Evidence map›Paper›PMID 34487276›Full record

ArticleClinical and experimental nephrology2022

Hemodialysis patients with coronavirus disease 2019: reduced antibody response.

Hiroko Beppu, Tatsuya Fukuda, Tomoko Kawanishi, Fumihiko Yasui, Minami Toda, Hitomi Kimura, Yuki Nakamura, Yuka Nakamura, Kaori Kojima, Hina Ogawa and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

2 citing papers in PubMed, 15 citations in OpenAlex.

  1. Observational
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 5 institutions in 1 country.

Hiroko BeppuDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Tatsuya FukudaDepartment of Endocrinology and Metabolism, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan. transatlantic0815@gmail.com.ORCID http://orcid.org/0000-0002-7468-317X
Tomoko KawanishiDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Fumihiko YasuiDepartment of Microbiology and Cell Biology, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Minami TodaDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Hitomi KimuraDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Yuki NakamuraDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Yuka NakamuraDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Kaori KojimaDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Hina OgawaDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Ayumi IshiwatariDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Yuiko KameiDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Toshie OgawaDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Yasutomo AbeDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Mariko EndoDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Tomohide HanawaDepartment of Pulmonary Medicine, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Rie MizobuchiDepartment of Pulmonary Medicine, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Chise SugitaDepartment of Pulmonary Medicine, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Koh OkamotoDepartment of Pulmonary Medicine, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Shuji HatakeyamaDepartment of Pulmonary Medicine, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Tetsusya YamadaDepartment of Molecular Endocrinology and Metabolism, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
Michinori KoharaDepartment of Microbiology and Cell Biology, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan.
Sachiko WakaiDepartment of Nephrology, Tokyo Metropolitan Health and Hospitals Corporation Okubo Hospital, Tokyo, Japan.
Ohkubo Hospital · JPTokyo Medical and Dental University · JPTokyo Metropolitan Institute of Medical Science · JPJichi Medical University · JPUniversity of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBecause patients on maintenance hemodialysis (HD) have an impaired immune response to pathogens, they are at higher risk of severe coronavirus disease 2019 (COVID-19). However, data on antibody production among HD patients with COVID-19 is scarce. Thus, we performed a retrospective cohort study evaluating severe acute respiratory syndrome coronavirus two antibody (SARS-CoV-2) production within 1 month after COVID-19 onset in hospitalized patients on HD.

methodsSARS-CoV-2-specific immunoglobulin (Ig) G levels were quantified using an iFlash 3000 Chemiluminescence Immunoassay analyzer (Shenzhen YHLO Biotech Co., Ltd.) to detect IgG antibodies specific for the S1 subunit of the spike protein (IgG-S1). Propensity score matching was used to balance covariate distribution in HD and non-HD patients. From April 2020 to February 2021, antibody testing was performed on 161 hospitalized patients with symptomatic COVID-19. Of them, 34 HD patients were matched to 68 non-HD patients.

resultsAfter propensity score matching, the median levels of IgG-S1 in the HD patients at 7-13 days after symptom onset were significantly lower than in non-HD patients, especially in those with severe disease. Among all patients, those with severe disease produced lower levels of IgG-S1 at 7-13 days compared with non-severe patients.

conclusionCOVID-19 patients with severe disease, especially those undergoing HD, had lower IgG-S1 production in the second week of the disease. Thus, the increased risk of severe COVID-19 in HD patients may be, in part, due to a slow and reduced antibody response.

Indexed as

Renal DialysisAdultAgedAged, 80 and overAntibodies, ViralBiomarkersCOVID-19FemaleHospitalizationHost-Pathogen InteractionsHumansImmunoglobulin GKidney DiseasesMaleMiddle AgedRetrospective StudiesAntibodies, ViralBiomarkersImmunoglobulin GAntibodyCOVID-19HemodialysisImmune responseSARS-CoV-2Severe disease

Identifiers

PMID34487276
PMCPMC8419388
OpenAlexW3196543229

What OpenQuestion holds

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Registered trials

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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.