Evidence map›Paper›PMID 40373041›Full record

ArticlePloS one2025

Polymorphisms in rs2069845 are associated with IL-6 and soluble IL-6 receptor levels during total joint replacement.

Kyle D Anderson, Bryan Dulion, John Wong, Niyati Patel, Anne DeBenedetti, Craig J Della Valle, Ryan D Ross

Abstract read
In one paragraph

Article in PloS one, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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

7 authors.

Kyle D AndersonDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, United States of America.ORCID 0000-0002-5312-7801
Bryan DulionDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, United States of America.
John WongDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, United States of America.
Niyati PatelDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, United States of America.
Anne DeBenedettiDepartment of Orthopedic Surgery, Rush University Medical Center, Chicago, Illinois, United States of America.
Craig J Della ValleDepartment of Orthopedic Surgery, Rush University Medical Center, Chicago, Illinois, United States of America.
Ryan D RossDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, Illinois, United States of America.ORCID 0000-0003-3760-234X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the number of patients undergoing total joint replacement (TJR) surgery increases, so does the number of revision surgeries. One driver of implant failure and subsequent revision surgery is peri-implant osteolysis, which is driven by inflammation-mediated bone loss. IL-6 is an inflammatory cytokine that is elevated during the peri-operative period. Early elevations in IL-6 levels have been linked to osteolysis development. The current study asked whether there is genetic contribution to the IL-6-related peri-operative inflammatory reaction to TJR surgery. Patients undergoing primary TJR (total hip or total knee) provided pre-operative and post-operative blood samples for measurement of the circulating levels of IL-6 and the soluble IL-6 receptor (sIL-6r), as well as evaluation of allele status of three single nucleotide polymorphisms (SNPs) linked to IL-6 or sIL-6r levels - rs2069845, rs2228145, and rs4537545. Circulating sIL-6r levels were associated with allele status in the rs2228145 SNP. More interestingly, allele status in the rs2069845 SNP was associated with the change in circulating IL-6 levels following TJR surgery. Specifically, patients with the A,A allele had increasing levels of IL-6, while those harboring the G,A allele had decreasing levels of IL-6. While implant survival was not assessed, the critical role of IL-6 in peri-implant osteolysis suggests that the rs2069845 allele may influence orthopedic implant success. rs2069845 polymorphisms may be a useful patient-specific marker of inflammatory response to TJR surgery.

Indexed as

Arthroplasty, ReplacementArthroplasty, Replacement, HipArthroplasty, Replacement, KneeInterleukin-6Polymorphism, Single NucleotideReceptors, Interleukin-6AgedAllelesFemaleHumansMaleMiddle AgedOsteolysisIL6 protein, humanIL6R protein, humanInterleukin-6Receptors, Interleukin-6

Identifiers

PMID40373041
PMCPMC12080868

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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.