Morphological changes of the limbic system associated with acute and chronic low‐back pain: A UK biobank imaging study

医学 边缘系统 扁桃形结构 生命银行 海马体 丘脑 慢性疼痛 腰痛 灰质 伏隔核 内科学 神经科学 中枢神经系统 物理疗法 心理学 病理 磁共振成像 生物信息学 白质 生物 替代医学 放射科
作者
Valeria Saccà,Thalia Celeste Chai‐Zhang,Sierra Hodges,Judith Amores,Şeyhmus Güler,Nevyana Todorova,Caroline Merritt McDonald,Tian Ge,Jian Kong
出处
期刊:European Journal of Pain [Wiley]
卷期号:28 (4): 608-619
标识
DOI:10.1002/ejp.2206
摘要

Abstract Background Low back pain (LBP) is a major public health issue that influences physical and emotional factors integral to the limbic system. This study aims to investigate the association between LBP and brain morphometry alterations as the duration of LBP increases (acute vs. chronic). Methods We used the UK Biobank data to investigate the morphological features of the limbic system in acute LBP ( N = 115), chronic LBP ( N = 243) and controls ( N = 358), and tried to replicate our findings with an independent dataset composed of 45 acute LBP participants evaluated at different timepoints throughout 1 year from the OpenPain database. Results We found that in comparison with chronic LBP and pain‐free controls, acute LBP was associated with increased volumes of the nucleus accumbens, amygdala, hippocampus, and thalamus, and increased grey matter volumes in the hippocampus and posterior cingulate gyrus. In the replication cohort, we found non‐significantly larger hippocampus and thalamus volumes in the 3‐month visit (acute LBP) compared to the 1‐year visit (chronic LBP), with similar effect sizes as the UK Biobank dataset. Conclusions Our results suggest that acute LBP is associated with dramatic morphometric increases in the limbic system and mesolimbic pathway, which may reflect an active brain response and self‐regulation in the early stage of LBP. Significance Our study suggests that LBP in the acute phase is associated with the brain morphometric changes (increase) in some limbic areas, indicating that the acute phase of LBP may represent a crucial stage of self‐regulation and active response to the disease's onset.

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