Evidence map›Paper›PMID 36518750›Full record

ArticleFrontiers in immunology2022

An interleukin-1 polymorphism additionally intensified by atopy as prognostic factor for aseptic non-mechanical complications in metal knee and hip arthroplasty.

B Summer, D Lill, K Remmel, A Schraml, C Schopf, I J Banke, H Kuechenhoff, T Maierhofer, S Endres, P Thomas

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 6 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

10 authors at 4 institutions in 2 countries.

B SummerDepartment of Dermatology and Allergology, University Hospital, Munich, Germany.
D LillDepartment of Dermatology and Allergology, University Hospital, Munich, Germany.
K RemmelDepartment of Orthopedic Surgery, Clinic Rummelsberg and Nürnberg, Rummelsberg, Germany.
A SchramlDepartment of Orthopedic Surgery, Clinic Rummelsberg and Nürnberg, Rummelsberg, Germany.
C SchopfDepartment of Orthopaedics, Physical Medicine and Rehabiliation University Hospital, Munich, Germany.
I J BankeClinic of Orthopedics and Sports Orthopedics, Klinikum rechts der Isar, Technical University of Munich (TUM), Munich, Germany.
H KuechenhoffStatistical Consulting Unit StaBLab, Department of Statistics, LMU, Munich, Germany.
T MaierhoferDepartment of Statistics, University of California, Los Angeles (UCLA), Los Angeles, CA, United States.
S EndresDivision of Clinical Pharmacology, University Hospital, Munich, Germany.
P ThomasDepartment of Dermatology and Allergology, University Hospital, Munich, Germany.
Ludwig-Maximilians-Universität München · DEMünchen Klinik · DETechnical University of Munich · DEUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In contrast to infection or mechanical issues joint replacement failure following inflammatory adverse reactions is poorly understood. Objective: To assess the association of IL-1β polymorphisms and history of allergy with aseptic non-mechanical complications following arthroplasty. Methods: In 102 patients with aseptic non-mechanically caused symptomatic knee or hip arthroplasty (SA) and 93 patients with asymptomatic arthroplasty (AA) questionnaire-based history, patch test with at least standard series, lymphocyte transformation test (LTT) with nickel, cobalt and chromium and interleukin-1 polymorphism analysis were done. Three polymorphisms of the IL1B gene [IL-1b -3954 (rs1143634), IL-1b -511 (rs16944) and IL-1b -31 (rs1143627)] and one polymorphism of the IL1RN gene [IL1RN intron 2, variable number of tandem repeats, VNTR (rs2234663)] were assessed by PCR and gel electrophoresis. Results: We found no significant difference in smoking history and atopy but 25% versus 10% of self-reported metal allergy in SA versus AA; the patch test (respective, LTT) for metal sensitivity was more often positive in SA patients. The allele 498 bp of the IL1RN polymorphism occurred significantly more often in the SA group (37% versus 11%; p < 0.0001). Upon additional presence of atopy, the difference was even greater (60% vs 10%) (p < 0.000001). There was no association of IL-1 polymorphisms with metal allergy. Conclusion: The IL1RN VNTR allele 498 bp was strongly associated with SA. In patients with a history of atopy, presence of the IL1RN VNTR allele 498 bp led to a four-fold higher SA prevalence compared to patients without this allele.

Indexed as

Arthroplasty, Replacement, HipArthroplasty, Replacement, KneeHypersensitivityInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinMetalsHumansPolymorphism, GeneticPrognosisIL1B protein, humanIL1RN protein, humanInterleukin-1betaInterleukin 1 Receptor Antagonist ProteinMetalsadverse reactionallergyarthroplastyatopycomplicationsgeneticsinterleukin-1polymorphism

Identifiers

PMID36518750
PMCPMC9742593
OpenAlexW4310230723

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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.