Department of Magnetic Resonance Imaging, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China; Zhengzhou Key Laboratory of brain function and cognitive magnetic resonance imaging, Zhengzhou, China; Henan Engineering Technology Research Center for detection and application of brain function, Zhengzhou, China; Henan Engineering Research Center of medical imaging intelligent diagnosis and treatment, Zhengzhou, China; Henan key laboratory of imaging intelligence research, Zhengzhou, China; Henan Engineering Research Center of Brain Function Development and Application, Zhengzhou, China.
Department of Psychiatry, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Prog Neuropsychopharmacol Biol Psychiatry. 2024 Aug 30;134:111052. doi: 10.1016/j.pnpbp.2024.111052. Epub 2024 Jun 11.
Depression is a neurodevelopmental disorder that exhibits progressive gray matter volume (GMV) atrophy. Research indicates that brain development is influential in depression-induced GMV alterations. However, the interaction between depression and age of onset is not well understood by the underlying molecular and neuropathological mechanisms. Thus, 152 first-episode depression individuals and matched 130 healthy controls (HCs) were recruited to undergo T1-weighted high-resolution magnetic resonance imaging for this study. By two-way ANOVA, age and diagnosis were used as factors when analyzing the interaction of GMV in the participants. Then, spatial correlations between neurotransmitter maps and factor-related volume maps are established. Results illustrate a pronounced antagonistic interaction between depression and age of onset in the right insula, superior temporal gyrus, anterior cingulate gyrus, and orbitofrontal gyrus. Depression-caused reductions in GMV are mainly distributed in thalamic-limbic-cortical regions, regardless of age. For the main effect of age, adults exhibit brain atrophy in frontal, cerebellum, parietal, and temporal lobe structures. Cross-modal correlations showed that GMV changes in the interactive regions were linked with the serotonergic system and dopaminergic systems. Summarily, our results reveal the interaction between depression and age of onset in neurobiological mechanisms, which provide hints for future treatment of different ages of depression.
抑郁症是一种神经发育障碍,表现为进行性灰质体积(GMV)萎缩。研究表明,大脑发育对抑郁引起的 GMV 改变有影响。然而,抑郁和发病年龄之间的相互作用的潜在分子和神经病理学机制尚不清楚。因此,本研究招募了 152 名首发抑郁症患者和 130 名匹配的健康对照者(HCs)进行 T1 加权高分辨率磁共振成像。通过双向方差分析,年龄和诊断被用作分析参与者 GMV 相互作用的因素。然后,建立了神经递质图谱与因子相关体积图谱之间的空间相关性。结果表明,右侧脑岛、颞上回、前扣带回和眶额回中抑郁和发病年龄之间存在明显的拮抗相互作用。无论年龄大小,抑郁引起的 GMV 减少主要分布在丘脑-边缘-皮质区域。对于年龄的主要影响,成年人的大脑在前额、小脑、顶叶和颞叶结构中出现萎缩。跨模态相关性表明,交互区域的 GMV 变化与 5-羟色胺能系统和多巴胺能系统有关。总之,我们的研究结果揭示了抑郁和发病年龄在神经生物学机制中的相互作用,为不同年龄的抑郁症的未来治疗提供了线索。