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      RISK FACTORS FOR INFECTION AND HEALTH IMPACTS OF THE COVID-19 PANDEMIC IN PEOPLE WITH AUTOIMMUNE DISEASES

      research-article
      , ScD 1 , 2 , , MD, MHS 3 , , BS 1 , , BS 1 , , BS 1 , , MD 3 , , MD 1 , , MD, PhD 1 , , MD, MHS 3 , , MD, MPH 1 , , MD 3 , , MD 3 , , MD, MHS 3 , , MD 3 , , MD 3 , , MD, MSc 3 , , MD 1 , , DO 1 , , MD, PhD 1 , , MD 1 , , MD, PhD 1 , , MD 1 , , MD 1 , , MD 4 , , MD, MAS 4 , , MBBCh 1 , , MD 5 , , MD, MHS 5 , , MD 6 , , MD 6 , , MD, MPH, PhD 2 , 3 , , MD 3 , , MD, MHS 3 , , MD, MCR 1 , 2
      medRxiv
      Cold Spring Harbor Laboratory

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          Abstract

          Background

          People with autoimmune or inflammatory conditions who take immunomodulatory/suppressive medications may have a higher risk of novel coronavirus disease 2019 (COVID-19). Chronic disease care has also changed for many patients, with uncertain downstream consequences.

          Objective

          Assess whether COVID-19 risk is higher among those on immunomodulating or suppressive agents and characterize pandemic-associated changes to care.

          Design

          Longitudinal registry study

          Participants

          4666 individuals with autoimmune or inflammatory conditions followed by specialists in neurology, rheumatology, cardiology, pulmonology or gastroenterology at Johns Hopkins

          Measurements

          Periodic surveys querying comorbidities, disease-modifying medications, exposures, COVID-19 testing and outcomes, social behaviors, and disruptions to healthcare

          Results

          A total of 265 (5.6%) developed COVID-19 over 9 months of follow-up (April-December 2020). Patient characteristics (age, race, comorbidity, medication exposure) were associated with differences in social distancing behaviors during the pandemic. Glucocorticoid exposure was associated with higher odds of COVID-19 in multivariable models incorporating behavior and other potential confounders (OR: 1.43; 95%CI: 1.08, 1.89). Other medication classes were not associated with COVID-19 risk. Diabetes (OR: 1.72; 95%CI: 1.08, 2.73), cardiovascular disease (OR: 1.68; 95%CI: 1.24, 2.28), and chronic kidney disease (OR: 1.76; 95%CI: 1.04, 2.97) were each associated with higher odds of COVID-19. Pandemic-related disruption to care was common. Of the 2156 reporting pre-pandemic utilization of infusion, mental health or rehabilitative services, 975 (45.2%) reported disruptions. Individuals experiencing changes to employment or income were at highest odds of care disruption.

          Limitations

          Results may not be generalizable to all patients with autoimmune or inflammatory conditions. Information was self-reported.

          Conclusions

          Exposure to glucocorticoids may increase risk of COVID-19 in people with autoimmune or inflammatory conditions. Disruption to healthcare and related services was common. Those with pandemic-related reduced income may be most vulnerable to care disruptions.

          Related collections

          Most cited references29

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          Neighborhood socioeconomic disadvantage and 30-day rehospitalization: a retrospective cohort study.

          Measures of socioeconomic disadvantage may enable improved targeting of programs to prevent rehospitalizations, but obtaining such information directly from patients can be difficult. Measures of U.S. neighborhood socioeconomic disadvantage are more readily available but are rarely used clinically.
            Bookmark
            • Record: found
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            Area deprivation and widening inequalities in US mortality, 1969-1998.

            G. Singh (2003)
            This study examined age-, sex-, and race-specific gradients in US mortality by area deprivation between 1969 and 1998. A census-based area deprivation index was linked to county mortality data. Area deprivation gradients in US mortality increased substantially during 1969 through 1998. The gradients were steepest for men and women aged 25 to 44 years and those younger than 25 years, with higher mortality rates observed in more deprived areas. Although area gradients were less pronounced for women in each age group, they rose sharply for women aged 25 to 44 and 45 to 64 years. Areal inequalities in mortality widened because of slower mortality declines in more deprived areas. Future research needs to examine population-level social, behavioral, and medical care factors that may account for the increasing gradient.
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              • Record: found
              • Abstract: found
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              Is Open Access

              Disease‐Modifying Therapies and Coronavirus Disease 2019 Severity in Multiple Sclerosis

              Objective This study was undertaken to assess the impact of immunosuppressive and immunomodulatory therapies on the severity of coronavirus disease 2019 (COVID‐19) in people with multiple sclerosis (PwMS). Methods We retrospectively collected data of PwMS with suspected or confirmed COVID‐19. All the patients had complete follow‐up to death or recovery. Severe COVID‐19 was defined by a 3‐level variable: mild disease not requiring hospitalization versus pneumonia or hospitalization versus intensive care unit (ICU) admission or death. We evaluated baseline characteristics and MS therapies associated with severe COVID‐19 by multivariate and propensity score (PS)‐weighted ordinal logistic models. Sensitivity analyses were run to confirm the results. Results Of 844 PwMS with suspected (n = 565) or confirmed (n = 279) COVID‐19, 13 (1.54%) died; 11 of them were in a progressive MS phase, and 8 were without any therapy. Thirty‐eight (4.5%) were admitted to an ICU; 99 (11.7%) had radiologically documented pneumonia; 96 (11.4%) were hospitalized. After adjusting for region, age, sex, progressive MS course, Expanded Disability Status Scale, disease duration, body mass index, comorbidities, and recent methylprednisolone use, therapy with an anti‐CD20 agent (ocrelizumab or rituximab) was significantly associated (odds ratio [OR] = 2.37, 95% confidence interval [CI] = 1.18–4.74, p = 0.015) with increased risk of severe COVID‐19. Recent use (<1 month) of methylprednisolone was also associated with a worse outcome (OR = 5.24, 95% CI = 2.20–12.53, p = 0.001). Results were confirmed by the PS‐weighted analysis and by all the sensitivity analyses. Interpretation This study showed an acceptable level of safety of therapies with a broad array of mechanisms of action. However, some specific elements of risk emerged. These will need to be considered while the COVID‐19 pandemic persists. ANN NEUROL 2021;89:780–789
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                Author and article information

                Journal
                medRxiv
                MEDRXIV
                medRxiv
                Cold Spring Harbor Laboratory
                05 February 2021
                : 2021.02.03.21251069
                Affiliations
                [1 ]Department of Neurology, Johns Hopkins School of Medicine, Baltimore, MD, USA
                [2 ]Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
                [3 ]Division of Rheumatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA
                [4 ]Division of Gastroenterology and Hepatology, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA
                [5 ]Division of Pulmonary and Critical Care Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA
                [6 ]Department of Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA
                Author notes
                Corresponding author: Kathryn C Fitzgerald, fitzgerald@ 123456jhmi.edu , 600 N Wolfe St, Pathology 627, Baltimore MD, 21287
                Article
                10.1101/2021.02.03.21251069
                7872366
                33564774
                23fdc052-dcb7-4533-bad2-d915f96e7587

                This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License, which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.

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