Evidence map›Paper›PMID 33744914›Full record

ArticleRheumatology (Oxford, England)2021

Multifocal calcific periarthritis with distinctive clinical and radiological features in patients with CD73 deficiency.

Cornelia D Cudrici, Kam A Newman, Elisa A Ferrante, Rebecca Huffstutler, Katherine Carney, Blas Betancourt, Markku Miettinen, Richard Siegel, James D Katz, Leon J Nesti and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. The Clinical Significance of CD73 in Cancer.International journal of molecular sciences · 2023
    Review
  6. An Alternate Explanation.The New England journal of medicine · 2023
    Article
  7. Article
  8. Review
  9. 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

16 authors at 6 institutions in 1 country.

Cornelia D CudriciNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.ORCID 0000-0002-9077-8195
Kam A NewmanNational Institutes of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, USA.
Elisa A FerranteNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Rebecca HuffstutlerNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Katherine CarneyNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Blas BetancourtNational Institutes of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, USA.
Markku MiettinenNational Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Richard SiegelNational Institutes of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, USA.
James D KatzNational Institutes of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, USA.
Leon J NestiWalter Reed National Military Medical Center, Clinical and Experimental Orthopaedics, Bethesda, MD, USA.
Cynthia St HilaireDepartment of Medicine, Division of Cardiology and Vascular Medicine Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Deepak LakshmipathyNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Han WenNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Mohammad H BagheriDepartment of Radiology and Imaging Sciences, Clinical Center, National Institutes of Health, Bethesda, MD, USA.
Manfred BoehmNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
Alessandra BrofferioNational Heart, Lung, and Blood Institute, Bethesda, MD, USA.
National Heart Lung and Blood Institute · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USNational Institutes of Health · USNational Institutes of Health Clinical Center · USUniversity of Pittsburgh · USWalter Reed National Military Medical Center · US

Funding

Genreal Surgical PathologyZIDBC011291 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MIETTINEN, MARKKU · 2010 to 2025
$30.3M
Clinical Training in RheumatologyZIEAR041176 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI COLBERT, ROBERT · 2009 to 2025
$29.8M
Immunohistochemical and genomic analysis of tumorsZIABC011427 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MIETTINEN, MARKKU · 2012 to 2025
$24.0M
X-ray micro tomography of pathology tissue samplesZIAHL006142 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI WEN, HAN · 2011 to 2025
$2.9M
Regulation of Vascular Calcification by Adenosine SignalingK22HL117917 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ST. HILAIRE, CYNTHIA · 2015 to 2017
$731k
NHLBI NIH HHS K22 HL117917
6 · The paper itself

Abstract

objectivesArterial calcification due to deficiency of CD73 (ACDC) is a hereditary autosomal recessive ectopic mineralization syndrome caused by loss-of-function mutations in the ecto-5'-nucleotidase gene. Periarticular calcification has been reported but the clinical characterization of arthritis as well as the microstructure and chemical composition of periarticular calcifications and SF crystals has not been systematically investigated.

methodsEight ACDC patients underwent extensive rheumatological and radiological evaluation over a period of 11 years. Periarticular and synovial biopsies were obtained from four patients. Characterization of crystal composition was evaluated by compensated polarized light microscopy, Alizarin Red staining for synovial fluid along with X-ray diffraction and X-ray micro tomosynthesis scanner for periarticular calcification.

resultsArthritis in ACDC patients has a clinical presentation of mixed erosive-degenerative joint changes with a median onset of articular symptoms at 17 years of age and progresses over time to the development of fixed deformities and functional limitations of small peripheral joints with, eventually, larger joint and distinct axial involvement later in life. We have identified calcium pyrophosphate and calcium hydroxyapatite (CHA) crystals in SF specimens and determined that CHA crystals are the principal component of periarticular calcifications.

conclusionThis is the largest study in ACDC patients to describe erosive peripheral arthropathy and axial enthesopathic calcifications over a period of 11 years and the first to identify the composition of periarticular calcifications and SF crystals. ACDC should be considered among the genetic causes of early-onset OA, as musculoskeletal disease signs may often precede vascular symptoms.

Indexed as

5'-NucleotidaseCalcinosisChild, PreschoolFemaleGPI-Linked ProteinsHumansJoint DiseasesMaleMiddle AgedPeriarthritisRadiographyVascular Diseases5'-NucleotidaseGPI-Linked ProteinsNT5E protein, humanACDCCD73crystal-induced arthritisperiarticular calcificationpseudogout

Identifiers

PMID33744914
PMCPMC8742829
OpenAlexW3138300603

What OpenQuestion holds

Textmetadata
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.