Evidence map›Paper›PMID 39424406›Full record

Observational studyRMD open2024

Comorbidity burden on mortality in patients with systemic sclerosis.

Thomas Fauthoux, Damien Brisou, Estibaliz Lazaro, Julien Seneschal, Joel Constans, Sophie Skopinski, Pierre Duffau, Elodie Blanchard, Cécile Contin-Bordes, Thomas Barnetche and 1 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in RMD open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02562079 (Vasculopathy, Inflammation and Systemic Sclerosis), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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.

NCT02562079 nacompletednot on this map

Vasculopathy, Inflammation and Systemic Sclerosis: The Role of Endothelial Cell Activation and OX40/OX40L in Modulation of T Lymphocyte Activation

TypeinterventionalSponsorUniversity Hospital, BordeauxRan2012 to 2016Enrolled350ConditionsSystemic SclerosisArmsBlood samples, Biopsy
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  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

11 authors.

Thomas FauthouxMédecine Interne, Hopital Saint-Antoine, Paris, France thomas.fauthoux@aphp.fr.ORCID 0009-0002-5727-0020
Damien BrisouPôle Biologie et Pathologie, CHU de Bordeaux, Bordeaux, France.
Estibaliz LazaroCHU de Bordeaux, Bordeaux, France.
Julien SeneschalDermatology, CHU de Bordeaux, Bordeaux, France.
Joel ConstansCHU de Bordeaux, Bordeaux, France.
Sophie SkopinskiCHU de Bordeaux, Bordeaux, France.
Pierre DuffauInternal Medicine Department, CHU de Bordeaux, Bordeaux, France.ORCID 0000-0002-4463-6583
Elodie BlanchardCHU de Bordeaux, Bordeaux, France.
Cécile Contin-BordesCIRID, UMR CNRS-5164, ImmunoConcEpT, CHU de Bordeaux, Bordeaux, France.ORCID 0000-0003-4652-2907
Thomas BarnetcheService de Rhumatologie, CHU de Bordeaux, Bordeaux, France.ORCID 0000-0002-0975-8534
Marie-Elise TruchetetRhumatologie, CHU de Bordeaux, Bordeaux, France.ORCID 0000-0001-8045-0180

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSystemic sclerosis (SSc) is a serious life-threatening tissue disease. A significant aspect of its mortality arises from comorbid conditions. Our study aimed at mapping out the prevalence of these comorbidities and their relation to mortality, thus creating a 'comorbidome'.

methodsIn our retrospective, single-centre observational study, we recorded each patient's data, including demographic informations, vital stats and SSc-related organ involvement, along with the presence or absence of 14 predefined comorbidities. We also documented the dates of their initial and most recent visits. To construct survival curves, we used the Kaplan-Meier method, followed by a Cox regression model for multivariate analysis.

resultsOur study involved 400 participants, 74 of whom unfortunately passed away. It is important to note that three specific comorbidities showed significant correlation to mortality: neoplasia, cardiovascular diseases and polypharmacy, as well as two SSc-specific organ involvements (lung and cardiac).

conclusionOur research led to the successful creation of the SSc comorbidome. Comorbidities are a major concern for patients suffering from SSc, particularly cardiovascular diseases and neoplasms. Our study highlights the effects of polypharmacy. The resultant comorbidome offers a comprehensive and analytical perspective on this complex issue and underscores the inter-relatedness of the data. Our study, however, was limited by a small sample size. Therefore, to confirm our findings, validation on a larger scale is necessary. This could potentially contribute to the creation of a future mortality scoring tool.

Indexed as

ComorbidityScleroderma, SystemicAdultAgedCardiovascular DiseasesFemaleHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasmsPrevalenceProportional Hazards ModelsRetrospective StudiesConnective Tissue DiseasesMortalityScleroderma, Systemic

Identifiers

PMID39424406
PMCPMC11492939

What OpenQuestion holds

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Registered trials

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.