Dual-energy computed-tomography-based discrimination between basic calcium phosphate and calcium pyrophosphate crystal deposition

Raman spectroscopy basic calcium phosphate calcium hydroxyapatite calcium pyrophosphate crystal-associated arthropathies dual-energy computed tomography

Journal

Therapeutic advances in musculoskeletal disease
ISSN: 1759-720X
Titre abrégé: Ther Adv Musculoskelet Dis
Pays: England
ID NLM: 101517322

Informations de publication

Date de publication:
2020
Historique:
received: 14 03 2020
accepted: 30 05 2020
entrez: 9 7 2020
pubmed: 9 7 2020
medline: 9 7 2020
Statut: epublish

Résumé

Dual-energy computed tomography (DECT) is being considered as a non-invasive diagnostic and characterization tool in calcium crystal-associated arthropathies. Our objective was to assess the potential of DECT in distinguishing between basic calcium phosphate (BCP) and calcium pyrophosphate (CPP) crystal deposition in and around joints A total of 13 patients with calcific periarthritis and 11 patients with crystal-proven CPPD were recruited prospectively to undergo DECT scans. Samples harvested from BCP and CPP calcification types were analyzed using Raman spectroscopy and validated against synthetic crystals. Regions of interest were placed in BCP and CPP calcifications, and the following DECT attenuation parameters were obtained: CT numbers (HU) at 80 and 140 kV, dual-energy index (DEI), electron density (Rho), and effective atomic number ( Raman spectroscopy enabled chemical fingerprinting of BCP and CPP crystals both DECT can help distinguish between crystal-proven BCP and CPP calcification types

Sections du résumé

BACKGROUND BACKGROUND
Dual-energy computed tomography (DECT) is being considered as a non-invasive diagnostic and characterization tool in calcium crystal-associated arthropathies. Our objective was to assess the potential of DECT in distinguishing between basic calcium phosphate (BCP) and calcium pyrophosphate (CPP) crystal deposition in and around joints
METHODS METHODS
A total of 13 patients with calcific periarthritis and 11 patients with crystal-proven CPPD were recruited prospectively to undergo DECT scans. Samples harvested from BCP and CPP calcification types were analyzed using Raman spectroscopy and validated against synthetic crystals. Regions of interest were placed in BCP and CPP calcifications, and the following DECT attenuation parameters were obtained: CT numbers (HU) at 80 and 140 kV, dual-energy index (DEI), electron density (Rho), and effective atomic number (
RESULTS RESULTS
Raman spectroscopy enabled chemical fingerprinting of BCP and CPP crystals both
CONCLUSION CONCLUSIONS
DECT can help distinguish between crystal-proven BCP and CPP calcification types

Identifiants

pubmed: 32636945
doi: 10.1177/1759720X20936060
pii: 10.1177_1759720X20936060
pmc: PMC7315653
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1759720X20936060

Informations de copyright

© The Author(s), 2020.

Déclaration de conflit d'intérêts

Conflict of interest statement: FB has received consulting fees from Horizon Therapeutics, unrelated to this work. The other authors declare that they have no competing interests.

Références

Orthopade. 1995 Jun;24(3):284-302
pubmed: 7617385
Ann Rheum Dis. 2018 Aug;77(8):1194-1199
pubmed: 29535120
Arthritis Res Ther. 2013;15(5):R103
pubmed: 24004678
Osteoarthritis Cartilage. 2019 Sep;27(9):1309-1314
pubmed: 31146015
Ann Rheum Dis. 2020 Jan;79(1):31-38
pubmed: 31167758
Nat Rev Rheumatol. 2018 Oct;14(10):592-602
pubmed: 30190520
Arthritis Rheumatol. 2018 Aug;70(8):1182-1191
pubmed: 29609209
Arthritis Rheum. 2011 Jan;63(1):10-8
pubmed: 20862682
Bone. 2005 May;36(5):893-901
pubmed: 15814305
Rheumatology (Oxford). 2016 Feb;55(2):379-80
pubmed: 26342227
Rheumatology (Oxford). 2019 Jun 1;58(6):1095-1098
pubmed: 30690553
Med Phys. 2020 Apr 24;:
pubmed: 32330301
Semin Musculoskelet Radiol. 2015 Dec;19(5):431-7
pubmed: 26696081
Arthritis Res Ther. 2017 Jul 21;19(1):171
pubmed: 28732526
Joint Bone Spine. 2019 Nov;86(6):665-668
pubmed: 31067507
Curr Rheumatol Rep. 2020 Apr 15;22(5):15
pubmed: 32291581
Rheumatology (Oxford). 2010 Mar;49(3):548-55
pubmed: 20032222
J Rheumatol. 2006 Feb;33(2):326-32
pubmed: 16465665
Arthritis Rheum. 2009 Sep;60(9):2694-703
pubmed: 19714647
Insights Imaging. 2018 Aug;9(4):477-492
pubmed: 29882050
N Engl J Med. 2016 Jun 30;374(26):2575-84
pubmed: 27355536
Rheumatology (Oxford). 2020 Jun 13;:
pubmed: 32533188
Arthritis Rheumatol. 2016 Jul;68(7):1751-7
pubmed: 26882173
AJR Am J Roentgenol. 2017 Nov;209(5):1088-1092
pubmed: 28834448
Arthritis Rheumatol. 2019 Jul;71(7):1158-1162
pubmed: 30714678
Rheumatology (Oxford). 2020 Apr 1;59(4):900-903
pubmed: 31630175
Radiology. 2018 Nov;289(2):293-312
pubmed: 30179101

Auteurs

Tristan Pascart (T)

Department of Rheumatology, Lille Catholic Hospitals, Saint-Philibert Hospital, University of Lille, Rue du Grand But, Lomme, F-59160, France.

Guillaume Falgayrac (G)

EA 4490, PMOI, Physiopathologie des Maladies Osseuses Inflammatoires, University of Lille, Lille, France.

Laurène Norberciak (L)

Department of Medical Research, Biostatistics, Lille Catholic Hospitals, University of Lille, Lomme, France.

Clément Lalanne (C)

Department of Orthopaedic Surgery, Lille Catholic Hospitals, University of Lille, Lomme, France.

Julie Legrand (J)

Department of Diagnostic and Interventional Radiology, Lille Catholic Hospitals, University of Lille, Lomme, France.

Eric Houvenagel (E)

Department of Rheumatology, Lille Catholic Hospitals, University of Lille, Lomme, France.

Hang-Korng Ea (HK)

Department of Rheumatology, Hôpital Lariboisière, AP-HP, Paris, France.

Fabio Becce (F)

Department of Diagnostic and Interventional Radiology, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.

Jean-François Budzik (JF)

EA 4490, PMOI, Physiopathologie des Maladies Osseuses Inflammatoires, University of Lille, Lille, France.

Classifications MeSH