of white adipose tissue in BD. Furthermore, higher CRP levels in BD I patients might induce leptin resistance. Collectively, our results implied vulnerability to inflammatory and metabolic diseases in patients with BD, especially BD I.
AB - Bipolar disorder (BD) and metabolic disturbance represent a chronic state of low-grade inflammation and corticostriatal circuitry alterations. Herein, we aimed to investigate whether plasma leptin, an adipokine that plays a key role in the interplay of metabolism and inflammation, is associated with corticostriatal connectivity in patients with BD. Twenty-eight BD I patients, 36 BD II patients and 66 healthy controls were enrolled and completed the Hamilton Depression Rating Scale, the Young Mania Rating Scale, and the Recent Life Change Questionnaire. Fasting plasma leptin and C-reactive protein (CRP) levels were measured, and corticostriatal connectivity was examined using functional magnetic resonance imaging (fMRI). The relationships between leptin, CRP and body mass index (BMI) identified in the controls and BD II patients were absent in the BD I patients. We did not find a significant group difference in the leptin level; nevertheless, the negative correlation between leptin level and corticostriatal connectivity (ventrolateral prefrontal cortex and inferior temporal gyrus) observed in the healthy controls was absent in the BD patients. The disproportionate increase in leptin level with increasing BMI in BD indicated a potential inflammatory role of white adipose tissue in BD. Furthermore, higher CRP levels in BD I patients might induce leptin resistance. Collectively, our results implied vulnerability to inflammatory and metabolic diseases in patients with BD, especially BD I.
UR - http://www.scopus.com/inward/record.url?scp=85144332206&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85144332206&partnerID=8YFLogxK
U2 - 10.1038/s41598-022-26233-8
DO - 10.1038/s41598-022-26233-8
M3 - Article
C2 - 36535988
AN - SCOPUS:85144332206
SN - 2045-2322
VL - 12
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 21898
ER -