Evidence map›Paper›PMID 35266034›Full record

ArticleRheumatology international2022

Differential efficacy of TNF inhibitors with or without the immunoglobulin fragment crystallizable (Fc) portion in rheumatoid arthritis: the ANSWER cohort study.

Yoichi Nakayama, Ryu Watanabe, Kosaku Murakami, Koichi Murata, Masao Tanaka, Hiromu Ito, Wataru Yamamoto, Kosuke Ebina, Kenichiro Hata, Yuri Hiramatsu and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  5. Ozoralizumab, a trivalent anti-TNFα NANOBODYFrontiers in immunology · 2026
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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

21 authors at 8 institutions in 1 country.

Yoichi NakayamaDepartment of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-8130-4350
Ryu WatanabeDepartment of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-1089-5296
Kosaku MurakamiDepartment of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0001-5981-4648
Koichi MurataDepartment of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-7896-3937
Masao TanakaDepartment of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-8942-2933
Hiromu ItoDepartment of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-1827-382X
Wataru YamamotoDepartment of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-0810-4221
Kosuke EbinaDepartment of Musculoskeletal Regenerative Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0002-2426-1024
Kenichiro HataDepartment of Internal Medicine IV, Division of Rheumatology, Osaka Medical College, Osaka, Japan.ORCID 0000-0002-7809-7637
Yuri HiramatsuDepartment of Internal Medicine IV, Division of Rheumatology, Osaka Medical College, Osaka, Japan.ORCID 0000-0003-0944-7186
Masaki KatayamaDepartment of Rheumatology, Osaka Red Cross Hospital, Osaka, Japan.ORCID 0000-0002-0773-7238
Yonsu SonFirst Department of Internal Medicine, Kansai Medical University, Osaka, Japan.ORCID 0000-0001-7244-7715
Hideki AmuroFirst Department of Internal Medicine, Kansai Medical University, Osaka, Japan.ORCID 0000-0002-7299-2884
Kengo AkashiDepartment of Rheumatology and Clinical Immunology, Kobe University Graduate School of Medicine, Hyogo, Japan.ORCID 0000-0002-5289-139X
Akira OnishiDepartment of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-3120-1273
Ryota HaraThe Center for Rheumatic Diseases, Department of Orthopaedic Surgery, Nara Medical University, Nara, Japan.ORCID 0000-0001-8000-3196
Keiichi YamamotoInformation Technology Center, Wakayama Medical University, Wakayama, Japan.ORCID 0000-0003-3278-5001
Koichiro OhmuraDepartment of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0003-2927-9159
Shuichi MatsudaDepartment of Orthopaedic Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0003-0802-1255
Akio MorinobuDepartment of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0002-4672-638X
Motomu HashimotoDepartment of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan. hashimoto.motomu@med.osaka-cu.ac.jp.ORCID 0000-0002-9241-060X
Kyoto University · JPKansai Medical University · JPOsaka Medical and Pharmaceutical University · JPKobe University · JPNara Medical University · JPOsaka Red Cross Hospital · JPThe University of Osaka · JPWakayama Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid factor (RF) binds to the fragment crystallizable (Fc) portion of immunoglobulin. It could bind to the Fc portion of anti-TNF inhibitors (TNFi) and attenuate the clinical efficacy. We tried to determine whether the therapeutic efficacy of TNFi with Fc might be lower than that of TNFi without Fc in rheumatoid arthritis (RA) patients with high titres of RF. The Kansai Consortium for Well-being of Rheumatic Disease Patients (ANSWER) cohort is an observational multi-center registry of patients with RA in the Kansai district of Japan. RA patients treated with TNFi were included and divided into two groups based on the structural characteristics between TNFi with Fc (infliximab, adalimumab, golimumab, and etanercept) and TNFi without Fc (certolizumab pegol). Patients were classified into 4 groups according to RF titre quartiles. The sequential disease activity score in 28 joints using erythrocyte sedimentation rate (DAS28-ESR) was compared by Mann-Whitney U test between TNFi with and without Fc in each RF titre group. Multiple linear regression analysis was used to analyze the effect of TNFi without Fc for the change of DAS28-ESR adjusted after potential confounders. A total of 705 RA patients were classified into four groups (RF

Indexed as

Antirheumatic AgentsArthritis, RheumatoidAdalimumabCohort StudiesEtanerceptHumansInfliximabRheumatoid FactorTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsAdalimumabAntirheumatic AgentsEtanerceptInfliximabRheumatoid FactorTumor Necrosis Factor-alphaTumor Necrosis Factor InhibitorsArthritis, RheumatoidRheumatoid factorTumor necrosis factor inhibitors

Identifiers

PMID35266034
OpenAlexW4220830168

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.