Quantitative assessment of interstitial lung disease in Sjögren's syndrome.
Journal
PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081
Informations de publication
Date de publication:
2019
2019
Historique:
received:
25
07
2019
accepted:
21
10
2019
entrez:
9
11
2019
pubmed:
9
11
2019
medline:
19
3
2020
Statut:
epublish
Résumé
Interstitial lung disease (ILD) is a frequent manifestation of Sjögren's syndrome (SS), an autoimmune disease of salivary and lacrimal glands, and affects approximately 20% of patients. No clinical or serological features appear to be useful to predict its presence, severity or progression, and chest high-resolution computed tomography (CT) remains the gold standard for diagnosis. Semiquantitative CT (SQCT) based on visual assessment (Goh and Taouli scoring) can estimate ILD extent, although it is burdened by relevant intra- and interobserver variability. Quantitative chest CT (QCT) is a promising alternative modality to assess ILD severity. To determine whether QCT assessment can identify extensive or limited lung disease in patients with SS and ILD. This multi-center, cross-sectional and retrospective study enrolled patients with SS and a chest CT scan. SQCT assessment was carried out in a blinded and centralized manner to calculate both Goh and Taouli scores. An operator-independent analysis of all CT scans with the open-source software platform Horos was used to evaluate the QCT indices. Patients were classified according to the extent of ILD and differences in QCT index distribution were investigated with non-parametric tests. From a total of 102 consecutive patients with SS, the prevalence of ILD was 35.3% (36/102). There was a statistically significant difference in QCT index distribution between the SS with ILD and SS without ILD groups (p<0.001). Moreover, SS-ILD patients with ILD >20% (by Goh score) had a QCT index statistically different from those with limited ILD extent (p<0.001). Finally, QCT indices showed a moderate-to-good correlation with the Goh and Taouli scores (from 0.44 to 0.65; p<0.001). QCT indices can identify patients with SS and ILD and discriminate those with lesser or greater lung disease.
Sections du résumé
BACKGROUND
Interstitial lung disease (ILD) is a frequent manifestation of Sjögren's syndrome (SS), an autoimmune disease of salivary and lacrimal glands, and affects approximately 20% of patients. No clinical or serological features appear to be useful to predict its presence, severity or progression, and chest high-resolution computed tomography (CT) remains the gold standard for diagnosis. Semiquantitative CT (SQCT) based on visual assessment (Goh and Taouli scoring) can estimate ILD extent, although it is burdened by relevant intra- and interobserver variability. Quantitative chest CT (QCT) is a promising alternative modality to assess ILD severity.
AIM
To determine whether QCT assessment can identify extensive or limited lung disease in patients with SS and ILD.
METHODS
This multi-center, cross-sectional and retrospective study enrolled patients with SS and a chest CT scan. SQCT assessment was carried out in a blinded and centralized manner to calculate both Goh and Taouli scores. An operator-independent analysis of all CT scans with the open-source software platform Horos was used to evaluate the QCT indices. Patients were classified according to the extent of ILD and differences in QCT index distribution were investigated with non-parametric tests.
RESULTS
From a total of 102 consecutive patients with SS, the prevalence of ILD was 35.3% (36/102). There was a statistically significant difference in QCT index distribution between the SS with ILD and SS without ILD groups (p<0.001). Moreover, SS-ILD patients with ILD >20% (by Goh score) had a QCT index statistically different from those with limited ILD extent (p<0.001). Finally, QCT indices showed a moderate-to-good correlation with the Goh and Taouli scores (from 0.44 to 0.65; p<0.001).
CONCLUSIONS
QCT indices can identify patients with SS and ILD and discriminate those with lesser or greater lung disease.
Identifiants
pubmed: 31703067
doi: 10.1371/journal.pone.0224772
pii: PONE-D-19-20968
pmc: PMC6839858
doi:
Banques de données
Dryad
['10.5061/dryad.sbcc2fr22']
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0224772Déclaration de conflit d'intérêts
Prof. Carlo Vanchieri is part of F. Hoffmann-La Roche Ltd. Scientific Board. He has received consulting fees and/or speaker fees from Astrazeneca, Boehringer Ingelheim, Chiesi, F. Hoffmann-La Roche Ltd and Menarini. Prof. Stefano Palmucci has reveived personal fees and honoraria for lectures from Boehringer Ingelheim, Delphi International srl and F. Hoffmann-La Roche Ltd. He has been included in the scientific board for Boehringer Ingelheim. This does not alter our adherence to PLOS ONE policies on sharing data and materials. None of the other authors have any potential conflicts of interest to disclose in relation to this work.
Références
PLoS Med. 2007 Oct 16;4(10):e296
pubmed: 17941714
Clin Rheumatol. 2018 Nov;37(11):2981-2988
pubmed: 30242640
Intern Emerg Med. 2017 Apr;12(3):327-331
pubmed: 27900604
Chest. 2009 Oct;136(4):1072-1078
pubmed: 19429722
Mod Rheumatol. 2015 Sep;25(5):724-30
pubmed: 25736361
N Engl J Med. 2018 Dec 6;379(23):2209-2219
pubmed: 30345907
Clin Exp Rheumatol. 2018 May-Jun;36 Suppl 112(3):121-129
pubmed: 30156546
Chest. 2018 Mar;153(3):e41-e43
pubmed: 29519308
Eur Radiol. 2002 Jun;12(6):1504-11
pubmed: 12042961
IEEE Trans Med Imaging. 2016 Jan;35(1):144-57
pubmed: 26208309
Ann Rheum Dis. 2017 Jun;76(6):1042-1050
pubmed: 27899373
Int J Rheum Dis. 2018 Jul;21(7):1423-1429
pubmed: 29968329
Autoimmun Rev. 2020 Feb;19(2):102447
pubmed: 31843713
Rheumatology (Oxford). 2017 Jun 1;56(6):922-927
pubmed: 28160007
J Immunol Res. 2018 Jun 7;2018:7510174
pubmed: 29977932
Arthritis Rheumatol. 2018 May;70(5):774-784
pubmed: 29361207
Respir Res. 2017 Mar 7;18(1):45
pubmed: 28264721
Multidiscip Respir Med. 2019 May 15;14:17
pubmed: 31114679
Br J Radiol. 2018 Feb;91(1083):20170644
pubmed: 29172671
J Chin Med Assoc. 2014 Feb;77(2):75-82
pubmed: 24342542
Respirology. 2018 Nov;23(11):1041-1048
pubmed: 30011421
Respiration. 2018;95(1):8-17
pubmed: 28918422
J Comput Assist Tomogr. 2009 Sep-Oct;33(5):731-8
pubmed: 19820502
Eur Respir Rev. 2016 Jun;25(140):110-23
pubmed: 27246587
Am J Respir Crit Care Med. 2008 Jun 1;177(11):1248-54
pubmed: 18369202
Medicine (Baltimore). 2018 Jun;97(24):e11003
pubmed: 29901591
Ann Rheum Dis. 2017 Jan;76(1):9-16
pubmed: 27789466
J Thorac Dis. 2018 Apr;10(4):2108-2117
pubmed: 29850114
Clin Exp Rheumatol. 2018 May-Jun;36 Suppl 112(3):94-101
pubmed: 29846161
Rheumatology (Oxford). 2015 Dec;54(12):2230-8
pubmed: 26231345
BMC Med. 2016 Nov 23;14(1):190
pubmed: 27876024
Adv Clin Exp Med. 2017 Oct;26(7):1101-1106
pubmed: 29211358
Clin Exp Rheumatol. 2018 May-Jun;36 Suppl 112(3):102-112
pubmed: 30156539
Arthritis Rheumatol. 2015 Apr;67(4):1084-95
pubmed: 25545990
Rheumatology (Oxford). 2013 Jan;52(1):155-60
pubmed: 23065360