Evidence map›Paper›PMID 30487997›Full record

ArticleRMD open2018

Uncovering the heterogeneity of disease impact in axial spondyloarthritis: bivariate trajectories of disease activity and quality of life.

Maike Imkamp, Valéria Lima Passos, Annelies Boonen, Suzanne Arends, Maxime Dougados, Robert Landewé, Sofia Ramiro, Filip Van den Bosch, Desirée van der Heijde, Freke R Wink and 2 more

Abstract read
In one paragraph

Article in RMD open, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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.

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

8 citing papers in PubMed.

  1. Observational
  2. Review
  3. Observational
  4. Article
  5. Article
  6. Secukinumab in axial spondyloarthritis: a narrative review of clinical evidence.Therapeutic advances in musculoskeletal disease · 2021
    Review
  7. Article
  8. 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.

Maike ImkampDepartment of Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, The Netherlands.
Valéria Lima PassosDepartment of Methodology and Statistics, Maastricht University, Maastricht, The Netherlands.
Annelies BoonenDepartment of Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, The Netherlands.
Suzanne ArendsDepartment of Rheumatology & Clinical Immunology, University Medical Center Groningen, University Groningen, Groningen, The Netherlands.
Maxime DougadosDepartment of Rheumatology, Cochin Hospital, Paris Descartes University, Paris, France.
Robert LandewéClinical Immunology and Rheumatology, Academic Medical Center, Amsterdam, The Netherlands.
Sofia RamiroDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Filip Van den BoschDepartment of Rheumatology, Ghent University and Ghent University Hospital, Ghent, Belgium.
Desirée van der HeijdeDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-5781-158X
Freke R WinkRheumatology, Medical Center Leeuwarden, Leeuwarden, The Netherlands.
Anneke SpoorenbergDepartment of Rheumatology & Clinical Immunology, University Medical Center Groningen, University Groningen, Groningen, The Netherlands.
Astrid van TubergenDepartment of Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe goal of managing axial spondyloarthritis (axSpA) is to improve and maintain patients' health-related quality of life (HRQoL), mainly through targeting towards low disease activity. Here, we aim to gain insight into the joint evolution of HRQoL and disease activity by identifying and characterising latent subgroups of patients with longstanding disease displaying similar trajectories throughout 8  years of follow-up.

methodsData from Outcome in Ankylosing Spondylitis (AS) International Study (n=161) and Groningen Leeuwarden AS cohort (n=264) were used. Biennially, HRQoL was assessed by AS Quality of Life (ASQoL) and disease activity by AS Disease Activity Score-C reactive protein (ASDAS-CRP). Bivariate trajectories of these outcomes were estimated by group-based trajectory modelling. Next, trajectories were profiled by comparing the latent groups with respect to baseline factors using analysis of variance and χ² test.

resultsFive bivariate trajectories were distinguished, in which ASQoL and ASDAS-CRP were tightly linked: (t1) low impact of disease; (t2) moderate impact; (t3) high impact with major improvement; (t4) high impact with some improvement; (t5) very high impact. Profiling revealed, for example, that (t1) was characterised by male gender and Human Leucocyte Antigen B27 positivity; (t3) by younger age, shorter symptom duration and biological intake and (t5) by the highest proportion of females.

conclusionsWe identified five bivariate trajectories of HRQoL and disease activity demonstrating a clear mutual relationship. The profiles revealed that both individual-related and disease-related features define the type of disease course in respect to HRQoL and disease activity in axSpA. This may provide clinicians insight into the differences among patients and help in the management of the disease.

Indexed as

axial spondyloarthritisdisease activitygroup-based multi-trajectory modellinghealth-related quality of lifetrajectories

Identifiers

PMID30487997
PMCPMC6241970

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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.