European League against Rheumatism (EULAR)/American College of Rheumatology (ACR) SLE classification criteria item performance

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3003233 118 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
European League against Rheumatism (EULAR)/American College of Rheumatology (ACR) SLE classification criteria item performance
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Background/objectives The European League Against Rheumatism (EULAR)/American College of Rheumatology (ACR) 2019 classification criteria for systemic lupus erythematosus system showed high specificity, while attaining also high sensitivity. We hereby analysed the performance of the individual criteria items and their contribution to the overall performance of the criteria. Methods We combined the EULAR/ACR derivation and validation cohorts for a total of 1197 systemic lupus erythematosus (SLE) and n=1074 non-SLE patients with a variety of conditions mimicking SLE, such as other autoimmune diseases, and calculated the sensitivity and specificity for antinuclear antibodies (ANA) and the 23 specific criteria items. We also tested performance omitting the EULAR/ACR criteria attribution rule, which defines that items are only counted if not more likely explained by a cause other than SLE. Results Positive ANA, the new entry criterion, was 99.5% sensitive, but only 19.4% specific, against a non-SLE population that included other inflammatory rheumatic, infectious, malignant and metabolic diseases. The specific criteria items were highly variable in sensitivity (from 0.42% for delirium and 1.84% for psychosis to 75.6% for antibodies to double-stranded DNA), but their specificity was uniformly high, with low C3 or C4 (83.0%) and leucopenia <4.000/mm³ (83.8%) at the lowest end. Unexplained fever was 95.3% specific in this cohort. Applying the attribution rule improved specificity, particularly for joint involvement. Conclusions Changing the position of the highly sensitive, non-specific ANA to an entry criterion and the attribution rule resulted in a specificity of >80% for all items, explaining the higher overall specificity of the criteria set. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.
Έτος δημοσίευσης:
2021
Συγγραφείς:
Aringer, M.
Brinks, R.
Dörner, T.
Daikh, D.
Mosca, M.
Ramsey-Goldman, R.
Smolen, J.S.
Wofsy, D.
Boumpas, D.T.
Kamen, D.L.
Jayne, D.
Cervera, R.
Costedoat-Chalumeau, N.
Diamond, B.
Gladman, D.D.
Hahn, B.
Hiepe, F.
Jacobsen, S.
Khanna, D.
Lerstrøm, K.
Massarotti, E.
McCune, J.
Ruiz-Irastorza, G.
Sanchez-Guerrero, J.
Schneider, M.
Urowitz, M.
Bertsias, G.
Hoyer, B.F.
Leuchten, N.
Schmajuk, G.
Tani, C.
Tedeschi, S.K.
Touma, Z.
Anic, B.
Assan, F.
Chan, T.M.
Clarke, A.E.
Crow, M.K.
Czirják, L.
Doria, A.
Graninger, W.
Halda-Kiss, B.
Hasni, S.
Izmirly, P.M.
Jung, M.
Kumánovics, G.
Mariette, X.
Padjen, I.
Pego-Reigosa, J.M.
Romero-Diaz, J.
Rúa-Figueroa, I.
Seror, R.
Stummvoll, G.H.
Tanaka, Y.
Tektonidou, M.G.
Vasconcelos, C.
Vital, E.M.
Wallace, D.J.
Yavuz, S.
Meroni, P.L.
Fritzler, M.J.
Naden, R.
Costenbader, K.
Johnson, S.R.
Περιοδικό:
Annals of the Rheumatic Diseases
Εκδότης:
BMJ Publishing Group
Τόμος:
80
Αριθμός / τεύχος:
6
Σελίδες:
775-781
Λέξεις-κλειδιά:
antinuclear antibody; complement component C3; complement component C4; double stranded DNA, Article; cohort analysis; controlled study; delirium; diagnostic test accuracy study; disease association; disease classification; disease course; Europe; fever; human; infection; leukopenia; major clinical study; malignant neoplasm; metabolic disorder; priority journal; psychosis; rheumatic disease; rheumatology; sensitivity and specificity; systemic lupus erythematosus
Επίσημο URL (Εκδότης):
DOI:
10.1136/annrheumdis-2020-219373
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