Bielau Hendrik, Trübner Kurt, Krell Dieter, Agelink Marcus W, Bernstein Hans-Gert, Stauch Renate, Mawrin Christian, Danos Peter, Gerhard Lieselotte, Bogerts Bernhard, Baumann Bruno
Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, Otto-von-Guericke-University of Magdeburg, Leipziger Strasse 44, 39120, Magdeburg, Germany.
Eur Arch Psychiatry Clin Neurosci. 2005 Dec;255(6):401-12. doi: 10.1007/s00406-005-0581-y. Epub 2005 Aug 17.
Structural changes in subcortical nuclei may underlie clinical symptoms of mood disorders. The goal was to determine whether macrostructural changes exist in brain areas assumed to be involved in regulation of mood and whether such changes differ between major depressive disorder and bipolar disorder. A case-control design was used to compare volumes of all major subcortical nuclei. Brains of patients with major depressive disorder (n = 9) or bipolar disorder (n = 11) or of individuals without a neuropsychiatric disorder (n = 22) were included. Exclusion criteria were a history of substance abuse or histological signs of neurodegenerative disorders. Volumes of the striato-pallidal nuclei, of the hypothalamus, thalamus, amygdala, hippocampus and basal limbic forebrain were determined in the right and left hemisphere by planimetry of 20 mum whole brain serial paraffin sections. Comparisons between patients with bipolar disorder, major depressive disorder and controls showed a significant (Lambda = 0.35, F(20,56) = 1.93, P = 0.028) overall difference in volumes of all investigated regions with strong effect sizes ( f > 0.40) contributed by the hypothalamus, external pallidum, putamen and thalamus. As compared to controls, a strong effect size (f > 0.40) was found in the bipolar group for smaller volumes of the hypothalamus, external pallidum, putamen and thalamus,whereas in patients with major depressive disorder a strong effect size was only found for a smaller volume of the external pallidum. In conclusion our data suggest that pathways presumably involved in mood regulation have structural pathology in affective disorders with more pronounced abnormalities in bipolar disorder.
皮层下核团的结构变化可能是情绪障碍临床症状的基础。本研究旨在确定假定参与情绪调节的脑区是否存在宏观结构变化,以及这些变化在重度抑郁症和双相情感障碍之间是否存在差异。采用病例对照设计比较所有主要皮层下核团的体积。纳入了重度抑郁症患者(n = 9)、双相情感障碍患者(n = 11)或无神经精神疾病的个体(n = 22)。排除标准为有药物滥用史或神经退行性疾病的组织学迹象。通过对20μm全脑连续石蜡切片进行平面测量,确定左右半球纹状体 - 苍白球核、下丘脑、丘脑、杏仁核、海马体和基底边缘前脑的体积。双相情感障碍患者、重度抑郁症患者和对照组之间的比较显示,所有研究区域的体积存在显著的总体差异(Lambda = 0.35,F(20,56) = 1.93,P = 0.028),下丘脑、外侧苍白球、壳核和丘脑的效应量较大(f > 0.40)。与对照组相比,双相情感障碍组下丘脑、外侧苍白球、壳核和丘脑体积较小,效应量较大(f > 0.40);而在重度抑郁症患者中,仅外侧苍白球体积较小,效应量较大。总之,我们的数据表明,推测参与情绪调节的通路在情感障碍中存在结构病理学改变,在双相情感障碍中异常更为明显。