SARS-CoV-2引起的冠状病毒感染中神经变性的分子模式

A. O. Mikhailov, N. Plekhova, S. Sokotun, A. Simakova, A. S. Bedareva
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引用次数: 0

摘要

背景:关于冠状病毒感染的神经和精神后果的报告由于其有限的可用性而具有特别的相关性。神经组织损伤的分子模式是理解神经退行性变潜在机制的重要任务。目的:研究冠状病毒感染患者急性期和长期神经变性和神经可塑性标志物含量的变化动态。材料与方法:共200例5183岁的患者被评估并分为两个年龄组:5165岁和6683岁。测定血清中神经变性标志物的水平:神经丝重链(NEFH)、S100 A6蛋白、S100 B蛋白、-淀粉样蛋白1-42 (A1-42)、微丝相关tau蛋白(MAPt)、血清淀粉样蛋白P (SAP)和神经可塑性:神经营养因子3 (NT3)、神经营养因子4 (NT4)。该研究在入院时疾病的急性期和出院后6个月和12个月进行了三次。结果:第一组患者在冠状病毒感染急性期,女性患者S100 A6(3.20.2)、S100 B(0.40.06)、NT3(1.10.1)、MAPt(0.130.02)浓度较高,男性患者NEFH(0.150.03)、A1-42(2.10.1)、SAP(4.50.06)浓度较高。从长期来看,与女性相比,年轻男性的神经退行性变和神经保护标志物长期持续高水平的总体趋势,表明康复期较长。12个月后,男性的钙结合蛋白S100 A6和S100 B水平分别为1.50.2 pg/mL和0.30.04 ng/mL,女性分别为1.10.1 pg/mL和0.20.04 ng/mL。12个月后,男性的SAP水平为4.30.1,女性为3.90.2 ng/mL,差异有统计学意义。第二组患者急性期S100 A6、A1-42水平较高,男性患者急性期S100 B、NT3、SAP水平较高。结论:冠状病毒感染患者急性期和晚期的变化表明不同年龄组的神经退行性变过程活跃,表现为血清中特异性蛋白浓度升高。
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Molecular patterns of neurodegeneration in coronavirus infection caused by SARS-CoV-2
BACKGROUND: The reports on the neurological and psychiatric consequences of coronavirus infection are of particular relevance owing to their limited availability. The molecular patterns of nerve tissue damage are an important task for understanding the underlying mechanisms of neurodegeneration. AIM: To study the dynamics of changes in the content of markers of neurodegeneration and neuroplasticity in patients with coronavirus infection in the acute and long-term periods. MATERIALS AND METHODS: A total of 200 patients aged 5183 years were assessed and categorized into two age groups: 5165 years and 6683 years. The levels of neurodegeneration markers were determined in the blood serum: neurofilament heavy chains (NEFH), S100 A6 protein, S100 B protein, -amyloid 1-42 (A1-42), microfilament associated tau protein (MAPt), serum amyloid P (SAP), and neuroplasticity: neurotrophin 3 (NT3), neurotrophin 4 (NT4). The study was performed thrice in the acute period of the disease at the time of admission to the hospital and at 6 and 12 months after discharge. RESULTS: In the first group of patients, in the acute period of coronavirus infection, women showed higher concentrations of S100 A6 (3.20.2), S100 B (0.40.06), NT3 (1.10.1), and MAPt (0.130.02), while the values for the men were NEFH (0.150.03), A1-42 (2.10.1), and SAP (4.50.06). In the long-term, a general tendency of long persistence of high levels of the markers of neurodegeneration and neuroprotection was noted in young men compared to women, indicating a long period of rehabilitation. After 12 months, the level of calcium-binding proteins S100 A6 and S100 B in men was 1.50.2 pg/mL and 0.30.04 ng/mL, which was 1.10.1 pg/mL and 0.20.04 ng/mL, respectively, in women. The level of SAP in men during the long-term period after 12 months was 4.30.1 versus 3.90.2 ng/mL in women, indicating a significant difference. Analyses of the results for the patients in the second group indicated a higher level of S100 A6 and A1-42 in the acute period for women, while men showed higher levels of S100 B, NT3, and SAP. CONCLUSION: The changes in patients with coronavirus infection both in the acute and late periods indicated active neurodegeneration processes in different age groups, which manifested as a result of an increase in the concentration of specific proteins in the blood serum.
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