Salsone Maria, Signorelli Carlo, Oldani Alessandro, Alberti Valerio Fabio, Castronovo Vincenza, Mazzitelli Salvatore, Minerva Massimo, Ferini-Strambi Luigi
Institute of Molecular Bioimaging and Physiology, National Research Council, 20125 Milan, Italy.
Sleep Disorders Center, Division of Neuroscience, San Raffaele Scientific Institute, 20127 Milan, Italy.
Vaccines (Basel). 2023 Oct 21;11(10):1621. doi: 10.3390/vaccines11101621.
In this Italian population-based study, we aimed to evaluate the neurological complications after the first and/or second dose of COVID-19 vaccines and factors potentially associated with these adverse effects.
Our study included adults aged 18 years and older who received two vaccine doses in the vaccination hub of Novegro (Milan, Lombardy) between 7 and 16 July 2021. The NEURO-COVAX questionnaire was able to capture the neurological events, onset and duration. That data that were digitized centrally by the Lombardy region were used to match the demographic/clinical characteristics and identify a vulnerability profile. Associations between vaccine lines and the development of complications were assessed. Digital healthcare system matching was also performed to evaluate severe neurological complications (Guillain-Barrè syndrome, Bell's palsy, transverse myelitis, encephalitis) and the incidence of hospital admissions and/or the mortality rate after two doses of the vaccines.
The NEURO-COVAX-cohort included 19.108 vaccinated people: 15.368 with BNT162b2, 2077 with mRNA-1273, 1651 with ChAdOx1nCov-19, and 12 with Ad26.COV2.S who were subsequently excluded. Approximately 31.2% of our sample developed post-vaccination neurological complications, particularly with ChAdOx1nCov-19. A vulnerable clinical profile emerged, where over 40% of the symptomatic people showed comorbidities in their clinical histories. Defining the neurological risk profile, we found an increased risk for ChAdOx1nCov-19 of tremors (vs. BNT162b2, OR: 5.12, 95% CI: 3.51-7.48); insomnia (vs. mRNA-1273, OR: 1.87, 95% CI: 1.02-3.39); muscle spasms (vs. BNT162b2, OR: 1.62, 95% CI: 1.08-2.46); and headaches (vs. BNT162b2, OR: 1.49, 95% CI: 0.96-1.57). For mRNA-1273, there were increased risks of parethesia (vs. ChAdOx1nCov-19, OR: 2.37, 95% CI: 1.48-3.79); vertigo (vs. ChAdOx1nCov-19, OR: 1.68, 95% CI: 1.20-2.35); diplopia (vs. ChAdOx1nCov-19, OR: 1.55, 95% CI: 0.67-3.57); and sleepiness (vs. ChAdOx1nCov-19, OR: 1.28, 95% CI: 0.98-1.67). In the period that ranged from March to August 2021, no one was hospitalized and/or died of severe complications related to COVID-19 vaccinations.
This study estimates the prevalence and risk for neurological complications potentially associated with COVID-19 vaccines, thus improving the vaccination guidelines and loading in future personalized preventive medicine.
在这项基于意大利人群的研究中,我们旨在评估接种第一剂和/或第二剂新冠疫苗后的神经并发症以及可能与这些不良反应相关的因素。
我们的研究纳入了2021年7月7日至16日在诺韦格罗(米兰,伦巴第)疫苗接种中心接种两剂疫苗的18岁及以上成年人。NEURO-COVAX问卷能够记录神经事件、发作情况和持续时间。由伦巴第地区集中数字化处理的数据用于匹配人口统计学/临床特征并确定易患特征。评估了疫苗种类与并发症发生之间的关联。还进行了数字医疗系统匹配,以评估严重神经并发症(格林-巴利综合征、贝尔麻痹、横贯性脊髓炎、脑炎)以及两剂疫苗接种后的住院率和/或死亡率。
NEURO-COVAX队列包括19108名接种疫苗的人:15368人接种BNT162b2,2077人接种mRNA-1273,1651人接种ChAdOx1 nCoV-19,12人接种Ad26.COV2.S,后12人被排除。我们样本中约31.2%的人出现了接种后神经并发症,尤其是接种ChAdOx1 nCoV-19疫苗的人。出现了一种易患临床特征,超过40%的有症状者在其临床病史中有合并症。在确定神经风险特征时,我们发现接种ChAdOx1 nCoV-19疫苗后震颤风险增加(与BNT162b2相比,比值比:5.12,95%置信区间:3.51-7.48);失眠风险增加(与mRNA-1273相比,比值比:1.87,95%置信区间:1.02-3.39);肌肉痉挛风险增加(与BNT162b2相比,比值比:1.62,95%置信区间:1.08-2.46);头痛风险增加(与BNT162b2相比,比值比:1.49,95%置信区间:0.96-1.57)。对于mRNA-1273,感觉异常风险增加(与ChAdOx1 nCoV-19相比,比值比:2.37,95%置信区间:1.48-3.79);眩晕风险增加(与ChAdOx1 nCoV-19相比,比值比:1.68,95%置信区间:1.20-2.35);复视风险增加(与ChAdOx1 nCoV-19相比,比值比:1.55,95%置信区间:0.67-3.57);嗜睡风险增加(与ChAdOx1 nCoV-19相比,比值比:1.28,95%置信区间:0.98-1.67)。在2021年3月至8月期间,没有人因新冠疫苗接种相关的严重并发症住院和/或死亡。
本研究估计了与新冠疫苗潜在相关的神经并发症的患病率和风险,从而改进了疫苗接种指南并为未来的个性化预防医学提供了依据。