Longitudinal analysis of ANA in the Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort.
Longitudinal analysis of ANA in the Systemic Lupus International Collaborating Clinics (SLICC) Inception Cohort.
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DOI:
10.1136/annrheumdis-2022-222168
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发表时间:
2022-08
影响因子:
27.4
通讯作者:
中科院分区:
文献类型:
--
作者:
A perception derived from cross-sectional studies of small SLE cohorts is that there is a marked discrepancy between antinuclear antibody (ANA) assays, which impacts on clinician’s approach to diagnosis and follow-up. We compared three ANA assays in a longitudinal analysis of a large international incident SLE cohort retested regularly and followed for five years. Demographic, clinical, and serological data was from 805 SLE patients at enrolment, year 3 and 5. Two HEp-2 indirect immunofluorescence assays (IFA1, IFA2), an enzyme-linked immunosorbent assay (ELISA), and SLE-related autoantibodies were performed in one central laboratory. Frequencies of positivity, titres/units, and IFA patterns were compared using McNemar, Wilcoxon, and kappa statistics, respectively. At enrolment, ANA positivity (≥1:80) was 96.1% by IFA1 (median titre 1:1280 [IQR 1:640–1:5120]), 98.3% by IFA2 (1:2560 [IQR 1:640–1:5120]), and 96.6% by ELISA (176.3AU [IQR 106.4–203.5]). At least one ANA assay was positive for 99.6% of patients at enrolment. At year 5, ANA positivity by IFAs (IFA1 95.2%; IFA2 98.9%) remained high, while there was a decrease in ELISA positivity (91.3%, p<0.001). Overall, there was >91% agreement in ANA positivity at all time points and ≥71% agreement in IFA patterns between IFA1 and IFA2. In recent-onset SLE, three ANA assays demonstrated commutability with a high proportion of positivity and titres/units. However, over five years follow-up, there was modest variation in ANA assay performance. In clinical situations where the SLE diagnosis is being considered, a negative test by either the ELISA or HEp-2 IFA may require reflex testing.
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影响因子:
4.7
作者:
Choi MY;Clarke AE;St Pierre Y;Hanly JG;Urowitz MB;Romero-Diaz J;Gordon C;Bae SC;Bernatsky S;Wallace DJ;Merrill JT;Isenberg DA;Rahman A;Ginzler EM;Petri M;Bruce IN;Dooley MA;Fortin PR;Gladman DD;Sanchez-Guerrero J;Steinsson K;Ramsey-Goldman R;Khamashta MA;Aranow C;Alarcón GS;Manzi S;Nived O;Zoma AA;van Vollenhoven RF;Ramos-Casals M;Ruiz-Irastorza G;Lim SS;Kalunian KC;Inanc M;Kamen DL;Peschken CA;Jacobsen S;Askanase A;Stoll T;Buyon J;Mahler M;Fritzler MJ
通讯作者:
Fritzler MJ
DOI:
10.1007/s13317-016-0075-0
发表时间:
2016-12
期刊:
Auto- immunity highlights
影响因子:
--
作者:
Damoiseaux J;von Mühlen CA;Garcia-De La Torre I;Carballo OG;de Melo Cruvinel W;Francescantonio PL;Fritzler MJ;Herold M;Mimori T;Satoh M;Andrade LE;Chan EK;Conrad K
通讯作者:
Conrad K
影响因子:
2.6
作者:
Isenberg, D. A.;Ramsey-Goldman, R.;Hanly, J. G.
通讯作者:
Hanly, J. G.
影响因子:
158.5
作者:
Arbuckle, MR;McClain, MT;Harley, JB
通讯作者:
Harley, JB
影响因子:
4.9
作者:
Fritzler MJ;Wiik A;Fritzler ML;Barr SG
通讯作者:
Barr SG