Cognitive impairment and a ered cerebral glucose metabolism in the subacute stage of COVID-19

被引:260
作者
Hosp, Jonas A. [1 ]
Dressing, Andrea [1 ,2 ]
Blazhenets, Ganna [3 ]
Bormann, Tobias [1 ]
Rau, Alexander [4 ]
Schwabenland, Marius [5 ]
Thurow, Johannes [3 ]
Wagner, Dirk [6 ]
Waller, Cornelius [7 ]
Niesen, Wolf D. [1 ]
Frings, Lars [3 ]
Urbach, Horst [4 ]
Prinz, Marco [5 ,8 ,9 ]
Weiller, Cornelius [1 ,2 ]
Schroeter, Nils [1 ]
Meyer, Philipp T. [3 ]
机构
[1] Univ Freiburg, Dept Neurol & Clin Neurosci, Med Ctr, Fac Med, Freiburg, Germany
[2] Univ Freiburg, Med Ctr, Fac Med, Freiburg Brain Imaging Ctr, Freiburg, Germany
[3] Univ Freiburg, Dept Nucl Med, Fac Med, Med Ctr, Freiburg, Germany
[4] Univ Freiburg, Dept Neuroradiol, Fac Med, Med Ctr, Freiburg, Germany
[5] Univ Freiburg, Fac Med, Inst Neuropathol, Freiburg, Germany
[6] Univ Freiburg, Div Infect Dis, Dept Internal Med 2, Med Ctr,Fac Med, Freiburg, Germany
[7] Univ Freiburg, Dept Internal Med 1, Fac Med, Med Ctr, Freiburg, Germany
[8] Univ Freiburg, Fac Med, Ctr Basics NeuroModulat NeuroModulBas, Freiburg, Germany
[9] Univ Freiburg, Signalling Res Ctr BIOSS & CIBSS, Freiburg, Germany
关键词
COVID-19; cognition; neurology; 18FDG PET; Montreal Cognitive Assessment; CYTOKINE STORM; TOOL;
D O I
10.1093/brain/awab009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
During the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, neurological symptoms increasingly moved into the focus of interest. In this prospective cohort study, we assessed neurological and cognitive symptoms in hospitalized coronavirus disease-19 (COVID-19) patients and aimed to determine their neuronal correlates. Patients with reverse transcription-PCR-confirmed COVID-19 infection who required inpatient treatment primarily because of non-neurological complications were screened between 20 April 2020 and 12 May 2020. Patients (age > 18 years) were included in our cohort when presenting with at least one new neurological symptom (defined as impaired gustation and/or olfaction, performance < 26 points on a Montreal Cognitive Assessment and/or pathological findings on clinical neurological examination). Patients with >= 2 new symptoms were eligible for further diagnostics using comprehensive neuropsychological tests, cerebral MRI and (18)fluorodeoxyglucose (FDG) PET as soon as infectivity was no longer present. Exclusion criteria were: premorbid diagnosis of cognitive impairment, neurodegenerative diseases or intensive care unit treatment. Of 41 COVID-19 inpatients screened, 29 patients (65.2 +/- 14.4 years; 38% female) in the subacute stage of disease were included in the register. Most frequently, gustation and olfaction were disturbed in 29/29 and 25/29 patients, respectively. Montreal Cognitive Assessment performance was impaired in 18/26 patients (mean score 21.8/30) with emphasis on frontoparietal cognitive functions. This was confirmed by detailed neuropsychological testing in 15 patients. (18)FDG PET revealed pathological results in 10/15 patients with predominant frontoparietal hypometabolism. This pattern was confirmed by comparison with a control sample using voxel-wise principal components analysis, which showed a high correlation (R-2 = 0.62) with the Montreal Cognitive Assessment performance. Post-mortem examination of one patient revealed white matter microglia activation but no signs of neuroinflammation. Neocortical dysfunction accompanied by cognitive decline was detected in a relevant fraction of patients with subacute COVID-19 initially requiring inpatient treatment. This is of major rehabilitative and socioeconomic relevance.
引用
收藏
页码:1263 / 1276
页数:14
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