Evidence map›Paper›PMID 39087364›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2024

Features Associated With Different Inflammatory Phenotypes of Calcium Pyrophosphate Deposition Disease: A Study Using Data From the International American College of Rheumatology/EULAR Calcium Pyrophosphate Deposition Classification Criteria Cohort.

Tristan Pascart, Augustin Latourte, Sara K Tedeschi, Nicola Dalbeth, Tuhina Neogi, Antonella Adinolfi, Uri Arad, Mariano Andres, Fabio Becce, Thomas Bardin and 23 more

Abstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2024. 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. Trial
  2. Observational
  3. Article
  4. Article
  5. Review
  6. Article
  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

33 authors.

Tristan PascartLille Catholic University, Saint-Philibert Hospital, Lille, France.ORCID https://orcid.org/0000-0002-8395-826X
Augustin LatourteUniversité Paris Cité, INSERM, UMR-S 1132 BIOSCAR and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.ORCID https://orcid.org/0000-0002-1087-7768
Sara K TedeschiBrigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.ORCID https://orcid.org/0000-0001-9475-1363
Nicola DalbethUniversity of Auckland, Auckland, New Zealand.ORCID https://orcid.org/0000-0003-4632-4476
Tuhina NeogiBoston University School of Medicine, Boston, Massachusetts.ORCID https://orcid.org/0000-0002-9515-1711
Antonella AdinolfiGrande Ospedale Metropolitano Niguarda, Milan, Italy.
Uri AradTe Whatu Ora-Health New Zealand Waikato and Waikato Clinical School, University of Auckland, Hamilton, New Zealand.ORCID https://orcid.org/0000-0002-2881-7739
Mariano AndresHospital General Universitario Dr. Balmis-ISABIAL, Universidad Miguel Hernández, Alicante, Spain.ORCID https://orcid.org/0000-0002-0219-9055
Fabio BecceLausanne University Hospital and University of Lausanne, Lausanne, Switzerland.ORCID https://orcid.org/0000-0001-8444-8504
Thomas BardinInstitut Mutualiste Montsouris, Paris, France.ORCID https://orcid.org/0000-0002-5080-4790
Edoardo CipollettaPolytechnic University of Marche, Ancona, Italy, and University of Nottingham, Nottingham, United Kingdom.ORCID https://orcid.org/0000-0002-6881-8197
Hang-Korng EaUniversité Paris Cité, INSERM, UMR-S 1132 BIOSCAR and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.
Georgios FilippouRheumatology Department, IRCCS Galeazzi, Sant'Ambrogio Hospital, Milan, Italy and Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.ORCID https://orcid.org/0000-0002-1647-2083
Emilio FilippucciPolytechnic University of Marche, Ancona, Italy.
John FitzGeraldUniversity of California and Veterans Administration for Greater Los Angeles, Los Angeles, California.ORCID https://orcid.org/0000-0002-8419-7538
Annamaria IagnoccoUniversità degli Studi di Torino, Turin, Italy.
Tim L JansenVieCuri Medical Centre, Venlo, The Netherlands, and Medical Cell BioPhysics Group, University of Twente, Enschede, The Netherlands.
Matthijs JanssenVieCuri Medical Centre, Venlo, The Netherlands, and Medical Cell BioPhysics Group, University of Twente, Enschede, The Netherlands.
Frédéric LiotéFeel'Gout, GH Paris Saint-Joseph and Université Paris Cité, INSERM, UMR-S 1132 BIOSCAR, Paris, France.
Alexander SoLausanne University Hospital, Lausanne, Switzerland.
Geraldine M McCarthySchool of Medicine and Medical Science, University College Dublin and Mater Misericordiae University Hospital, Dublin, Ireland.
Roberta RamondaUniversity of Padova, Padova, Italy.ORCID https://orcid.org/0000-0002-9683-8873
Pascal RichetteUniversité Paris Cité, INSERM, UMR-S 1132 BIOSCAR and Service de Rhumatologie, AP-HP, Lariboisière Hospital, Paris, France.
Ann RosenthalMedical College of Wisconsin, Milwaukee.
Carlo ScirèItalian Society for Rheumatology, Milan, Italy.ORCID https://orcid.org/0000-0001-7451-0271
Ettore SilvagniUniversity of Ferrara, Ferrara, Italy, and Azienda Ospedaliera-Universitaria di Ferrara, Cona, Italy.ORCID https://orcid.org/0000-0001-7654-8222
Silvia SirottiIRCCS Istituto Ortopedico Galeazzi, Milan, Italy.ORCID https://orcid.org/0000-0001-9795-131X
Francisca SiveraHospital General Universitario Elda, Elda, Spain, and Department of Clinical Medicine, Universidad Miguel Hernandez, Elche, Spain.
Lisa K StampUniversity of Otago Christchurch, Christchurch, and Te Whatu Ora Waitata, Christchurch, New Zealand.ORCID https://orcid.org/0000-0003-0138-2912
William J TaylorUniversity of Otago Christchurch, Christchurch, and Te Whatu Ora Waitata, Christchurch, New Zealand.ORCID https://orcid.org/0000-0001-6075-8479
Robert TerkeltaubUniversity of California, San Diego.
Hyon K ChoiHarvard Medical School, Boston, Massachusetts.
Abhishek AbhishekUniversity of Nottingham, Nottingham, United Kingdom.ORCID https://orcid.org/0000-0003-0121-4919

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe study objective was to examine the disease, demographic, and imaging features associated with different inflammatory phenotypes of calcium pyrophosphate deposition (CPPD) disease, ie, recurrent acute calcium pyrophosphate (CPP) crystal arthritis, chronic CPP crystal inflammatory arthritis, and crowned dens syndrome (CDS).

methodsData from an international cohort (assembled from 25 sites in 7 countries for the development and validation of the 2023 CPPD classification criteria from the American College of Rheumatology/EULAR) that met the criteria were included. Three cross-sectional studies were conducted to determine the phenotypic characteristics of recurrent acute CPP crystal arthritis, chronic CPP crystal inflammatory arthritis, and CDS. Multivariable logistic regression analysis was used to calculate adjusted odds ratio (aOR) and 95% confidence interval (CI) to examine the association between potential risk factors and the inflammatory phenotype.

resultsAmong the 618 people included (56% female; mean age [standard deviation] 74.0 [11.9] years), 602 (97.4%) had experienced acute CPP crystal arthritis, 332 (53.7%) had recurrent acute arthritis, 158 (25.6%) had persistent inflammatory arthritis, and 45 (7.3%) had had CDS. Recurrent acute CPP crystal arthritis associated with longer disease duration (aOR 2.88 [95% CI 2.00-4.14]). Chronic CPP crystal inflammatory arthritis was associated with acute wrist arthritis (aOR 2.92 [95% CI 1.81-4.73]), metacarpophalangeal joint osteoarthritis (aOR 1.87 [95% CI 1.17-2.97]), and scapho-trapezo-trapezoid (STT) joint osteoarthritis (aOR 1.83 [95% CI 1.15-2.91]), and it was negatively associated with either metabolic or familial risk for CPPD (aOR 0.60 [95% CI 0.37-0.96]). CDS was associated with male sex (aOR 2.35 [95% CI 1.21-4.59]), STT joint osteoarthritis (aOR 2.71 [95% CI 1.22-6.05]), and more joints affected with chondrocalcinosis (aOR 1.46 [95% CI 1.15-1.85]).

conclusionCPPD disease encompasses acute and chronic inflammatory phenotypes, each with specific clinical and imaging features that need to be considered in the diagnostic workup.

Indexed as

ChondrocalcinosisPhenotypeAcute DiseaseAgedAged, 80 and overArthritisCalcium PyrophosphateChronic DiseaseCohort StudiesCross-Sectional StudiesFemaleHumansInflammationLogistic ModelsMaleMiddle AgedCalcium Pyrophosphate

Identifiers

PMID39087364
PMCPMC11605267

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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.