中重度COVID-19对未接种疫苗患者深部灰质微观结构的影响:来自MRI T1制图的见解

IF 3.7 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Masia Fahim, Elke Hattingen, Alina Jurcoane, Jan R Schüre, Svenja Klinsing, Julia Koepsell, Kolja Jahnke, Michael W Ronellenfitsch, Ulrich Pilatus, Maria J G T Vehreschild, Ralf Deichmann, Christophe T Arendt
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引用次数: 0

摘要

背景:研究2019冠状病毒病(COVID-19)康复患者深部灰质定量T1松弛时间(qT1)的变化。方法:使用3- t磁共振成像检查血清阳性≥3个月未接种COVID-19疫苗的参与者和年龄和性别匹配的对照组。自动分割后,从qT1图中提取丘脑、白球、壳核、尾状核和伏隔核以及海马的双侧测量。评估神经功能(标准化考试)、嗅觉能力(4项口袋嗅觉测试)、抑郁(贝克抑郁量表- ii)、嗜睡(Epworth嗜睡量表)、睡眠质量(匹兹堡睡眠质量指数)、健康相关生活质量(EQ-5D)和认知表现(蒙特利尔认知评估)的基线特征和结果。结果:145名受试者(中位年龄46岁;纳入73例女性)(2020年11月- 2021年12月):69例COVID-19后康复,76例对照组(年龄,p = 0.532;性别,p = 0.799),总体qT1值无显著差异(所有p值> 0.050)。年龄≥40岁的参与者亚组分析(年龄,p = 0.675;性别,p = 0.447)显示,与对照组(47/76)相比,先前住院的COVID-19受试者的左右尾状核qT1值更高(23/69)(p = 0.009;P = 0.027)、左侧伏隔核(P = 0.017)、右侧壳核(P = 0.041)、右侧海马(P = 0.020)。与宏观影像学表现、既往病史、自COVID-19诊断以来的时间、住院治疗时间或检测结果均无相关性。结论:T1图谱揭示了欧米克隆时代前未接种疫苗且年龄≥40岁的中重度COVID-19康复者纹状体和海马区的微结构变化。相关声明:本研究阐明了严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染后的大脑受累,强调需要进一步的纵向分析来评估这些发现的潜在可逆性、稳定性或恶化。关键点:我们假设COVID-19后深部灰质T1松弛时间改变。≥40岁未接种疫苗的参与者在中重度COVID-19后表现出更高的纹状体和海马qT1。未发现qT1与住院时间、既往疾病或神经(心理)逻辑测试相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact on the microstructure of deep gray matter in unvaccinated patients after moderate-to-severe COVID-19: insights from MRI T1 mapping.

Background: To determine changes in quantitative T1 relaxation times (qT1) in deep gray matter in patients recovered from coronavirus disease 2019 (COVID-19).

Methods: Unvaccinated COVID-19 participants ≥ 3 months after seropositivity and age- and sex-matched controls were examined using 3-T magnetic resonance imaging. Bilateral measures of thalamus, pallidum, putamen, caudate and accumbens nuclei, and hippocampus were extracted from qT1 maps after automated segmentation. Baseline characteristics and results of tests assessing neurological functions (standardized exam), ability to smell (4-Item Pocket Smell Test), depression (Beck Depression Inventory-II), sleepiness (Epworth Sleepiness Scale), sleep quality (Pittsburgh Sleep Quality Index), health-related quality of life (EQ-5D), and cognitive performance (Montreal Cognitive Assessment) were evaluated.

Results: One hundred forty-five subjects (median age, 46 years; 73 females) were included (11/2020-12/2021): 69 recovered after COVID-19 and 76 controls (age, p = 0.532; sex, p = 0.799), without significant differences in qT1 values overall (all p-values > 0.050). Subgroup analysis of participants aged ≥ 40 (age, p = 0.675; sex, p = 0.447) revealed higher qT1 values in previously hospitalized COVID-19 subjects (23/69) compared to controls (47/76) in left and right caudate nuclei (p = 0.009; p = 0.027), left accumbens nucleus (p = 0.017), right putamen (p = 0.041), and right hippocampus (p = 0.020). No correlations were found with macroscopic imaging findings, pre-existing conditions, time since COVID-19 diagnosis, inpatient treatment duration, or test results.

Conclusion: T1 mapping revealed microstructural changes in striatal and hippocampal regions of unvaccinated individuals aged ≥ 40 who recovered from moderate-to-severe COVID-19 during the pre-Omicron era.

Relevance statement: This study elucidates brain involvement following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, underscoring the need for further longitudinal analyses to assess the potential reversibility, stability or deterioration of these findings.

Key points: We hypothesized altered T1 relaxation times in deep gray matter after COVID-19. Unvaccinated participants ≥ 40 years exhibited higher striatal, hippocampal qT1 after moderate-to-severe COVID-19. No qT1 correlations were found with hospitalization duration, pre-existing conditions, or neuro-(psycho)logical tests.

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来源期刊
European Radiology Experimental
European Radiology Experimental Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
6.70
自引率
2.60%
发文量
56
审稿时长
18 weeks
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