Haichen Yang1, Linling Li2, Hongjun Peng3, Tiebang Liu4, Allan H Young5, Jules Angst6, Rong Ye7, Han Rong8, Erni Ji8, Yunhai Qiu2, Lingjiang Li9. 1. Mental Health Institute, Second Xiangya Hospital, Central South University, Changsha, China; Department for Affective Disorders, Shenzhen Mental Health Centre, Shenzhen Key Lab for Psychological Healthcare, Shenzhen, China. 2. Research Centre for Neural Engineering, Institute of Biomedical and Health Engineering, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China. 3. Mental Health Institute, Second Xiangya Hospital, Central South University, Changsha, China; Guangzhou Hui'ai Hospital, Affiliated Hospital of Guangzhou Medical College, Guangzhou, China. 4. Department for Affective Disorders, Shenzhen Mental Health Centre, Shenzhen Key Lab for Psychological Healthcare, Shenzhen, China. Electronic address: liutbsz@126.com. 5. Centre for Affective Disorders, Department of Psychological Medicine, Institute of Psychiatry, King's College, London, United Kingdom. 6. Zurich University Psychiatric Hospital, Zurich, Switzerland. 7. Department of Neuroimaging, King's College London, London, United Kingdom. 8. Department for Affective Disorders, Shenzhen Mental Health Centre, Shenzhen Key Lab for Psychological Healthcare, Shenzhen, China. 9. Mental Health Institute, Second Xiangya Hospital, Central South University, Changsha, China. Electronic address: llj2920@163.com.
Abstract
BACKGROUND: Bipolar disorder (BD) is difficult to diagnose in the early stages of the illness, with the most frequent misdiagnosis being major depressive disorder (MDD). We aimed to use a regional homogeneity (ReHo) approach with resting-state functional magnetic resonance imaging (rs-fMRI) to investigate the features of spontaneous brain activity in MDD patients screening positive on the 32-item Hypomania Checklist (HCL-32). METHODS: Nineteen MDD patients screening positive (HCL-32(+); 9 males; 24.9±5.7 years) and 18 patients screening negative (HCL-32(-); 9 males; 27.1±6.7 years), together with 24 healthy controls (HC; 11 males; 26.4±3.9 years) were studied. ReHo maps were compared and an receiver operating characteristic (ROC) analysis was conducted to confirm the utility of the identified ReHo differences in classifying the patients. RESULTS: The MDD versus HC showed different ReHo in many brain areas, especially in the frontal and parietal cortex. The HCL-32(+) versus HCL-32(-) showed significant increase of ReHo in the right medial superior frontal cortex, left inferior parietal cortex and middle/inferior temporal cortex, and decrease of ReHo in the left postcentral cortex and cerebellum. ROC analysis showed good sensitivity and specificity for distinguishing these two subgroups of MDD. LIMITATIONS: Recruited patients were all on antidepressants and standard mania rating scales were not performed to assess their hypomanic symptoms. CONCLUSIONS: The rs-fMRI measurement of ReHo in distributed brain regions may be putative biomarkers which could differentiate subthreshold BD from MDD.
BACKGROUND:Bipolar disorder (BD) is difficult to diagnose in the early stages of the illness, with the most frequent misdiagnosis being major depressive disorder (MDD). We aimed to use a regional homogeneity (ReHo) approach with resting-state functional magnetic resonance imaging (rs-fMRI) to investigate the features of spontaneous brain activity in MDDpatients screening positive on the 32-item Hypomania Checklist (HCL-32). METHODS: Nineteen MDDpatients screening positive (HCL-32(+); 9 males; 24.9±5.7 years) and 18 patients screening negative (HCL-32(-); 9 males; 27.1±6.7 years), together with 24 healthy controls (HC; 11 males; 26.4±3.9 years) were studied. ReHo maps were compared and an receiver operating characteristic (ROC) analysis was conducted to confirm the utility of the identified ReHo differences in classifying the patients. RESULTS: The MDD versus HC showed different ReHo in many brain areas, especially in the frontal and parietal cortex. The HCL-32(+) versus HCL-32(-) showed significant increase of ReHo in the right medial superior frontal cortex, left inferior parietal cortex and middle/inferior temporal cortex, and decrease of ReHo in the left postcentral cortex and cerebellum. ROC analysis showed good sensitivity and specificity for distinguishing these two subgroups of MDD. LIMITATIONS: Recruited patients were all on antidepressants and standard mania rating scales were not performed to assess their hypomanic symptoms. CONCLUSIONS: The rs-fMRI measurement of ReHo in distributed brain regions may be putative biomarkers which could differentiate subthreshold BD from MDD.