奥米克隆前后僵人综合征谱系障碍患者的 COVID-19 风险因素和结果。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Hanyeh Afshar, Alexandra Simpson, Elena Taylor, Ashley Miles, Herbert R Chen, Scott D Newsome
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引用次数: 0

摘要

背景:僵人综合征谱系障碍(SPSD)是一种罕见的致残性神经系统疾病,与冠状病毒病2019(COVID-19)的风险因素有关。然而,关于COVID-19对SPSD总体影响的数据有限:方法:纳入约翰-霍普金斯大学SPS中心随访的SPSD和COVID-19患者。记录人口统计学特征、SPSD 特征以及 COVID-19 的特异性数据:研究期间共报告了 35 例 SPSD 和 COVID-19 病例。患者平均年龄为 56 岁(SD ± 10),大多数为女性(66.7%)。80%的 COVID-19 病例通过检测得到确诊,其余病例高度提示 COVID-19。COVID-19 患者的合并症包括高血压(6 例)、糖尿病(6 例)、肥胖(5 例)和心血管疾病(4 例)。大多数参与者正在使用免疫疗法和/或苯二氮卓类药物。在报告的病例中,只有 2 例需要住院治疗,其中 2 例均患有糖尿病,1 例正在接受免疫抑制治疗。大多数病例都是在全面接种疫苗后出现的。发热是最常见的 COVID-19 相关症状。此外,还报告了短暂的神经系统症状:结论:SPSD 感染严重 COVID-19 的风险因素似乎与普通人群的历史数据相同。重要的是,COVID-19 似乎与 COVID-19 后 SPSD 的恶化无关。接种疫苗可能在预防严重的 COVID-19 病例方面发挥了作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 risk factors and outcomes in individuals with stiff person syndrome spectrum disorders before and after omicron.

Background: Stiff person syndrome spectrum disorders (SPSD) are rare, disabling disorders of the nervous system that are associated with risk factors for Coronavirus disease 2019 (COVID-19). However, limited data exist on the overall impact of COVID-19 on SPSD.

Methods: Patients with SPSD and COVID-19 who are followed at Johns Hopkins SPS Center were included. Demographics and SPSD characteristics along with COVID-19-specific data were recorded.

Results: Thirty-five cases of SPSD with COVID-19 cases were reported during the study time period. Mean age of the cohort was 56 (SD ± 10) and most were female (66.7%). Eighty percent of the COVID-19 cases were confirmed with testing, and the rest were highly suggestive of COVID-19. COVID-19 comorbidities among patients were hypertension (n = 6), diabetes (n = 6), obesity (n = 5), and cardiovascular disease (n = 4). The majority of participants were on immune therapies and/or benzodiazepines. Out of the cases reported, only 2 required hospitalization, both of whom had diabetes, and one was on immunosuppressive therapy. The majority of cases were post-full-vaccination cases. Fever was the most common COVID-19-associated symptom. Transient neurological symptoms were also reported.

Conclusion: Risk factors for developing severe COVID-19 in SPSD appear to be the same as historical data in the general population. Importantly, COVID-19 did not appear to be associated with worsening SPSD post-COVID-19. Vaccination may have played a role in preventing severe cases of COVID-19.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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