Trajectories of Inflammatory Markers and Post-COVID-19 Cognitive Symptoms: A Secondary Analysis of the CONTAIN COVID-19 Randomized Trial.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY Neurology® Neuroimmunology & Neuroinflammation Pub Date : 2024-05-01 Epub Date: 2024-04-16 DOI:10.1212/NXI.0000000000200227
Jennifer A Frontera, Rebecca A Betensky, Liise-Anne Pirofski, Thomas Wisniewski, Hyunah Yoon, Mila B Ortigoza
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Abstract

Background and objectives: Chronic systemic inflammation has been hypothesized to be a mechanistic factor leading to post-acute cognitive dysfunction after COVID-19. However, little data exist evaluating longitudinal inflammatory markers.

Methods: We conducted a secondary analysis of data collected from the CONTAIN randomized trial of convalescent plasma in patients hospitalized for COVID-19, including patients who completed an 18-month assessment of cognitive symptoms and PROMIS Global Health questionnaires. Patients with pre-COVID-19 dementia/cognitive abnormalities were excluded. Trajectories of serum cytokine panels, D-dimer, fibrinogen, C-reactive peptide (CRP), ferritin, lactate dehydrogenase (LDH), and absolute neutrophil counts (ANCs) were evaluated over 18 months using repeated measures and Friedman nonparametric tests. The relationships between the area under the curve (AUC) for each inflammatory marker and 18-month cognitive and global health outcomes were assessed.

Results: A total of 279 patients (N = 140 received plasma, N = 139 received placebo) were included. At 18 months, 76/279 (27%) reported cognitive abnormalities and 78/279 (28%) reported fair or poor overall health. PROMIS Global Mental and Physical Health T-scores were 0.5 standard deviations below normal in 24% and 51% of patients, respectively. Inflammatory marker levels declined significantly from hospitalization to 18 months for all markers (IL-2, IL-2R, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12, IL-13, INFγ, TNFα, D-dimer, fibrinogen, ferritin, LDH, CRP, neutrophils; all p < 0.05), with the exception of IL-1β, which remained stable over time. There were no significant associations between the AUC for any inflammatory marker and 18-month cognitive symptoms, any neurologic symptom, or PROMIS Global Physical or Mental health T-scores. Receipt of convalescent plasma was not associated with any outcome measure.

Discussion: At 18 months posthospitalization for COVID-19, cognitive abnormalities were reported in 27% of patients, and below average PROMIS Global Mental and Physical Health scores occurred in 24% and 51%, respectively. However, there were no associations with measured inflammatory markers, which decreased over time.

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炎症标记物和 COVID-19 后认知症状的轨迹:CONTAIN COVID-19 随机试验的二次分析。
背景和目的:慢性全身性炎症被认为是导致 COVID-19 后急性认知功能障碍的一个机制性因素。然而,评估纵向炎症标志物的数据却很少:我们对 CONTAIN 随机试验中收集的 COVID-19 住院患者疗养血浆数据进行了二次分析,包括完成 18 个月认知症状评估和 PROMIS 全球健康问卷调查的患者。COVID-19之前患有痴呆症/认知异常的患者被排除在外。使用重复测量和弗里德曼非参数检验对 18 个月内血清细胞因子、D-二聚体、纤维蛋白原、C 反应肽 (CRP)、铁蛋白、乳酸脱氢酶 (LDH) 和绝对中性粒细胞计数 (ANC) 的变化轨迹进行了评估。评估了每种炎症标记物的曲线下面积(AUC)与 18 个月认知和总体健康结果之间的关系:共纳入 279 例患者(N = 140 例接受血浆治疗,N = 139 例接受安慰剂治疗)。18个月后,76/279(27%)例患者出现认知异常,78/279(28%)例患者总体健康状况一般或较差。分别有 24% 和 51% 的患者的 PROMIS 全球心理和身体健康 T 分数低于正常水平 0.5 个标准差。从住院到18个月期间,所有炎症标志物水平均显著下降(IL-2、IL-2R、IL-4、IL-5、IL-6、IL-8、IL-10、IL-12、IL-13、INFγ、TNFα、D-二聚体、纤维蛋白原、铁蛋白、LDH、CRP、中性粒细胞;均 p < 0.05),只有 IL-1β 保持稳定。任何炎症标记物的AUC与18个月的认知症状、任何神经症状或PROMIS全球生理或心理健康T-评分之间均无明显关联。接受康复血浆与任何结果测量均无关联:讨论:COVID-19患者入院后18个月时,27%的患者出现认知异常,24%和51%的患者PROMIS全球身心健康评分低于平均水平。然而,这与所测量的炎症标志物没有关联,炎症标志物会随着时间的推移而降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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