Evidence map›Paper›PMID 33741041›Full record

ArticleArthritis research & therapy2021

The troubling liaison between cancer and metabolic syndrome in chronic inflammatory rheumatic diseases.

Giovanni Cioffi, Ombretta Viapiana, Luigi Tarantini, Giovanni Orsolini, Luca Idolazzi, Federica Ognibeni, Andrea Dalbeni, Davide Gatti, Angelo Fassio, Giovanni Adami and 2 more

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
0.4field-weighted citation impact, top 35% 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, 2 syntheses or guidelines pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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

12 authors at 1 institution in 1 country.

Giovanni CioffiRheumatology Section, Department of Medicine, University of Verona, Verona, Italy. dottcioffi@gmail.com.ORCID 0000-0002-2805-9982
Ombretta ViapianaRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Luigi TarantiniDepartment of cardiology, Ospedale civile S. Martino, Belluno, Italy.
Giovanni OrsoliniRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Luca IdolazziRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Federica OgnibeniRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Andrea DalbeniDepartment of Medicine, General Medicine and Hypertension Unit, University of Verona & Azienda Ospedaliera Universitaria Integrata of Verona, Verona, Italy.
Davide GattiRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Angelo FassioRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Giovanni AdamiRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Maurizio RossiniRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
Alessandro GiolloRheumatology Section, Department of Medicine, University of Verona, Verona, Italy.
University of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral studies on community populations found that metabolic syndrome (MetS) is associated with higher risk for total incident cancer with a predisposition for specific types of cancer. These findings have never been analyzed in patients with chronic inflammatory rheumatic and musculoskeletal diseases (RMD). We assessed prevalence/incidence and factors related to the development of cancer in a large cohort of these patients and evaluate whether MetS and its components were associated with cancer independent of traditional markers of inflammation.

methodsBetween March 2014 and April 2016, 474 patients with RMD involved in a cardiovascular primary prevention program were consecutively recruited into this ambispective (combination of retrospective/prospective) study. They underwent clinical, laboratory, and echocardiographic evaluations. MetS was diagnosed according to the ATPIII criteria.

resultsDuration of follow-up was 42 [18-60] months. Patients with a diagnosis of cancer (made before recruitment or during follow-up) were 46 (9.7%). Cancer was diagnosed in 22/76 patients (29%) with MetS and in 24/398 patients (6%, p < 0.001) without MetS; nearly two thirds of malignancies belonged to those traditionally related to MetS. MetS was the strongest cancer risk factor. Cancer was positively associated with the number of MetS components identified in each patient. Beyond MetS, cancer was associated to older age and increased inflammatory disease activity; this information allowed to build a simple performance indicator highly sensitive for cancer development.

conclusionIn light of our results, an increasingly accurate assessment of MetS would be required in patients with RMD as potential measure of clinical outcomes including the risk of cancer.

Indexed as

Metabolic SyndromeNeoplasmsRheumatic DiseasesAgedHumansPrevalenceProspective StudiesRetrospective StudiesRisk FactorsAnkylosing spondylitisCancerDisease activityInflammatory autoimmune diseasesMetabolic syndromePsoriatic arthritisRheumatoid arthritis

Identifiers

PMID33741041
PMCPMC7977293
OpenAlexW3137294291

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.