Evidence map›Paper›PMID 39479725›Full record

ArticleEuropean journal of rheumatology2024

Factors Associated with the Development of Anti-drug Antibodies to TNFi and the Consequences for Axial Spondyloarthritis: A Two-year Follow-up Study.

Elif Durak Ediboğlu, Muhammed Çınar, Didem Kozacı, Dilek Solmaz, Gökhan Sargın, Ömer Karadağ, Gülay Kınıklı, Umut Kalyoncu, Sedat Yılmaz, Taşkın Şentürk and 11 more

Abstract read
In one paragraph

Article in European journal of rheumatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Elif Durak EdiboğluDivision of Rheumatology, Department of Internal Medicine, Izmir Katip Celebi University Faculty of Medicine, Izmir, Türkiye.
Muhammed ÇınarDivision of Rheumatology, Department of Internal Medicine, University of Health Sciences, Gulhane Faculty of Medicine, Ankara, Türkiye.
Didem KozacıDepartment of Biochemistry, Yıldırım Beyazit University Faculty of Medicine, Ankara, Türkiye.
Dilek SolmazDivision of Rheumatology, Department of Internal Medicine, Izmir Katip Celebi University Faculty of Medicine, Izmir, Türkiye.
Gökhan SargınDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydın, Türkiye.
Ömer KaradağDivision of Rheumatology, Department of Internal Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
Gülay KınıklıDivision of Rheumatology, Department of Internal Medicine, Ankara University Faculty of Medicine, Ankara, Türkiye.
Umut KalyoncuDivision of Rheumatology, Department of Internal Medicine, Hacettepe University Faculty of Medicine, Ankara, Türkiye.
Sedat YılmazDivision of Rheumatology, Department of Internal Medicine, University of Health Sciences, Gulhane Faculty of Medicine, Ankara, Türkiye.
Taşkın ŞentürkDivision of Rheumatology, Department of Internal Medicine, Adnan Menderes University Faculty of Medicine, Aydın, Türkiye.
Gökhan KabadayıDivision of Rheumatology, Department of Internal Medicine, Izmir Katip Celebi University Faculty of Medicine, Izmir, Türkiye.
Gökhan KeserDivision of Rheumatology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir, Türkiye.
Gülen HatemiDivision of Rheumatology, Department of Internal Medicine, Istanbul University Faculty of Medicine, Istanbul, Türkiye.
Kübra KayaDepartment of Biochemistry, Yıldırım Beyazit University Faculty of Medicine, Ankara, Türkiye.
Mustafa ÖzmenDivision of Rheumatology, Department of Internal Medicine, Izmir Katip Celebi University Faculty of Medicine, Izmir, Türkiye.
Figen YargucuDivision of Rheumatology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir, Türkiye.
Yeşim ÖzgülerDivision of Rheumatology, Department of Internal Medicine, Istanbul University Faculty of Medicine, Istanbul, Türkiye.
Ayşe CefleDivision of Rheumatology, Department of Internal Medicine, Kocaeli University Faculty of Medicine, Kocaeli, Türkiye.
Önay GerçikDivision of Rheumatology, Department of Internal Medicine, Izmir Demokrasi University Faculty of Medicine, Izmir, Türkiye.
Bünyamin KısacıkDivision of Rheumatology, Department of Internal Medicine, Medicalpark Hospital, Gaziantep, Türkiye.
Servet AkarDivision of Rheumatology, Department of Internal Medicine, Izmir Katip Celebi University Faculty of Medicine, Izmir, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To evaluate the development of anti-drug antibodies (ADAb) against tumor necrosis factor inhibitors (TNFi) therapy during a 2-year period and search the factors linked to patients with axial spondyloarthritis (axSpA). Methods: Biologic-naive patients with axSpA were included in this observational study. Serum drug levels and ADAb were measured at weeks 12, 24, 52, and 104 of treatment by enzyme-linked immunosorbent assay (ELISA). The development of ADAb and factors related to ADAb over time were investigated using generalized estimating equations (GEE). Results: A total of 180 patients with axSpA (116 male, mean (±SD) 45.6 (±11.9) years) who started TNFi treatment (etanercept (32.2%), adalimumab (27.2%), golimumab (20.6%), infliximab (20%)) were included. In the etanercept treatment group, only 1 patient had ADAb at 12 weeks and 24 weeks. Anti-drug antibodies against TNFi drugs were present in the adalimumab group in 32.7% of patients and in the infliximab group in 21.2% of patients at 12 weeks, and the proportion of ADAb-positive patients were found to be stable throughout the follow-up for adalimumab- and infliximab-treated patients. In the golimumab group, one patient had ADAb against golimumab at 12 weeks and the proportion of ADAb-positive patients increased throughout follow-up. In longitudinal analysis, baseline age, TNFi type, longitudinal Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and ASDAS-CRP scores, serum C-eeactive protein (CRP) levels, presence of adverse events and treatment discontinuation were associated with the presence of ADAb. Conclusion: The development of ADAb against TNFi therapy is associated with younger age, high disease activity, the development of adverse events and more common treatment discontinuation in patients with axSpA during 2-year follow-up.

Indexed as

anti-drug antibodyAxial spondyloarthritistumor necrosis factor inhibitors

Identifiers

PMID39479725
PMCPMC11562142

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