Shreya Mukherjee, Tracey Singer, Aditi Venkatesh, Natasha A Choudhury, Gina S Perez Giraldo, Millenia Jimenez, Janet Miller, Melissa Lopez, Barbara A Hanson, Aasheeta P Bawa, Ayush Batra, Eric M Liotta, Igor J Koralnik
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Among PNP patients, 87% had a pre-vaccination infection and 13% had a breakthrough infection post-vaccination. Among the NNP patients, 70.7% had a pre-vaccination infection and 29.3% had a breakthrough infection. Both PNP and NNP breakthrough infection patients had more frequent pre-existing depression/anxiety than their respective pre-vaccination infection groups, and NNP breakthrough infection patients also had more frequent comorbidities of headache, lung and gastrointestinal diseases than the NNP pre-vaccination infection group. An average of 10 months after symptom onset, the three most common neurological symptoms for PNP patients were brain fog (86.5%), numbness/tingling (56.5%) and headache (56.5%). Of all Neuro-PASC symptoms, PNP breakthrough infection more frequently reported anosmia compared to PNP pre-vaccination infection patients (69.2 versus 37.9%; <i>P</i> = 0.005). For NNP patients, the three most common neurological symptoms were brain fog (83.9%), headache (70.9%) and dizziness (53.8%). NNP pre-vaccination infection reported anosmia (56.6 versus 39.1%; <i>P</i> < 0.0001) and dysgeusia (53.3 versus 37.3%; <i>P</i> < 0.0001) more frequently than breakthrough infection patients. NNP breakthrough infection more frequently reported dizziness compared to NNP pre-vaccination infection patients (61.5 versus 50.6%; <i>P</i> = 0.001). Both PNP and NNP patients had impaired quality-of-life in cognitive, fatigue, sleep, anxiety and depression domains with no differences between pre-vaccination infection and breakthrough infection groups. PNP patients performed worse on National Institutes of Health Toolbox tests of processing speed, attention, executive function and working memory than a US normative population whereas NNP patients had lower results in processing, speed, attention and working memory, without differences between pre-vaccination infection and breakthrough infection groups. These results indicate that vaccination prior to SARS-CoV-2 infection does not affect the neurologic manifestations of long COVID in either PNP or NNP patients. Minor differences in neurologic symptoms between pre-vaccination infection and breakthrough infection groups may be caused by SARS-CoV-2 strains evolution. 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COVID-19 vaccines reduce the gravity of ensuing SARS-CoV-2 infections. However, whether vaccines also have an impact on PASC remain unknown. We investigated whether vaccination prior to infection alters the subsequent neurologic post-acute sequelae of SARS-CoV-2 infection (Neuro-PASC). We studied prospectively the first consecutive 200 post-hospitalization Neuro-PASC (PNP) and 1100 non-hospitalized Neuro-PASC (NNP) patients evaluated at our neuro-COVID-19 clinic between May 2020 and January 2023. Among PNP patients, 87% had a pre-vaccination infection and 13% had a breakthrough infection post-vaccination. Among the NNP patients, 70.7% had a pre-vaccination infection and 29.3% had a breakthrough infection. Both PNP and NNP breakthrough infection patients had more frequent pre-existing depression/anxiety than their respective pre-vaccination infection groups, and NNP breakthrough infection patients also had more frequent comorbidities of headache, lung and gastrointestinal diseases than the NNP pre-vaccination infection group. An average of 10 months after symptom onset, the three most common neurological symptoms for PNP patients were brain fog (86.5%), numbness/tingling (56.5%) and headache (56.5%). Of all Neuro-PASC symptoms, PNP breakthrough infection more frequently reported anosmia compared to PNP pre-vaccination infection patients (69.2 versus 37.9%; <i>P</i> = 0.005). For NNP patients, the three most common neurological symptoms were brain fog (83.9%), headache (70.9%) and dizziness (53.8%). NNP pre-vaccination infection reported anosmia (56.6 versus 39.1%; <i>P</i> < 0.0001) and dysgeusia (53.3 versus 37.3%; <i>P</i> < 0.0001) more frequently than breakthrough infection patients. NNP breakthrough infection more frequently reported dizziness compared to NNP pre-vaccination infection patients (61.5 versus 50.6%; <i>P</i> = 0.001). Both PNP and NNP patients had impaired quality-of-life in cognitive, fatigue, sleep, anxiety and depression domains with no differences between pre-vaccination infection and breakthrough infection groups. PNP patients performed worse on National Institutes of Health Toolbox tests of processing speed, attention, executive function and working memory than a US normative population whereas NNP patients had lower results in processing, speed, attention and working memory, without differences between pre-vaccination infection and breakthrough infection groups. 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引用次数: 0
摘要
COVID-19后的持续症状构成长COVID综合征,也称为SARS-CoV-2感染急性后后遗症(PASC)。COVID-19疫苗降低了随后的SARS-CoV-2感染的严重性。然而,疫苗是否对PASC也有影响尚不清楚。我们调查了感染前接种疫苗是否会改变SARS-CoV-2感染后的神经系统急性后后遗症(neuropasc)。我们前瞻性研究了2020年5月至2023年1月在我们的神经- covid -19诊所评估的首批连续200例住院后神经- pasc (PNP)和1100例非住院神经- pasc (NNP)患者。在PNP患者中,87%的人在接种前感染,13%的人在接种后出现突破性感染。在NNP患者中,接种前感染占70.7%,突破感染占29.3%。PNP和NNP突破感染患者的既往抑郁/焦虑发生率均高于接种前感染组,NNP突破感染患者的头痛、肺部和胃肠道疾病合并症发生率均高于接种前感染组。症状出现后平均10个月,PNP患者最常见的3种神经系统症状为脑雾(86.5%)、麻木/刺痛(56.5%)和头痛(56.5%)。在所有神经- pasc症状中,与接种前感染PNP的患者相比,PNP突破感染更频繁地报告嗅觉缺失(69.2 vs 37.9%;P = 0.005)。NNP患者最常见的3种神经系统症状为脑雾(83.9%)、头痛(70.9%)和头晕(53.8%)。NNP疫苗接种前感染报告嗅觉缺失(56.6%对39.1%;P < 0.0001)和发音困难(53.3 vs 37.3%;P < 0.0001)高于突破感染患者。与NNP疫苗接种前感染患者相比,NNP突破感染更频繁地报告头晕(61.5%对50.6%;P = 0.001)。PNP和NNP患者在认知、疲劳、睡眠、焦虑和抑郁领域的生活质量受损,接种前感染组和突破感染组之间没有差异。PNP患者在美国国立卫生研究院工具箱测试的处理速度、注意力、执行功能和工作记忆方面的表现低于美国正常人群,而NNP患者在处理、速度、注意力和工作记忆方面的结果低于接种前感染组和突破感染组。这些结果表明,在感染SARS-CoV-2之前接种疫苗对PNP或NNP患者的长冠状病毒神经系统表现没有影响。疫苗接种前感染组与突破感染组神经系统症状的微小差异可能是由SARS-CoV-2毒株进化引起的。突破性感染后发生神经pasc的患者有更高的合并症负担,突出了不同的危险因素,需要有针对性的管理。
Vaccination prior to SARS-CoV-2 infection does not affect the neurologic manifestations of long COVID.
Persistent symptoms after COVID-19 constitute the long COVID syndrome, also called post-acute sequelae of SARS-CoV-2 infection (PASC). COVID-19 vaccines reduce the gravity of ensuing SARS-CoV-2 infections. However, whether vaccines also have an impact on PASC remain unknown. We investigated whether vaccination prior to infection alters the subsequent neurologic post-acute sequelae of SARS-CoV-2 infection (Neuro-PASC). We studied prospectively the first consecutive 200 post-hospitalization Neuro-PASC (PNP) and 1100 non-hospitalized Neuro-PASC (NNP) patients evaluated at our neuro-COVID-19 clinic between May 2020 and January 2023. Among PNP patients, 87% had a pre-vaccination infection and 13% had a breakthrough infection post-vaccination. Among the NNP patients, 70.7% had a pre-vaccination infection and 29.3% had a breakthrough infection. Both PNP and NNP breakthrough infection patients had more frequent pre-existing depression/anxiety than their respective pre-vaccination infection groups, and NNP breakthrough infection patients also had more frequent comorbidities of headache, lung and gastrointestinal diseases than the NNP pre-vaccination infection group. An average of 10 months after symptom onset, the three most common neurological symptoms for PNP patients were brain fog (86.5%), numbness/tingling (56.5%) and headache (56.5%). Of all Neuro-PASC symptoms, PNP breakthrough infection more frequently reported anosmia compared to PNP pre-vaccination infection patients (69.2 versus 37.9%; P = 0.005). For NNP patients, the three most common neurological symptoms were brain fog (83.9%), headache (70.9%) and dizziness (53.8%). NNP pre-vaccination infection reported anosmia (56.6 versus 39.1%; P < 0.0001) and dysgeusia (53.3 versus 37.3%; P < 0.0001) more frequently than breakthrough infection patients. NNP breakthrough infection more frequently reported dizziness compared to NNP pre-vaccination infection patients (61.5 versus 50.6%; P = 0.001). Both PNP and NNP patients had impaired quality-of-life in cognitive, fatigue, sleep, anxiety and depression domains with no differences between pre-vaccination infection and breakthrough infection groups. PNP patients performed worse on National Institutes of Health Toolbox tests of processing speed, attention, executive function and working memory than a US normative population whereas NNP patients had lower results in processing, speed, attention and working memory, without differences between pre-vaccination infection and breakthrough infection groups. These results indicate that vaccination prior to SARS-CoV-2 infection does not affect the neurologic manifestations of long COVID in either PNP or NNP patients. Minor differences in neurologic symptoms between pre-vaccination infection and breakthrough infection groups may be caused by SARS-CoV-2 strains evolution. Patients developing Neuro-PASC after breakthrough infection have a higher burden of comorbidities, highlighting different risk factors warranting targeted management.