Evidence map›Paper›PMID 41931245›Full record

ArticleClinical rheumatology2026

Evaluation of the efficacy of various hepatitis B dosage regimens in spondyloarthritis patients undergoing immunomodulatory treatment.

Gizem Varkal, Ipek Türk, Elif Altunel Kılınç, Gizem Kırmızıer, Ferit Kuşçu, Behice Kurtaran, Süleyman Özbek

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Article in Clinical rheumatology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Gizem VarkalFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Cukurova University, Adana, Turkey. dr.gizem.varkal@gmail.com.ORCID http://orcid.org/0000-0003-2270-102X
Ipek TürkFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Cukurova University, Adana, Turkey.ORCID http://orcid.org/0000-0001-5192-9045
Elif Altunel KılınçFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Cukurova University, Adana, Turkey.ORCID http://orcid.org/0000-0003-2501-2473
Gizem KırmızıerFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Cukurova University, Adana, Turkey.ORCID http://orcid.org/0000-0003-0092-8645
Ferit KuşçuFaculty of Medicine, Department of Infectious Diseases and Clinical Microbiology, Cukurova University, Adana, Turkey.ORCID http://orcid.org/0000-0001-5662-8305
Behice KurtaranFaculty of Medicine, Department of Infectious Diseases and Clinical Microbiology, Cukurova University, Adana, Turkey.ORCID http://orcid.org/0000-0002-2081-4664
Süleyman ÖzbekFaculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Cukurova University, Adana, Turkey.ORCID http://orcid.org/0000-0002-8548-8126

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the serologic response to different double-dose hepatitis B vaccination protocols in patients with axial spondyloarthritis receiving biologic therapy. MATERIALS AND

methodsThis single-center, retrospective study included patients diagnosed with axial spondyloarthritis (axSpA) according to ASAS classification criteria. Patients receiving biologic therapy who were non-immune to hepatitis B virus were vaccinated with double-dose hepatitis B vaccine (40 µg) using one of three different vaccination schedules: 0-1-6 months, 0-1-2-12 months, or 0-7-21-365 days. A reference group of axSpA patients treated with nonsteroidal anti-inflammatory drugs and/or conventional DMARDs received the standard-dose hepatitis B vaccine (20 µg) according to the conventional schedule. Anti-hepatitis B surface antibody (anti-HBs) levels were measured one month after completion of vaccination, and an anti-HBs level ≥ 10 IU/L was considered indicative of a protective immune response.

resultsAmong 103 biologic-treated patients with axSpA, 91 patients (88.3%) achieved a protective anti-HBs response following double-dose hepatitis B vaccination, while 12 patients (11.7%) were classified as non-responders. Serologic response rates did not differ significantly among the three double-dose vaccination protocols. In bivariate analyses, non-response was more frequently observed in patients receiving infliximab and certolizumab pegol; however, no independent predictors of non-response were identified in multivariate logistic regression analysis. All patients in the reference group, consisting of biologic-naïve axSpA patients, achieved protective anti-HBs titers following standard-dose hepatitis B vaccination.

conclusionDouble-dose hepatitis B vaccination is associated with high serologic response rates in patients with axial spondyloarthritis receiving biologic therapy, regardless of the vaccination schedule applied. These findings support the use of intensified hepatitis B vaccination strategies in axSpA patients undergoing biologic treatment. Key Points • In biologic-treated axial spondyloarthritis patients, double-dose (40 µg) hepatitis B vaccination achieved a high seroprotection rate of 88.3%. • Similar immune responses across vaccination schedules indicate that antigen dose, rather than timing, is the main determinant of seroprotection.

Indexed as

Axial SpondyloarthritisHepatitis BHepatitis B VaccinesSpondylarthritisAdultAntirheumatic AgentsFemaleHepatitis B AntibodiesHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeVaccinationAntirheumatic AgentsHepatitis B AntibodiesHepatitis B VaccinesBiologic therapyDouble-dose hepatitis B vaccineHepatitis BSpondyloarthritisVaccination

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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.