IL8和IL18(而非IL6)的围术期水平与手术三个月后的基底核萎缩有关

IF 5.2 3区 医学 Q1 NEUROSCIENCES Journal of Neuroimmune Pharmacology Pub Date : 2024-03-14 DOI:10.1007/s11481-024-10110-4
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引用次数: 0

摘要

摘要 过去的研究发现,外科手术后可能会加速脑萎缩。此外,还有人描述了全身炎症与神经变性之间的关系。我们假设,术后血液循环中的白细胞介素(IL)水平以及围手术期白细胞介素水平的变化与作为大脑皮层乙酰胆碱主要来源的大细胞基底核(NBM)术后萎缩程度的增加有关。我们分析了 BioCog 队列的数据,该队列包括年龄≥ 65 岁、接受择期大手术(≥ 60 分钟)的患者。我们在手术前和术后第一天采集了血液样本。在手术前和术后三个月的随访中进行了脑部磁共振成像和神经心理学评估。我们使用线性回归分析确定了三种白细胞介素(IL6、IL8 和 IL18)与 NBM 萎缩(从术前基线到随访期间体积变化的百分比)的关系,并研究了 NBM 萎缩和体积与术后认知能力和围手术期认知变化的关系。使用接收器操作曲线来确定术前白细胞介素水平的预后价值。对于 IL8(N = 97)和 IL18(N = 217),而非 IL6(N = 240),我们观察到术后第一天较高的 IL 水平与术后三个月较高的 NBM 萎缩有显著关联。随后的分析表明,在 IL8 和 IL18 中,这种关联是由长期升高的 IL 水平和 NBM 萎缩(反映在术前 IL 浓度上)这一更普遍的关联驱动的,而不是 IL 对手术的反应(以术前和术后 IL 浓度之差衡量)。随访时,NBM体积与认知能力水平呈正相关,但NBM萎缩与围手术期的认知变化无明显关系。术前 IL 浓度对 NBM 萎缩的预后价值较低。我们的研究结果表明,术后白细胞介素水平与 NBM 萎缩的关系是由术前炎症导致的术前白细胞介素升高引起的,而不是围手术期白细胞介素水平随手术和麻醉的变化而变化。BioCog研究已于2014年10月15日在clinicaltrials.gov上注册(NCT02265263)。 图表摘要
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Perioperative Levels of IL8 and IL18, but not IL6, are Associated with Nucleus Basalis Magnocellularis Atrophy Three Months after Surgery

Abstract

Past studies have observed that brain atrophy may accelerate after surgical procedures. Furthermore, an association of systemic inflammation with neurodegeneration has been described. We hypothesize that postoperative interleukin (IL) levels in circulation as well as the perioperative change in interleukin levels are associated with increased postoperative atrophy in the Nucleus basalis magnocellularis (of Meynert, NBM) which is the major source of cortical acetylcholine. We analyzed data from the BioCog cohort which included patients ≥ 65 years presenting for elective major surgery (≥ 60min). Blood samples were taken before surgery and on the first postoperative day. Magnetic resonance imaging of the brain and neuropsychological assessments were conducted before surgery and after three months follow-up. We used linear regression analysis to determine the association of three interleukins (IL6, IL8 and IL18) with NBM atrophy (in % volume change from baseline before surgery to follow-up), as well as to examine the associations of NBM atrophy and volume with postoperative cognitive ability and perioperative cognitive change. Receiver-operating curves were used to determine the prognostic value of preoperative interleukin levels. For IL8 (N = 97) and IL18 (N = 217), but not IL6 (N = 240), we observed significant associations of higher postoperative IL levels at the first postoperative day with higher NBM atrophy at three months after surgery. Subsequent analyses suggested that in both IL8 and IL18, this association was driven by a more general association of chronically elevated IL levels and NBM atrophy, reflected by preoperative IL concentrations, rather than IL response to surgery, measured as the difference between pre- and postoperative IL concentrations. At follow-up, NBM volume was positively associated with the level of cognitive performance, but NBM atrophy was not significantly related to perioperative cognitive change. Prognostic value of preoperative IL concentrations for NBM atrophy was low. Our results suggest that an association of postoperative interleukin levels with NBM atrophy is driven by preoperatively elevated interleukins due to pre-existing inflammation, rather than perioperative change in interleukin levels in response to surgery and anesthesia. The BioCog study has been registered at clinicaltrials.gov on Oct 15, 2014 (NCT02265263).

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来源期刊
CiteScore
13.60
自引率
0.00%
发文量
18
审稿时长
6-12 weeks
期刊介绍: The aims of the Journal of Neuroimmune Pharmacology are to promote the dissemination, interest, and exchange of new and important discoveries for the pharmacology and immunology of the nervous system. The aims parallel that of the Society on NeuroImmune Pharmacology by increasing the fundamental understanding of neurologic and neuropsychiatric disorders affected by the immune system or vice versa and towards pharmacologic measures that lead, either to a better understanding of disease mechanisms, or by improving disease outcomes. The scope of JNIP includes all primary works and reviews into the etiology, prevention, and treatment of neuroimmune and nervous system diseases affected by disordered immunity. Original studies serving to define neuroimmune modulation of environmental or endogenous cues such as toxins and drugs of abuse, hormones, and cytokines are welcome. JNIP will serve as a reliable source of interdisciplinary information bridging the fields of pharmacology, immunology, and neuroscience.
期刊最新文献
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