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

被引:25
|
作者
Iaffaldano, Pietro [1 ]
Lucisano, Giuseppe [1 ]
Manni, Alessia [1 ]
Paolicelli, Damiano [1 ]
Patti, Francesco [3 ]
Capobianco, Marco [4 ,5 ]
Morra, Vincenzo Brescia [6 ]
Sola, Patrizia [7 ]
Pesci, Ilaria [8 ]
Lus, Giacomo [2 ]
De Luca, Giovanna [9 ,10 ]
Lugaresi, Alessandra [11 ,12 ]
Cavalla, Paola [13 ]
Montepietra, Sara [4 ,5 ]
Maniscalco, Giorgia Teresa [15 ]
Granella, Franco [16 ]
Ragonese, Paolo [17 ]
Vianello, Marika [18 ]
Brambilla, Laura [19 ]
Totaro, Rocco [20 ]
Toscano, Simona [3 ]
Malucchi, Simona [14 ]
Petracca, Maria [24 ]
Moiola, Lucia [21 ]
Ferraro, Diana [22 ]
Lepore, Vito [23 ]
Mosconi, Paola [23 ]
Ponzio, Michela [6 ]
Tedeschi, Gioacchino [25 ]
Comi, Giancarlo [26 ]
Battaglia, Mario Alberto [27 ]
Filippi, Massimo [21 ]
Amato, Maria Pia [28 ,29 ]
Trojano, Maria [1 ]
机构
[1] Univ Bari Aldo Moro, Neurosci & Sense Organs, Dept Basic Med Sci, Bari, Italy
[2] CORESEARCH, Pescara, Italy
[3] Univ Catania, Ctr Sclerosi Multipla, Sez Neurosci, GF Ingrassia,Dipartimento Sci Med & Chirurg & Tec, Catania, Italy
[4] AOU San Luigi, SCDO Neurol, Orbassano, TO, Italy
[5] AOU San Luigi, Ctr Riferimento Reg Sclerosi Multipla CRESM, Orbassano, TO, Italy
[6] Federico II Univ Naples, Reprod & Odontos Tomatol Sci, Dept Neurosci, Naples, Italy
[7] Azienda Osped Univ Modena OCB, UO Neurol, Ctr Malattie Demielinizzanti, Modena, Italy
[8] AUSL PR, Osped Vaio, Ctr SM UO Neurol, Fidenza, Italy
[9] Univ Naples 2, Dept Clin & Expt Med, Div Neurol 2, Multiple Sclerosis Ctr, Naples, Italy
[10] Policlin SS Annunziata, Clin Neurol, Ctr Sclerosi Multipla, Chieti, Italy
[11] UOSI Riabilitaz Sclerosi Multipla, IRCCS Ist Sci Neurol Bologna, Bologna, Italy
[12] Univ Bologna, Dipartimento Sci Biomed & Neuromotorie, Bologna, Italy
[13] AOU Citta Salute & Sci Torino, Neurol DU 1, Ctr SM, Turin, Italy
[14] AUSL IRCCS Reggio Emilia, Arcispedale Santa Maria Nuova, Ctr SM, SOC Neurol, Reggio Emilia, Italy
[15] Cardarelli Hosp, Neurol Clin & Multiple Sclerosis Ctr, Naples, Italy
[16] Azienda Osped Univ Parma, Ctr Sclerosi Multipla, Parma, Italy
[17] Univ Palermo, Dept Biomed, Neurosci & Adv Diagnost, Palermo, Italy
[18] Ctr Sclerosi Multipla UO Neurol Osped, Treviso, Italy
[19] Fdn IRCCS Ist Neurol C Besta UO Neuroimmunol & Ma, Milan, Italy
[20] Osped San Salvatore, Clin Neurol, Ctr Malattie Demielinizzanti, Laquila, Italy
[21] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Neurofisiol & Neuroriabilitaz, Dipartimento Neurol, Milan, Italy
[22] Univ Modena & Reggio Emilia, Metab & Neurosci, Dept Biomed, Reggio Emilia, Italy
[23] Ist Ric Farmacol Mario Negri IRCCS, Milan, Italy
[24] Italian Multiple Sclerosis Fdn, Sci Res Area, Genoa, Italy
[25] Univ Campania Luigi Vanvitelli, MRI Res Ctr SUN FISM, AOU, Div Neurol 1,Dept Adv Med & Surg Sci, Naples, Italy
[26] IRCCS San Raffaele Hosp, Inst Expt Neurol, Milan, Italy
[27] Univ Siena, Dept Life Sci, Siena, Italy
[28] Univ Florence, Dept NEUROFARBA, Florence, Italy
[29] IRCCS Fdn Don Carlo Gnocchi, Florence, Italy
来源
关键词
DISEASE-MODIFYING THERAPIES;
D O I
10.1212/NXI.0000000000001141
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
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