多发性硬化症患者感染COVID-19的风险:一项病例对照研究

IF 7.5
Pietro Iaffaldano, Giuseppe Lucisano, Alessia Manni, Damiano Paolicelli, Francesco Patti, Marco Capobianco, Vincenzo Brescia Morra, Patrizia Sola, Ilaria Pesci, Giacomo Lus, Giovanna De Luca, Alessandra Lugaresi, Paola Cavalla, Sara Montepietra, Giorgia Teresa Maniscalco, Franco Granella, Paolo Ragonese, Marika Vianello, Laura Brambilla, Rocco Totaro, Simona Toscano, Simona Malucchi, Maria Petracca, Lucia Moiola, Diana Ferraro, Vito Lepore, Paola Mosconi, Michela Ponzio, Gioacchino Tedeschi, Giancarlo Comi, Mario Alberto Battaglia, Massimo Filippi, Maria Pia Amato, Maria Trojano
{"title":"多发性硬化症患者感染COVID-19的风险:一项病例对照研究","authors":"Pietro Iaffaldano,&nbsp;Giuseppe Lucisano,&nbsp;Alessia Manni,&nbsp;Damiano Paolicelli,&nbsp;Francesco Patti,&nbsp;Marco Capobianco,&nbsp;Vincenzo Brescia Morra,&nbsp;Patrizia Sola,&nbsp;Ilaria Pesci,&nbsp;Giacomo Lus,&nbsp;Giovanna De Luca,&nbsp;Alessandra Lugaresi,&nbsp;Paola Cavalla,&nbsp;Sara Montepietra,&nbsp;Giorgia Teresa Maniscalco,&nbsp;Franco Granella,&nbsp;Paolo Ragonese,&nbsp;Marika Vianello,&nbsp;Laura Brambilla,&nbsp;Rocco Totaro,&nbsp;Simona Toscano,&nbsp;Simona Malucchi,&nbsp;Maria Petracca,&nbsp;Lucia Moiola,&nbsp;Diana Ferraro,&nbsp;Vito Lepore,&nbsp;Paola Mosconi,&nbsp;Michela Ponzio,&nbsp;Gioacchino Tedeschi,&nbsp;Giancarlo Comi,&nbsp;Mario Alberto Battaglia,&nbsp;Massimo Filippi,&nbsp;Maria Pia Amato,&nbsp;Maria Trojano","doi":"10.1212/NXI.0000000000001141","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>Several studies have assessed risk factors associated with the severity of COVID-19 outcomes in people with multiple sclerosis (PwMS). The potential role of disease-modifying therapies (DMTs) and demographic and clinical factors on the risk of acquiring SARS-CoV-2 infection has not been evaluated so far. The objective of this study was to assess risk factors of contracting SARS-CoV-2 infection in PwMS by using data collected in the Italian MS Register (IMSR).</p><p><strong>Methods: </strong>A case-control (1:2) study was set up. Cases included PwMS with a confirmed diagnosis of COVID-19, and controls included PwMS without a confirmed diagnosis of COVID-19. Both groups were propensity score-matched by the date of COVID-19 diagnosis, the date of last visit, and the region of residence. No healthy controls were included in this study. COVID-19 risk was estimated by multivariable logistic regression models including demographic and clinical covariates. The impact of DMTs was assessed in 3 independent logistic regression models including one of the following covariates: last administered DMT, previous DMT sequences, or the place where the last treatment was administered.</p><p><strong>Results: </strong>A total of 779 PwMS with confirmed COVID-19 (cases) were matched to 1,558 PwMS without COVID-19 (controls). In all 3 models, comorbidities, female sex, and a younger age were significantly associated (<i>p</i> < 0.02) with a higher risk of contracting COVID-19. Patients receiving natalizumab as last DMT (OR [95% CI]: 2.38 [1.66-3.42], <i>p</i> < 0.0001) and those who underwent an escalation treatment strategy (1.57 [1.16-2.13], <i>p</i> = 0.003) were at significantly higher COVID-19 risk. Moreover, PwMS receiving their last DMT requiring hospital access (1.65 [1.34-2.04], <i>p</i> < 0.0001) showed a significant higher risk than those taking self-administered DMTs at home.</p><p><strong>Discussion: </strong>This case-control study embedded in the IMSR showed that PwMS at higher COVID-19 risk are younger, more frequently female individuals, and with comorbidities. Long-lasting escalation approach and last therapies that expose patients to the hospital environment seem to significantly increase the risk of SARS-CoV2 infection in PwMS.</p><p><strong>Classification of evidence: </strong>This study provides Class III evidence that among patients with MS, younger age, being female individuals, having more comorbidities, receiving natalizumab, undergoing an escalating treatment strategy, or receiving treatment at a hospital were associated with being infected with COVID-19. Among patients with MS who were infected with COVID-19, a severe course was associated with increasing age and having a progressive form of MS, whereas not being on treatment or receiving an interferon beta agent was protective.</p>","PeriodicalId":520720,"journal":{"name":"Neurology(R) neuroimmunology & neuroinflammation","volume":" ","pages":""},"PeriodicalIF":7.5000,"publicationDate":"2022-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cb/55/NEURIMMINFL2021039360.PMC8771668.pdf","citationCount":"22","resultStr":"{\"title\":\"Risk of Getting COVID-19 in People With Multiple Sclerosis: A Case-Control Study.\",\"authors\":\"Pietro Iaffaldano,&nbsp;Giuseppe Lucisano,&nbsp;Alessia Manni,&nbsp;Damiano Paolicelli,&nbsp;Francesco Patti,&nbsp;Marco Capobianco,&nbsp;Vincenzo Brescia Morra,&nbsp;Patrizia Sola,&nbsp;Ilaria Pesci,&nbsp;Giacomo Lus,&nbsp;Giovanna De Luca,&nbsp;Alessandra Lugaresi,&nbsp;Paola Cavalla,&nbsp;Sara Montepietra,&nbsp;Giorgia Teresa Maniscalco,&nbsp;Franco Granella,&nbsp;Paolo Ragonese,&nbsp;Marika Vianello,&nbsp;Laura Brambilla,&nbsp;Rocco Totaro,&nbsp;Simona Toscano,&nbsp;Simona Malucchi,&nbsp;Maria Petracca,&nbsp;Lucia Moiola,&nbsp;Diana Ferraro,&nbsp;Vito Lepore,&nbsp;Paola Mosconi,&nbsp;Michela Ponzio,&nbsp;Gioacchino Tedeschi,&nbsp;Giancarlo Comi,&nbsp;Mario Alberto Battaglia,&nbsp;Massimo Filippi,&nbsp;Maria Pia Amato,&nbsp;Maria Trojano\",\"doi\":\"10.1212/NXI.0000000000001141\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objectives: </strong>Several studies have assessed risk factors associated with the severity of COVID-19 outcomes in people with multiple sclerosis (PwMS). The potential role of disease-modifying therapies (DMTs) and demographic and clinical factors on the risk of acquiring SARS-CoV-2 infection has not been evaluated so far. The objective of this study was to assess risk factors of contracting SARS-CoV-2 infection in PwMS by using data collected in the Italian MS Register (IMSR).</p><p><strong>Methods: </strong>A case-control (1:2) study was set up. Cases included PwMS with a confirmed diagnosis of COVID-19, and controls included PwMS without a confirmed diagnosis of COVID-19. Both groups were propensity score-matched by the date of COVID-19 diagnosis, the date of last visit, and the region of residence. No healthy controls were included in this study. COVID-19 risk was estimated by multivariable logistic regression models including demographic and clinical covariates. The impact of DMTs was assessed in 3 independent logistic regression models including one of the following covariates: last administered DMT, previous DMT sequences, or the place where the last treatment was administered.</p><p><strong>Results: </strong>A total of 779 PwMS with confirmed COVID-19 (cases) were matched to 1,558 PwMS without COVID-19 (controls). In all 3 models, comorbidities, female sex, and a younger age were significantly associated (<i>p</i> < 0.02) with a higher risk of contracting COVID-19. Patients receiving natalizumab as last DMT (OR [95% CI]: 2.38 [1.66-3.42], <i>p</i> < 0.0001) and those who underwent an escalation treatment strategy (1.57 [1.16-2.13], <i>p</i> = 0.003) were at significantly higher COVID-19 risk. Moreover, PwMS receiving their last DMT requiring hospital access (1.65 [1.34-2.04], <i>p</i> < 0.0001) showed a significant higher risk than those taking self-administered DMTs at home.</p><p><strong>Discussion: </strong>This case-control study embedded in the IMSR showed that PwMS at higher COVID-19 risk are younger, more frequently female individuals, and with comorbidities. Long-lasting escalation approach and last therapies that expose patients to the hospital environment seem to significantly increase the risk of SARS-CoV2 infection in PwMS.</p><p><strong>Classification of evidence: </strong>This study provides Class III evidence that among patients with MS, younger age, being female individuals, having more comorbidities, receiving natalizumab, undergoing an escalating treatment strategy, or receiving treatment at a hospital were associated with being infected with COVID-19. Among patients with MS who were infected with COVID-19, a severe course was associated with increasing age and having a progressive form of MS, whereas not being on treatment or receiving an interferon beta agent was protective.</p>\",\"PeriodicalId\":520720,\"journal\":{\"name\":\"Neurology(R) neuroimmunology & neuroinflammation\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2022-01-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/cb/55/NEURIMMINFL2021039360.PMC8771668.pdf\",\"citationCount\":\"22\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurology(R) neuroimmunology & neuroinflammation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1212/NXI.0000000000001141\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/3/1 0:00:00\",\"PubModel\":\"Print\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurology(R) neuroimmunology & neuroinflammation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1212/NXI.0000000000001141","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/3/1 0:00:00","PubModel":"Print","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 22

摘要

背景和目的:几项研究评估了与多发性硬化症(PwMS)患者COVID-19结局严重程度相关的危险因素。疾病修饰疗法(dmt)以及人口统计学和临床因素对获得SARS-CoV-2感染风险的潜在作用迄今尚未得到评估。本研究的目的是利用意大利多发性硬化症登记册(IMSR)收集的数据,评估多发性硬化症患者感染SARS-CoV-2的危险因素。方法:建立病例-对照(1:2)研究。病例包括确诊为COVID-19的PwMS,对照组包括未确诊为COVID-19的PwMS。两组均按COVID-19诊断日期、最后一次就诊日期和居住地区进行倾向评分匹配。本研究未纳入健康对照。通过包括人口统计学和临床协变量在内的多变量logistic回归模型估计COVID-19风险。DMT的影响在3个独立的逻辑回归模型中进行评估,包括以下协变量之一:最后一次给药的DMT,以前的DMT序列,或最后一次治疗的地方。结果:779名确诊的PwMS(病例)与1558名未确诊的PwMS(对照组)匹配。在所有3种模型中,合并症、女性性别和较年轻的年龄与感染COVID-19的高风险显著相关(p < 0.02)。接受natalizumab作为最后一次DMT的患者(OR [95% CI]: 2.38 [1.66-3.42], p < 0.0001)和接受升级治疗策略的患者(1.57 [1.16-2.13],p = 0.003)的COVID-19风险显着增加。此外,PwMS最后一次接受DMT时需要到医院就诊(1.65 [1.34-2.04],p < 0.0001)的风险明显高于在家自行接受DMT的患者。讨论:这项纳入IMSR的病例对照研究表明,罹患COVID-19风险较高的PwMS患者更年轻,更常见的是女性,并伴有合并症。长期升级方法和使患者暴露于医院环境的最后治疗似乎显著增加了PwMS患者感染SARS-CoV2的风险。证据分类:本研究提供的III类证据表明,在MS患者中,年龄较小、女性、合并症较多、接受natalizumab治疗、接受升级治疗策略或在医院接受治疗与感染COVID-19相关。在感染COVID-19的多发性硬化症患者中,病程严重与年龄增长和多发性硬化症进展有关,而未接受治疗或接受干扰素β制剂则具有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Risk of Getting COVID-19 in People With Multiple Sclerosis: A Case-Control Study.

Risk of Getting COVID-19 in People With Multiple Sclerosis: A Case-Control Study.

Risk of Getting COVID-19 in People With Multiple Sclerosis: A Case-Control Study.

Risk of Getting COVID-19 in People With Multiple Sclerosis: A Case-Control Study.

Background and objectives: Several studies have assessed risk factors associated with the severity of COVID-19 outcomes in people with multiple sclerosis (PwMS). The potential role of disease-modifying therapies (DMTs) and demographic and clinical factors on the risk of acquiring SARS-CoV-2 infection has not been evaluated so far. The objective of this study was to assess risk factors of contracting SARS-CoV-2 infection in PwMS by using data collected in the Italian MS Register (IMSR).

Methods: A case-control (1:2) study was set up. Cases included PwMS with a confirmed diagnosis of COVID-19, and controls included PwMS without a confirmed diagnosis of COVID-19. Both groups were propensity score-matched by the date of COVID-19 diagnosis, the date of last visit, and the region of residence. No healthy controls were included in this study. COVID-19 risk was estimated by multivariable logistic regression models including demographic and clinical covariates. The impact of DMTs was assessed in 3 independent logistic regression models including one of the following covariates: last administered DMT, previous DMT sequences, or the place where the last treatment was administered.

Results: A total of 779 PwMS with confirmed COVID-19 (cases) were matched to 1,558 PwMS without COVID-19 (controls). In all 3 models, comorbidities, female sex, and a younger age were significantly associated (p < 0.02) with a higher risk of contracting COVID-19. Patients receiving natalizumab as last DMT (OR [95% CI]: 2.38 [1.66-3.42], p < 0.0001) and those who underwent an escalation treatment strategy (1.57 [1.16-2.13], p = 0.003) were at significantly higher COVID-19 risk. Moreover, PwMS receiving their last DMT requiring hospital access (1.65 [1.34-2.04], p < 0.0001) showed a significant higher risk than those taking self-administered DMTs at home.

Discussion: This case-control study embedded in the IMSR showed that PwMS at higher COVID-19 risk are younger, more frequently female individuals, and with comorbidities. Long-lasting escalation approach and last therapies that expose patients to the hospital environment seem to significantly increase the risk of SARS-CoV2 infection in PwMS.

Classification of evidence: This study provides Class III evidence that among patients with MS, younger age, being female individuals, having more comorbidities, receiving natalizumab, undergoing an escalating treatment strategy, or receiving treatment at a hospital were associated with being infected with COVID-19. Among patients with MS who were infected with COVID-19, a severe course was associated with increasing age and having a progressive form of MS, whereas not being on treatment or receiving an interferon beta agent was protective.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信