BOLD-fMRI study on the function analysis of the brain in major depression disorder and#br#
their first-degree relatives
SONG Yu-lu1, MU Xin-nuan2, SONG Xiao-lei1, FANG Jun-fang2, MAO Ning3, WANG Bin1
1. Department of Radiology, Yantai Affiliated Hospital of Binzhou Medical University, Yantai Shandong 264003, China;
2. Medical Imaging Center of Binzhou Affiliated Hospital of Binzhou Medical University, Binzhou Shandong 256600, China;
3. Yantai Yuhuangding Hospital, Yantai Shandong 264000, China
Abstract:Objective: We studied the characteristics and differences of the regional homogeneity(ReHo) of the major depression disorder(MDD) and their first-degree relatives in the resting state by functional magnetic resonance imaging(fMRI), in order to understand the early changes of the brain function in patients with MDD. Methods: The experiments were performed by 3.0T fMRI in 15 patients with MDD(the depression group), 15 first-degree relatives of MDD(the first-degree relatives group) and 15 healthy volunteers(the control group). A statistics analysis of ReHo was performed subsequently. Results: The ReHo values measured in right middle frontal gyrus, right precentral gyrus, right superior frontal gyrus, right anterior cingulate cortex, right insular, left putamen, left superior temporal gyrus, left middle temporal gyrus, left dorsal cingulate cortex of MDD group were significantly lower than those of the first-degree relatives group(P<0.05). The ReHo values measured in left postcentral gyrus, left superior temporal gyrus, left middle temporal gyrus, left inferior frontal gyrus, left orbitofrontal cortex, left dorsal cingulate cortex, right precentral gyrus, right medial prefrontal cortex, right superior frontal gyrus, the middle frontal gyrus, the anterior cingulate cortex, right insular of MDD group were significantly lower than those of the control group(P<0.05). The ReHo values measured in left anterior lobe of cerebellum, left middle temporal gyrus, left inferior frontal gyrus, left orbitofrontal cortex, left superior frontal gyrus, left dorsal cingulate cortex, left insular, right middle frontal gyrus, right anterior cingulate cortex of the first-degree relatives group were significantly lower than those of the control group(P<0.05). Conclusion: With the widespread abnormal ReHo values of brain in MDD and first-degree relatives, we can get a hypothesis that these abnormalities may be associated with cognitive network disorders and emotional distress in MDD.
宋玉璐1,穆新暖2,宋筱蕾1,房俊芳2,毛 宁3,王 滨1. 运用fMRI对抑郁症及一级亲属的静息态脑功能分析研究[J]. 中国临床医学影像杂志, 2017, 28(10): 716-721.
SONG Yu-lu1, MU Xin-nuan2, SONG Xiao-lei1, FANG Jun-fang2, MAO Ning3, WANG Bin1. BOLD-fMRI study on the function analysis of the brain in major depression disorder and#br#
their first-degree relatives. JOURNAL OF CHINA MEDICAL IMAGING, 2017, 28(10): 716-721.
[1]Jacobs RH, Barba A, Gowins JR, et al. Decoupling of the amygdala to other salience network regions in adolescent-onset recurrent major depressive disorder[J]. Psychol Med, 2016, 46(5): 1055-1067.
[2]Jones NP, Chase HW, Fournier JC. Brain mechanisms of anxiety’s effects on cognitive control in major depressive disorder[J]. Psychol Med, 2016, 46(11): 2397-2409.
[3]Hammar A, Neto E, Clemo L, et al. Striatal hypoactivation and cognitive slowing in patients with partially remitted and remitted major depression[J]. Psych J, 2016, 5(3): 191-205.
[4]Bullmore E, Sporns O. The economy of brain network organization[J]. Nat Rev Neurosci, 2012, 13(5): 336-349.
[5]Yao Z, Wang L, Lu Q, et al. Regional homogeneity in depression and its relationship with separate depressive symptom clusters: a resting-state fMRI study[J]. J Affect Disord, 2009, 115(3): 430-438.
[6]Guo Z, Liu X, Jia X, et al. Regional coherence changes in Alzheimer’s disease patients with depressive symptoms: a resting-state functional MRI study[J]. J Alzheimers Dis, 2015, 48(3): 603-611.
[7]Yuan Y, Zhu W, Zhang Z, et al. Regional gray matter changes are associated with cognitive deficits in remitted geriatric depression: an optimized voxel-based morphometry study[J]. Biol Psychiatry, 2008, 64(6): 541-544.
[8]Liu CH, Ma X, Wu X, et al. Regional homogeneity of resting-state brain abnormalities in bipolar and unipolar depression[J]. Prog Neuropsychopharmacol Biol Psychiatry, 2013, 41(1): 52-59.
[9]Phillips ML, Ladouceur CD, Drevets WC. A neural model of voluntary and automatic emotion regulation: implications for understanding the pathophysiology and neurodevelopment of bipolar disorder[J]. Mol Psychiatry, 2008, 13(9): 833-857.
[10]Kupfer DJ, Frank E, Phillips ML. Major depressive disorder: new clinical, neurobiological, and treatment perspectives[J]. Lancet, 2012, 379(9820): 1045-1055.
[11]Frodl T, Scheuerecker J, Albrecht J, et al. Neuronal correlates of emotional processing in patients with major depression[J]. World J Biol Psychiatry, 2009, 10(3): 202-208.
[12]Li CT, Lin CP, Chou KH, et al. Structural and cognitive deficits in remitting and non-remitting recurrent depression: a voxel-based morphometric study[J]. Neuroimage, 2010, 50(1): 347-356.
[13]Leung KK, Lee TM, Wong MM, et al. Neural correlates of attention biases of people with major depressive disorder: a voxel-based morphometric study[J]. Psychol Med, 2009, 39(7): 1097-1106.
[14]Tao H, Guo S, Ge T, et al. Depression uncouples brain hate circuit[J]. Mol Psychiatry, 2013, 18(1): 101-111.
[15]Cullen KR, Gee DG, Klimes-Dougan B, et al. A preliminary study of functional connectivity in comorbid adolescent depression[J]. Neurosci Lett, 2009, 460(3): 227-231.
[16]Rogers MA, Bradshaw JL, Pantelis C, et al. Frontostriatal deficits in unipolar major depression[J]. Brain Res Bull, 1998, 47(4): 297-310.
[17]Herwig U, Bruhl AB, Kaffenberger T, et al. Neural correlates of pessimistic attitude in depression[J]. Psychol Med, 2010, 40(5): 789-800.
[18]Abe O, Yamasue H, Kasai K, et al. Voxel-based analyses of gray/white matter volume and diffusion tensor data in major depression[J]. Psychiatry Res, 2010, 181(1): 64-70.
[19]Qin J, Wei M, Liu H, et al. Abnormal hubs of white matter networks in the frontal-parieto circuit contribute to depression discrimination via pattern classification[J]. Magn Reson Imaging, 2014, 32(10): 1314-1320.
[20]Hampshire A, Chamberlain SR, Monti MM, et al. The role of the right inferior frontal gyrus: inhibition and attentional control[J]. Neuroimage, 2010, 50(3): 1313-1319.
[21]Hajek T, Alda M, Hajek E, et al. Functional neuroanatomy of response inhibition in bipolar disorders—combined voxel based and cognitive performance meta-analysis[J]. J Psychiatr Res, 2013, 47(12): 1955-1966.
[22]Hummer TA, Hulvershorn LA, Karne HS, et al. Emotional response inhibition in bipolar disorder: a functional magnetic resonance imaging study of trait- and state-related abnormalities[J]. Biol Psychiatry, 2013, 73(2): 136-143.
[23]Penfold C, Vizueta N, Townsend JD, et al. Frontal lobe hypoactivation in medication-free adults with bipolar Ⅱ depression during response inhibition[J]. Psychiatry Res, 2015, 231(3): 202-209.
[24]Foland-Ross LC, Thompson PM, Sugar CA, et al. Investigation of cortical thickness abnormalities in lithium-free adults with bipolar Ⅰ disorder using cortical pattern matching[J]. Am J Psychiatry, 2011, 168(5): 530-539.
[25]van To MJ, vander Wee NJ, vanden Heuvel OA, et al. Regional brain volume in depression and anxiety disorders[J]. Arch Gen Psychiatry, 2010, 67(10): 1002-1011.
[26]Yuan Y, Zhang Z, Bai F, et al. Abnormal neural activity in the patients with remitted geriatric depression: a resting-state functional magnetic resonance imaging study[J]. J Affect Disord, 2008, 111(2-3): 145-152.
[27]Papmeyer M, Giles S, Sussmann JE, et al. Cortical thickness in individuals at high familial risk of mood disorders as they develop major depressive disorder[J]. Biol Psychiatry, 2015, 78(1): 58-66.
[28]Buyukdura JS, Mc Clintock SM, Croarkin PE. Psychomotor retardation in depression: biological underpinnings, measurement, and treatment[J]. Prog Neuropsychopharmacol Biol Psychiatry, 2011, 35(2): 395-409.