Evidence map›Paper›PMID 33481783›Full record

ArticlePloS one2021

Contribution of viral infection to risk for cancer in systemic lupus erythematosus and multiple sclerosis.

Deborah K Johnson, Kaylia M Reynolds, Brian D Poole, Matthew D Montierth, Vera M Todd, April Barnado, Mary F Davis

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 20 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

7 authors at 2 institutions in 1 country.

Deborah K JohnsonDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.ORCID 0000-0002-4575-9841
Kaylia M ReynoldsDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.
Brian D PooleDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.ORCID 0000-0002-3205-640X
Matthew D MontierthDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.ORCID 0000-0002-0860-1420
Vera M ToddDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.ORCID 0000-0002-3791-9606
April BarnadoDivision of Rheumatology & Immunology, Vanderbilt University Medical Center, Nashville, TN, United States of America.
Mary F DavisDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.ORCID 0000-0003-3344-0013
Brigham Young University · USVanderbilt University Medical Center · US

Funding

Using the electronic health record to risk-stratify patients with systemic lupus erythematosusK08AR072757 · NIAMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BARNADO, APRIL LYNN · 2018 to 2022
$817k
NIAMS NIH HHS K08 AR072757
6 · The paper itself

Abstract

Patients with autoimmune disorders (AD) have altered cancer risks compared to the general population. Systemic lupus erythematosus and multiple sclerosis lead to a heightened risk for hematological malignancies and decreased risk for breast, ovarian, and prostate malignancies. Often patients with autoimmune disease have dysregulated antiviral immune responses, including against oncogenic viruses. To uncover the relationship between viral incidence and cancer risk in the context of autoimmune disease, we extracted electronic health records (EHR) from Vanderbilt University. ICD-9/10 codes and laboratory values were collected for hematological, lung, anal-vaginal, thyroid, hepatobiliary, bladder, prostate, and breast cancers; and viruses including Epstein Barr virus (EBV), Human papilloma virus (HPV), and Hepatitis A/B/C (Hep). Only viral infections that led to a physician visit or laboratory test were entered into the EMR; therefore, only clinically relevant cases were noted and considered positive in this study. The relationship between virus infection and cancer in an SLE cohort (SLE-cases n = 2,313, and SLE-controls n = 5,702) and an MS cohort (MS-case n = 7,277, MS-control n = 7,277) was examined by multilinear logistic regression. Viral infection was strongly associated with increased risk for cancer overall. SLE and MS patients were more susceptible to all viral infections. MS patients trended toward increased risk for cancers overall, while decreased risk for hormone-based cancers in SLE patients non-significantly reduced their risk for overall cancer. Both SLE and MS patients had increased clinically relevant EBV infection, which was associated with risk for hematological cancers. Preventing viral infections by vaccination may be especially helpful in controlling risk for cancer in SLE and MS patients.

Indexed as

Cohort StudiesConfidence IntervalsHumansIncidenceLogistic ModelsLupus Erythematosus, SystemicMultiple SclerosisOdds RatioRisk FactorsVirus Diseases

Identifiers

PMID33481783
PMCPMC7822541
OpenAlexW3122949784

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.