Evidence map›Paper›PMID 32555638›Full record

ArticlePloS one2020

Increased risk of cervical dysplasia in females with autoimmune conditions-Results from an Australia database linkage study.

Emma Foster, Michael J Malloy, Vilija G Jokubaitis, C David H Wrede, Helmut Butzkueven, Joe Sasadeusz, Sharon Van Doornum, Finlay Macrae, Gary Unglik, Julia M L Brotherton and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

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  15. The MSBase pregnancy, neonatal outcomes, and women's health registry.Therapeutic advances in neurological disorders · 2021
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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

11 authors at 4 institutions in 1 country.

Emma FosterDepartment of Neurology, MS and Neuroimmunology Service, Alfred Health, Melbourne, Australia.
Michael J MalloyVictorian Cervical Screening Registry, VCS Population Health, VCS Foundation, Melbourne, Australia.
Vilija G JokubaitisDepartment of Neurology, MS and Neuroimmunology Service, Alfred Health, Melbourne, Australia.
C David H WredeDepartment of Oncology and Dysplasia, Royal Women's Hospital, Melbourne, Australia.
Helmut ButzkuevenDepartment of Neurology, MS and Neuroimmunology Service, Alfred Health, Melbourne, Australia.
Joe SasadeuszVictorian Infectious Diseases Service, The Royal Melbourne Hospital, Melbourne, Australia.
Sharon Van DoornumRheumatology Department, The Royal Melbourne Hospital, Melbourne, Australia.
Finlay MacraeColorectal Medicine and Genetics, The Royal Melbourne Hospital, Melbourne, Australia.
Gary UnglikDepartment of Clinical Immunology and Allergy, The Royal Melbourne Hospital, Melbourne, Australia.
Julia M L BrothertonVictorian Cervical Screening Registry, VCS Population Health, VCS Foundation, Melbourne, Australia.
Anneke van der WaltDepartment of Neurology, MS and Neuroimmunology Service, Alfred Health, Melbourne, Australia.ORCID 0000-0002-4278-7003
The Royal Melbourne Hospital · AUAlfred Health · AUThe University of Melbourne · AURoyal Women's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutoimmune conditions (AICs) and/or their treatment may alter risk of human papilloma virus (HPV) infection and females with AICs are therefore at an increased risk of cervical dysplasia. However, inclusion of these at-risk populations in cervical cancer screening and HPV-vaccination guidelines, are mostly lacking. This study aimed to determine the prevalence of cervical dysplasia in a wide range of AICs and compare that to HIV and immunocompetent controls to support the optimisation of cervical cancer preventive health measures.

methodsData linkage was used to match cervical screening episodes to emergency department records of females with AICs or HIV to immunocompetent controls over a 14-year period. The primary outcome was histologically confirmed high-grade cervical disease. Results, measured as rates by cytology and histology classification per 1,000 females screened, were analysed per disease group, and intergroup comparisons were performed.

resultsFemales with inflammatory bowel disease (2,683), psoriatic and enteropathic arthropathies (1,848), multiple sclerosis (MS) (1,426), rheumatoid arthritis (1,246), systemic lupus erythematosus and/or mixed connective tissue disease (SLE/MCTD) (702), HIV (44), and 985,383 immunocompetent controls were included. SLE/MCTD and HIV groups had greater rates of high-grade histological and cytological abnormalities compared to controls. Increased rates of low-grade cytological abnormalities were detected in all females with AICs, with the exception of the MS group.

conclusionsFemales with SLE/MCTD or HIV have increased rates of high-grade cervical abnormalities. The increased low-grade dysplasia rate seen in most females with AICs is consistent with increased HPV infection. These findings support expansion of cervical cancer preventative programs to include these at-risk females.

Indexed as

AdultArthritis, RheumatoidAustraliaAutoimmune DiseasesDatabases, FactualFemaleHIV InfectionsHumansImmunocompetenceLupus Erythematosus, SystemicMiddle AgedNeoplasm GradingPrevalenceRisk FactorsUterine Cervical Dysplasia

Identifiers

PMID32555638
PMCPMC7302686
OpenAlexW3036896642

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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.