加速老化沿着感觉运动关联皮层轴在精神分裂症中展开:多位点研究。

Haonan Pei,Sisi Jiang,Changyue Hou,Hechun Li,Zhihuan Yang,Roberto Rodriguez-Labrada,Mingjun Duan,Dezhong Yao,Cheng Luo
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引用次数: 0

摘要

背景:由于衰老加速,精神分裂症与平均寿命缩短有关。早期的研究主要集中在全球大脑年龄差距上,限制了我们对特定区域衰老的理解。此外,加速衰老与精神分裂症疾病进展之间的关系尚未得到直接研究。目的:我们的目的是研究精神分裂症患者衰老和疾病进展过程中的皮层时空模式。方法利用多位点静息状态功能磁共振成像数据,分析2353名健康对照者和546名精神分裂症患者的内在活动波动。我们评估了健康对照组大脑活动衰老轨迹的规范模型,并检查了精神分裂症患者在疾病进展过程中偏离规范参考范围的发育轨迹。结果两组的衰老轨迹均表现出沿感觉运动-关联皮层轴的时空变异性,其特征是年轻时跨模式关联皮层迅速衰退,随后随着年龄的增长初级皮层加速衰退。然而,精神分裂症在整个大脑皮层表现出更快的下降速度,特别是在短时间阶段。进一步的分析表明,疾病引起的衰老偏差的空间变异性在整个疾病进展过程中沿着感觉运动关联皮层轴持续存在。包括多巴胺和血清素在内的神经递质系统的过早参与,可能是加速衰老的基础。结论我们的工作揭示了沿感觉运动关联皮层轴组织的区域衰老轨迹,并为精神分裂症的非典型衰老和疾病进展机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Accelerated ageing unfolds along the sensorimotor-association cortical axis in schizophrenia: multi-site study.
BACKGROUND Schizophrenia is associated with a reduced average lifespan due to accelerated ageing. Early studies have predominantly focused on the global brain age gap, limiting our understanding of region-specific ageing. Moreover, the relationship between accelerated ageing and schizophrenia disease progression has not been directly examined. AIMS Our aim was to investigate the cortical spatiotemporal patterns in ageing and disease progression in schizophrenia. METHOD Using multi-site, resting-state functional magnetic resonance imaging data, we analysed intrinsic activity fluctuations in 2353 healthy controls and 546 subjects with schizophrenia. We assessed normative models of ageing trajectories in brain activities in healthy controls, and examined the developmental trajectory of deviations from normative reference ranges with disease progression in schizophrenia. RESULTS The ageing trajectories of both groups demonstrated spatiotemporal variability unfolding along the sensorimotor-association cortical axis, characterised by a rapid decline in transmodal association cortices at younger ages and followed by an accelerated decline in primary cortices at older ages. However, schizophrenia exhibited a more rapid rate of decline across the entire cerebral cortex, particularly during the short-duration stage. Further analysis revealed that the spatial variability of disease-induced ageing deviations persisted along the sensorimotor-association cortical axis throughout disease progression. The premature involvement of neurotransmitter systems, including dopamine and serotonin, may underlie accelerated ageing. CONCLUSIONS Our work uncovers regional ageing trajectories organised along the sensorimotor-association cortical axis, and provides new insights into the mechanisms of atypical ageing and disease progression in schizophrenia.
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