Clinical and Experimental Neuropsychology Laboratory, Faculty of Psychology, University of Geneva, Geneva, Switzerland.
Department of Clinical Neurosciences, Neurology Department, Geneva University Hospitals, Switzerland.
J Glob Health. 2024 Mar 8;14:05008. doi: 10.7189/jogh.14.05008.
Despite numerous observations of neuropsychological deficits immediately following severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, little is known about what happens to these deficits over time and whether they are affected by changes in fatigue and any psychiatric symptoms. We aimed to assess the prevalence of neuropsychological deficits at 6-9 months and again at 12-15 months after coronavirus disease 2019 (COVID-19) and to explore whether it was associated with changes in fatigue and psychiatric symptoms.
We administered a series of neuropsychological tests and psychiatric questionnaires to 95 patients (mean age = 57.12 years, standard deviation (SD) = 10.68; 35.79% women) 222 (time point 1 (T1)) and 441 (time point 2 (T2)) days on average after infection. Patients were categorised according to the severity of their respiratory COVID-19 symptoms in the acute phase: mild (no hospitalisation), moderate (conventional hospitalisation), and severe (hospitalisation in intensive care unit (ICU) plus mechanical ventilation). We ran Monte-Carlo simulation methods at each time point to generate a simulated population and then compared the cumulative percentages of cognitive disorders displayed by the three patient subgroups with the estimated normative data. We calculated generalised estimating equations for the whole sample to assess the longitudinal associations between cumulative neuropsychological deficits, fatigue, and psychiatric data (anxiety, depressive symptoms, posttraumatic stress disorder, and apathy).
Most participants (>50%) exhibited a decrease in their neuropsychological impairments, while approximately 25% showed an escalation in these cognitive deficits. At T2, patients in the mild subgroup remained free of accumulated neuropsychological impairments. Patients with moderate severity of symptoms displayed a decrease in the magnitude of cumulative deficits in perceptual and attentional functions, a persistence of executive, memory and logical reasoning deficits, and the emergence of language deficits. In patients with severe symptoms, perceptual deficits emerged and executive deficits increased, while attentional and memory deficits remained unchanged. Changes in executive functions were significantly associated with changes in depressive symptoms, but the generalised estimating equations failed to reveal any other significant effect.
While most cumulative neuropsychological deficits observed at T1 persisted and even worsened over time in the subgroups of patients with moderate and severe symptoms, a significant proportion of patients, mainly in the mild subgroup, exhibited improved performances. However, we identified heterogeneous neuropsychological profiles both cross-sectionally and over time, suggesting that there may be distinct patient phenotypes. Predictors of these detrimental dynamics have yet to be identified.
尽管有大量观察表明,在严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染后会出现神经认知缺陷,但对于这些缺陷随时间推移的变化,以及它们是否受到疲劳和任何精神症状变化的影响,知之甚少。我们旨在评估新冠肺炎(COVID-19)后 6-9 个月和 12-15 个月时的神经认知缺陷的发生率,并探讨其是否与疲劳和精神症状的变化有关。
我们对 95 名患者(平均年龄 57.12 岁,标准差(SD)=10.68;35.79%为女性)在感染后平均 222(时间点 1(T1))和 441(时间点 2(T2))天进行了一系列神经心理学测试和精神科问卷。根据急性阶段呼吸 COVID-19 症状的严重程度将患者分类:轻症(无需住院)、中症(常规住院)和重症(入住重症监护病房(ICU)加机械通气)。我们在每个时间点运行蒙特卡罗模拟方法,生成一个模拟人群,然后将三个患者亚组显示的认知障碍的累积百分比与估计的正常数据进行比较。我们对整个样本进行了广义估计方程,以评估累积神经认知缺陷、疲劳和精神数据(焦虑、抑郁症状、创伤后应激障碍和冷漠)之间的纵向关联。
大多数参与者(>50%)表现出神经认知障碍的减轻,而大约 25%的患者表现出这些认知缺陷的加重。在 T2 时,轻症患者亚组没有累积的神经认知障碍。中症患者的感知和注意力功能的累积缺陷程度降低,执行、记忆和逻辑推理缺陷持续存在,语言缺陷出现。重症患者出现感知缺陷,执行缺陷增加,而注意力和记忆缺陷保持不变。执行功能的变化与抑郁症状的变化显著相关,但广义估计方程未显示出任何其他显著影响。
虽然在中症和重症患者亚组中,T1 时观察到的大多数累积神经认知缺陷在随时间推移而持续存在,甚至恶化,但主要在轻症患者亚组中,相当一部分患者的表现有所改善。然而,我们发现无论是在横断面还是随时间推移,都存在异质的神经认知特征,这表明可能存在不同的患者表型。这些不良动态的预测因素尚未确定。