Evidence map›Paper›PMID 35948984›Full record

ArticleArthritis research & therapy2022

Cytomegalovirus infection is a risk factor for venous thromboembolism in ANCA-associated vasculitis.

C King, R Patel, C Mendoza, J K Walker, E Y Wu, P Moss, M D Morgan, D O'Dell Bunch, L Harper, D Chanouzas

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 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
0.8field-weighted citation impact, top 28% 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.

  1. Article
  2. Review
  3. Review
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.

C KingDepartment of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK. catherine.king4@nhs.net.ORCID 0000-0001-8918-0404
R PatelDepartment of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.
C MendozaUniversity of North Carolina Gillings School of Global Public Health, Chapel Hill, NC, USA.
J K WalkerDepartment of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.
E Y WuUniversity of North Carolina Pediatric Allergy, Immunology, and Rheumatology, Chapel Hill, USA.
P MossInstitute of Immunology and Immunotherapy, University of Birmingham, Cancer Sciences Building, Edgbaston, Birmingham, B15 2TT, UK.
M D MorganHull York Medical School, University of Hull, Hull, UK.
D O'Dell BunchUniversity of North Carolina Department of Medicine, Kidney Centre, Chapel Hill, NC, USA.
L HarperDepartment of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.
D ChanouzasDepartment of Renal Medicine, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, UK.
Queen Elizabeth Hospital Birmingham · GBUniversity of North Carolina at Chapel Hill · USUniversity of Birmingham · GBUniversity of Hull · GB

Funding

Translation of Knowledge on the Pathogenesis of ANCA Disease into NovelP01DK058335 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NACHMAN, PATRICK H · 2000 to 2019
$25.9M
Medical Research Council MR/R011230/1NIDDK NIH HHS P01 DK058335
6 · The paper itself

Abstract

backgroundVenous thromboembolism (VTE) is a common complication in patients with anti-neutrophil cytoplasm antibody (ANCA)-associated vasculitides (AAV) and confers significant morbidity and mortality. Both acute and past cytomegalovirus (CMV) infection have been identified as risk factors for VTE in immunocompetent and immunosuppressed individuals. Here, we examine whether past exposure to CMV is a risk factor for VTE amongst patients with AAV.

methodsWe retrospectively analysed outcomes of patients with a new diagnosis of AAV from a UK cohort. All confirmed cases of VTE where CMV IgG serology was available were recorded. Retrospective collection of the same data for patients at a North American centre was used as a validation cohort.

resultsVTE was common with 12% of patients from the study cohort (total 259 patients) developing an event during the median follow-up period of 8.5 years of which 60% occurred within the first 12 months following diagnosis. Sixteen percent of CMV seropositive patients developed a VTE compared with 5% of patients who were seronegative (p = 0.007) and CMV seropositivity remained an independent predictor of VTE in multivariable analysis (HR 2.96 [1.094-8.011] p = 0.033). CMV seropositivity at diagnosis was confirmed as a significant risk factor for VTE in the American validation cohort (p = 0.032).

conclusionsVTE is common in patients with AAV, especially within the first year of diagnosis. Past infection with CMV is an independent risk factor associated with VTE in AAV.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisCytomegalovirus InfectionsVenous ThromboembolismCytomegalovirusHumansRetrospective StudiesRisk FactorsANCACytomegalovirusThrombosisVasculitis

Identifiers

PMID35948984
PMCPMC9364516
OpenAlexW4291398829

What Socratic 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 Socratic graph.