Evidence map›Paper›PMID 34392059›Full record

Observational studyMultiple sclerosis and related disorders2021

Outcomes of COVID-19 infection in multiple sclerosis and related conditions: One-year pandemic experience of the multicenter New York COVID-19 Neuroimmunology Consortium (NYCNIC).

Sylvia Klineova, Asaff Harel, Rebecca Straus Farber, Tracy DeAngelis, Yinan Zhang, Roland Hentz, Tung Ming Leung, Kathryn Fong, Tyler Smith, Richard Blanck and 1 more

Open access · bronzeAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Multiple sclerosis and related disorders, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.3field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 22 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Sylvia KlineovaThe Corinne Goldsmith Dickinson Center for MS at Icahn School of Medicine at Mount Sinai Hospital New York, USA. Electronic address: sylvia.klineova@mssm.edu.
Asaff HarelDivision of Neuro-Immunology, Department of Neurology, Lenox Hill Hospital, North Shore University Hospital, Zucker School of Medicine at Hofstra/Northwell, New York, USA.
Rebecca Straus FarberColumbia University Multiple Sclerosis Center, Columbia University Irving Medical Center, New York, USA.
Tracy DeAngelisNeurological Associates of Long Island, USA.
Yinan ZhangThe Corinne Goldsmith Dickinson Center for MS at Icahn School of Medicine at Mount Sinai Hospital New York, USA.
Roland HentzBiostatistics Unit, Feinstein Institutes for Medical Research, Great Neck, New York, USA.
Tung Ming LeungBiostatistics Unit, Feinstein Institutes for Medical Research, Great Neck, New York, USA.
Kathryn FongColumbia University Multiple Sclerosis Center, Columbia University Irving Medical Center, New York, USA.
Tyler SmithNYU Multiple Sclerosis Comprehensive Care Center, NYU Langone Health, New York, New York, USA.
Richard BlanckNeurological Associates of Long Island, USA.
Lana Zhovtis-RyersonNYU Multiple Sclerosis Comprehensive Care Center, NYU Langone Health, New York, New York, USA.
Columbia University Irving Medical Center · USFeinstein Institute for Medical Research · USMount Sinai Hospital · USMultiple Sclerosis Center Of Northeastern New York · USNorth Shore University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine outcomes of COVID-19 in patients with Multiple Sclerosis (MS) and related conditions, and to determine predictors of these outcomes.

methodsThis was a multicenter, observational cohort study of patients with MS or related CNS autoimmune disorders who developed confirmed or highly suspected COVID-19 infection from 2/1/2020 to 12/31/2020. MAIN OUTCOME AND MEASURE: The primary outcome measure was hospitalization status due to COVID-19. Severity of infection was measured using a 4-point ordinal scale: 1. home care; 2. hospitalization without mechanical ventilation; 3. hospitalization and mechanical ventilation, and 4. death.

resultsOf 474 patients in the study, 63.3% had confirmed COVID-19 infection and 93.9% were diagnosed with an MS phenotype. Mean age was 45 ± 13 (mean±SD) years, 72% were female, and 86% were treated with a DMT at the time of infection. 58 patients (12.2%) were hospitalized. 24 patients (5.1%) were critically ill (requiring ICU care or outcome of death), of which 15 patients (3.2%) died. Higher neurological disability and older age independently predicted hospitalization. 85% (102/120) of patients with known antibody results not treated with anti-CD20 therapies were seropositive while only 39.5% (17/43) of patients treated with anti-CD20 demonstrated seropositivity (p < 0.0001). Only 25% (2/8) of patients with PCR-confirmed COVID-19 being treated with anti-CD20 therapies demonstrated seropositivity.

conclusionsNeurological disability and older age independently predicted hospitalization due to COVID-19. Additionally, the results demonstrate that anti-CD20 therapies significantly blunt humoral responses post-infection, a finding that carries implications with regards to natural or vaccine-mediated immunity.

Indexed as

COVID-19Multiple SclerosisAdultAgedFemaleHospitalizationHumansMiddle AgedNew YorkPandemicsSARS-CoV-2AntibodyAnti-CD20 therapyCOVID-19Multiple Sclerosis

Identifiers

PMID34392059
PMCPMC8286899
OpenAlexW3184560672

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.