Evidence map›Paper›PMID 36835000›Full record

ArticleInternational journal of molecular sciences2023

Plasma N-Cleaved Galectin-9 Is a Surrogate Marker for Determining the Severity of COVID-19 and Monitoring the Therapeutic Effects of Tocilizumab.

Hiroko Iwasaki-Hozumi, Yosuke Maeda, Toshiro Niki, Haorile Chagan-Yasutan, Gaowa Bai, Takashi Matsuba, Daisuke Furushima, Yugo Ashino, Toshio Hattori

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

9 authors at 6 institutions in 1 country.

Hiroko Iwasaki-HozumiResearch Institute of Health and Welfare, Kibi International University, Takahashi 716-8508, Japan.ORCID 0000-0002-5682-6835
Yosuke MaedaViral Section, Department of Microbiology, Faculty of Life Sciences, Kumamoto University, Kumamoto 860-8556, Japan.
Toshiro NikiDepartment of Immunology, Faculty of Medicine, Kagawa University, Kagawa 761-0793, Japan.ORCID 0000-0003-4531-1331
Haorile Chagan-YasutanResearch Institute of Health and Welfare, Kibi International University, Takahashi 716-8508, Japan.
Gaowa BaiResearch Institute of Health and Welfare, Kibi International University, Takahashi 716-8508, Japan.
Takashi MatsubaDepartment of Animal Pharmaceutical Science, School of Pharmaceutical Science, Kyusyu University of Health and Welfare, Nobeoka 882-8508, Japan.
Daisuke FurushimaFaculty of Medicine School of Health Science, Kagoshima University, Kagoshima 890-8544, Japan.ORCID 0000-0002-1112-4821
Yugo AshinoDepartment of Respiratory Medicine, Sendai City Hospital, Sendai 982-8502, Japan.
Toshio HattoriResearch Institute of Health and Welfare, Kibi International University, Takahashi 716-8508, Japan.ORCID 0000-0003-0947-7625
Kibi International University · JPKagawa University · JPKagoshima University · JPKumamoto University · JPKyushu University of Health and Welfare · JPSendai City Hospital · JP

Funding

Japan Society for the Promotion of Science JP17H01690
6 · The paper itself

Abstract

Galectin-9 (Gal-9) is known to contribute to antiviral responses in coronavirus disease 2019 (COVID-19). Increased circulating Gal-9 in COVID-19 is associated with COVID-19 severity. In a while, the linker-peptide of Gal-9 is susceptible to proteolysis that can cause the change or loss of Gal-9 activity. Here, we measured plasma levels of N-cleaved-Gal9, which is Gal9 carbohydrate-recognition domain at the N-terminus (NCRD) with attached truncated linker peptide that differs in length depending on the type of proteases, in COVID-19. We also investigated the time course of plasma N-cleaved-Gal9 levels in severe COVID-19 treated with tocilizumab (TCZ). As a result, we observed an increase in plasma N-cleaved-Gal9 levels in COVID-19 and its higher levels in COVID-19 with pneumonia compared to the mild cases (healthy: 326.1 pg/mL, mild: 698.0 pg/mL, and with pneumonia: 1570 pg/mL). N-cleaved-Gal9 levels were associated with lymphocyte counts, C-reactive protein (CRP), soluble interleukin-2 receptor (sIL-2R), D-dimer, and ferritin levels, and ratio of percutaneous oxygen saturation to fraction of inspiratory oxygen (S/F ratio) in COVID-19 with pneumonia and discriminated different severity groups with high accuracy (area under the curve (AUC): 0.9076). Both N-cleaved-Gal9 and sIL-2R levels were associated with plasma matrix metalloprotease (MMP)-9 levels in COVID-19 with pneumonia. Furthermore, a decrease in N-cleaved-Gal9 levels was associated with a decrease of sIL-2R levels during TCZ treatment. N-cleaved-Gal9 levels showed a moderate accuracy (AUC: 0.8438) for discriminating the period before TCZ from the recovery phase. These data illustrate that plasma N-cleaved-Gal9 is a potential surrogate marker for assessing COVID-19 severity and the therapeutic effects of TCZ.

Indexed as

COVID-19COVID-19 Drug TreatmentPatient AcuityPneumoniaAntibodies, Monoclonal, HumanizedBiomarkersGalectinsHumansReceptors, Interleukin-2SARS-CoV-2Antibodies, Monoclonal, HumanizedBiomarkersGalectinsLGALS9 protein, humanReceptors, Interleukin-2tocilizumabcoronavirus disease 2019C-reactive proteinmatrix metalloprotease-9N-cleaved-Gal9proteolysisseveritysoluble interleukin-2 receptorsurrogate markertherapeutic effectstocilizumab

Identifiers

PMID36835000
PMCPMC9964849
OpenAlexW4320493765

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.